Endothelial Progenitor Cells for Rotator Cuff Healing
by
Hui Tung Tony Lin
A thesis submitted in conformity with the requirements for the degree of Master of Science
Institute of Medical Science University of Toronto
© Copyright by Hui Tung Tony Lin 2014
ii
Endothelial Progenitor Cells for Rotator Cuff Healing
Hui Tung Tony Lin
Master of Science
Institute of Medical Science
University of Toronto
2014
Abstract
The avascular environment at the tendon-bone interface is a major concern for rotator cuff
healing, contributing to the high re-tear rate. We hypothesized that better tendon-bone healing
would occur with transplantation of endothelial progenitor cells, a population of angiogenic cells,
during rotator cuff repair in rats. The surgical procedure involved a unilateral detachment and
repair of the supraspinatus tendon in a syngeneic population of Fischer 344 rats. The EPC group
received one 106 EPCs and the Fibrin (negative control) group received none. Biomechanical and
histological analyses were performed at two, four, and six weeks post mortem. At 6 weeks, there
was a statistically significant difference in the tendon attachment strength. While no significant
difference was found in histology, the EPC groups showed a trend of increased vascularity. The
EPCs provide improvements in tendon-bone attachment 6 weeks after the repair. However, such
biomechanical improvement was not detectable via conventional histological methods.
iii
Acknowledgments
I owe my deepest gratitude to my supervisors and mentors, Dr Emil Schemitsch and Dr Aaron
Nauth, for their guidance, encouragement, and support. The years in the Musculoskeletal (MSK)
Research Laboratory at St Michael’s Hospital (SMH) have been a wonderful learning
experience. My graduate study has been challenging at times, but Dr Schemitsch and Dr Nauth
were always positively optimistic. Their dedication to research and scholarship is nothing but
inspirational. Without their supervision and mentorship, a suffix “MSc” after my name would not
have been possible.
I would also like to express my gratitude to my program advisory committee members, Dr Jed
Davies and Dr Cari Whyne, for their time, expertise, constructive criticisms, and trips to my
meeting during the dreaded Toronto rush hour.
The companionship and camaraderie of members and former members of the MSK Research Lab
– Erica Giles, Michael Glick, Charles Godbout, and Sarah Ketcheson – shall always be
cherished. Our countless hours in the Vivarium, the lab, the culture hood, and the pub
contributed to the completion of my thesis project and a phenomenal research experience. In
addition, the contribution of our lab rats to scientific advancements will not be forgotten.
Dr Vladimir Iakovlev at Pathology, St Michael’s Hospital, Jian Wang at Dentistry, University of
Toronto, and Lily Morikawa at Toronto Centre for Phenogenomics, were key to my data
collection and analyses. Radovan Zdero of St Michael’s Hospital Biomechanics Lab was
extremely helpful providing guidance in biomechanics. The staff at the Core Research Facility at
SMH had been especially patient with me, taking me step by step through the methods.
Moreover, I am in debt to all the science nerds at SMH for lending their hands and equipment.
I would like to extend my thanks to my friends in fish bowl office 412, Lidice and Alaa, whom I
spent three years sharing my coffee maker with; and Trifecta, cough…Shariq and Yian…cough,
without them, I would have graduated a year earlier.
Finally, I would like to thank my family for their unconditional support and love throughout my
study and life.
iv
Table of Contents
Acknowledgments ____________________________________________________________ iii
Table of Contents _____________________________________________________________ iv
Contributions ________________________________________________________________ vii
List of Abbreviations __________________________________________________________ viii
List of Tables __________________________________________________________________ x
List of Figures ________________________________________________________________ xi
List of Appendices ____________________________________________________________ xiv
1 Introduction _____________________________________________________________ 1
1.1 The Rotator Cuff _____________________________________________________________ 1
1.1.1 Anatomy and Function ______________________________________________________________ 2
1.1.2 Healthy Tendon Insertion ____________________________________________________________ 4
1.1.3 Vascular Supply to the Rotator Cuff ____________________________________________________ 8
1.2 Rotator Cuff Pathology _______________________________________________________10
1.2.1 Clinical Spectrum of Disease _________________________________________________________ 10
1.2.2 Pathophysiology of Rotator Cuff Disease _______________________________________________ 12
1.2.3 Treatment Options ________________________________________________________________ 17
1.2.4 Biology of Rotator Cuff Healing _______________________________________________________ 19
1.2.5 Vascularity of the Rotator Cuff _______________________________________________________ 28
1.3 Rotator Cuff Repair Model ____________________________________________________31
1.3.1 Animal Models and the Rat Model ____________________________________________________ 31
1.3.2 Cell Therapy in the Rat Rotator Cuff Repair Model _______________________________________ 34
1.4 Angiogenesis and Endothelial Progenitor Cells ____________________________________39
1.4.1 Capillaries ________________________________________________________________________ 39
1.4.2 Angiogenesis _____________________________________________________________________ 41
1.4.3 Endothelial Progenitor Cells _________________________________________________________ 44
1.4.4 Applications of Endothelial Progenitor Cells ____________________________________________ 49
1.5 Rationale, Hypothesis, and Objectives __________________________________________53
1.5.1 Rationale ________________________________________________________________________ 53
v
1.5.2 Hypothesis _______________________________________________________________________ 54
1.5.3 Objectives _______________________________________________________________________ 54
2 Methods _______________________________________________________________ 56
2.1 Study Design _______________________________________________________________56
2.1.1 Statistical Significance of the Study ___________________________________________________ 58
2.1.2 Sample Size Calculation _____________________________________________________________ 59
2.2 Cell Isolation _______________________________________________________________60
2.2.1 Endothelial progenitor cell isolation ___________________________________________________ 60
2.2.2 Flow cytometry ___________________________________________________________________ 61
2.2.3 Functional assays __________________________________________________________________ 65
2.2.4 Cell survival in fibrin sealant _________________________________________________________ 67
2.3 Surgery ___________________________________________________________________68
2.4 End Points, Sacrifices, and Dissections __________________________________________71
2.5 Biomechanical Testing _______________________________________________________72
2.6 Histological Analysis _________________________________________________________76
2.6.1 Hematoxylin and Eosin Staining ______________________________________________________ 78
2.6.2 Safranin O/ Fast Green FCF Staining ___________________________________________________ 79
2.6.3 Collagen Birefringence _____________________________________________________________ 80
2.6.4 Vessel Staining ____________________________________________________________________ 82
2.7 Cell Tracking _______________________________________________________________83
3 Results _________________________________________________________________ 85
3.1 Endothelial Progenitor Cells ___________________________________________________85
3.1.1 Flow cytometry ___________________________________________________________________ 85
3.1.2 Functional Assays _________________________________________________________________ 87
3.1.3 Cell survival in fibrin sealant _________________________________________________________ 90
3.2 Biomechanical Testing _______________________________________________________91
3.2.1 Ultimate Load ____________________________________________________________________ 92
3.2.2 Interface Area and Ultimate Stress ____________________________________________________ 94
3.2.3 Stiffness _________________________________________________________________________ 98
3.3 Histological Analyses _______________________________________________________101
3.3.1 Hematoxylin and Eosin Staining _____________________________________________________ 101
vi
3.3.2 Safranin O staining _______________________________________________________________ 102
3.3.3 Picrosirius Red Staining ____________________________________________________________ 103
3.3.4 Vessel Staining ___________________________________________________________________ 106
3.4 Cell Tracking ______________________________________________________________108
4 Discussion _____________________________________________________________ 110
4.1 Endothelial Progenitor Cells __________________________________________________112
4.2 Biomechanical Testing ______________________________________________________113
4.3 Histology _________________________________________________________________115
4.4 Cell Tracking ______________________________________________________________118
4.5 Limitations _______________________________________________________________119
4.6 Clinical Relevance __________________________________________________________121
5 Conclusion and Future Directions __________________________________________ 122
5.1 Conclusion________________________________________________________________122
5.2 Future Directions __________________________________________________________122
5.2.1 Identifying the Angiogenic Mechanisms _______________________________________________ 123
5.2.2 The Mesenchymal Lineage _________________________________________________________ 124
5.2.3 Clinical Application _______________________________________________________________ 125
References ________________________________________________________________ 128
Appendix A ________________________________________________________________ 146
Appendix B ________________________________________________________________ 148
vii
Contributions
The figure of rotator cuff vascular anatomy was modified and adapted from Rothman and Parke.
Clin Orthop Relat Res. 1965 Jul-Aug;41:176-86.
The F344-Tg(UBC-EGFP)F455Rrrc (RRRC#: 307) rats were provided by the Rat Resource and
Research Center P40OD011062, Columbia, MO, USA.
viii
List of Abbreviations
AcLDL Acetylated-low density lipoprotein
APC Allophycocyanin
bFGF Basic fibroblastic growth factor
BMP Bone morphogenetic protein
BSA Bovine serum albumin
CCN Connective tissue growth factor/cysteine-rich 61/nephroblastoma
over-expressed protein
COMP Cartilage oligomeric matrix protein
CTGF Connective tissue growth factor
DAB 3, 3'-diaminobenzidine
DAPI 4', 6-diamidino-2-phenylindole
DiI-AcLDL 1,1' -dioctadecyl -3,3,3',3' -tetramethyl-indocarbocyanine
perchlorate
DNA Deoxyribonucleic acid
EGM2-MV Endothelial Growth Medium 2-MV
EPC Endothelial progenitor cell
FITC Fluorescein isothiocyanate
Flk-1 Fetal liver kinase-1
FMO Fluorescent minus one
GFP Green Fluorescent protein
GH joint Glenohumeral joint
ix
HRP Horseradish peroxidase
IGF Insulin-like growth factor
miRNA Micro ribonucleic acid
MRI Magnetic resonance imaging
MSC Mesenchymal stem cells
MMP Matrix metalloproteinase
MT1-MMP Membrane type 1 matrix metalloproteinase
NSAID Non-steroidal anti-inflammatory drug
PBS Phosphate buffered saline
PCR Polymerase chain reaction
PDGF Platelet derived growth factor
PE Phycoerythrin
PECAM-1 Platelet endothelial cell adhesion molecule 1
PRFM Platelet-rich fibrin matrix
PROM-1 Prominin 1
PRP Platelet-rich plasma
RCF Relative centrifugal force
Scx Scleraxis gene
TGF Transforming growth factor
TIMMP tissue inhibitors of matrix metalloproteinase
UEA-1 Ulex europaeus 1 agglutinin
VEGF Vascular endothelial growth factor
VEGFR-2 Vascular endothelial growth factor receptor-2
x
List of Tables
Table 1-1. Biomechanical results of rotator cuff studies using mesenchymal stem cells
Table 1-2. Histological results of rotator cuff studies using mesenchymal stem cells
Table 2-1. Staining Protocol for flow cytometry
Table 2-2. Tissue dehydration process by Leica TP1020
Table 2-3. Hematoxylin and eosin staining protocol using Lecia Autostainer XL
Table 2-4. Deparaffinization and rehydration of slides using Leica Autostainer XL
Table 2-5. Dehydration of slides using Leica Autostainer XL
Table 3-1. Ultimate Load (N)
Table 3-2. Interface Cross-Sectional Area (mm2)
Table 3-3. Ultimate Stress of Tendon-Bone Interface (N/mm2 or MPa)
Table 3-4. Stiffness of Tendons (N/mm)
Table 3-5. Summary of biomechanical values for 2, 4, and 6 Week Groups
Table 3-6. Collagen birefringence measured in mean optical density
Table 3-7. Vascular density (vessels/mm2)
xi
List of Figures
Figure 1-1. Cross-section (coronal plane) of the shoulder illustrating the relationships of the
glenohumeral joint, the joint capsule, the subacromial bursa, and the rotator cuff (supraspinatus
tendon). Figure adapted from http://what-when-how.com/rheumatology/periarticular-disorders-
of-the-extremities-disorders-of-the-joints-and-adjacent-tissues-rheumatology/
Figure 1-2. Pictorial representation of the tendon-bone transition (safranin O staining). At a
mature fibrocartilaginous enthesis, there are four distinctive, but continuous zones of specialized
tissues: dense fibrous connective tendinous tissue, unmineralized fibrocartilage, mineralized
fibrocartilage, and bone.
Figure 1-3. The vascular anatomy of the rotator cuff insertions (adapted from Rothman. Clin
Orthop Relat Res. 1965 Jul-Aug;41:176-86)
Figure 1-4. The ultimate load to failure at the insertion. The mesenchymal stem cells transduced
with MT1-MMP gene and Scx gene increase insertion strength at 4 weeks after the repair
compared to the control group/MSC group (MSC group was the baseline value for subsequent
genetic modifications). Mesenchymal stem cells alone were not sufficient to improve healing.
Figure 1-5. Surface antigens and possible angiogenic mechanisms of endothelial progenitor cells.
The conventional surface markers are CD 34, CD 133, and Flk-1 (VEGFR2). The mechanisms
for angiogenesis are endothelial differentiation and angiogenic signaling.
Figure 2-1. The study design.
Figure 2-2. Biomechanical apparatus setup.
Figure 3-1. Flow cytometry analysis: 98.3 % of the cultured cells expressed CD 34 on the surface
(left); of these CD 34 expressing cells, 96.8 % of the cells expressed CD 133 and Flk-1 (right). In
summary, 95 % of the cultured cells expressed all three surface antigens.
Figure 3-2. AcLDL and lectin stains: DiI-AcLDL (red fluorescence) staining and DAPI (blue
fluorescence) staining (top); GS-II lectin DAPI (green fluorescence) staining and DAPI DAPI
(blue fluorescence) staining (bottom). Bar = 50 μm.
Figure 3-3. Tube formation assay 24 hours after seeding: endothelial progenitor cells (after ten
days of culturing, left) and mesenchymal stem cells (right). The endothelial progenitor cells
formed tube-like structures while the mesenchymal stem cells were in isolated colonies.
xii
Figure 3-4. Cell survival: cells suspended in fibrin for 24 hours (left) and cell proliferation at 48
hours (right). After the cells were placed into a flask after being in the fibrin clot for 24 hours,
they were able to adhere, resume monolayer morphology, and proliferate.
Figure 3-5. The weight of rats. The weights of the rats in EPC groups and Fibrin groups were not
significantly different at any of the time points. Error bars represent standard deviations.
Figure 3-6. The ultimate load at the insertions. The ultimate load to failure is significantly higher
in the EPC treated repairs at 6 weeks (t-test, p = 0.0025). Error bars represent standard
deviations. The dotted line represents the ultimate load for healthy tendon, 26.39 N.
Figure 3-7. Area of tendon-bone attachments. No differences in the insertion area were found at
any time point. Error bars represent standard deviations. The dotted line represents the area of
tendon-bone attachment for healthy insertions, 2.71 mm2.
Figure 3-8. Ultimate stress at the insertion. The stress significantly higher in the EPC group 6
weeks after the repair (p < 0.0001). Error bars represent standard deviations. The stress for
healthy insertions is 9.84 MPa (not shown on the graph).
Figure 3-9. The stiffness of the tendons. No differences in stiffness were found at any time point.
Error bars represent standard deviations. The dotted line represents the stiffness for healthy
insertions, 23.17 N/mm.
Figure 3-10. Hematoxylin and eosin, Safranin O, picrosirius red, and CD 31 antigen staining
(from left to right) of healthy rotator cuff tendons. Bar = 2 mm.
Figure 3-11. Hematoxylin and eosin. The orientation and the depth of the shoulder sections were
appropriate. Bar = 2 mm.
Figure 3-12. Safranin O and fast green staining. No cartilage formation was detected at the
tendon-bone interface. Bar = 2 mm.
Figure 3-13. Picrosirius red staining. The organization of collagen fibers was assessed under
polarized light. There was no difference in collagen organization between the Fibrin and the EPC
groups. Bar = 2mm.
Figure 3-14. Polarization of tendinous insertion. No significant differences were found between
the groups at any time point. Error bars represent standard deviations.
Figure 3-15. CD 31 staining. The insertion region was selected for analysis. The EPC group
showed an increase in vascularity from Week 4 to Week 6. Bar = 2 mm.
xiii
Figure 3-16. Number of blood vessels per millimeter squared (vascular density) at the insertion
site as identified by CD 31 immunohistochemistry staining. Although the differences were not
statistically significant, the density of vessels was increased in the EPC group at both time points
and the EPC group showed a trend towards increasing vessel density from 4 to 6 weeks, whereas
the Fibrin group showed a decrease in vessel density from 4 to 6 weeks. Error bars represent
standard deviations.
Figure 3-17. The brown HRP-DAB stain indicated GFP-expressing endothelial progenitor cells
(transplanted cells) at Week 2 in the scar tissue at the injury site. Few of the GFP positive cells
incorporated into the endothelium as indicated by the red arrows.
xiv
List of Appendices
Appendix A: Flow cytometry analysis for CD 31, CD 34, CD 133, and Flk-1
Appendix B: Bonferroni’s multiple comparison test
1
1 Introduction
Rotator cuff pathology can cause serious disability in occupational and athletic settings as well as
a major functional impairment for those performing their daily activities. Rotator cuff pathology
is the most common soft tissue injury of the shoulder, and is ranked only second to back and
neck pain in workplace related injuries 86
. Over stressing of rotator cuff muscles by excessive
load during repetitive overhead motion or as a result of acute trauma can cause a rotator cuff tear.
Depending on the severity of the tear, surgical repair may be necessary to restore rotator cuff
function.
With more than 75,000 surgical repairs of the rotator cuff performed annually at an average cost
of $10,605 per operation 195
, the health care utility cost of rotator cuff treatment is estimated to
be over 800 million US dollars alone. The overall economic burden would be much higher as
rotator cuff disability limits physical movement and can have significant impact on work
productivity and sick days. It also compromises daily living activities and severely reduces the
quality of life.
1.1 The Rotator Cuff
The range of motion of the glenohumeral (GH) joint is second to none in the human body.
Ligaments and capsule at the joint provide passive resistance to instability. Active stabilization is
2
primarily provided by a group of four muscles and their tendons, collectively termed the rotator
cuff. From anterior to posterior, these muscles and tendons are the subscapularis, supraspinatus,
infraspinatus, and teres minor. Each of the four muscles and tendons are responsible for the fine
control and the dynamic stability of humeral movements. They centre the humeral head to the
glenoid and prevent excessive glenohumeral translation in addition to rotating the humeral head
about the GH joint. Weak or damaged rotator cuff muscles often lead to limited shoulder range
of motion, poor GH joint stability, and compromised function at the shoulder.
1.1.1 Anatomy and Function
The rotator cuff originates from various bony surfaces of the scapula and inserts into the
proximal region of the humerus. The subscapularis muscle originates from the medial two-thirds
of anterior scapula, which is commonly termed the subscapular fossa. It inserts onto the lesser
tuberosity of proximal humerus. As the sole anterior component of the rotator cuff, the
subscapularis muscle serves to internally rotate and flex the humerus at the GH joint as well as
limit anterior translation of the humeral head. On the posterior surface of the scapula, the
infraspinatus and the teres minor muscles are external rotators and extenders of the humerus. The
two muscles originate from the medial aspect of the infraspinatus fossa and insert into the middle
and lower facet of the greater tuberosity of proximal humerus.
The most superiorly situated muscle of the rotator cuff is the supraspinatus muscle. Originating
from the postero-superior surface of the scapular that is superior to the scapular spine, the
supraspinatus muscle inserts onto the superior facet of the greater tuberosity. The tendinous
3
insertion at the greater tuberosity is not completely separate from infraspinatus and teres minor.
It primarily participates in the abduction of the humerus as well as limits, to some extent, inferior
translation of the humeral head. In addition, the supraspinatus muscle compresses the humeral
head against the glenoid fossa when the arm is in an adducted position; the inferiorly directed
component force serves to depress the humeral head. Due to the complex nature of the bony
structures at the shoulder, the supraspinatus muscle/tendon passes through the subacromial
space. The distal portion of the supraspinatus tendon is wrapped around the contour of the
articular surface of the humeral head, where the articular surface of the tendon is subjected to
compressive forces in addition to tension during the initial phase of humeral abduction.
