The Role of Vacuolar Type H + -ATPase (V-ATPase) in Hair Cell Development A Thesis Project Submitted in Partial Fulfillment of the Requirements of the Renée Crown University Honors Program at Syracuse University Victoria-Marie Berlandi-Short Candidate for B.S. in Nutrition Science Candidate for B.S. in Neuroscience and Renée Crown University Honors May 2020 Honors Thesis Project in Developmental Biology and Neuroscience Thesis Project Advisor: _________________________ Thesis Project Reader: _________________________ Honors Director: __________________________
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The Role of Vacuolar Type H+-ATPase (V-ATPase) in Hair Cell Development
A Thesis Project Submitted in Partial Fulfillment of the Requirements of the Renée Crown University Honors Program at
Syracuse University
Victoria-Marie Berlandi-Short Candidate for B.S. in Nutrition Science
Candidate for B.S. in Neuroscience and Renée Crown University Honors
May 2020
Honors Thesis Project in Developmental Biology and Neuroscience
Thesis Project Advisor: _________________________
Thesis Project Reader: _________________________
Honors Director: __________________________
Date: April 24, 2020
RUNNING HEAD: The role of V-ATPase in Hair Cell Development
The Role of V-ATPase in Hair Cell Development 2
The Role of Vacuolar Type H+-ATPase
(V-ATPase) in Hair Cell Development
Victoria Berlandi-Short
Syracuse University
The Role of V-ATPase in Hair Cell Development 3
Abstract
The vacuolar type H+-ATPase (V-ATPase) is a membrane-bound proton (H+) pump that exists in several isoforms, allowing it to perform many critical cellular processes such as acidifying intracellular domains, receptor-mediated endocytosis, vesicle trafficking, protein degradation, prohormone processing, sperm maturation, small molecule uptake (e.g. neurotransmitters), and many others (Jefferies et al., 2008; Toei et al., 2010). Current literature suggests that V-ATPase activity is important in pH regulation of certain organelles, but functions of V-ATPase during embryonic development are poorly understood. Interestingly, patients with mutations in V-ATPase have been reported to develop sensorineural deafness among other related phenotypes (Colacurcio et al., 2016). To investigate potential underlying mechanisms for this phenotype, we have started characterizing the effects of V-ATPase loss via genetic knockout on the hair cells within two zebrafish auditory regions, the inner ear macula and lateral line neuromast. We have observed a significant reduction of hair cells in the neuromast of mutant embryos, but this relationship is not as pronounced in the inner ear macula. We have also found significant reductions in the amount and length of hair bundles in the mutant lines (featuring V-ATPase loss) in both the inner ear macula and neuromast. Furthermore, we tested the presence of mitotic support cells and found that there was also no statistical significance between actively dividing support cells and V-ATPase presence in the wild type and mutant lines at both the inner ear macula and neuromast.
The purpose of these experiments was to study the role of V-ATPase in both the inner ear macula and lateral line neuromast hair cells, then observe differences in hair cell development between these two regions of zebrafish morphology. The results of these experiments suggest that V-ATPase inhibition may have more influence over the survival of the neuromast hair cells, and hair bundles of both the neuromast and inner ear macula. though it may not influence other structures, such as support cells, to the same magnitude. The results presented here alongside the clinical significance of hair cell damage from V-ATPase inhibition suggest that there is much about V-ATPase functionality and hair cell development that needs to be investigated, though a negative correlation between V-ATPase, hair cell survival, and mechanotransduction is plausible.
This cell and developmental biology thesis project explored the relationship between a
well-known, proton-dependent and pH regulating transmembrane protein, known as V-ATPase,
and its influence on the development, proliferation, and survival of a specific cell type, the
auditory hair cell. The hair cells we studied were in two locations across the zebrafish- the
organism used to perform our experiments- the inner ear macula (IE) and lateral line neuromast
(NM). Researching the effects of V-ATPase loss in the same cell type, but in different locations,
allowed us to make further comparisons between development, proliferation, and survival
between the wild type (with V-ATPase) and mutant (V-ATPase loss) groups.
Clinically, patients with mutations, or adverse genetic alterations to the DNA, of the V-
ATPase protein within inner ear hair cell membranes exhibit sensorineural hearing loss. As of
2014, hearing loss was the most common sensory deficit in humans (Stawicki et al., 2014). Since
hair cells are the beginning of the pathway in the auditory system in which sound is converted to
a neural signal, loss of functional hair cells would prevent the auditory stimulus from being sent
to the nerve. The clinical presentation of this mutation provides significance and reason to study
this protein; the more we understand about its functionality, the more likely we are to someday
be able to treat those with this specific type of hearing loss more effectively.