The subacromial space is defined by the acromion, the acromioclavicular joint, the clavicle, and
the coracoid. Situated between the acromion process and the rotator cuff tendons are the
subacromial and the subdeltoid bursae that help to reduce friction between the structures. In
addition to padding, the bursae also take part in the inflammatory response and provide a
potential vascular source during rotator cuff healing. However, adhesion of the subacromial
bursa to the rotator cuff tendons can effectively narrow the subacromial space and cause
impingement of the tendons.
4
Figure 1-1. Cross-section (coronal plane) of the shoulder illustrating the relationships of the
glenohumeral joint, the joint capsule, the subacromial bursa, and the rotator cuff (supraspinatus
tendon). Figure adapted from http://what-when-how.com/rheumatology/periarticular-disorders-
of-the-extremities-disorders-of-the-joints-and-adjacent-tissues-rheumatology/
1.1.2 Healthy Tendon Insertion
A typical healthy tendon consists roughly of 20 % cellular material and 80 % extracellular matrix
by volume. It is a regular dense connective tissue with relatively few resident cells known as
5
tenocytes. Tenocytes are responsible for producing the extracellular components of the tendon
matter.
A healthy tendon is 55 to 70 % water by weight 96, 162
and 95% of its dry mass is type I collagen.
Type III collagen accounts for less than 5 % of the tendon dry mass in a normal cadaver rotator
cuff tendon. Together, the collagen molecules comprise the majority of solid substance in the
extracellular matrix. The ratio of type III to type I collagen, however, increases with the severity
of degeneration, tendon injury, and age 102
.
In addition to the collagen molecules, the extracellular matrix contains a number of various
macromolecules, termed ground substances, which help stabilize the structural and material
properties. These major ground substances can be classified into two large molecular families,
proteoglycans and glycoproteins. Proteoglycans are shaped like a bottle brush: a core protein
with various glycosaminoglycan chains stemming from it. Glycosaminoglycans are linear
polysaccharides containing repeating units of disaccharides. The negatively charged
proteoglycan molecules are hydrophilic, and thus help retain water in the tissue. Of the
proteoglycan family, decorin and aggrecan are in the tendon and the fibrocartilage 144
.
The glycoproteins are branched molecules which are responsible in maintaining and repairing the
tendon structure. These structural glycoproteins facilitate interaction between cells and their
neighbours as well as cell adhesion to the specific tissues. For instance, fibronectin provides
binding sites for fibroblasts and collagen, and chondronectin is essential for adhesion of
chondrocytes to type II collagen.
Macroscopically, as the rotator cuff tendons approach their skeletal attachment, their
extracellular matrix composition changes. The skeletal attachment of the rotator cuff tendons are
fibrocartilaginous in nature. At a mature fibrocartilaginous enthesis, there are four distinctive,
6
but continuous zones of specialized tissues: dense fibrous connective tendinous tissue,
unmineralized fibrocartilage, mineralized fibrocartilage, and bone. This transition zone is
commonly referred to as the enthesis, footprint, osteotendinuous junction, or tendon-bone
interface. Microscopically, the biochemical composition in the extracellular matrix at the tendon
insertion reflects mechanical demands present at the soft and hard tissue interface. The interface
facilitates the force transmission from tendon to the bone while resisting bending forces when the
line of pull is not parallel to the insertion.
The tendon-bone insertion is where the two type I collagen-rich tissues, the bone and the tendon,
join. At this interface, the calcified and uncalcified fibrocartilage is rich in type II collagen, and
thus presenting a gap phenomenon with immunohistochemical staining of collagen molecules.
Other ground substances such as glycosaminoglycans and proteoglycans help to dissipate the
bending forces away from the insertion to the more flexible tendon body.
7
Tendon
Unmineralized fibrocartilage
Mineralized fibrocartilage
Bone
Figure 1-2. Pictorial representation of the tendon-bone transition (safranin O staining). At a
mature fibrocartilaginous enthesis, there are four distinctive, but continuous zones of specialized
tissues: dense fibrous connective tendinous tissue, unmineralized fibrocartilage, mineralized
fibrocartilage, and bone.
8
1.1.3 Vascular Supply to the Rotator Cuff
The head of humerus receives its blood supply mainly from the axillary artery. Anatomic studies
have demonstrated that the axillary artery branches into six vessels, with the suprascapular and
the anterior and posterior humeral circumflex arteries being the largest contributor of blood
supply to the head of humerus 148
. The ascending arcuate branch of anterior humeral artery
provides the major source of proximal humeral vascularity and the greater tuberosity and the
insertion of the cuff tendons. Immediately proximal to the supraspinatus tendon insertion, there
is an identified anastomotic area known as the critical zone where vascular deficiency is
observed. Most degenerative changes and tears occur in this area. It is believed that the
avascularity at this region compromises the tendon’s metabolic activity and its ability to heal
after micro-trauma. Studies have identified that this critical zone in the supraspinatus tendon
renders it prone to tear 43, 100, 142, 148
. A possible decrease in vascularity was observed in patients
up to six months after surgery 50
.
9
Figure 1-3. The vascular anatomy of the rotator cuff insertions (adapted from Rothman. Clin
Orthop Relat Res. 1965 Jul-Aug;41:176-86)
10
1.2 Rotator Cuff Pathology
While the etiology of pathological changes are still debated, the current proposed causes for
rotator cuff diseases fall under two categories, intrinsic and extrinsic factors. Intrinsic changes
suggest the alteration of tendon chemical environment which compromises the structural
integrity. Extrinsic insults, on the other hand, describe the mechanical influences that result in
structural wear and tear. These factors, in combination, contribute to the pathological progression
in rotator cuff degeneration.
1.2.1 Clinical Spectrum of Disease
The major clinical presentations of rotator cuff diseases include impingement, chronic tears, and
acute tears. Primary impingement implies a decrease in the subacromial space in which the cuff
tendons passes through. Increased friction with the surrounding tissues causes accelerated wear
and tear. The symptoms show characteristics of Neer’s three-stage classification for
impingement: (I) edema and hemorrhage, (II) fibrosis and tendinitis, and (III) degeneration, bony
changes, and tendon ruptures. Instability at the glenohumeral joint capsule or lagging of scapular
stabilizers can result in unfavourable humeral head translations, and consequently, secondary
impingement of the cuff tendons. Excessive contact with the bony structures such as the postero-
11
superior glenoid rim frequently causes partial tearing of the supraspinatus and infraspinatus
tendons.
Long term repetitive use in overhead motions combined with the inherent poor blood supply to
the rotator cuff tendons can lead to degenerative changes and ultimately chronic tears. The
disease here manifests in poor tendon property and compromised healing capacity, commonly
seen in overhead workers and the in elderly population. In contrast, acute tears of the rotator cuff
tendons are often the result of traumatic incidences such as glenohumeral joint dislocation.
Incidences of rotator cuff tears have been observed in cadaveric specimens over the age of 50 to
be between 39 and 60 % 40
. It was estimated that the prevalence of rotator cuff tears may be up to
40 % of asymptomatic individuals over the age of 50 202
. Recent magnetic resonance imaging
studies of rotator cuff tears in populations reported that 37 % of the patients had tears of the
supraspinatus and infraspinatus tendons 154
, and found that the majority of these tears (70%)
were at the rotator cuff insertion 194
.
Clinically rotator cuff tendon tears are categorized into either partial-thickness or full-thickness
(complete) tears. The Ellman classification 47
of partial-thickness tears indicates the location
(articular, bursal surfaces, or intrasubstance) of the tear. Then according to severity, the tears are
sub-classified into Grade I tear (tears less than 3 mm deep), Grade II lesion (tears 3 to 6 mm
deep), and Grade III lesion (tears greater 6 mm deep). Here the normal cuff tendon thickness is
considered to be between 10 to 12 mm. If, however, the tears are full-thickness, a separate but
similar classification system, the Cofield classification 41
, is used. A full-thickness tear suggests a
complete tear involving one or more cuff tendons. A small full-thickness tear is less than 1 cm in
size, a medium tear between 1 to 3 cm in size, a large tear between 3 to 5 cm, and a massive tear
greater than 5 cm.
12
1.2.2 Pathophysiology of Rotator Cuff Disease
Intrinsic Factors of Rotator Cuff Disease
From a histolopathological point of view, rotator cuff tendinopathy often manifests in
degenerative changes, and is widely believed to be the major factor leading to rotator cuff tendon
tears. Structural and chemical alterations can be detected using biochemical and histological
analyses. It is uncertain, however, if degeneration is the initiating pathology or secondary to
other conditions such as impingement or chronic overuse.
The proposed intrinsic factors include the cuff quality reflected by the collagen composition and
the presence of fatty infiltration, cytokines and inflammatory markers, tendon remodeling
molecules the matrix metalloproteinases and their inhibitors, and genetics, diet, and lifestyle
factors.
i. Rotator cuff quality
To determine the pathological progression of rotator cuff tendinopathy, markers of degeneration
are used to assess the tendon quality. Signs of degeneration can manifest in the absence of
inflammatory cells, lack of fibril structural organization, atrophy of fibrils, changes in cellularity,
cell apoptosis, glycosaminoglycan accumulation, and fatty infiltration. With no changes in the
expression of cytokines and receptors, however, inflammation is absent in the degenerative state.
It is not known whether inflammatory response has taken place in earlier stages. Evidence
13
suggests that the extracellular matrix turnover in chronic tendinopathy reflects the cell-mediated
remodeling process, but with prolonged impaired remodeling and gradual deterioration 144
.
Those tendons suffering from injury or degeneration have a higher ratio of type III to type I
collagen. High levels of type III collagen, along with increased hydroxylysine content and
excessive cross-links in collagen fibers, are characteristic features of mechanically weaker scar
tissue. In addition, changes in water content can be indicative of tendon pathology. Injured
tendon will synthesize more extracellular matrix proteins in an attempt to maintain structural
integrity. Consequently, these proteins draw water into the tendon, thereby altering the
mechanical property.
Torn rotator cuff tendons may lead to degenerative fat accumulation in the corresponding
muscles. Fatty infiltration reduces tendon quality and predisposes repaired tendon to re-tear. The
degree of fatty infiltration is associated with the severity of the tear, the type of tendon lesion, the
age of the patient, and the chronicity of the tear. While accumulation of fat can be arrested upon
successful repair and restoration of tendon function, the existing fatty content is not always
reversible 61, 205
.
ii. Cytokines and inflammation
In the early phase of inflammatory response, the key modulators are the signaling molecules –
cytokines. They act as molecular agents to promote cellular proliferation, metabolism, apoptosis,
and extracellular matrix protein turnover in tendon tissue. The degree of inflammation and
angiogenesis, however, is inversely proportional to the age of the patient, particularly on the
articular side. In degenerative tendinopathy, imbalances of cytokine levels and inflammatory
responses fails to trigger repair in the tendon, resulting in poor tendon quality 60, 102
. Chronic
14
overuse and repetitive stress significantly reduces the number of resident tendon cells, causing
impairment to the tendinous repair process. Specifically, oxidative stress, inflammatory
cytokines and regulators, and apoptotic mediators are potential factors for stress-induced
apoptosis of fibroblast-like cells 116, 197, 210
. The inflammatory response is a double edged sword
which may initially be detrimental to the healing of tendon and triggering tendon cell apoptosis,
but the process is essential for the repair of tendon tissue. The absence of acute inflammation
results in poor clinical outcome in pathologic supraspinatus tendons. The relations between
tendon degeneration, tendinopathy, and inflammatory responses have yet to be clearly
delineated.
Growth factors are biochemical molecules which stimulate cellular activities, namely in
proliferation and differentiation. Researchers have been trying to identify the roles of the various
growth factors that contribute to the process of tendon-to-bone healing. Well-defined spatial and
temporal expression of relevant growth factors will aid the progress in targeted treatment
modalities. The early phase temporal expression of growth factors and tendon-associated
proteins were examined at the tendon-bone interface in a rat supraspinatus repair model 203
.
These proteins include basic fibroblastic growth factor (bFGF), bone morphogenetic proteins
(BMP) -12, -13, and -14, cartilage oligomeric matrix protein, connective tissue growth factor,
platelet-derived growth factor-β (PDGF- β), and transforming growth factor-β (TGF- β). Their
temporal profiles are thought to correspond to the various stages and the associated responses of
acute tendon-bone healing. Increased levels of these proteins were found in the first week post-
operation, but the levels returned to the normal values by four months. These growth factors
have been independently investigated in many studies as well (see Biology of Rotator Cuff
Healing section).
15
iii. Matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases
Tendons undergo continuous remodeling, and the tendons that experience high mechanical stress
such as the supraspinatus tendon will exhibit a greater extracellular matrix protein turnover rate
than those subjected to lesser stress, such as the distal biceps tendon. Extracellular matrix
metabolism is a balance between catabolic and anabolic activities. The major class of enzyme in
tendon degradation is the matrix metalloproteinases (MMPs). Their activity is rivaled by tissue
inhibitors of matrix metalloproteinases (TIMMPs). MMPs are found at low levels in normal
tendon tissue but high amounts are seen in injured tissues 39
. Elevated MMP-1 synthesis in
tendon cells is associated with up-regulation of cytokines and inflammatory modulators 197
. The
expression of TIMMPs acts in a reciprocal manner to MMPs in torn tendons 39, 57
. The imbalance
between these extracellular matrix enzymes and inhibitors reduces tendon quality and results in
the progression of degeneration.
iv. Genetics, lifestyle, and diet
Other possible factors which lead to degenerative changes in the rotator cuff tendons have been
investigated. Studies have proposed genetic predisposition to the pathogenesis of rotator cuff
disease. For instance, Harvie and co-workers found that familial influence doubled the risk of
developing rotator cuff tears and increased the chance to experience symptoms five folds
between patients and their siblings 69
. Not surprisingly, lifestyle choice such as smoking
increases tearing risk in a dose-dependent manner even after adjustment for age 13
. Longo et al
investigated rotator cuff tears in association to patient lipid and glucose profiles. In both the
16
prospective serum lipid level study and the case control plasma glucose study, there seemed to be
a trend towards a correlation between high values and the prevalence of rotator cuff tears 101
.
While no direct histological or pathological correlation was made, the studies alluded to macro-
circulatory and micro-circulatory impairment mediated tendon degeneration. However,
atherosclerosis, a macro-circulatory disease, did not correlate with rotator cuff tears 44
. Lastly,
hypertension is believed to be a potential factor for rotator cuff tear and its severity 67
. It was
postulated that circulatory impairment may initiate degenerative changes in the footprint, and the
hypoxic condition in the tendon was exacerbated by the administration of antihypertensive drugs.
Extrinsic factors of Rotator Cuff Disease
Intrinsic factors play a role in the degenerative changes of the tendons. However, the other major
contributor to rotator cuff disorders are the extrinsic factors that contribute to tendon damage.
Structural wear and tear often results from mechanical compression of the supraspinatus tendon
against the coracoacromial ligament and the anterior acromion. Neer observed bony
impingement in rotator cuff tears and this mechanical characteristic has been described as an
extrinsic factor potentially contributing to rotator cuff pathology. Subsequent classification of
acromial morphology showed correlation between hooked and curved acromions with rotator
cuff tendon tears 125
. The shape of the acromion can be congenital or acquired through age-
related changes. Excessive mechanical stress between the anatomical structures aided by
pathophysiological conditions at the acromial region may encourage the pathogenic progression
to a hooked acromion as well as the growth of acromial bony spurs.
17
Repetitive injuries and chronic overuse are recognized associations with rotator cuff pathology.
The micro-trauma theory proposed by Nho and colleagues suggested that small injuries
accumulate over time to result in significant structural deterioration, predisposing the tendon to
acute tear 126
. The overuse injury is frequently observed in the shoulder of the dominant arm in
patients. In one study, about 75 % of the patients presented full-thickness tear on their dominant
side, and 36 % to 50 % of the patients had bilateral tears 40
.
1.2.3 Treatment Options
Non-operative treatment is usually the first-line of treatment for most of the tears, with the
exception of large, acute tear in young and active patients. When non-operative management
fails, surgical intervention may be considered in hopes to reduce pain and restore function. The
standard surgical repair of rotator cuff tears involves approximating the remains of the ruptured
tendon to the humeral head and inserting them into a bony trough on the greater tuberosity.
Within recent decades, surgical methods have evolved from open, to mini-open, to arthroscopic
repairs. The attachment techniques have changed over the years as well, from transosseous
suture repairs to single rows and double rows of suture anchors, and recently the suture bridge
technique.
Generally, strenuous overhead activities are avoided for at least four to six weeks post-surgery
for most of the repairs. Passive range of motion exercise is prescribed for six weeks followed by
active motion in physiotherapy. As the shoulders approaches full range of motion, a more
aggressive rehabilitative program is prescribed. At least a six month recovery prior to return to
18
sports is recommended. Despite all the precautionary and rehabilitative strategies, functional
recovery to original strength is, however, is infrequent.
Re-tear
Despite the evolution of surgical techniques and improved repair methods, structural healing of
the rotator cuff tendon to the humeral head still remains a challenge. While studies have found
the tendons to heal after the rotator cuff repair, the incidence of re-tear is a major concern for
current repair methods. A recent systematic review of post-operative outcomes indicates
recurrence rates from 13 % in small tear less than 1 cm to 61 % in massive tears over 5 cm 45
.
The causes of re-tearing after repair have been proposed: mechanical failure of repair construct
and biological failure of healing at tendon-bone interface 117
. Re-tears that occur within three
months after the repair are attributed to mechanical failure; recurrences after the initiation of
physical therapy are more reflective of the failure of biological healing to provide adequate
mechanical strength.
The success of surgical repair relies heavily on the functional healing of the injury site, the
maintenance of contact between the separated structures, and the regeneration of the enthesis 92,
181, 182. The hypovascular and hypocellular nature of tendons may be the primary reason for poor
healing and lack of regeneration of a specialized tissue to connect tendon and bone 180
.
Insufficient blood supply hinders reparative activities at the injury site and the lack of resident
cells impedes healing and remodeling processes. Immature scar tissues are not replaced by the
strong, mature collagen types appropriate at the tendon-bone interface. This predisposes the
19
repair to failure in the future as the presence of fibrovascular scar tissue renders the interface
mechanically weaker than the native fibrocartilaginous attachment.
1.2.4 Biology of Rotator Cuff Healing
The process of tendon healing follows closely the general sequence for soft tissue healing:
inflammation, proliferation, and remodeling. Hematoma usually occurs immediately after the
initial trauma. While the platelets clot the damaged vessels to contain erythrocytes within the
circulatory system, the platelets release chemotactic factors to promote the infiltration of
inflammatory cells, mainly the monocytes and the macrophages. Angiogenesis and residential
tenocyte proliferation are initiated at this stage as well as fibroblast recruitment and collagen
synthesis. A few days after the initial trauma, the injured site enters the proliferative stage in
which fibroblasts and tenocytes are rapidly recruited with type III collagen synthesis reaching its
peak. During this stage, neovascularization reaches its peak as the metabolic demand is high. At
this point the wound becomes scar-like. The remodeling stage occurs weeks after the injury as
the overall cellularity and type III collagen decrease. Type III collagen is progressively replaced
by the structurally organized type I collagen to yield superior mechanical strength. The water
content and extracellular matrix components approach the normal levels of a tendon tissue. This
remodeling and maturation process may take up to four months 162
.
Although the healing process is slow, it is essential that the tendon remodeling achieves a
structure and content which is similar to the uninjured counterpart. Unfortunately, in many cases,
20
the healed tendon is unlikely to reach its original biomechanical capacity as scar tissue is inferior
to the native tendon tissue.
Growth Factors
Growth factors are biochemical molecules which stimulate cellular activities, namely in
proliferation and differentiation. Researchers have been trying to identify the roles of the various
growth factors that contribute to the process of tendon-to-bone healing. Well-defined spatial and
temporal expression of relevant growth factors will aid the progress in targeted treatment
modalities. The temporal expressions of eight early-phase growth factors in supraspinatus
tendon-to-bone healing were characterized by Würgler-Hauri et al 203
. In addition, Oliva et al has
recently compiled a list of known growth factors expressed in the three defined healing stages
127.
i. Basic fibroblastic growth factor
Consisting of a single chain polypeptide of 146 amino acids, basic fibroblastic growth factor
(bFGF) has been shown to promote wound healing via its angiogenic activity 10, 186
and induction
of a proliferative response 28, 183, 186
. The proliferative effect on tenocytes was confirmed by
Takahashi et al., but the administration of bFGF suppressed collagen synthesis in vitro 174, 183
.