Furthermore, V-ATPase is a very common protein across complex organisms, such as
humans, mammals, amphibians, and reptiles, and is seen in the structure of insects, plants, and
fungi (Finbow et al., 1997). While it is found in multiple areas of the same cell in an organism, it
can also be present across different cell types of that same organism. For example, in humans V-
ATPase is found in the IE as mentioned, but also lies in kidney tubules, osteoclasts (bone cells
responsible for breaking down and releasing calcium, phosphate, and vitamin D from bone), and
the male reproductive tract for sperm maturation (Toei et al., 2010). Mutations in various
The Role of V-ATPase in Hair Cell Development 5
subunits of V-ATPase lead to renal tubular acidosis (Chen et al., 2020), osteopetrosis (a rare
condition in which bones harden, making them more prone to fracture), depression, (Duan et al.,
2018) and even in processes such as tumor metastasis, among a plethora of others (Toie et al.,
2010).
To provide further clarification on hair cell anatomy, it should be noted that there are
several structures included within the hair cell that are relevant for discussion. First, hair cells
develop in bundles, and are observed in this fashion in both the inner ear and neuromasts.
Second, each hair cell contains up to 100 projections extending from the top, or apical, side of
the cell; these are known as stereocilia, (Bear et al., 2007; Gillespie et al., 2005), and are grouped
in hair cell bundles. Third, there is one additional projection at the end of the stereocilia stalk,
called the kinocilium. It is longer than the stereocilia, and during sound conduction, all
stereocilia bend towards this kinocilium in response to the auditory stimulus in order to send the
sound signal to the brain (Bear et al., 2007; Gillespie et al., 2005). Lastly, there are supporting
cells that surround the hair cell bundles, and research has shown that they develop into hair cells
and can also replace hair cells in the case of damage and/or death (Thomas et al., 2014).
In this thesis three experiments to characterize the development, proliferation, and
survival of hair cells, containing V-ATPase, in the inner ear macula and lateral line neuromast
are presented. All three experiments provide two comparisons: the first investigates hair cell
survival and proliferation of the IE and NM between the wild type (WT) and mutants (v1f). The
second compares the development of WT and v1f hair cells by calculating the amount and length
of hair bundles that protrude from the hair cells. The third experiment examines a route of cell
differentiation by studying the amount of mitotic, or dividing support cells between the WT and
v1f of both regions.
The Role of V-ATPase in Hair Cell Development 6
Overall, the results suggested that V-ATPase has a much greater role in hair cell survival
in the NM than in the IE. Also, it appears to significantly affect hair bundle amount and length;
the mutants show reductions in both of these characteristics at both regions. V-ATPase was
shown to not be influential in the mitotic activity of support cells, suggesting that its effect on
cell differentiation is minimal. To test for proliferation, more experiments are necessary at earlier
times in embryonic development. Most importantly however, the more that we know about V-
ATPase and its functionality across multiple cell and tissue types, the more effectively we can
provide treatment for clinical presentations of its damage in a patient.
Table of ContentsAbstract…………………………………………………………………………………...3Executive Summary……………………………………………………………………...4Acknowledgments………………………………………………………………………...8
The Role of V-ATPase in Hair Cell Development 7
Introduction……………………………………………………………………...……….10Methods and Materials…………………...……………………………………………...19Results…………………………………………………………………………………….24 Discussion………………………………………………………………………………...32Conclusion………………………………………………………………………………..35List of Abbreviations………………………………………………………………….....36Appendix………………………………………………………………………………….37References………………………………………………………………………………...38
Acknowledgements
The Role of V-ATPase in Hair Cell Development 8
I would like to give a huge thanks to the Principal Investigator of the lab I studied in, Dr.
Jeffrey Amack, and to PhD candidate, my mentor, Peu Santra. Your constant encouragement and
willingness to answer questions and spur critical thinking for the preparation of these
experiments developed me so much as a student and as a researcher. There is something purely
special about being in an academic environment in which all you can do is learn every day and
find the challenge consistently humbling. Working in a lab taught me a great deal of what
methodic, benchwork science is really like, and a lot about life that I would not learn anywhere
else. My appreciation for that is endless.
Thank you to Alexis Whellan and Justin Cox for showing me the way around the lab,
teaching me valuable protocols, several times over. I wish you both the most exciting and well-
rounded careers out there.