The delivery of exogenous bFGF gene into tenocytes, however, significantly increased the
expression of type I and III collagen gene in vitro 198
. In vivo studies of rotator cuff healing
showed the peak of bFGF expression at week one 90, 203
, and another increase at week eight 203
.
21
Recent in vivo investigation of bFGF application in a rat supraspinatus model demonstrated
accelerated tendon-to-bone repair 79, 80
.
ii. Bone morphogenetic proteins
The bone morphogenetic proteins (BMPs) were first identified in bone extracts, and named
according to their ability to directly induce ectopic bone formation, although they have also been
found to participate in the growth and development of other tissues. BMPs constitute the largest
subfamily of the transforming growth factor beta (TGF-β) superfamily, with over twenty
identified members to date 23, 32
. With respect to their sequential similarity and functions, BMPs
are typically divided in four smaller groups: BMP-2/ -4, BMP-5/ -6/ -7/ -8a/ -8b, BMP-9/ -10,
and BMP-12/ -13/ -14. Within the smaller groups, BMP-12/ -13/ -14 are believed to be involved
in tendon regeneration 52, 122, 200
. Acute increase of these BMPs at the supraspinatus tendon-to-
bone attachment site within the first 2 weeks post-operation was reported by Würgler-Hauri et al,
with the changes of BMP-12 being the most significant 203
. BMP-2 and BMP-7 induced
moderate anabolic activities in rotator cuff tendon cells in vitro which were favourable for the
healing of the tendon 133
. In a sheep rotator cuff repair model, BMP-12 was found to improve
tissue healing and biomechanical properties 160
. Adenovirus-mediated BMP13 delivery to rotator
cuff tendon repair in rats resulted in up-regulation of the tendon matrix gene expression and
improved biomechanical strength 211
.
22
iii. Cartilage oligomeric matrix protein
Cartilage oligomeric matrix protein (COMP) is the fifth member of the thrombospondin protein
family, and is therefore also known as thrombospondin-5. It is a non-collagenous pentameric
glycoprotein present in the extra-cellular matrix of both tendon and cartilage 24
. It binds to both
type I and II collagen, the major components of fibrocartilagous tissues. Södersten et al observed
a positive correlation between the ultra-structural distribution of COMP in horse digital flexor
tendons with respect to age, maturation, and training 158
. A similar correlation was found in the
expression of COMP and the exercise load in rat Achilles tendons 159
. Although the function of
COMP has yet to be clearly defined, current evidences suggest its role in supporting structural
integrity of tissues. The expression of COMP is found in cultured monolayer chondrocyte,
tendon and ligament cells. In the study of temporal expression of growth factors, Würgler-Hauri
et al reported a significant increase of COMP level the first week immediate to the surgery 203
.
iv. Connective tissue growth factor
Connective tissue growth factor (CTGF) belongs to the connective tissue growth factor/cysteine-
rich 61/nephroblastoma over-expressed protein (CCN) family 24
. While CNN proteins have
similar structures, their biological functions vary greatly and are very dependent on the local
cellular context. Their participation in angiogenesis 25
, chrondrogenesis 121
, wound healing and
fibrosis 199
has been implicated in many studies. CTGF is a promoting factor for anabolic activity
of the extracellular matrix, including fibroblast and endothelial cell proliferation, migration,
adhesion, and survival 104, 118, 121, 163
. The expression of CTFG in mesenchymal stem cells
(MSCs) was able to direct the MSCs down the fibroblastic differentiating pathway 94
. Elevated
23
expression of CTFG was found in tendons after acute exercise 72
or injury 31
. The observations
were consistent with the report of an initial increase of CTGF in the supraspinatus tendon
insertion site at one week post-surgery 203
.
v. Platelet-derived growth factors
Platelet-derived growth factors (PDGFs) are a group of mitogens and chemo-attractants for cells
of mesenchymal origin. The PDGF family is composed of four structurally and functionally
similar polypeptides, designated PDGF-A/ -B/ -C/ -D, and the polypeptides can be joined by
disulphide-bonded to form dimers. The expression of PDGF-BB has been observed in tendon
healing models in close association with other growth factors such as bFGF, TGF-β, and IGF in
vitro209
and in vivo 90, 203
. Genetic modification in tenocytes to express PDGF-B 192
or the
addition of PDGF-BB to fibroblasts 185
enhanced collagen gene expression in vitro.
Thomopoulos et al investigated flexor tendon repair and found that PDGF-BB promoted cell
proliferation and collagen remodeling 188
as well as biomechanical properties 184
. The efficacy of
PDGF on rotator cuff tendon healing has been tested by two groups. Uggen et al evaluated both
in vitro and in vivo application of genetically transduced tendon fibroblasts, and reported a
significant increase in collagen synthesis in cell culture and accelerated rotator cuff repair
histomorphologically in rats 192
. The other study by Hee et al demonstrated superior
biomechanical and histological properties at the infraspinatus tendon insertion 70
.
24
vi. Transforming growth factors
As their names suggest, the transforming growth factor-βs (TGF-βs) gained their reputation from
their ability to induce and transform the growth of fibroblasts 151, 170
. With the discovery of more
structurally and functionally related proteins, the TGF-βs now represent one of the four major
subfamilies of the big TGF-β family of over 40 members 151
. Three isoforms of TGF-βs have
been identified in mammals: TGF-β1, TGF-β2, and TGF-β3. The TGF-βs play important roles in
the regulation of collagen synthesis during wound healing, tissue synthesis, fibrosis, and scarring
as well as many other cellular processes.
In vitro studies provided evidence for the fibrogenic potential of TGF-β1 in tendons 29, 88, 89
.
TGF-β1 has been widely associated with aggressive inflammation and wound healing responses
30, 151. The response of collagen formation, however, varies with cells isolated from different
parts of a tendon, as shown by Klass et al with rabbit flexor tendon cells 88, 89
. There is a general
consensus that over-expression of TGF-β1 may have adverse effect by increasing type III to type
I collagen ratio and tendon adhesion 30, 87-89
. Many studies of the supraspinatus tendon model
confirmed transient and localized increase of TGF-β1 one week after surgery or injury 54, 203
,
suggesting the role of TGF-β1 in the initial phase of tendon healing. Peak cell proliferation and
cellularity at the injury site coincided with the increased level of TGF-β1 90
.
Studies have noted the phenomenon that fetal wound healing is achieved in a regenerative
manner, often termed scarless healing, while post-natal healing is achieved in a scar-mediated
process 161, 168
. This difference in fetal and adult healing property can be attributed to expression
of growth factors unique to the different stages of development 20, 161
. Manning et al attempted to
mimic the fetal development and scarless healing stimulus via exogenous addition of TGF-β3.
25
They hypothesized the sustained delivery of TGF-β3 would stimulate regeneration of
fibrocartilage at the adult tendon-to-bone insertion rather than proliferation of scar tissue at the
region. The administration of TGF-β3, however, was insufficient to create a biochemical milieu
which promotes scarless healing in mature rat rotator cuff enthesis. In fact, Manning et al found
increased disorganized scar fibres at the fibrocartilaginous transition zone. The authors
speculated the importance of the role of tissue environment and cellular composition which
affected the healing property in the presence of TGF-β3. Nonetheless, early structural and
biomechanical advantages were observed. Compiling their observations, the data suggested an
accelerated response of all phases in the healing process with the addition of TGF-β3 111
. Kim et
al, however, reported that the application of exogenous TGF-β3 and neutralizing antibodies to
TGF-β1 and -β2 did not improve supraspinatus tendon-to-bone healing 87
. It is important to
better define the healing properties of the TGF-βs and the other key factors to modulate and
augment early tendon healing.
vii. Insulin-like growth factor
Insulin-like growth factors (IGFs) are liver-made proteins that participate in growth,
development, and metabolic activity of various tissues. The stimulatory effects of IGF-I have
been identified in musculoskeletal tissues. IGF-I has been implicated as a mediator in phases of
wound healing of various tissues. Analyses of temporal expression of growth factors revealed
that IGF-I expression occurred early on during the inflammatory phase 31, 90
, and then peaked
again at four weeks 37
. Other studies have found increased extra-cellular matrix synthesis and
protein turnover in vitro 1, 2
, and accelerated tendon healing in rat models in vivo 93
. To date,
26
studies on IGF-I applications have yet to examine their efficacy on the healing at the tendon-to-
bone interface.
viii. Matrix metalloproteinases
The matrix metalloproteinases (MMPs) are a family of zinc endopeptidases found in a range of
multicellular organisms. MMPs are responsible for timely degradation of extra-cellular matrix in
development, morphogenesis, tissue repair, and remodeling. A compilation of the MMPs and
their association to orthopaedic applications was provided by Pasternak and Aspenberg 132
, and
Garofalo et al 58
. It is commonly believed that general inhibition of MMPs will impair tendon
healing. Modulating the levels of MMPs present at the injury may facilitate tendon healing. Bedi
and coworkers reported a distinct histomorphologic difference at the supraspinatus tendon-to-
bone insertion with local delivery of a universal MMP inhibitor, α-2-macroglobulin protein.
They found greater fibrocartilage formation and collagen organization, and a significant
reduction in collagen degradation within four weeks while no biomechanical advantage was
detected at the insertion 17
. Gulotta et al took a different approach by introducing the
developmental gene MT1-MMP into mesenchymal stem cells before transplanting them to the
tendon-bone insertion in a rat supraspinatus tendon. At four weeks, they obtained a higher
presence of fibrocartilage and an improved biomechanical property at the tendon-bone insertion
site 64
. Future investigations are necessary to better characterize the effects of the different
MMPs to the structural integrity of the repair. Modulation of MMP activity in the perioperative
period may offer a novel biologic pathway to augment tendon-bone healing after rotator cuff
repair.
27
Platelet-Rich Plasma
Platelet-rich plasma (PRP) is a natural storage vehicle of growth factors. The current working
definition of PRP is a volume of autologous plasma with a platelet concentration of more than
106 platelets/μL
112. It is obtained from whole blood by separating red and white blood cells from
the plasma and platelets, and subsequently concentrating the plasma contents and platelets.
Taylor et al compiled a list of GFs and bioactive proteins found in PRP: TGF-β1, PDGF, bFGF,
VEGF, IGF-1, epithelial growth factor, and hepatocyte growth factor 177
. Many clinical studies
have been done with the application of PRP on musculoskeletal injuries, but only a handful have
focused on rotator cuff tendon repair 81, 110, 141
. The most recent study which investigated the
efficacy of PRP found that PRP application during arthroscopic repair of supraspinatus tendon
did not result in accelerated recovery 81
. These clinical studies and randomized controlled trials
81, 110, 141 have failed to demonstrate improved healing with PRP application at the time of rotator
cuff repair.
A variation of PRP, termed platelet-rich fibrin matrix (PRFM), is also being used in attempt to
augment rotator cuff repair. The safety and efficacy of the use of PRFM has been evaluated in
randomized controlled trials 27, 145
as well as in other clinical investigations 12, 21
. The randomized
trials by Castricini et al 27
and Rodeo et al 145
, and the clinical trial by Bergeson et al 12
found that
PRFM did not improve shoulder functions while Barber and colleagues showed lowered
incidents of re-tear rates 21
. However, no significant adverse effect was observed in any of the
studies. It should be noted that there are considerable difference exist amongst various
commercial PRP constructs available for use. Variability may present in the density of platelets
and growth factors, the presence of anticoagulants, and the leukocyte infusion.
28
1.2.5 Vascularity of the Rotator Cuff
Similar to other tissues of the body, vascular changes are indicative of tissue health and
condition. Normal tendon is relatively hypovascular when compared to its adjacent
musculoskeletal structures, the bone and the muscle. The vascular supply to the supraspinatus
tendon and the presence of its critical hypoxic zone has been the spotlight of debate. Rotator cuff
tears often involve the supraspinatus tendon, and some speculate the presence of a hypoxic
region which contributes to the progression of tendon degeneration in a similar fashion to
hypoxic degenerative tendinopathy in the Achilles tendon.
However, the theories of hypovascularity and predisposition to degeneration and injury of the
rotator cuff tendon in this region remain a source of controversy. The traditional description of
the critical zone corresponds to a region of anastomoses between skeletal and tendinous blood
supplies at the supraspinatus tendon. The area of hypovascularity at the supraspinatus tendon is
between 5 mm proximal to the humeral insertion and the musculotendinous junction. The critical
zone was more evident at the articular side of the tendon where almost no vessels were present
distally in comparison to the bursal side. It was suggested that this deficient vascularization
predisposes the supraspinatus to degenerative pathologies. Furthermore, full adduction of the
arm compresses the supraspinatus tendon against the humeral head and increased pressure on the
supraspinatus tendon effectively reduces perfusion to the articular side of the tendon 107, 142
.
The concept of enhancing blood flow to injured regions has been applied to therapeutic
treatments of chronic Achilles tendinopathy 130, 131
, patellar tendinopathy 171
, and lateral
29
epicondylitis 113
. Glyceryl trinitrate, a topical drug, was used in various studies to induce local
vasodilation and hence increase blood flow to the applied area. A double-blinded randomized
controlled trial examined the effect of glyceryl trinitrate for chronic rotator cuff tendinopathy,
and found positive effects including force and functional measures in patient outcomes 129
.
Recently, the use of contrast-enhanced ultrasonography allowed a better visualization of the
vascular dynamics of the rotator cuff tendon in human subjects, confirming a hypovascular zone
in the supraspinatus tendon. Studies have evaluated the spatial distribution and age-related
changes to circulation of the supraspinatus tendon in healthy adults as well as alternations after
tendon tear or repair 4, 55, 149
. There was a consistent region of decreased vascularity at the
articular medial margin of the asymptomatic rotator cuff tendons. While all regions experienced
an enhanced blood flow after exercise, the response at the articular medial region was
considerably lower in comparison to the articular, lateral and bursal aspects of the tendon.
Funakoshi et al did a longitudinal characterization of the vascular pattern at the supraspinatus
tendon and its associated anatomy and found unique temporal vascular responses in the
investigated structures 53
. The vascular response of the bursal aspect of the supraspinatus tendon
peaked one month after the surgery. The peak response for the articular aspect, however,
occurred at two months. The vascular activity decreased globally by three months after the
surgery in the supraspinatus tendon. In contrast, the vascularity at the anchor hole which was at
the region of tendon and bone contact showed elevated responses over the period of the study.
Proper blood supply is a pre-requisite for maintaining tendon quality. Hence, blood supply has
becoming an emphasized therapeutic target for preventing degeneration and promoting healing
of the rotator cuff tendon. Understanding the vascular dynamics of the rotator cuff will allow
researchers and physicians to gain deeper insights to the pathophysiology of degenerative
30
changes and potentially lead to novel therapeutic strategies. However, at the present time there
are no therapeutic options available for increasing vascularity in rotator cuff repair.
31
1.3 Rotator Cuff Repair Model
An appropriate rotator cuff model that is representative of the human rotator cuff consists of the
following criteria: the shoulder musculature of the rotator cuff and its surrounding muscles (the
biceps and deltoid muscles), the shoulder bony structures (the acromion, clavicle, coracoids, and
humerus), the articulations of the bony structures, and the motions of the joints.
1.3.1 Animal Models and the Rat Model
Various animal models have been explored in attempt to recapitulate the disease and healing
progression of the rotator cuff. Some of these animal models include the rabbit, the sheep, the
canine, the primate, and the most popularized – the rat.
The rabbit rotator cuff model was employed to examine muscular fatty infiltration and
degenerative changes, tendon-bone enthesis regeneration, and rotator cuff biologic augmentation
68. The sheep rotator cuff was large enough in size to introduce large tears and monitor its effect
and healing progression comparable to the timeline for humans 59
. Additionally, sheep rotator
cuff muscles experience degenerative changes similar to that of chronic tears in humans. This
model allows for temporal molecular analysis of pathological mechanisms after rotator cuff tear
51. The canine rotator cuff model provided a functional assessment of the scaffold augmentations
as the animals place load to the rotator cuff which reflects the stress experience by human
32
conditions 42
. While many of the quadrupedal models have similar shoulder architecture as the
human shoulder, their rotator cuff tendons insert onto the humeral head separately, and therefore
do not form a “true cuff” structure as that of the human rotator cuff 167
.
Non-human primates have the shoulder anatomy and physiology most similar to that of the
human shoulder 166, 204
. The cost, complexity of facility management, and ethical considerations
comprise the reasons for the lack of use of this model.
While the rats are also quadrupeds, their unique shoulder anatomy makes them a suitable animal
model for rotator cuff studies. The rat shoulder shares similar morphology with a human
shoulder, with the supraspinatus tendon passing through the subacromial space 169
. Expanding
from the rat supraspinatus model, an acute surgical repair model has been developed to
specifically examine the healing at the insertion 181
. The model has been extensively used to
examine the various factors in and strategies for tendon healing.
The use of biological approaches to enhance tendon-bone integration has been a popular theme
for the rat supraspinatus acute repair model. The surgery involves detachment of the
supraspinatus from its humeral insertion immediately followed by a bone tunnel suture repair.
Interventions are usually administered during the surgeries: growth factors and bioactive
molecules in healthy or diseased-condition, pharmacological drugs, and cell therapies. Outcome
measurements have included tendon biomechanical properties and histological examinations.
The characterization of early phase of supraspinatus tendon-bone healing in this model allowed
the characterization of the temporal expression profiles of growth factors 203
. Several studies
have investigated the application of fibroblastic growth factor 79, 80
, bone morphogenetic protein-
13 66
, insulin-like growth factor and platelet-derived growth factor-β 192
, and transforming
33
growth factor-β 111
in this model. All but the bone morphogenetic protein-13 study found that the
growth factors were moderately beneficial for tendon healing. However, platelet-rich plasma,
which contains a variety of growth factors that stimulates anabolic activities in tissues, was
found to have no effect on the tendon-bone strength after surgery 14
. Bioactive molecules such as
the recombinant human parathyroid hormone 73
(a hormone that increases osteogenesis and
chrondrogenesis) and alpha-2-macroglobulin 17
(a large generic protease inhibitor) yielded
superior macroscopic healing at the tendon-bone junction, but failed to increase strength,
suggesting the formation of bone and fibrocartilage at the enthesis was not sufficient to translate
into biomechanical improvements.
Diabetic and osteopenic conditions for the rat supraspinatus model have been developed.
Diabetes mellitus significantly compromises healing at the tendon-bone interface, resulting in
lower biomechanical load to failure and inferior tissue characteristics 16
. Although the study by
Cadet and co-workers did not perform surgical detachments of the rotator cuff tendons, estrogen
deficiency induced osteopenia at the greater tuberosity resulted in negative changes at the
insertion histomorphologically 26
. The failure stress, however, did not show statistical
significance.
Pharmacological agents such as bisphosphonate and non-steroidal anti-inflammatory drugs
(NSAIDs) were administered to examine their effects on tendon-bone healing. In the same study,
Cadet and co-workers also used zoledronic acid (bisphosphonate) to improve bone density at the
insertion of the supraspinatus tendon 26
. They found stronger mechanical strength at the tendon-
bone junction with increased bone density at the supraspinatus footprint. It is important,
however, to note that their study did not involve detachment and repair of the supraspinatus
tendon. Further investigation to address the efficacy of bisphosphonate drugs in tendon-bone
34
healing is necessary to delineate the relation. Cohen et al conducted an experiment to examine
the effect of NSAIDs on tendon-bone healing in the rat supraspinatus repair model 34
. Both of the
anti-inflammatory drugs indomethacin and celecoxib compromised soft tissue healing, including
some that failed to heal. The study confirmed the links between tendon-bone healing and the
production of cyclooxygenase-2.
As mentioned in the previous chapter, cell therapy is an attractive therapeutic for regenerative
medicine, especially when the cells themselves are both renewable and differentiable. The
following section will discuss the application of cell therapies to the rat supraspinatus repair
model.
1.3.2 Cell Therapy in the Rat Rotator Cuff Repair Model
Gulotta and colleagues investigated the use of mesenchymal stem cells (MSCs) during rotator
cuff repair to improve tendon-bone healing 63
. MSCs are speculated to differentiate into cells
associated with the tendon-bone interface and augment the tissue quality at the injury site.
However, they found that MSCs showed no benefit over the control groups. Gulotta and
colleagues then conducted a series of three subsequent studies with rotator cuff repair by
genetically modifying the MSCs: MSCs transduced with the membrane type 1 matrix
metalloproteinase gene (MSC-MT1-MMP) 64
, MSCs transduced with the scleraxis gene (MSC-
Scx) 65
, and MSCs transduced with the bone morphogenetic protein-13 gene (MSC-BMP13) 66
.
MSC-MT1-MMP and MSC-Scx demonstrated stronger interfaces, while MSC-BMP13 had no
improvement.
35
It was found that MSCs alone were insufficient to improve the attachment strength of the
supraspinatus tendon at 2 weeks and 4 weeks after repair. The following table provides a
summary of the biomechanical results of these studies.
Table 1-1. Biomechanical results of rotator cuff studies using mesenchymal stem cells
2 Weeks Control63
MSC63-66
MSC-
BMP1366
MSC-MT1-
MMP64
MSC-Scx
65
Load (N) 11.2 ± 2.3 10.5 ± 2.4 11.2 ± 2.5 12 13
Stress (MPa) 1.9 ± 0.6 1.7 ± 0.7 1.6 2.1 2.6 ± 0.9*
Stiffness
(N/mm) 5.7 ± 2.3 4.9 ± 1.8 5.1 6 8.4 ± 2.9*
4 Weeks Control63
MSC63-66
MSC-
BMP1366
MSC-MT1-
MMP64
MSC-Scx
65
Load (N) 22.1 ± 3.5 20.8 ± 4.4 20.8 ± 4.4 27.3 ± 4.2* 26.7 ± 4.6*
Stress (MPa) 3.5 ± 1.0 3.5 ± 1.0 3.9 5.0 ± 1.3* 4.7 ± 1.3*
Stiffness
(N/mm) 9.8 ± 4.7 9.3 ± 3.3 8.2 13.3 ± 5.1* 15.3 ± 3.4*
* significant compared to the control group/MSC group (MSC group was the baseline value for
subsequent genetic modifications)
36
0
5
10
15
20
25
30
35Fo
rce
Tendon Strength
2 Weeks
4 Weeks
*F
orc
e (
N)
Figure 1-4. The ultimate load to failure at the insertion. The mesenchymal stem cells transduced
with MT1-MMP gene and Scx gene increase insertion strength at 4 weeks after the repair
compared to the control group/MSC group (MSC group was the baseline value for subsequent
genetic modifications). Mesenchymal stem cells alone were not sufficient to improve healing.
Histologically, the MSCs were tracked using Ad-LacZ transduction prior to transplantation.
Their presence was evaluated by the activity of β-galactosidase post-mortem. Exposure to β-
galactosidase turned X-Gal solution from colourless to blue, indicating the presence of
metabolically active MSC-LacZ. The amount of blue was significantly more in the specimens
treated with MSC-LacZ than MSC-Null, and the β-galactosidase activity was lower at 4 weeks
comparing to that at 2 weeks.
37
At 4 weeks, the tendon-bone interface tissue was more robust than those at 2 weeks even under
gross observation. The continuity between the repaired tendon and the bone was observed and
the natural healing progression without intervention was noted.
The collagen fibre organization and the area of fibrocartilaginous tissue were quantified using
birefringence represented in gray scale and Safranin O/Fast Green FCF staining respectively.
The following table provides a summary of the histological results from these studies.
38
Table 1-2. Histological results of rotator cuff studies using mesenchymal stem cells
2 Weeks Control63
MSC63-66
MSC-
BMP1366
MSC-MT1-
MMP64
MSC-Scx
65
Organization
(gray scale) 16.5 ± 5.5 20.3 ± 5.9 20.2 ± 3.6 24.4 ± 4.4 22.1 ± 3.5
Fibrocartilage
(mm2)
0.342 ± 0.201
0.596 ± 0.192 0.603 ± 0.294 0.514 ± 0.305 0.528 ± 0.407
4 Weeks Control63
MSC63-66
MSC-
BMP1366
MSC-MT1-
MMP64
MSC-Scx
65
Organization
(gray scale) 24.8 ± 2.5 26.5 ± 5.5 26.5 ± 5.4 34.5 ± 3.5* 25.9 ± 6.3
Fibrocartilage
(mm2)
0.438 ± 0.115 0.343 ± 0.217 0.451 ± 0.215 1.047 ±
0.384*
0.729 ±
0.050*
* significant compared to the control group/MSC group (MSC group was the baseline value for
subsequent genetic modifications)
The mesenchymal stem cells alone did not statistically improve the biomechanical strength of the
repaired tendons. The hypoxic environment leading to compromised cell activities was likely a
factor for the result. Alternative cell types were considered and it was hypothesized that the issue
of poor vascularity should be addressed.
39
1.4 Angiogenesis and Endothelial Progenitor Cells
1.4.1 Capillaries
The microvasculature of the body is the site of interchange between the circulation and the body
tissues. These specialized vessels are called capillaries. The total diameter of the capillaries in a
human body is 800 times longer than that of the aorta, and their total surface area is roughly
6000 metres squared. Accordingly, the flow speed in the capillaries is 0.3 millimetres per second
whereas the average flow speed is 320 millimetres per second in the aorta. Their dimensions are
7 to 9 micrometres in diameter and 0.25 to 1 millimetres in length. Structural variations of
capillaries in different tissues reflect a variety of complex metabolic demand and function of the
associated tissues and organs.
The general structure of capillaries is composed of a layer of endothelium and a basement
membrane. The endothelium consists of a single layer of endothelial cells of mesenchymal
origin. Endothelial cells are polygonal in shape and elongated in the direction of blood flow.
They rest on basal lamina, are held together by zonula occludens (tight junctions), and are in
contact with neighbours through gap junctions. On the luminal membrane of endothelial cells is
surface proteins which are immunogenic and coagulating modulators. Present along some
locations surrounding the capillary endothelial cells are pericytes. These mesenchymal cells
possess the capacity to transform into cells associated with blood vessels.
40
The structure of the capillaries dictates the function of the capillaries: the macromolecule
permeability, the metabolic activities, and the anti-thrombogenic role. Accordingly, the various
types of capillaries include the continuous (somatic) capillary, the fenestrated (visceral)
capillary, renal fenestrated capillary, and the discontinuous sinusoidal capillary. Continuous
capillary is the major capillary type in muscles, connective tissues, and nervous tissues. The
prominent characteristic of the continuous capillary is the absence of fenestrae in the
endothelium. Here, exchanges between the blood and tissues rely heavily on pinocytotic vesicles
in the endothelial cells. Fenestrated, or visceral, capillaries are often seen in organs that allow
rapid interchange of substances such as in kidneys and intestinal organs. From 60 to 80
nanometres in diameter, fenestrations closed by a thin diaphragm in the endothelium enable
small molecules to cross freely. The renal fenestrated capillary is a specialized version of
fenestrated capillary, which is encapsulated by the glomerulus. Lastly, the discontinuous
sinusoidal capillary is marked by tortuous path, fenestration lacking diaphragms, enlarged lumen
from 30 to 40 micrometres in diameter, and presence of macrophages along the endothelium.
These capillaries have discontinued endothelium and basement membrane that allow
mobilization of cells and higher levels material exchange, especially mid-sized plasma proteins
such as albumin. Discontinued sinusoidal capillaries are present in the liver and hematopoietic
tissues and organs such as the bone marrow and the spleen.
The second component of the capillary, the basement membrane, is a connective tissue which is
by large composed of the extra-cellular matrix. The membrane provides structural integrity, acts
as a filtration barrier, and regulates cell attachment and chemotaxis. The membrane is rich in
collagen fibrils: type I and type III collagen.
41
1.4.2 Angiogenesis
The growth of vessels via pre-existing capillaries is termed angiogenesis. It is a complex process
that involves proliferation, migration, and remodeling of endothelial cells into functional
vasculature, and the tight balances between pro-angiogenic and angiostatic molecules.
Angiogenesis is regulated by cytokines and chemokines, the extracellular matrix as well as
physical forces of the vascular environment.
The most potent angiogenic cytokines are the vascular endothelial growth factors (VEGFs).
VEGFs can induce vasodilation, increased permeability of and fenestration in the endothelium,
activation of endothelial cells to a proliferative state 190
. On the surfaces of endothelial cells are
VEGF tyrosine kinase receptors, specifically, the VEGF receptor-2 which binds to the VEGF-A
isoform. Some of the major bioactive molecules involved in angiogenesis include fibroblastic
growth factors, transforming growth factor-β, insulin-like growth factor-1, platelet-derived
growth factors, angiopoeitin, erythropoietin, and tumor necrosis factor-α. Each drives the
angiogenic activity through various signaling pathways and downstream effects. The actions of
the molecules are not independent of each other, but work in concert to facilitate microvascular
expansion.
Successful migration and invasion of endothelial cells into the perivascular tissue is dependent
on the proteolysis and remodeling of the extracellular matrix. The extracellular matrix offers
molecular directional cues for angiogenesis as well as binding sites that provides spatial
information to the cells 190
. Present on the cell surface are transmembrane protein integrins which
modulate the motility and affinity of the cells through the extracellular matrices.
42
Lastly, hemodynamic forces in the vessels can affect the angiogenesis and subsequent
remodeling processes. Shear stress is essential for the maintenance of endothelial integrity and
responses; forms of shear stress can induce different angiogenic responses via distinct signaling
pathways 109
. Local inflammatory response alters the hemodynamics of the tissues, and the
capillary network remodels to accommodate the environment. It is observed that once the
inflammation subsides, the network remodels again to its original hemostatic architecture.
Mechanisms of Angiogenesis
Once the endothelial cells have been stimulated for angiogenesis, a cascade of events follows as
the vessels prepare for neovascularization. There are two identified physiological angiogenic
processes: sprouting and intussusceptive angiogenesis. Both types of microvascular growth have
been observed in vivo.
Sprouting angiogenesis, as the name suggests, involves paracrine induced migration of a tip cell
supported by lateral stalks cells into the perivascular tissue. Upon activation of the tip cell by
angiogenic stimulation, the adjacent basement membrane is degraded by proteases. The direction
of sprouting is guided toward higher gradient of growth factors until cellular contact is made
with other capillary sprouts. Trailing the tip cell, the stalk cells form the lumen of the vessel and
line the endothelium. Pericytes are recruited as the vessel architecture undergoes remodeling and
maturation. The tip and stalk cell phenotypes are transient and highly regulated by notch
signaling; the process of angiogenesis requires dynamic transitions between the endothelial, tip,
and stalk cell phenotypes 138
.
43
The other process of angiogenesis, intussusceptive angiogenesis, occurs via splitting the pre-
existing vascular network or capillary plexus. The characteristic hallmark of intussusceptive
angiogenesis is the formation of multiple intraluminal pillars from invaginations of opposing
vessel walls in its initial stages 38
. When the inter-endothelial junctions are re-organized, the core
of each pillar is perforated to allow mural cell invasion and growth factor trafficking. As the
pillar expands with increasing extracellular matrix deposition, it fuses with nearby pillars to
create bifurcation in a vessel.
Both sprouting and intussusceptive angiogenesis rely on pre-existing vasculature. While
intussusceptive angiogenesis is more limited in a sense that it can only occur in capillary
plexuses developed from vasculogenesis or sprouting angiogenesis, its process is much faster
and energy efficient. Capillary splitting does not require the disruption of basement membrane or
extensive proliferation of endothelial cells to line the endothelium. Microvascular growth studies
have identified the predominance of capillary sprouting in the early stages of vascular growth,
followed by extensive hierarchical splitting of vessel during remodeling 106
. The novel evidence
suggests the temporal dependence of the angiogenic mechanisms.
It is plausible that during tendon healing in which metabolic resource is scarce, there is a
tendency for the fibrovascular tissue to derive vessels via intussusceptive angiogenesis.
However, the tendon is hypovascular, leaving the bone and the bursa as the major sources for
pre-existing vasculature. The hypovascular nature of the tendon itself may impair its ability to
heal.
44
1.4.3 Endothelial Progenitor Cells
Cell therapy is an attractive therapeutic avenue for regenerative medicine, especially when the
cells themselves have the capacity to renew and differentiate. Stem cells and progenitor cells are
populations of cells which possess such capabilities. Much excitement was generated when
endothelial progenitor cells were identified. The first published detailed description for
endothelial progenitor cell isolation is by Asahara and colleagues in 1997 6. It sparked a new
paradigm in utilizing endothelial progenitor cells as a cellular strategy for therapeutic
neovascularization. It is believed that these cells can induce angiogenesis via the secretion of
angiogenic factors or by directly participating in the lining of endothelium. Endothelial
progenitor cells are a rare but normal component of the elements that make up the circulating
blood cells.
There are a several sources from which these cells can be isolated. These include the peripheral
blood 6, 77, 99
, the bone marrow 140
, and the umbilical cord blood 22, 123, 134
In addition, endothelial
progenitor cells have been found to reside in tissues and organs such as fat 134, 137
and vascular
tissues 150
, the fetal liver 134
, and the heart19
.
Currently, there is not a well-defined set of surface immune-phenotyping or functional assays to
identify putative populations of endothelial progenitor cells. Various combinations of cell surface
antigens or markers were used in attempt to characterize the cells. Most of these markers are not
endothelial lineage specific; the marker profile reflects the hematopoietic lineage 189
.
Nonetheless, the conventional positive markers for detection are CD 34, CD 133, and vascular
endothelial growth factor receptor-2 (VEGFR2) or fetal liver kinase-1 (Flk-1) 75, 189
. CD 34
45
positivity indicates that the putative population is of the hematopoietic stem/progenitor cell
population. The second marker, CD 133, also known as Prominin-1 or AC 133, is a strict
character for early hematopoietic stem/progenitor cell that reside in the bone marrow, fetal liver,
or in circulation 207
. Lastly, the presence of vascular endothelial growth factor receptor-2 on the
membrane warrants the ability for the cells to respond to vascular endothelial growth factor, a
potent signaling molecule for angiogenesis.
46
Endothelial Progenitor Cells
CD133
CD34
Endothelial progenitor cell
Endothelial cells
Paracrineeffect
Flk-1
Figure 1-5. Surface antigens and possible angiogenic mechanisms of endothelial progenitor cells.
The conventional surface markers are CD 34, CD 133, and Flk-1 (VEGFR2). The mechanisms
for angiogenesis are endothelial differentiation and angiogenic signaling.
In addition to surface immune-phenotyping, assays are often performed to demonstrate
functional characteristics of putative cells of the endothelial lineage. The uptake of acetylated-
low density lipoprotein (AcLDL) labeled with fluorescent probe 1,1' -dioctadecyl -3,3,3',3' -
tetramethyl-indocarbocyanine perchlorate (DiI-AcLDL), the binding of lectin Ulex europaeus 1
agglutinin (UEA-1), and forming tubes in 3 dimensional matrices are frequently used in vitro
behaviours 35, 74, 189
. In contrast to the surface markers which correlate more to that of the
hematopoietic stem cell phenotypes, the functional assays are indicative of endothelial
properties. AcLDL uptake occurs through the scavenger cell pathway of lipid metabolism. While
47
internalizing AcLDL is a property of endothelial cells, monocytes and macrophages are also
know to scavenge AcLDL macromolecules. Likewise, UEA-1 binds to glycoproteins that are
found predominately on the endothelial cell surface, but are present on epithelial cells and other
blood-derived cells. Accordingly, either of the functional assays alone is sufficient to distinguish
endothelial progenitor cells from other hematopoietic cells. In vitro tubulogenesis assay is
considered to be a very informative test; other cells do not typically form tubes in fibrous
matrices. Endothelial progenitor cells, when in contact with extracellular matrix components,
have the capacity to assemble and form a network of tubes that resembles the microvasculature
in vivo 74
.
Under the conventional isolation protocols, two distinct populations of endothelial progenitor
cells have been identified. Early and late endothelial progenitor cells, named according to their
time-dependent appearance in vitro, share common endothelial surface phenotypes but display
different functional potentials 77, 208
. Early endothelial progenitor cells have a shorter life span
(about 4 weeks) and higher levels of cytokine secretion. They are, however, poor in forming
tubes in vitro. Late endothelial progenitor cells, also known as late outgrowth cells, have better
endothelial incorporating and tubulogenic capacities; they are representative of mature
endothelial cells yet still maintain proliferative angiogenic characteristics. The contrasting
angiogenic profiles suggest the different roles during neovascularization 119
. The paracrine and
autocrine effects of the early cells augment the proliferation, migration, and incorporation of the
late cells. This synergistic interaction of the mixed populations has been demonstrated in vivo.
The transplantation of both types of progenitor cells together led to better perfusion than either of
the cells alone 208
.
48
The exact origin of endothelial progenitor cells is still uncertain. The cells are believed to be
derived from the bone marrow, as observed in gender-mismatched marrow transplant patients 99
.
There are two proposed sources, the mesenchymal and the hematopoietic differentiations. The
cells from the mesenchymal lineage lacked the early hematopoietic markers and were able to
differentiate in vitro into osteocytes and adipocytes 128, 143
. When they were cultured for
endothelial differentiation, the cells expressed endothelial antigens and formed vascular tubes
when plated on extracellular matrix 5, 128, 143
. In addition to the mesenchymal origin, the
hematopoietic origin has been indicated as an alternative source for endothelial progenitor cells.
A wealth of literature has described the hematopoietic stem cell-myeloid progenitor-monocyte
pathway for endothelial precursor differentiation 48, 139, 156
. Surface markers and angiogenic
assays confirmed the plasticity of monocytes to give rise to vasculogenic cells 135
. Myeloid
progenitors are also found to contribute to endothelial progenitor cell differentiation and
contribute to the vascular endothelium 11, 103
. The close association between the two cell lineages
in the bone marrow could explain the phenotypic overlap of their progenies. A recent study
highlighted the trans-differentiating potential from the mesenchymal lineage precursor
(mesenchymoangioblast) to the hematopoietic lineage precursor (hemangioblast) given the
appropriate stimulation 164
.
49
1.4.4 Applications of Endothelial Progenitor Cells
Bone marrow transplant experiment showed that endothelial progenitor cells have 0.2 to 0.4 %
engraftment rates in the vascular endothelium after four months 36
. Tissue specific vascular
progenitor cells may result in different cell responses and fates during neovascularization 108
.
Various animal models have been used for pre-clinical investigations of endothelial progenitor
cell therapy in ischemic conditions. Increased micro-vasculature in the myocardium, improved
myocardial remodeling and function, and reduced scarring were observed with the addition of
endothelial progenitor cells to ischemic heart condition 84, 85, 91, 157
. Similarly, anti-fibrogenesis,
remodeling, and hepatic regeneration were associated with the transplantation of endothelial
progenitor cells to the cirrhotic liver model 120, 175, 191
. The authors speculated that the secretion
of angiogenic growth factors and enhanced vascularization lead to the improvement in liver
function and animal survival. Additionally, extensive studies have examined the effects of
delivering endothelial progenitor cells in ischemic hind limb models. Capillary density and limb
blood flow increased, and the rate of limb loss was reduced 83, 155, 193
.
The pre-clinical animal studies done using endothelial progenitor cells have revolved around the
theme of re-vascularizing injured tissues to enhance the tissue’s innate reparative ability.
Increased vascular density and blood supply to target tissues along with ameliorated tissue
quality were the results. Indeed, the endothelial progenitor cell population was expected to
provide a source of angiogenic growth factors that stimulates endothelial proliferation. While
these studies have confirmed the angiogenic effects of introducing endothelial progenitor cells to
50
these tissues, more studies are needed to delineate the specific mechanisms by which the cells
promote neovascularization.
i. Clinical trials
Vascular progenitor cells have been investigated in clinical trials for critical limb ischemia and
heart diseases. Randomized controlled trials have been conducted to evaluate angiogenic cell
therapy in critical limb ischemia. Two sources of mononuclear cells were used in the studies:
bone marrow mononuclear cells 176
and peripheral blood mononuclear cells 76
. Both trials
demonstrated feasibility and safety of treatment.
Clinical trials for angiogenic cell therapy in heart diseases have been divided into two categories
165: acute myocardial infarction and chronic heart disease. Major trials for acute myocardial
infarction include TOPCARE-AMI 8, 152
, BOOST 114, 115, 201
, ASTAMI 18, 105
, and REPAIR-AMI
49, 153. On the other hand, for chronic ischemic heart diseases, there are TOPCARE-CHD
7 and
FOCUS-CCTRN 18, 105, 136
. All trials but ASTAMI and FOCUS-CCTRN showed positive
functional outcomes for the heart.
Two trials, TOPCARE-AMI and TOPCARE-CHD, employed both the bone marrow and the
peripheral blood endothelial progenitor cells, and both found favourable improvements in the left
ventricular function. Interestingly, the TOPCARE-CHD study compared circulating progenitor
cells with bone marrow progenitor cells and found better outcome in left ventricular ejection
fraction with the bone marrow progenitor cells 7. The long term results of TOPCARE-AMI
demonstrated safety and efficacy with progenitor cell restored cardiac function 95
.
51
ii. Orthopaedic applications
Vascular strategies have received much attention in the field of orthopaedics recently. The use of
vascular progenitor cells to promote neovascularization in tissues with poor or deficient
vascularity has been a major focus of recent investigations. This includes osteonecrosis of the
femoral head, segmental bone defects, and transected ligament.
While the etiology of osteonecrosis is multifaceted and not yet fully understood, circulatory
impediment is a widely accepted theory of pathogenesis 82
. The addition of endothelial
progenitor cells has shown beneficial effects on osteonecrosis of the femoral head in animal
models 173, 179
. Both osteogenic and angiogenic responses have been reported. Clinically, bone
marrow mononuclear cells containing endothelial progenitor cells have been continuously
investigated over the years 56, 196, 206
. While endothelial progenitor cell transplantations have
showed promises, more studies are required to ensure efficacy and safety.
Endothelial progenitor cell therapy has demonstrated great potential to heal segmental bone
defects in the rat femur. The addition of endothelial progenitor cells aided the healing of the bone
defect, while the control group without these cells did not heal 9, 98
. A subsequent study showed
that endothelial progenitor cell therapy enhanced expression of various VEGF isoforms in a bone
defect model 97
. The findings of these studies suggested that the endothelial progenitor cells
encouraged early osteogenesis via the facilitation of angiogenesis.
Ligaments are known for their hypovascularity under normal physiological conditions. Healing
of the medial collateral ligament was augmented by administering an endothelial progenitor cell-
enriched population 178
. The local transplantation of the CD 34-positive cells aided ligament
52
healing by increasing angiogenic activities and improving macroscopic, histological, and
biomechanical results. Real-time reverse transcription polymerase chain reaction also revealed
higher expressions of ligament-specific markers, collagen1A2 and tenomodulin, in the treatment
group. The addition of CD 34-positive cells could alter the local environment to one that is
favourable for ligament healing.
Gomes and colleagues investigated the supplement of bone marrow mononuclear cells during
conventional transosseous rotator cuff repair in a clinical trial 46
. The idea of using these
mononuclear cells was that they could revitalize tendons that have undergone avascular
degeneration after the repair. The patients demonstrated functional improvements and tendon
integrity after a twelve month follow up. The magnetic resonance imaging (MRI) results also
suggested the formation of new tissue at the footprint in some of the patients. Although the
preliminary results indicated positive clinical outcomes and MRI findings, the study did not
include a control group and were unable to provide definitive evidence for tissue quality.
To our knowledge, the use of endothelial progenitor cells to augment rotator cuff repair has not
been investigated. In vivo studies are necessary to assess the effectiveness of endothelial
progenitor cell transplantation during rotator cuff repair.
53
1.5 Rationale, Hypothesis, and Objectives
1.5.1 Rationale
Biological strategies for the augmentation of rotator cuff tendon repair have been a popular topic
of pre-clinical and clinical investigations, many of which employ growth factor supplementation
33, 172, extra-cellular matrices
146, 160, and/or anabolic progenitor cells
63, 64. Due to their absence of
immunogenic responses, autologous cell-based therapies have received much attention. With
recent investigations of mesenchymal stem cells (MSCs) strategies yielding disappointing
results63
, potentially due to impaired vascularization at the site of tendon-bone healing3, 78
,
alternative cell lines warrant consideration.
Endothelial progenitor cells are a population of heterogeneous cells that can be isolated from the
bone marrow and the peripheral blood. Endothelial progenitor cells are believed to promote
angiogenic activities through secretion of angiogenic factors (paracrine) and differentiation into
vascular endothelial cells 74
. This cell population has become a popular vehicle for
supplementation of angiogenic growth factors. Studies in animal models of ischemia have shown
their efficacy to induce vascular growth in tissues.
Recent orthopaedic application of endothelial progenitor cells showed superior bone healing
compared to using mesenchymal stem cells9, 124
. The endothelial progenitor cells increased
vascularity in the animals (on the basis of Laser Doppler) and demonstrated superior healing of
54
bone. Given the relevant literature, it stands to reason that the addition of endothelial progenitor
cells at the tendon-bone reattachment site in rotator cuff repair could enhance the vascular
response and improve healing. Endothelial progenitor cell therapy could have a therapeutic effect
on the hypovascular condition of the tendon and aid osteogenesis on the bone end to improve
tendon-bone integration. However, the use of endothelial progenitor cells for the biological
augmentation of rotator cuff repair has not previously been investigated. Our study aimed to
investigate the augmentation rotator cuff repair and vascularity with the therapeutic application
of endothelial progenitor cells.
1.5.2 Hypothesis
Our hypothesis was that the application of endothelial progenitor cells during rotator cuff repair
would increase the biomechanical strength at the tendon-bone interface and increase
angiogenesis during the early phase of rotator cuff healing.
1.5.3 Objectives
It was postulated that by promoting angiogenesis at the tendon-bone site, the endothelial
progenitor cell-treated subjects would yield better tendon repair in a rotator cuff model. The
study addressed the efficacy of endothelial progenitor cells to augment surgical rotator cuff
55
repair and also sought to investigate the fate of the transplanted endothelial progenitor cells. Our
first objective was to confirm the endothelial progenitor cell population from our isolation using
flow cytometry and functional assays. Our second objective was to assess the effect of
endothelial progenitor cell transplantation on the biomechanical strength and histology of the
healing rotator cuff tendon after surgical repair in a rat model. Our third objective was to
evaluate the effect of endothelial progenitor cell transplantation on the vascularity at the repair
site using immunohistochemistry. Our final objective was to examine the fate of the transplanted
endothelial progenitor cells using genetically labeled cells.
56
2 Methods
2.1 Study Design
The study aimed to complete three objectives: evaluate the effect of endothelial progenitor cell
transplantation on the strength and quality of healing tissue, quantify the angiogenic response,
and monitor cell survival at the injury site. Accordingly, the study was designed to address these
objectives.
All animals(80)
EPC(32)
Biomechanics (24)
Week 2(4)
Week 4(10)
Week 6(10)
Histology(8)
Week 4(4)
Week 6(4)
Fibrin(32)
Biomechanics (24)
Week 2(4)
Week 4(10)
Week 6(10)
Histology(8)
Week 4(4)
Week 6(4)
Tracking(16)
GFP-EPC(8)
Day 3 (2)
Week 1(2)
Week 2(2)
Week 4(2)
EPC(8)
Day 3 (2)
Week 1(2)
Week 2(2)
Week 4(2)
Figure 2-1. The study design.
57
A population of syngeneic Fischer 344 rats was used to allow the transplantation of endothelial
progenitor cells between specimens. They were mature healthy rats between 250 to 300 grams
when ordered which roughly translates to three months of age. The animals were housed in pairs
upon arrival from Charles River, and were allowed to acclimatize for at least two days prior to
their surgery. All rats were allowed normal weight bearing and cage activities, standard diet and
water ad libitum. The study was approved by the Animal Care Committee and the Research
Vivarium, St. Michael’s Hospital.
The rats were divided into three groups. The first group (experimental group) received
endothelial progenitor cells delivered in fibrin sealant during the surgical repair of the
supraspinatus tendon. The second group (control group) received only the fibrin sealant. These
two groups were allocated for biomechanical testing and histomorphometric analysis to answer
the first two study questions. The third group, which was used to track cells, received endothelial
progenitor cells which expressed green fluorescent protein delivered in fibrin sealant. This group
was dedicated only for histology examination for the presence of the fluorescent protein.
58
2.1.1 Statistical Significance of the Study
The primary outcome measure for the study was biomechanical strength of the rotator cuff
repair, specifically the ultimate load to failure at 4 weeks. Previous studies have set a 20 %
increase in biomechanical strength as the threshold for significance, and this was felt to be a
clinically significant difference. Accordingly, the statistical significance for this study was set at
20 % increase in biomechanical strength at 95 % confidence (α = 0.05) and 80 % power (β =
0.2).
59
2.1.2 Sample Size Calculation
The calculation for sample size with respect to estimated standard deviation and expected
differences was the following:
where α = the confidence interval; β = power; σ = the standard deviation; and δ = the expected
difference.
The pre-determined level of significance is 95 % with a power at 80 % gives
The same size variables were derived from previous data with regards to supraspinatus tendon
strength at 4 weeks 63
.
Therefore, the determined sample size for each group (the experimental and fibrin groups) was
ten.
60
2.2 Cell Isolation
2.2.1 Endothelial progenitor cell isolation
The endothelial progenitor cell isolation was performed following the developed protocol in the
Musculoskeletal Research Laboratory as previously described 9, 124
.
Syngeneic Fischer 344 rats (Charles River Laboratories, Wilmington, Massachusetts, USA) were
used for cell isolation to allow for transplantation without immunogenic complications.
Endothelial progenitor cells were isolated from rat long bone marrow. Rats were anaesthetized
with isoflurane and euthanized via cervical dislocation. Bilateral femurs and tibiae were carefully
disarticulated and soft tissues were sharply removed post-mortem under sterile conditions.
Dissected femurs and tibiae were immediately immersed in sterile phosphate buffered solution
(Dulbecco’s Phosphate-Buffered Saline, Gibco, Carlsbad, California, USA) and transferred to a
culture hood.
Bone marrow cells were obtained by flushing the intramedullary canals of the long bones with
PBS. The collected solution was centrifuged at 220 relative centrifugal force (RCF) for 5
minutes at room temperature. The supernatant was discarded and the pellet was suspended in
Endothelial Growth Medium 2-MV (EGM2-MV, Gibco, Carlsbad, California, USA), and
transferred into a tube containing Ficoll (Ficoll-Paque Plus, GE Healthcare, Little
Chalfont, United Kingdom) without disturbing the interface between the two solutions. The tube
was centrifuged at 400 RCF, 30 minutes, room temperature. The middle buffy layer containing
61
mononuclear cells was extracted, rinsed in EGM-2-MV, and centrifuged at 100 RCF for 10
minutes, room temperature. The pellet was re-suspended and rinsed once more, and centrifuged
at 100 RCF for 10 minutes, room temperature.
The mononuclear cells were re-suspended in EGM-2-MV and seeded on to human fibronectin-
coated (Discovery Labware, Billerica, Massachusetts, USA) culture flasks and incubated at 37°C
for four days to allow selection of endothelial progenitor cells via fibronectin adhesion and
endothelial cell-specific medium before washing non-adhering cells. Medium was changed every
two days after the initial four days. The cells were cultured for 9 to 10 days before
transplantation, by which time they reach 80 % confluence.
2.2.2 Flow cytometry
Once the endothelial progenitors cells were cultured in the flask for 9 to 10 days, they were
trypsinized (Trypsin-EDTA 1x, Mediatech, Manasass, Virginia, USA) for 5 minutes, harvested,
and rinsed. They were then transferred into microcentrifuge tubes (200 000 cells/tube). The cells
were pelleted and the supernatant was removed. A volume of 100 microlitres of 1 % bovine
serum albumin (Sigma-Aldrich, St Louis, Missouri, USA) in phosphate buffered saline
(BSA/PBS) was used to suspend the cells for each tube. The four antibodies were added
accordingly. The tubes were incubated at 4°C in the dark for 20 minutes to allow antibodies to
bind. The cell suspensions were transferred to flow tubes for analysis.
62
The cells were analyzed with MACSQuant flow cytometer. The event readings were selected for
single cells only, and their fluorescence was gated using the fluorescent minus one (FMO)
groups and the single stains. The surface antigens chosen for flow cytometry were CD 31, CD
34, CD 133, and Flk-1. The excitation formats for CD 31, CD 34, CD 133, and Flk-1 were
fluorescein isothiocyanate (FITC), AlexaFluor 647, phycoerythrin (PE), and VioBlue (v450)
respectively.
i. CD 31
Platelet endothelial cell adhesion molecule 1 (PECAM-1), designated CD 31, is a common
endothelial marker. It is a type I integral membrane glycoprotein (130 kDa) and a member of the
immunoglobulin family that is expressed at high concentrations on the surfaces and between cell
junctions. CD 31 mediates homophilic and heterophilic cell-cell adhesion. CD 31 mediated
endothelial cell-cell interactions are involved in angiogenesis in rats and mice. Accordingly, CD
31 antibodies are often used to measure angiogenesis in association with physiological processes
such as tumor growth. However, in addition to endothelial cells, CD 31 is also expressed on
platelets and subsets of leukocytes.
ii. CD 34
CD 34 is a type I transmembrane glycoprotein (110-120 kDa) of the CD 34/Podocalyxin family
of sialomucin proteins. It is recognized as a highly glycosylated hematopoietic stem/ progenitor
cell antigen. The surface glycoprotein functions as a cell-cell adhesion factor, which mediates the
63
attachment of stems cells to the bone marrow extracellular matrix or directly to stromal cells. CD
34 is also expressed on the endothelium of capillaries.
iii. CD 133
CD 133 (117 kDa), or prominin 1 (PROM-1), is a 5-transmembrane glycoprotein specifically
localized to cellular protrusions. Originally known as AC 133, CD 133 expression is restricted to
a subset of CD3 4 stem/ progenitor cells in the hematopoietic system in liver, bone marrow, cord
blood, and peripheral blood. Only a small portion of CD 34- CD 133
+ cells are found in these
tissues. CD 133 is present on circulating endothelial progenitor cells, fetal neural stem cells, and
other tissue specific stem cells.
iv. Fetal liver kinase-1/Vascular endothelial growth factor receptor-2
Fetal liver kinase-1 (Flk-1), also known as vascular endothelial growth factor receptor-2
(VEGFR-2), is a receptor protein tyrosine kinase of the immunoglobulin family. It is closely
related to CD 177 (c-kit) and CD 140a (PDGF receptor α chain). As the name VEGFR-2
suggests, Flk-1 is a receptor for vascular endothelial growth factor (VEGF). It is expressed on
endothelial cells, and in embryonic and adult tissues. In vivo and in vitro studies indicate that
Flk-1 is required for embryonic development of hematopoietic and vascular endothelial cells as
VEGF is an important signaling protein involved in vasculogenesis and angiogenesis.
64
Table 2-1. Staining Protocol for flow cytometry
Antibody CD 31 CD 34 CD 133 Flk-1
Manufacturer AbSeroTech BD Horizon Miltenyi Biotech BD Horizon
Stock concentration 0.1 mg/mL 0.5 mg/mL 0.022 mg/mL 0.2 mg/mL
Format FITC AlexaFluor 647 PE VioBlue
Aliquoted stock per tube (µL) 5 4 20 10
Aliquoted BSA/PBS per tube (µL) 15 16 0 10
Aliquoted volume (µL) 20 20 20 20
Total stock prepared (µL) 30 24 100 60
Added BSA/PBS prepared (µL) 90 96 0 60
Total diluted volume (µL) 120 120 100 120
Added Aliquoted Volume in µL
Stains Tube number Antibodies CD 31 CD 34 CD 133 Flk-1 BSA/PBS Total
Control 1 - 0 0 0 0 100 100
Single
2 CD 31 20 0 0 0 80 100
3 CD 34 0 20 0 0 80 100
4 CD 133 0 0 20 0 80 100
5 Flk-1 0 0 0 20 80 100
FMO
6 CD 31, 34, 133 20 20 20 0 40 100
7 CD 31, 34, Flk-1 20 20 0 20 40 100
8 CD 31, 133, Flk-1 20 0 20 20 40 100
9 CD 34, 133, Flk-1 0 20 20 20 40 100
Quadruple 10 CD 31, 34, 133, Flk-1 20 20 20 20 20 100
Total 100 100 100 100
65
2.2.3 Functional assays
Functional assays were performed to evaluate the putative endothelial progenitor cell
populations. Both AcLDL uptake and lectin binding assays were carried out on the same slides.
i. AcLDL uptake and lectin binding assays
The isolated endothelial progenitor cell population was evaluated for the uptake of acetylated-
low density lipoprotein labeled with fluorescent probe 1,1' -dioctadecyl -3,3,3',3' -tetramethyl-
indocarbocyanine perchlorate (DiI-AcLDL, Invitrogen, Carlsbad, California, USA) and the
binding of lectin GS II (Lectin GS II Alexa Fluor 488 Conjugate, Invitrogen, Carlsbad,
California, USA). Two-well chamber slides were coated with human fibronectin (10 µg/mL) and
cells were seeded at a density of 8000 cells per square centimetre with endothelial growth
medium at 37°C overnight.
The next morning, stock DiI-AcLDL was diluted to 10 µg/mL with culture medium, and 500 µL
of the solution was added to the appropriate chambers. The control chambers received 500 µL of
endothelial growth medium. They were all incubated at 37°C for four hours followed by three
phosphate buffered saline (PBS) rinses. The cells were then fixed with 2 % paraformaldehyde for
ten minutes, and washed three times with PBS.
The lectin molecule, GS II, was used for lectin binding. Stock GS II was diluted to 20 µg/mL
using PBS with calcium and magnesium (Dulbecco’s Phosphate-Buffered Saline with calcium
and magnesium, Gibco, Carlsbad, California, USA). The solution was added to the appropriate
66
chambers (500 µL/well) and the control chambers received only PBS, and were kept at 4°C
overnight on a shaker. The next morning, the chambers were washed three times with PBS. The
chambers were disassembled and the slide was allowed to air dry in the dark. 4', 6-diamidino-2-
phenylindole in permount (ProLong Gold with DAPI, Invitrogen, Carlsbad, California, USA)
was added to each slide (80 µL), and cover slips were placed on. When the slides were imaged
under fluorescent microscopy, the DiI-AcLDL appeared red, the GS II appeared green, and the
nucleus appeared blue.
ii. In vitro tube formation assay
The isolated population of endothelial progenitor cells was plated on basement membrane
Matrigel (BD Sciences, Bedford, Massachusetts, USA) for tube formation assay. Stock Matrigel
was diluted 1:1 with sterile cold PBS. Diluted Matrigel was aliquoted into a 24-well plate (300
µL/well) and was incubated for 30 minutes to allow polymerization. Endothelial progenitor cells
were seeded at 48 000 cells per well (cell density of approximately 25 000 cells/cm2) with 500
µL of endothelial growth medium. They were incubated for 24 hours and imaged with a
microscope. Mesenchymal stem cells were used as the negative control. The number of tubes
formed was counted and the total length was calculated.
67
2.2.4 Cell survival in fibrin sealant
Fibrin sealant has been widely used as cell delivery agent, namely with mesenchymal stem cells.
Endothelial progenitor cells, however, have yet to be delivered via this method. To ensure
endothelial progenitor cell survival in this delivery agent, the fibrin sealant, the following
procedure was performed.
Commercial fibrin sealant (Evicel, Johnson & Johnson, Somervile, New Jersey, USA) is
composed of two ingredients: (1) human clottable protein (often termed fibrinogen), and (2)
human thrombin. Human clottable protein is activated upon exposure to thrombin in the presence
of calcium ions, causing the mixture to clot.
The endothelial progenitor cells were trypsinized and counted. One million cells were re-
suspended with 12.5 microlitres of thrombin, as it is the less viscous of the 2 components of
fibrin sealant. The same volume of fibrinogen was added to the thrombin-cell suspension and
incubated at 37°C without endothelial growth medium for 24 hours. Five millilitres of
endothelial growth medium was added after 24 hours and the cells were incubated for another
day. The cell survival was assessed at 24 hours and 48 hours by examining cell morphology
(normal healthy cell appearance – adherence to flask, flat monolayer).
68
2.3 Surgery
Endothelial progenitor cells were prepared immediately prior to surgeries. After 9 to 10 days of
in vitro expansion, the cells were harvested by trypsinization, and washed in endothelial basal
medium without fetal bovine serum. For each rat, one million endothelial progenitor cells were
mixed in 12.5 microlitres of thrombin solution of fibrin sealant and kept on ice. The delivery of
the cells involved pipetting the 12.5 microlitres of thrombin and cell mixture with 12.5
microlitres of viscous fibrinogen solution to the central hole made on the greater tuberosity
during surgery.
The surgical procedure involves a unilateral detachment of the supraspinatus tendon from its
humeral insertion followed by a transosseous suture repair. The surgical model has been
developed by Thomopoulos and colleagues to examine tendon-bone healing at the insertion 181
.
During the surgery, 10 day-old endothelial progenitor cells expanded in vitro were delivered in
fibrin sealant. All surgical procedures were approved by the Animal Care Committee and the
Research Vivarium, St. Michael’s Hospital.
Prior to the surgeries, endothelial progenitors were harvested from the culture flasks and
suspended in thrombin, the less viscous solution of the fibrin sealant components. They were
then kept on ice until use.
All the surgeries were performed in the same manner. In each surgery, once the rat had been
anaesthetized with isoflurane (5 %) in combination with oxygen (2 L/min) in the induction
chamber, it was weighted and given a pre-operation dose of buprenorphine (0.05 mg/kg) via
69
intraperitoneal injection. The rat was shaved from the elbow to the neck to expose the skin,
disinfected with Betadine (povidone-iodine) and alcohol. The rat was transferred to the operating
table and was maintained anesthetized with isoflurane (2 %) in combination with oxygen (2
L/min) through the nose cone.
A three centimetre skin incision was made with a scalpel blade at the anterolateral aspect of the
rat’s right shoulder to expose the deltoid-acromion structure. The humerus of the rat was kept in
adduction and external rotation, and a longitudinal incision was made on the deltoid muscle,
splitting the muscle without detaching the deltoid from its acromion origin. Access to the
supraspinatus tendon was created. The supraspinatus tendon insertion on the greater tuberosity of
the proximal humerus could be effectively visualized by placing the humerus in adduction and
internal rotation at the glenohumeral joint.
Before detaching the supraspinatus tendon from it insertion, a Mason-Allen stitch to the distal
tendon was made using a 3-0 Ethicon suture (Johnson & Johnson, Somervile, New Jersey, USA).
Subsequently the tendon was sharply detached from the proximal humerus with a scalpel blade,
and any residual fibrocartilage at the footprint was removed by gently decorticating the greater
tuberosity to expose the bone marrow with a 1.0 mm crosscut burr (Stryker, Kalamazoo,
Michigan, USA). A bone tunnel was made using the burr at the anterior margins of the insertion
two millimetres from the articular surface. Both ends of the suture from the Mason-Allen stitch
were passed through this tunnel and tied over a bony bridge on the lateral aspect of the proximal
humerus.
Prior to securing the tendon repair, the rat was randomized to one of the groups to receive either
the fibrin sealant carrying endothelial progenitor cells or fibrin sealant only. The experimental
group received 106 endothelial progenitor cells suspended in 25 microlitres of the fibrin sealant
70
carrier and the fibrin group received only 25 microlitres of the fibrin sealant carrier. The cells
were first suspended in 12.5 microlitres of thrombin, and then injected at the central hole
simultaneously with 12.5 microlitres of fibrinogen. The clot formed at the bony trough made by
decorticating the fibrocartilaginous footprint. The supraspinatus tendon was approximated to the
exposed marrow by pulling the suture and tying it over the humeral metaphyseal cortex. The
quality of the repair was evaluated by applying slight tension to the tendon. The deltoid muscle
and the skin were closed separately using a standard suturing technique with 5-0 Ethicon suture
(Johnson & Johnson, Somervile, New Jersey, USA).
The rat was then transferred to the recovery chamber until it recovered from the anaesthesia, and
was then housed individually. Two doses of buprenorphine (0.05 mg/kg) were administrated to
each rat during the post-operative period for two days. All rats were allowed normal weight
bearing and cage activities, standard diet and water ad libitum.
71
2.4 End Points, Sacrifices, and Dissections
There were three end points for biomechanical testing (two, four, and six weeks after rotator cuff
repair), and two for histological analysis (four and six weeks after rotator cuff repair). End points
for cell tracking were three days, one week, two weeks, and four weeks after rotator cuff repair.
From the experimental and the fibrin control groups, ten rats were dedicated for biomechanics
and the other four for histology at each end point.
All dissections were performed post mortem. The rats were sacrificed via anaesthesia with
isoflurane (5 %) in combination with oxygen (2 L/min) in the induction chamber followed by
cardiac injection of a dose of diluted euthanizing agent, T61. Each rat received 0.5 millilitres of
T61 diluted with 0.5 millilitres of saline. The shoulder regions were then shaved to fully expose
the skin.
For biomechanics, the rat shoulders were dissected of irrelevant tissues; each specimen contained
only the humerus, the supraspinatus tendon, and the supraspinatus muscle. Each specimen was
immediately wrapped in gauze which was soaked in phosphate buffered saline, and kept in -80°C
freezer until use.
For histology, the rat shoulders were harvested en bloc; each specimen included the humerus, the
scapula, and the adjacent soft tissues. Each specimen was immediately immersed in 10 % neutral
buffered formalin and kept at room temperature for at least five days before any subsequent
tissue processing.
72
2.5 Biomechanical Testing
The rotator cuff specimens, consisting of the supraspinatus tendon attached to the humerus, were
stored in the -80°C freezer. The suture was removed and was not included in the testing. Before
the biomechanical testing, the specimens were thawed overnight in the 4°C refrigerator. They
were warmed to room temperature prior to testing. The area of the tendon-bone interface
(enthesis) was measured using a digital caliper. The area was estimated to be rectangular and
length and width were recorded for each specimen. The greater tuberosity of the humerus was
used as the main landmark for tendon/scar length measurement. Additionally, the central tunnel
for transosseous sutures was present in all repaired shoulders, and was used to approximate the
width of the healing tendon/scar.
i. Specimen mounting
The tendon end was stripped of muscle tissue, gripped with sandpaper and ethyl cyanoacrylate
adhesive (crazy glue), and clamped with custom screw grip. The tendon was aligned to the
humerus in a linear fashion 63
(see Figure 2-2). The tendon footprint area was measured using a
digital caliper.
73
ii. Tendon loading
The testing protocol included a preload to secure the tendon, a session of cyclic preconditioning
to obtain a consistent tendon loading history followed by a ramp to failure to determine the
ultimate load.
In detail, the tendons were preloaded to 0.10 N to eliminate the slack. Ten preconditioning cycles
from 0.10 N to 0.50 N at a rate of 1.0 mm/min were given to each of the tendon to reach a steady
state of mechanical equilibrium. The ramp to failure was performed at a rate of 1.0 mm/min.
Two sites of failure were anticipated: at the enthesis and at the tendon. An enthesis failure can be
a disruption at the tendon-bone interface with or without bony fragments attached. Disruption at
the tendon body can be considered tendon rupture, and the load to failure was not included in the
final analysis.
74
Grip
Jig
Clamps to secure the humerus
Humerus
Supraspinatus tendon
Figure 2-2. Biomechanical apparatus setup.
iii. Parameters
The measured parameters included the area of the footprint, tendon displacement, load, and
ultimate tensile load. The calculated parameters included the stiffness and stress.
(1) Tendon stress: tendon force relative to the tendon cross sectional area
75
(2) Tendon stiffness: change in tendon length in relation to the force applied to the tendon
These parameters were subjected to statistical analysis, comparing the experimental and the
fibrin control groups using the t-test for four and six weeks animals (n = 10 in each group), and
non-parametric test for two weeks animals (n = 4 in each group). Analysis of variance (ANOVA)
and multiple comparison test (Bonferroni’s test) were performed to compare the effect of healing
over time.
76
2.6 Histological Analysis
The specimens for histology consisted of the scapula, the humerus, the distal portion of the
clavicle, and all the attached musculature. The specimens were kept in 10 % neutral buffered
formalin and stored at room temperature for a minimum of five days. The shoulders were
processed in groups for consistency. After fixation, the specimens were trimmed of irrelevant
tissues and decalcified in Immunocal (Decal, Congers, New York, USA) for one week minimum.
The dehydration process was executed using Leica TP1020, an automated tissue processing
machine. The specimens were secured in a plastic cassette and went through 12 stations of
various solvents or solutions. See table below for details in each station.
Table 2-2. Tissue dehydration process by Leica TP1020
Station Reagent Duration (hr) Vacuum
1 Formalin 1 No
2 Formalin 1 No
3 70% EtOH 1.5 No
4 80% EtOH 1.5 No
5 95% EtOH 1.5 No
6 95% EtOH 1.5 No
7 100% EtOH 1.5 No
8 100% EtOH 2 No
9 Xylene 1.5 No
10 Xylene 2 No
11 Paraffin 60°C 1.5 Yes
12 Paraffin 60°C 2 Yes
77
After the specimens completed the dehydration process, they were embedded in paraffin in a
geometry which the supraspinatus was approximately perpendicular to the shaft of the humerus.
The specimens were positioned for sectioning in the coronal plane. The positioning of the tissue
sample was achieved with fast solidification of the paraffin wax on ice using Leica EG 1160.
The embedded samples were then stored at room temperature.
The sectioning was performed using a low profile blade on Leica RM 2235. Each section was
five microns thick in the coronal plane, cutting through the head of humerus, the tendon-bone
junction, and the supraspinatus tendon. The sections were mounted on positively charged
microscope slides.
78
2.6.1 Hematoxylin and Eosin Staining
The hematoxylin and eosin staining was performed using Leica Autostainer XL. Slides were then
examined for proper section orientation and depth as well as infection.
Table 2-3. Hematoxylin and eosin staining protocol using Lecia Autostainer XL
Station Reagent Time (min:sec) Exact Dips
Oven 65°C 10:00 No -
1 Xylene 3:00 No 3
2 Xylene 2:00 No 3
3 Xylene 3:00 No 3
4 100% EtOH 1:00 No 3
5 100% EtOH 1:00 No 3
6 95% EtOH 1:00 No 3
Wash 1 H2O 1:30 No 3
8 HAEMATOXYLIN 2:00 Yes 3
Wash 5 H2O 1:00 No 3
9 DEFINE 0:35 Yes 3
Wash 4 H2O 1:00 No 3
10 BLUE BUFFER 0:45 Yes 3
Wash 3 H2O 1:00 No 3
11 95% EtOH 1:00 No 3
12 EOSIN 1:00 Yes 3
13 100% EtOH 1:00 No 3
14 100% EtOH 1:00 No 3
16 100% EtOH 1:00 No 3
17 Xylene 1:00 No 3
18 Xylene 1:00 No 3
22 EXIT - - -
79
2.6.2 Safranin O/ Fast Green FCF Staining
The staining for cartilage involved three parts: (1) deparaffinization/rehydration, (2) cartilage
staining, and (3) dehydration. The deparaffinization/rehydration steps were a replication of
haematoxylin staining using Leica Autostainer XL.
Table 2-4. Deparaffinization and rehydration of slides using Leica Autostainer XL
Station Reagent Time (min:sec) Exact Dips
Oven 65°C 10:00 No -
1 Xylene 3:00 No 3
2 Xylene 2:00 No 3
3 Xylene 3:00 No 3
4 100% EtOH 1:00 No 3
5 100% EtOH 1:00 No 3
6 95% EtOH 1:00 No 3
Wash 1 H2O 1:30 No 3
22 Exit - - -
After the slides were retrieved, the cartilaginous tissues were stained with Safranin O and fast
green FCF. First the slides were submerged in 0.1 % aqueous fast green FCF stain (OmniPur,
EMD Chemicals, Darmstadt, Germany) for 3 minutes followed by an acetic acid (1 %) wash for
30 seconds. Then they were submerged in 0.1% aqueous Safranin O (Harleco, EMD Chemicals,
Darmstadt, Germany) for 5 minutes.
For the dehydration process, the slides were transferred to the Leica Autostainer XL.
Table 2-5. Dehydration of slides using Leica Autostainer XL
80
Station Reagent Time (min:sec) Exact Dips
Wash 3 H2O 1:00 No 3
11 95% EtOH 1:00 No 3
13 100% EtOH 1:00 No 3
14 100% EtOH 1:00 No 3
16 100% EtOH 1:00 No 3
17 Xylene 1:00 No 3
18 Xylene 1:00 No 3
22 EXIT - - -
The proteoglycans in the cartilage/fibrocartilage stained red, the nuclei stained black, and the
cytoplasm stained green.
Safranin O binds to proteoglycans in the fibrocartilage and presents a contrasting red colour
against the green background. The fibrocartilage was outlined on three sequential slides for each
rotator cuff with a software program and the area for each slide was calculated. The mean area
and the standard deviation for each group were determined and compared.
2.6.3 Collagen Birefringence
The collagen parallelism was examined with polarized light microscopy. When a beam of light
passes through a polarizing filter, the light will exist with vibration in one direction. When it
encounters another polarizing filter with a main axis perpendicular to that of the first filter, the
light will not pass through, resulting in the dark field effect. Collagen has the ability to rotate the
axis of light passing through called birefringence. Once the vibration direction of the light has
81
been rotated, the light will pass through the second filter, and collagen appears bright against the
dark background.
The parallelism of the collagen fibres close to the insertion can be evaluated with the parallelism
index. The index is calculated based on the amount of light signal fluctuation. Higher fluctuation
indicates more organized fibre directions as light intensity is greatest when collagen fibres are
parallel (anisotropy). Likewise, unorganized fibres will generate smaller fluctuation of light
intensity as multiple fibre orientations are represented.
The slides were first deparaffinized/rehydrated using Leica Autostainer XL, then stained in
picrosirius red (Sirius red, Sigma-Aldrich, St Louis, Missouri, USA) for one hour and washed
twice with an acetic acid (1 %) wash for 30 seconds each. The slides were dehydrated using the
Leica Autostainer XL.
Picrosirius red staining was used to enhance the birefringent property of collagen. The light
intensity, the rotation of the filter, and the focus of the camera were standardized for all the
measurements. The specimens were orientated so that the tendons were parallel to the edge of the
stage. The field of view was imaged and the mean light intensity was recorded for each specimen
using an image analysis program based on language IDL 6.3 ( ITT Visual Information Solutions,
Boulder, Colorado). The mean and the standard deviation for each group was determined and
compared.
82
2.6.4 Vessel Staining
The tissues were stained for CD 31 (PECAM-1). The slides were deparaffinized/rehydrated in
the same manner as before using the Leica AutoStainer XL. The antigen retrieval step involved
incubating the slides with 10 mM of sodium citrate at 98°C for 20 minutes. The slides were then
treated with 3 % hydrogen peroxide for 30 minutes to quench the endogenous peroxide. They
were washed thoroughly and followed by incubation with Dako protein block (Dako, Glostrup,
Denmark)) for 30 minutes. The serum was wiped off and the rabbit anti-CD 31 antibody
(Abcam, Cambridge, England, United Kingdom) was applied to the slides. After incubation
overnight at 4°C, the slides were washed and the secondary antibody (Goat anti-rabbit antibody:
Biotinylated, Dako, Glostrup, Denmark) was added at 1:200 dilution and incubated at room
temperature for 30 minutes. The VECTORSTAIN Elite ABC System (Vector Labs, Burlingame,
CA, USA) was used for detection. Solutions A and B were both diluted 1:50 for avidin-
biotin/horse raddish peroxidase binding. The DAB reagent was then applied for colour
development, incubated at room temperature for 10 minutes. The slides were rinsed, dehydrated,
and mounted for analysis.
Images of the new tendon insertion (the area of interest where the tendon boardered the bone and
the adjacent tendinous tissues) were captured and selected, and the vascular objects were counted
as vascular density (vessel/mm2) using an image analysis program, Visiopharm Integrator
System (Visiopharm, Hoersholm, Denmark). The mean and the standard deviation for each
group were determined and compared.
83
2.7 Cell Tracking
Green fluorescent protein (GFP) was used to track transplanted endothelial progenitor cells. The
endothelial progenitor cells were isolated from the bone marrow of transgenic GFP Fischer 344
rats [F344-Tg(UBC-EGFP)F455Rrrc, RRRC#: 307; Rat Resource and Research Center,
Columbia, MO, USA] using the same isolation techniques and procedure as previously
described. Additionally, GFP cell pellets were collected for positive control staining. The GFP
positive endothelial progenitor cells were cultured in the same manner, and delivered to the
rotator cuff tendon insertion with fibrin sealant. The rats were allowed to heal for three days, one
week, two weeks, and four weeks. Two rats were allocated per time point. Regular non-GFP
fluorescent endothelial progenitor cells were used for control.
Once the shoulders were dissected, they were processed in the same manner as previously
described for histology. Again, the specimens consisted of the scapula, the humerus, the distal
portion of the clavicle, and all the attached musculature. They were then fixed, decalcified, and
embedded. Five micron sections were cut in preparation to stain for GFP protein using
immunohistochemistry.
After the slides were cut, they were deparaffinized and rehydrated. The antigen retrieval step
involved incubating the slides with 10 mM of sodium citrate at 98°C for 20 minutes. Then the
endogenous hydrogen peroxidases were blocked with 3 % hydrogen peroxide solution for 30
minutes. Dako protein block (Dako, Glostrup, Denmark) was applied and incubated for 30
minutes at room temperature. The primary antibody (Chicken IgY anti-GFP antibody,
84
Invitrogen, Carlsbad, California, USA) was added at 1:500 dilution and incubated at 4°C
overnight. The secondary antibody (Goat anti-chicken antibody: Biotinylated, Vector Labs,
Burlingame, CA, USA) was added at 1:200 dilution and incubated at room temperature for 30
minutes. The VECTORSTAIN Elite ABC System (Vector Labs, Burlingame, CA, USA) was
used for detection. Solutions A and B were both diluted 1:50 for avidin-biotin/horse raddish
peroxidase binding. The DAB reagent was then applied for colour development, incubated at
room temperature for 10 minutes. The slides were rinsed, dehydrated, and mounted for analysis.
The transplanted endothelial progenitor cells (GFP-expressing) were identified by the presence
of the brown stain under a microscope.
85
3 Results
3.1 Endothelial Progenitor Cells
3.1.1 Flow cytometry
Cells were selected out of all detected events in the flow cytometry. Then single cells, CD 34
positive, and CD 133 and Flk-1 positives, and lastly, CD 31 positive cells were gated. The
analysis found 98.3 % of single cells positive for CD 34. Of the CD 34 positive cells, 96.8 %
were positive for both CD 133 and Flk-1. These antigens indicated progenitor and endothelial
characteristics. The “stemness” of the progenitor cells was illustrated by the high expression of
CD 34 and CD 133, reflective of the hematopoietic lineage. The presence of Flk-1, also known
as vascular endothelial growth factor receptor-2 (VEGFR-2), indicated the response to
angiogenic signals. With respect to the total single cell population, 98 % of the cells were
positive for all three surface antigens.
Lastly, CD 31 was gated to determine endothelial commitment. CD 31, platelet endothelial cell
adhesion molecule 1 (PECAM-1), is a mature endothelium marker. This set of surface antigen
profile in the EPC population indicated its origin from the hematopoietic lineage and
commitment to the endothelial lineage. The level of CD 31 expression, 60 % positivity, was not
as high as the other markers because the endothelial progenitor cells have yet to lose their
86
stem/progenitor cell phenotype. The cells possessed more of the characteristics of stem cells than
the terminally differentiated endothelial cells.
Please refer to Appendix A for the full cytometric analysis.
CD 34 CD 133
Flk-
1
Sid
e Sc
atte
r
Figure 3-1. Flow cytometry analysis: 98.3 % of the cultured cells expressed CD 34 on the surface
(left); of these CD 34 expressing cells, 96.8 % of the cells expressed CD 133 and Flk-1 (right). In
summary, 95 % of the cultured cells expressed all three surface antigens.
87
3.1.2 Functional Assays
i. AcLDL and lectin
The isolated cell population was identified by DAPI, staining the nucleus blue. The cells showed
high positivity for both DiI-AcLDL and Alexa Fluor 488 conjugated GS-II, suggesting the
uptake of AcLDL and the binding to lectin molecules. AcLDL uptake and lectin binding are
characteristics of the endothelial cell lineage. The results indicate that the isolation population
possesses endothelial phenotypes.
88
Figure 3-2. AcLDL and lectin stains: DiI-AcLDL (red fluorescence) staining and DAPI (blue
fluorescence) staining (top); GS-II lectin DAPI (green fluorescence) staining and DAPI DAPI
(blue fluorescence) staining (bottom). Bar = 50 μm.
89
ii. Tube formation
The angiogenic potential of the progenitor cells was assessed by their ability to form tube-like
structures on the basement membrane matrices, Matrigel. The mesenchymal stem cell control did
not have tube-like structure 24 hours after seeding.
Figure 3-3. Tube formation assay 24 hours after seeding: endothelial progenitor cells (after ten
days of culturing, left) and mesenchymal stem cells (right). The endothelial progenitor cells
formed tube-like structures while the mesenchymal stem cells were in isolated colonies.
90
3.1.3 Cell survival in fibrin sealant
The cells survived the clot formation from adding thrombin to fibrinogen. The general cell shape
remained intact at 24 hours after mixing the components to produce fibrin. After the growth
media was supplemented, the endothelial progenitor cells were able to proliferate at the edges of
the fibrin clot. They were able to find a surface to adhere to and assumed the cell adherent
morphology. The cells remained active after 48 hours in the fibrin clot.
When delivered in vitro, the fibrin clot is expected to be disintegrated by the host within a day.
The cells will then be exposed to the host tissue environment which will provide the essential
nutrients and oxygen for metabolism. From this result, the endothelial progenitor cells could be
expected to survive the delivery and remain active in the host.
Figure 3-4. Cell survival: cells suspended in fibrin for 24 hours (left) and cell proliferation at 48
hours (right). After the cells were placed into a flask after being in the fibrin clot for 24 hours,
they were able to adhere, resume monolayer morphology, and proliferate.
91
3.2 Biomechanical Testing
The average weight of the Fibrin group at the time of repair was 283 ± 21 g. The weight of the
Fibrin group at the three respective endpoints, two, four, and six weeks, was 297 ± 16 g, 319 ±
20 g, and 331 ± 14 g. The average weight of the EPC group at the time of repair was 281 ± 13 g.
The weight of the EPC group at the three respective endpoints, two, four, and six weeks, was 293
± 16 g, 315 ± 10 g, and 332 ± 18 g. There were no differences between the Fibrin and the EPC
groups at the time of the repair or at the endpoints.
W e ig h t o f R a ts
We
igh
t (g
)
S u r g e r y W e e k 2 W e e k 4 W e e k 6
0
1 0 0
2 0 0
3 0 0
4 0 0
F ib r in G ro u p
E P C G ro u p
W e ig h t o f R a ts
We
igh
t (g
)
S u r g e r y W e e k 2 W e e k 4 W e e k 6
0
1 0 0
2 0 0
3 0 0
4 0 0
F ib r in G ro u p
E P C G ro u p
Figure 3-5. The weight of rats. The weights of the rats in EPC groups and Fibrin groups were not
significantly different at any of the time points. Error bars represent standard deviations.
92
3.2.1 Ultimate Load
For the healthy contra-lateral shoulders, the failure sites were either at the physis or the tendinous
tissue close to the interface. Only the ones that failed at the tendon-bone interface were included.
However, the failure modes of the biomechanical tests for the operated tendons (with sutures
removed) were consistently at the tendon-bone interface. The fibrous scar at the attachment was
significantly weaker than the tendinous tissue.
The healthy shoulders tended to have a clean slope to failure with one distinctive peak and a
characteristic drop in force, indicating a complete rupture. The operated shoulders, however,
displayed discontinuous ramps, multiple peaks, and a gradual decrease in force.
The healthy insertions had an average ultimate force of 26.39 ± 5.27 N with a sample size of 10
specimens. For the Fibrin group, the ultimate force at two, four, and six weeks was determined to
be 9.33 ± 3.86 N, 10.67 ± 3.29 N, and 19.09 ± 3.48 N. The ultimate load for the EPC group at
two, four, and six weeks was 9.14 ± 3.00 N, 11.58 ± 2.74 N, and 24.64 ± 3.58 N*. However, at
six weeks, there was an appreciable difference between the Fibrin and the EPC groups
(p=0.0025). ANOVA and Bonferroni’s multiple comparison test indicated no differences in
ultimate force between at two and four weeks, but significant increase in ultimate force from four
to six weeks in both groups. Refer to Appendix B for details of Bonferroni’s multiple
comparison test.
93
Table 3-1. Ultimate Load (N)
Time Point Fibrin Group EPC Group
Week 2 9.33 ± 3.86 N 9.14 ± 3.00 N
Week 4 10.67 ± 3.29 N 11.58 ± 2.74 N
Week 6 19.09 ± 3.48 N 24.64 ± 3.58 N*
Significance: * p = 0.0025
Figure 3-6. The ultimate load at the insertions. The ultimate load to failure is significantly higher
in the EPC treated repairs at 6 weeks (t-test, p = 0.0025). Error bars represent standard
deviations. The dotted line represents the ultimate load for healthy tendon, 26.39 N.
94
3.2.2 Interface Area and Ultimate Stress
The area of the tendon-bone interface was significantly smaller in the healthy insertions
compared to the operated groups. These healthy insertions were better defined and their
boundaries were clear. On the other hand, the operated insertions in the Fibrin and the EPC
groups were filled with scar tissues. For the Fibrin group, the interface area at two, four, and six
weeks was determined to be 7.69 ± 0.49 mm2, 6.08 ± 0.76 mm
2, and 6.71 ± 0.49 mm
2. The
interface area for the EPC group at two, four, and six weeks was 7.58 ± 0.51 mm2, 6.24 ± 1.22
mm2, and 6.43 ± 0.54 mm
2. There was no significant difference in the area between the groups.
The interface area remained larger than that of the healthy tendon insertion at all the time points.
ANOVA and Bonferroni’s multiple comparison test indicated a decrease in the cross sectional
area in the Fibrin group from two to four weeks. The difference was not significant in the EPC
group due to large standard deviation. However, there were no significant differences between
the EPC and the Fibrin groups in either time point. Refer to Appendix B for details of
Bonferroni’s multiple comparison test.
95
Table 3-2. Interface Cross-Sectional Area (mm2)
Time Point Fibrin Group EPC Group
Week 2 7.69 ± 0.49 mm2
7.58 ± 0.51 mm2
Week 4 6.08 ± 0.76 mm2 6.24 ± 1.22 mm
2
Week 6 6.71 ± 0.49 mm2 6.43 ± 0.54 mm
2
Figure 3-7. Area of tendon-bone attachments. No differences in the insertion area were found at
any time point. Error bars represent standard deviations. The dotted line represents the area of
tendon-bone attachment for healthy insertions, 2.71 mm2.
96
The ultimate stress was determined by dividing the ultimate load with the corresponding tendon-
bone interface area. This normalized the attachment strength with respect to the size of the
insertion. For the Fibrin group, the ultimate stress at two, four, and six weeks was determined to
be 1.21 ± 0.52 MPa, 1.79 ± 0.66 MPa, and 2.83 ± 0.35 MPa. The ultimate stress for the EPC
group at two, four, and six weeks was 1.20 ± 0.33 MPa, 1.89 ± 0.44 MPa, and 3.83 ± 0.43 MPa*.
Significant difference was detected at six weeks, with the EPC group demonstrating significantly
higher ultimate stress (p<0.0001). ANOVA and Bonferroni’s multiple comparison test indicated
gradual improvements from two weeks to six weeks in the EPC group over time. The Fibrin
group did not show significant differences between two and four week due to large standard
deviation. However, differences between the Fibrin and EPC groups were not seen until six
weeks. Refer to Appendix B for details of Bonferroni’s multiple comparison test.
97
Table 3-3. Ultimate Stress of Tendon-Bone Interface (N/mm2 or MPa)
Time Point Fibrin Group EPC Group
Week 2 1.21 ± 0.52 MPa 1.20 ± 0.33 MPa
Week 4 1.79 ± 0.66 MPa 1.89 ± 0.44 MPa
Week 6 2.83 ± 0.35 MPa 3.83 ± 0.43 MPa*
Significance: * p < 0.0001
Stress
*
Figure 3-8. Ultimate stress at the insertion. The stress significantly higher in the EPC group 6
weeks after the repair (p < 0.0001). Error bars represent standard deviations. The stress for
healthy insertions is 9.84 MPa (not shown on the graph).
98
3.2.3 Stiffness
The stiffness of the tendon and scar tissues were determined by the largest value of slope in the
linear region of the ramp to failure. For the Fibrin group, the stiffness at two, four, and six weeks
was determined to be 6.77 ± 2.23 N/mm, 8.17 ± 3.11 N/mm, and 13.17 ± 3.93 N/mm. The
stiffness for the EPC group at two, four, and six weeks was 8.11 ± 1.75 N/mm, 8.56 ± 2.62
N/mm, and 12.78 ± 2.68 N/mm. There was no significant difference between the Fibrin and the
EPC group. ANOVA and Bonferroni’s multiple comparison test indicated no differences in
stiffness between at two and four weeks, but significant increase in stiffness from four to six
weeks in both groups. Refer to Appendix B for details of Bonferroni’s multiple comparison test.
99
Table 3-4. Stiffness of Tendons (N/mm)
Time Point Fibrin Group EPC Group
Week 2 6.77 ± 2.23 N/mm 8.11 ± 1.75 N/mm
Week 4 8.17 ± 3.11 N/mm 8.56 ± 2.62 N/mm
Week 6 13.17 ± 3.93 N/mm 12.78 ± 2.68 N/mm
Figure 3-9. The stiffness of the tendons. No differences in stiffness were found at any time point.
Error bars represent standard deviations. The dotted line represents the stiffness for healthy
insertions, 23.17 N/mm.
100
Table 3-5. Summary of biomechanical values for 2, 4, and 6 Week Groups
2 Week Groups Fibrin (n=4) EPC (n=4)
Ultimate Load (N) 9.33 ± 3.86 9.14 ± 3.00
Stiffness (N/mm) 6.77 ± 2.23 8.11 ± 1.75
Insertion Area (mm2) 7.69 ± 0.49 7.58 ± 0.51
Stress (N/mm2) 1.21 ± 0.52 1.20 ± 0.33
4 Week Groups Fibrin (n=10) EPC (n=10)
Ultimate Load (N) 10.67 ± 3.29 11.58 ± 2.74
Stiffness (N/mm) 8.17 ± 3.11 8.56 ± 2.62
Insertion Area (mm2) 6.08 ± 0.76 6.24 ± 1.22
Stress (N/mm2) 1.79 ± 0.66 1.89 ± 0.44
6 Week Groups Fibrin (n=10) EPC (n=10)
Ultimate Load (N) 19.09 ± 3.48 24.64 ± 3.58*
Stiffness (N/mm) 13.17 ± 3.93 12.78 ± 2.68
Insertion Area (mm2) 6.71 ± 0.49 6.43 ± 0.54
Stress (N/mm2) 2.83 ± 0.35 3.83 ± 0.43**
Significance: * p = 0.0025; ** p < 0.0001
101
3.3 Histological Analyses
All stains were performed on the operated shoulders as well as the unoperated, healthy
contralateral shoulders.
Figure 3-10. Hematoxylin and eosin, Safranin O, picrosirius red, and CD 31 antigen staining
(from left to right) of healthy rotator cuff tendons. Bar = 2 mm.
3.3.1 Hematoxylin and Eosin Staining
Qualitative analysis of the shoulder indicated that the operated tendons were damaged, and that
scar tissue was apparent. The central hole in the humeral head at the native tendon insertion was
obvious in the operated samples. The sections made were of the correct orientation and at similar
depth.
102
Fibrin Group EPC Group
Week 4
Week 6
Figure 3-11. Hematoxylin and eosin. The orientation and the depth of the shoulder sections were
appropriate. Bar = 2 mm.
3.3.2 Safranin O staining
No fibrocartilage was observed at the insertion site at four or six weeks after the repair in both
the Fibrin and the EPC groups.
103
Fibrin Group EPC Group
Week 4
Week 6
Figure 3-12. Safranin O and fast green staining. No cartilage formation was detected at the
tendon-bone interface. Bar = 2 mm.
3.3.3 Picrosirius Red Staining
The polarization birefringence property was enhanced using picrosirius red staining. The
measured brightness intensity demonstrated that there was no difference between the Fibrin and
the EPC groups, indicating that the degree of collagen immaturity and disorganization were
similar.
104
Fibrin Group EPC Group
Week 4
Week 6
Figure 3-13. Picrosirius red staining. The organization of collagen fibers was assessed under
polarized light. There was no difference in collagen organization between the Fibrin and the EPC
groups. Bar = 2mm.
105
Table 3-6. Collagen birefringence measured in mean optical density
Time Point Fibrin Group EPC Group
Week 4 89.82 ± 20.22 96.69 ± 12.30
Week 6 108.20 ± 9.52 91.23 ± 7.35
Figure 3-14. Polarization of tendinous insertion. No significant differences were found between
the groups at any time point. Error bars represent standard deviations.
106
3.3.4 Vessel Staining
There was no significant difference between the Fibrin and the EPC groups in the number of
vessels. Although the values did not reach statistical significance, the vascular density was
higher in the EPC group and both time points. In addition, an increase of vascularity was
observed in the EPC group between four and six weeks, while the Fibrin group exhibited the
opposite trend.
Fibrin Group EPC Group
Week 4
Week 6
Figure 3-15. CD 31 staining. The insertion region was selected for analysis. The EPC group
showed an increase in vascularity from Week 4 to Week 6. Bar = 2 mm.
107
Table 3-7. Vascular density (vessels/mm2)
Time Point Fibrin Group EPC Group
Week 4 279 ± 141 (n = 4) 376 ± 126 (n = 3)
Week 6 188 ± 78 (n = 4) 457 ± 146 (n = 3)
Figure 3-16. Number of blood vessels per millimeter squared (vascular density) at the insertion
site as identified by CD 31 immunohistochemistry staining. Although the differences were not
statistically significant, the density of vessels was increased in the EPC group at both time points
and the EPC group showed a trend towards increasing vessel density from 4 to 6 weeks, whereas
the Fibrin group showed a decrease in vessel density from 4 to 6 weeks. Error bars represent
standard deviations.
108
3.4 Cell Tracking
Green fluorescent protein (GFP) positive endothelial progenitor cells were observed at the rotator
cuff repair site at three days, one week, two weeks, and four weeks. The presence of the cells
indicates survival and retention at the site of injury.
Most GFP positive cells were surrounded by tendinous scar tissues. Only a few were
incorporated into the endothelium.
109
Figure 3-17. The brown HRP-DAB stain indicated GFP-expressing endothelial progenitor cells
(transplanted cells) at Week 2 in the scar tissue at the injury site. Few of the GFP positive cells
incorporated into the endothelium as indicated by the red arrows.
110
4 Discussion
Rotator cuff retear is a common complication after surgical repair. Causes for retear have been
proposed and strategies to augment tendon healing have been investigated. Scaffolds, biological
factors, surgical techniques, cells, and even rehabilitation have been indicated in variable studies
to improve integration of the tendinous and bony tissues at the insertion. However, there is
currently a lack of clinically effective means to augment rotator cuff repair biologically.
Recently, there has been significant interest in the investigation of adult pluripotent stem cells to
aid rotator cuff tendon healing. Cell-based therapies are of a particular interest among other
therapeutic strategies because of their ability to contribute to healing through self-renewal,
paracrine effects, and/or differentiation into tissue-specific cells that contribute to the healing
process.
Our study was built on previous findings of restricted blood supply to the supraspinatus tendon
insertion and the therapeutic angiogenic effect of endothelial progenitor cells. Vascular ingrowth
is critical to facilitate the delivery of nutrients and cells that respond to the requirements of the
stages of healing. Since the successful identification of endothelial progenitor cells by Asahara et
al 6, there has been a wealth of evidence that these cells induce angiogenic responses in various
in vivo models. With endothelial progenitor cells and their known ability for neovascularization,
we hoped to develop a novel cell therapy for rotator cuff repair to augment healing at the poorly
vascularized tendon-bone interface.
111
The rat rotator cuff repair model is a well-established surgical model for the investigation of
tendon-bone healing and therapeutic interventions 63, 169, 181
. The fibrin sealant delivery method
and the survival of transplanted cells were assessed in previous studies 187
. The use of autologous
progenitor cells minimized immunogenic responses in the host. No adverse immunogenic
response was observed in the animals.
The tracking of the transplanted green fluorescent protein-expressing endothelial progenitor cells
using immunohistochemistry at three days indicated the survival of the transplanted cells.
However, the survival percentage of transplanted cells is not quantified. Determining the survival
percentage should give light to the effectiveness of cell delivery through fibrin sealant.
112
4.1 Endothelial Progenitor Cells
The Ficoll density separation limited the cells collected from the bone marrow to be strictly
mononuclear, which contains the progenitor cells including endothelial progenitor cells as well
as mesenchymal stem cells. The fibronectin coating and the growth media supplementation
favoured the adherence and proliferation of endothelial progenitor cells in vitro culturing.
The high expression of CD 34 and CD 133 suggested that the isolated endothelial progenitor
cells possessed the characteristics of stem cell characteristics, especially that of the
hematopoietic lineages. As importantly, the presence of vascular endothelial growth factor
receptor-2 (VEGFR-2) indicated response to angiogenic signals. The same population of
endothelial progenitor cells also demonstrated endothelial capacity: expression of CD 31
(PECAM-1), uptake of AcLDL and binding of lectin, and in vitro tube formation. Collectively
these assays confirmed that the population of cells isolated from the bone marrow was indeed
functional endothelial progenitor cells.
The cells were only cultured for ten days prior to surgery, and thus were considered early
endothelial progenitor cells. Cells that were cultured for more than two weeks would be
considered late endothelial progenitor cells. Early endothelial cells are believed to predominantly
provide paracrine effects, and the presence of these cytokine secreting early endothelial
progenitor cells was important for in vivo angiogenic mechanisms 208
. The result in this study
supports the paracrine effects of transplanted early endothelial progenitor cells (see Chapter 4.4).
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4.2 Biomechanical Testing
The ultimate force for this rat rotator cuff repair model is considered the most appropriate
biomechanical outcome as it is the most repeatable measurement with the least source of error.
The injury no doubt weakened the strength at the tendon-bone interface. All operated specimens
ruptured at the tendon-bone interface (repair site, sutures removed). Even at six weeks after the
repair, the attachment (Fibrin group) remained weaker than the healthy, uninjured insertions. In
this study, the percentage of strength recovered at each time point are 35 %, 43 %, and 72 % of
the normal insertion strength, versus the reported value at 22 % and 52 % at two and four weeks
15. Additionally, Gulotta et al found no benefits of applying fibrin sealant during rat rotator cuff
repair 63
.
We found no significant differences between the Fibrin and the EPC groups at two or four weeks
in the ultimate force, interface cross-sectional area, stiffness, and ultimate stress. Similar results
were reported by Gulotta and colleagues when they used mesenchymal stem cells alone in the
same rotator cuff repair model 63
. From gross observation, it is evident that fibrous tissues filled
the interface and attached over the greater tuberosity of the humeral head in a disorganized
fashion. The coverage area was much larger than the original insertion, likely a reparative
mechanism to compensate for the weaker scar fibers, providing stability during the initial stages
of healing. Results of rotator cuff repair using cell therapy by Gulotta et al also indicated large
amount of scar at the attachment 63
.
Significant improvements in the tendon ultimate load and stress were detected after six weeks of
healing with the addition of endothelial progenitor cells. The ultimate load of the rotator cuff
114
insertion in the EPC group (24.64 ± 3.58 N) was comparable to that in the healthy insertions
(26.34 ± 5.27 N). Manning and co-workers have reported that the attachment strength in repaired
tendon insertions (TGF-treated and control groups) approaches the normal/uninjured strength at
28.8 N eight weeks after repair 111
. The large cross-sectional area of these fibrous tissues at the
tendon-bone interface offered strength to the attachment more so than the quality of the tendon
tissue. Extensive scar formation was observed in studies using the same rotator cuff model 54, 63,
181. Consequently, the ultimate stress at six weeks (3.83 ± 0.43 N/mm
2) remained inferior to that
of the healthy insertions (9.84 ± 2.15 N/mm2).
The trend showed a slow healing progress in the first four weeks followed by a rapid increase in
strength. This is likely from the effect of the remodeling phase in which the weaker type III
collagen fibrils were replaced by the stronger, more organized type I collagen fibrils. Galatz and
colleagues reported an increased expression of mRNA and protein contents in both types I and
III collagen at ten days post-surgery 54
. Between two to four weeks, there was a drop in type I
collagen content and synthesis and that of the type III collagen plateaued. After four weeks,
types I and III collagen synthesis exhibited opposing trends, with increasing type I and
decreasing type III, suggesting structural remodeling. The biomechanical effect in our study was
consistent with the trend observed in the previous literature.
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4.3 Histology
The histology results indicated that there was no significant difference between the Fibrin group
and the EPC group. At four weeks, the literature reported high type III collagen content and
synthesis 54
. Disorganized fibers were present in abundance even at six weeks in our study.
Collagen birefringence showed less dense and less mature collagen fibers at the insertion of
repaired shoulders compared to the healthy, non-injured tendons. Scarring has been associated
with transforming growth factor beta (TGF-β) signaling. TGF-β1 level peaked at day ten after
rotator cuff repair, corresponding to the peak cell proliferation and extracellular matrix synthesis
54. The administration of TGF-β3 during tendon-bone healing led to increased formation of
fibrovascular scar tissue 111
. It seems that scarring is an inevitable process in adult rotator cuff
healing, and provides stability and strength to the injured tissue prior to structural remodeling as
suggested in the previous TGF-β3 study. Whether or not having abundant scar tissue at this stage
of healing is therapeutic would require longer endpoints fully assess.
We did not observe fibrocartilage at the repair site in either treatment group. Ide et al did not find
safranin O-stained fibrocartilage in the FGF-untreated shoulders at two or six weeks 79
. Using
unmodified mesenchymal stem cells alone did not result in increased fibrocartilage 63
. In the cell
therapy studies where increased fibrocartilage was detected 64, 65
, molecular signaling
(transduction of MT1-MMP gene or Scleraxis gene into mesenchymal stem cells) was
incorporated to induce tissue regeneration. Collectively, this evidence suggests that early
regeneration of this fibrocartilaginous transition zone between the tendon and the bone requires
more than just the host’s intrinsic anabolic cells and the transplanted adult stem cells. The repair
116
site likely lacks the critical biological factors/molecules and the appropriate reparative cells to
recreate a fibrocartilaginous insertion. It is, however, uncertain if angiogenic therapy will
promote the recreation of the native fibrocartilaginous insertion due to the nature of the
hypovascular transition zone.
The attempt to increase the blood supply to this region did not improve the healing response or
encourage early remodeling at four weeks. While the vascularity data did not reach statistical
significance in either time point, it is apparent that the EPC group had increasing vascularity at
the injury site between four to six weeks after the repair. At the same time the Fibrin group
showed decreasing vascularity. The endothelial progenitor cells were capable of sustaining
vascular supply, and possibly enhancing it, weeks after the surgery when the tendon naturally
progresses into its “hypovascular state”. The presence of the avascular critical zone in healthy
insertions is believed to have negative impact on the subsequent rotator cuff tendon-bone
healing. The questionable blood supply to the repair site, especially after massive rotator cuff
repairs, has been implicated in repair failure in clinical studies 71
. Other clinical studies have
found increased vascular distribution to the repair site compared to the uninjured states; however,
the studies showed either delayed 55
or a lower magnitude of response than the surrounding
tissues at the repair site 53
. In our study, the observed increase in vascularity correlated with the
mechanical advantages of the attachment site seen in the biomechanical testing. It is plausible
that prolonged supply of nutrient and cellular access to the attachment was responsible for the
superior strength. The alteration of the vascular environment perhaps allowed reparative cells to
engage in a higher anabolic level, for a longer period of time, than those without. The finding
here confirms that the lack of sustained vascular supply during insertion healing could have
detrimental consequences. However, given the histological findings in the tissue quality at the
117
repair site, the specific mechanism by which vascular supply improves attachment strength
remains unclear.
The conventional histological methods were unable to detect differences between the Fibrin and
the EPC groups. This suggests that the increase in strength is independent of the presence of
fibrocartilage or better collagen fibre organization. It seems that more sensitive and targeted
histological techniques are required to detect changes in the healing rotator cuff tendons.
Immunohistochemical characterization of collagen types (eg. types I, II, III, and X) and
tendinous ground substances (eg. aggrecan, decorin, and biglycan) at the insertion may shed light
on small changes in repair tissue and the distribution of these extracellular matrix molecules.
Changes in tissue levels of matrix metalloproteinases, modulators of tendon remodeling, may
help uncover the remodeling processes that led to stronger attachments. Moreover, the transition
zone includes the tendon and the bone, and endothelial progenitor cells have been shown to
promote bone healing. While we did not specifically assess bone healing at the insertion
histologically, such healing may have contributed to the increase in attachment strength
observed.
118
4.4 Cell Tracking
The ubiquitous green fluorescent protein (GFP) expression allows the identification of the
transplanted endothelial progenitor cells in regular non-GFP expressing Fischer 344 rats. The
GFP positive endothelial progenitor cells were seen at all cell tracking time points, suggesting
survival in the host environment without adverse immunogenic responses. Endothelial
incorporation was not observed on day 3, but was seen at one, two, and four weeks. This is
consistent with reports in the literature that peak capillary proliferation was seen at seven days
post-surgery 54
. However, most of the GFP positive endothelial progenitor cells were stray cells
in the scar tissue rather than incorporating into endothelium, suggesting that their activity may be
limited to paracrine effects, such as secreting molecular factors beneficial to the repair process.
More studies are needed to delineate the fate of transplanted endothelial progenitor cells in
rotator cuff tendon healing.
Gulotta et al used the metabolism of β-galactosidase to determine the presence of transplanted
mesenchymal stem cells (MSCs) at the rotator cuff tendon repair site 187
. While the metabolism
of β-galactosidase indicated that the cells were alive and metabolically active at the site of injury,
neither the cells’ location nor morphology could be determined using such method. Our detection
of transplanted endothelial progenitor cells via immunohistochemistry allowed us to identify and
locate the cells in the shoulder sections. It also revealed cell fate (incorporation into the
endothelium) after transplantation.
119
4.5 Limitations
The study has several limitations that require consideration. As previously mentioned, several
potential sources of error are inherent to the biomechanical testing. While the testing was
performed in a consistent manner, variability between specimens was inevitable. This is
especially the case when mounting the specimens (gauge length) and measuring the attachment
area. The distribution glue between the sand paper and the tendons, the time needed for the glue
to dry, and the penetration of glue into the tissues are examples of potential variability. The
graphs of the biomechanical test results were not “clean” load to failure curves, making stiffness
calculations problematic. This likely contributed to the variability in stiffness and ultimate stress,
although the variability observed in this study was actually quite low. It is also important to note
that a single load-to-failure test construct used in this study (and others in the literature) does not
represent what the clinical population experiences on a daily basis. Continuous cyclic loading
may be a better testing regime for replicating tendon overuse.
While the shoulder sections were made by experienced technicians and the sample orientation
and depth were examined by the pathologist during the cut to the best of their abilities, these
variables could have affected our histological data. The histology serves as supplementary results
to support our biomechanical findings. Thus, the histology by itself cannot provide conclusive
results of rotator cuff healing. In spite of our biomechanical finding, our histology methods may
not have been sensitive enough to detect differences in the healing tissues.
In this study, a single dose of one million endothelial progenitor cells was used for
transplantation. This number was chosen in accordance to previous studies of cell therapy for
120
rotator cuff repairs 63, 64, 65, 66
. Varying numbers of cells were not tested. It is likely that more than
one million cells are required to result in detectable histological differences. However, it is
expected that at some point the aggregation of transplanted cells will become a burden to
healing. A dose-response curve will be crucial to determine the optimal amount of cells before
becoming detrimental to tendon healing.
Another potential limitation of this study is that the model used healthy young rats. This may not
be representative of the older population who often experiences rotator cuff tears. Compromised
healing rat models should be investigated in future studies. These may include diabetic models,
steroid or collagenase injections to simulate tendon degeneration, and induced overuse via
activity. Aged rats are expected to show slower healing due to their diminished cellular activities.
The augmentation of blood supply in these conditions will perhaps have a greater effect in
healing and result in further statistical significance.
121
4.6 Clinical Relevance
We found the transplantation of autologous endothelial progenitor cells during rotator cuff repair
to result in improved biomechanical strength without adverse effects or immunogenic responses.
The difference in the ultimate load to failure between the EPC group (24.64 N) and the Fibrin
group (19.09 N) is 5.55 N, a 29 % increase from the Fibrin group. This improvement in insertion
strength is considered clinically significant as we previously defined clinical significance to be
20 % or more, in agreement with the literature 15, 16, 34, 62, 63, 73
. Although it is unfortunate that we
cannot directly link the difference in insertion strength to retear rates in a clinical setting, we can
associate stronger attachment with better tendon-bone integration, and a higher threshold for re-
rupture. While the regeneration of the fibrocartilaginous transitional zone has been regarded as
the hallmark for the regeneration of native tendon-bone insertion 34, 62, 64, 79, 80
, we found
attachment strength increase to be independent of fibrocartilage formation at the insertion site in
this study.
122
5 Conclusion and Future Directions
5.1 Conclusion
The delivery of endothelial progenitor cells during rotator cuff repair improves the attachment
strength at the supraspinatus insertion six weeks after the surgery without detrimental effects to
the tendinous tissue. Further studies are required to gain a better understanding of the multiple
facets of tendon-bone healing and to ultimately lead to effective biological therapies for rotator
cuff repair.
5.2 Future Directions
Attributing a single factor or cause to rotator cuff injury is difficult due to the large number of
pathogenic factors that may come into play. Targeting each pathogenic condition is necessary for
individualized medical treatment. Similarly, while rotator cuff tears can be treated surgically or
managed non-operatively, the post-operation treatments will need to address the various facets of
the condition for the rotator cuff healing to be optimized.
123
In this experiment, a cellular strategy for vascular enhancement was investigated. Endothelial
progenitor cells have been shown this study, and many others, to have the ability to induce and
enhance localized vascular growth in injured tissues. The cells are appropriate candidates for
therapeutic angiogenesis.
5.2.1 Identifying the Angiogenic Mechanisms
The current study sought to address the functional outcome via biomechanical testing. The load
to failure represents the strength that the healing tendinous structure can sustain before it
detaches completely. Biomechanical testing is the most clinically representative outcome, as
functional strength is a well-defined clinical assessment for rotator cuff injuries. In this study, the
histomorphometric analyses provide only supplementary confirmation of tissue healing.
Histology generates pictures for the healing phases, and histological grading can be related to
biomechanical functions 147
.
The study draws connections between the transplanted cells and the outcomes. The cellular
mechanism by which vessel growth is promoted by the endothelial progenitor cell population is
still yet to be fully delineated. Possible mechanisms include secretion of angiogenic growth
factors such as vascular endothelial growth factors, angiopoeitin-1, and platelet derived growth
factor, and the recently proposed mechanism of secreting vesicles containing miRNA, and
differentiation into endothelial cells to aid the expansion of the local vascular network.
124
The factors responsible for the angiogenic mechanisms could be confirmed by genetically
modifying the endothelial progenitor cells to enhance the synthesis of angiogenic molecules,
such as vascular endothelial growth factors, angiopoeitin-1, and platelet derived growth factor.
Pharmaceutical agents, alternatively, could be employed to block the activity or production of
angiogenic molecules to more precisely define the downstream effect of the factors at play.
5.2.2 The Mesenchymal Lineage
The transition zone helps transfer mechanical forces from the tendon to the bone by minimizing
stress concentration at the interface. Accordingly, for optimal healing at the tendon-bone
interface, the regeneration of this specialized tendon-bone transition zone must occur. In addition
to meeting the metabolic and vascular demands, this healing process requires the proliferation
and hypertrophy of chondrocytes at the interface, proper mineral deposition in the extra-cellular
matrices, and remodeling of collagenous structures.
The current study focused on the augmentation of vascular supply in hopes that this would set
stage for the following healing and remodeling processes. Indeed, meeting the local metabolic
demands of the tissue is crucial for optimizing tendon-bone healing. However, fibrocartilage
chrondrogenesis and structural remodeling are other facets of the healing that could be targeted.
In the future, a mixture of endothelial progenitor cells and mesenchymal stem cells could be
investigated. Both cell types are found in the bone marrow mononuclear cell population. The
functions and effects of the endothelial progenitor cells are described previously. The
125
mesenchymal stem cells can differentiate into the various stromal cell lineages that aid the repair
of musculoskeletal tissues; osteoblasts, chondrocytes, and tenocytes/fibroblasts that are essential
for the production of extracellular matrix of the tendon-bone junction. This is where blood
supply plays a crucial role in meeting the metabolic demands of these active cells. As previously
mentioned, the fact that autologous transplantation of mesenchymal stem cells alone did not
yield superior healing 63
is possibly due to the discrepancy between nutrient supply and
metabolic demand at the repair site. With the presence of endothelial progenitor cells, the
vascularized tendon-bone interface would possibly support the high metabolic requirement of
active cells at the repair site.
While the mononuclear cell population has already been employed in clinical studies, endothelial
progenitor cells constitute only a small fraction of the population 46
. Given the results of this
study, it would reasonable to investigate an endothelial progenitor cell-enriched as well as
mesenchymal stem cell-enriched mononuclear population in rotator cuff tendon healing after
surgery.
5.2.3 Clinical Application
Moving forward, a dose-response relationship between the quantity of endothelial progenitor
cells and the healing/angiogenic response needs to be established. The study was done in an
animal model in which the rats received one million endothelial progenitor cells for their
treatment. Whether the positive effect can be seen in a much larger scale in that of a human
rotator cuff is still unknown. A recent study of mesenchymal stem cell therapy in human rotator
126
cuff repair has shown successful healing with an average of 51 000 cells given to each patient 212
compared to the one million mesenchymal stem cells given in previous studies. Various amounts
of endothelial progenitor cells need to be transplanted to determine a curve that will indicate the
appropriate dose of endothelial progenitor cells to administer to the patients.
The cells are rare and their phenotype alters during in vitro expansion, and thus finding the
optimal number cells for transplantation requires ensuring the quality of the cells as well as the
quantity. Accordingly, it is crucial to standardize and optimize methods to rapidly and efficiently
acquire sufficient endothelial progenitor cells from the bone marrow with or without in vitro
culturing for use during the surgery. Maintaining early endothelial progenitor cell phenotypes
may be key to higher levels of angiogenic secretions. In addition, investigations of multiple
deliveries over the span of the recovery period could further determine the best treatment regime.
While the first dose of endothelial progenitor cells could be given during the surgery, subsequent
doses would have to be administered via local injection or intravenous delivery. Accordingly, the
method of cell delivery is also a topic that requires further investigation.
Most importantly, not all rotator cuff injuries should be treated the same. Identifying the patients
who would be most likely to benefit from endothelial progenitor cell transplantation during
rotator cuff repair is paramount. Older populations suffering from tendon degeneration are more
likely to benefit from the addition of endothelial progenitor cells than the young, athletic
population with traumatic rotator cuff injury. Comparisons of healing potential between aged rat,
diabetic rats, and young mature rats will confirm the possible different responses to endothelial
progenitor cell therapy.
The use of endothelial progenitor cells in surgical settings to aid the healing of rotator cuff
tendon is feasible as the cell population can be extracted from autologous sources: the bone
127
marrow and the blood. Employing adult stem cell-like progenitor cells for rotator cuff surgeries
bypasses the many ethical issues and technical issues that surround the use of embryonic stem
cells and induced pluripotent stem cells. Nonetheless, the cost-efficiency of such procedure
would need to be addressed.
128
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Appendix A
Flow cytometry analysis for CD 31, CD 34, CD 133, and Flk-1
Forward Scatter – Area
Forw
ard
Sca
tter
–H
eigh
t
Forward Scatter – Area
CD 133CD 34
Flk-
1
Sid
e Sc
atte
r –
Are
aSi
de
Scat
ter –
Are
a
The first gate selected cells from the total events registered by the flow cytometer (top left). The
second gate limited the analysis to single cells only (top right). Using unstained cells as well as
fluorescence minus one (FMO) samples, we determined the threshold for CD 34 positivity to be
at 103 (bottom left). Cells with a fluorescence of 10
3 or higher were considered CD 34 positive.
The analysis indicated 98.3 % of the single cells express CD 34. Then we gated for both CD 133
and Flk-1 at the same time (bottom right). Again, using unstained cells as well as FMO samples,
we determined the threshold for CD 34 positivity to about 103. The analysis indicated 96.8 % of
the CD 34 expressing cells express both CD 133 and Flk-1. In other words, approximately 95 %
of the single cells express all three markers.
147
CD 31 is a mature endothelial marker. In this study, CD 31 was
used to evaluate endothelial commitment of the endothelial
progenitor cells.
The unstained endothelial progenitor cell population exhibited
some level of auto-fluorescence (top picture). The gating
showed that approximately 60 % (after accounting for auto-
fluorescence) of the endothelial progenitor cells were positive
for CD 31 (middle picture). While the shift in fluorescence was
small, the detection of CD 31 with the antibody was sensitive as
indicated by overlapping the unstained cell data with the stained
(bottom picture).
Flow cytometry showed that most cells possessed the
endothelial progenitor cell markers CD 34, CD 133, and Flk-1,
but only some expressed the endothelial marker C 31. This
indicates that the cell population exhibited stronger
stem/progenitor cell characteristics than the terminally
differentiated endothelial cells.
148
Appendix B
Bonferroni’s Multiple Comparison Test
Ultimate Force
Fibrin Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -1.341 No > 0.9999
Week 2 vs. Week 6 -9.761 Yes 0.0003
Week 4 vs. Week 6 -8.42 Yes < 0.0001
EPC Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -2.44 No 0.6187
Week 2 vs. Week 6 -15.5 Yes < 0.0001
Week 4 vs. Week 6 -13.06 Yes < 0.0001
Stiffness
Fibrin Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -1.397 No > 0.9999
Week 2 vs. Week 6 -6.395 Yes 0.0133
Week 4 vs. Week 6 -4.998 Yes 0.0103
EPC Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -0.453 No > 0.9999
Week 2 vs. Week 6 -4.67 Yes 0.0161
Week 4 vs. Week 6 -4.217 Yes 0.0039
149
Cross Sectional Area
Fibrin Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 1.612 Yes 0.0008
Week 2 vs. Week 6 0.9835 Yes 0.0429
Week 4 vs. Week 6 -0.628 No 0.1046
EPC Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 1.346 No 0.0569
Week 2 vs. Week 6 1.158 No 0.1206
Week 4 vs. Week 6 -0.188 No > 0.9999
Ultimate Stress
Fibrin Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -0.5802 No 0.233
Week 2 vs. Week 6 -1.62 Yes 0.0001
Week 4 vs. Week 6 -1.04 Yes 0.0008
EPC Group Mean Diff. Significant? Adjusted P Value
Week 2 vs. Week 4 -0.6939 Yes 0.0322
Week 2 vs. Week 6 -2.638 Yes < 0.0001
Week 4 vs. Week 6 -1.944 Yes < 0.0001