Thank you to Dr. Robin Jones, who introduced me to neuroscience several years ago and
through her classes, reminded me of my potential and competence in the field. Thank you for the
real and true dialogue, and for taking on the arduous task of being my thesis reader amidst your
hectic schedule. Knowing that your door is always open, and that you are always in my corner
means the most.
Lastly, thank you to Dr. Margaret Voss, I genuinely believe that I would not be in this
position if it were not for you. Your passion for the sciences is radiant and authentic; it has
helped me persevere regardless of the discipline I am studying. I find myself actively seeking
knowledge purely for curiosity over any other reason that’s often found in academia. My
ambition to learn for the sake of learning is wholly inspired by you. As a senior, I am ecstatic
knowing that I am graduating with two degrees from Syracuse University, and that is in no small
part due to your encouragement and faith in me over the past three years. My professional and
The Role of V-ATPase in Hair Cell Development 9
personal goal to be as well-rounded, literate, and grounded as possible is because of you. Thank
you, truly, for everything.
I would be remiss if I did not mention the pivotal contributions to this thesis from my
mentor, Peu, whom I worked closely over the past year and a half to collect and analyze data for
this project. She assisted with immunostaining, confocal microscopy, image analysis, statistics
and analyses. Thank you for introducing me to the start of my professional career.
Introduction
The Role of V-ATPase in Hair Cell Development 10
V-ATPase
V-ATPase (Figure 1) is an enzyme complex divided into two regions: V0 on the
extracellular or luminal side of the membrane, and V1 on the cytoplasmic side (Jefferies et al.,
2008). V1 comprises a minimum of eight subunits: A through H (Jefferies et al., 2008; Horng et
al., 2007) while V0 has six subunits responsible for proton translocation (Toei et al., 2010). When
the V1 region hydrolyzes ATP (adenosine triphosphate) into ADP (adenosine diphosphate) and Pi
(inorganic phosphate), a structural change in the A subunit occurs that propels rotation of the
central stalk. Upon this rotation, cytoplasmic H+ are translocated into the lumens of organelles,
or into the extracellular space in the case of plasma membrane V-ATPases (Horng et al., 2007).
The resulting pH of V-ATPase-containing organelles or the extracellular space decreases, thus
increasing acidity.
Figure 1. V-ATPase and subunits. The superior portion, or V1 is cytoplasmic, while the inferior portion, V0 is extracellular. (Bing.com, 2019).
Prior literature has shown that V-ATPase pumps are pivotal for maintaining intracellular
and intra-organellar pH in a plethora of systems across eukaryotes (Lin et al., 2019; Stawicki et
The Role of V-ATPase in Hair Cell Development 11
al., 2014). V-ATPase pumps are found within the membranes of organelles such as vacuoles,
lysosomes, and vesicles budding from the Golgi apparatus (Horng et al., 2007). Though
ubiquitous across differentiated cell types, the specific concentration of V-ATPases within
organelles, cell and tissue types depends on the necessity of pH regulation for that region (Duan
et al., 2018). Their role in pH regulation is associated with that cells’ individual survival and
ability to operate normally. Any deviation in the structure, and thus function of V-ATPase will
likely result in impaired pH regulation of the organelle or cell it is embedded in. This will result
in a major impairment of a multitude of pH-dependent processes occurring in that space. At the
organismal level, such loss of V-ATPase functionality affects tissues and the corresponding
organ, thus altering the overall quality of life and the ability of the organism to survive.
Mechanotransduction and the Inner Ear
V-ATPase, in regard to both the mammalian and fish auditory systems, is associated with
mechanotransduction. At its foundation, this is the process by which external auditory stimuli,
including gravity and head orientation (Kawashima et al., 2011; Paluch et al., 2015), are
mechanically propagated to the inner ear, where it is then converted to an electrochemical signal
and transmitted to the brain via afferent neurons for perception and response (Iskratsch et al.,
2014; Olt et al., 2016). While this definition includes both the auditory and vestibular systems,
the focus of the research presented here is on the auditory system.
In humans, all stimuli are funneled into the ear via the external auditory meatus, through
the air-filled auditory canal, and reverberate off the tympanic membrane of the middle ear
(Ballachanda et al., 2013; Bear et al., 2007). Vibrations from the tympanic membrane move
The Role of V-ATPase in Hair Cell Development 12
through the three auditory ossicles of the middle ear: the malleus, incus, and stapes (Figure 2).
While all three ossicles participate in amplifying the external signal as it moves towards the inner
ear, the stapes specifically contains a piston-like apparatus that vibrates against the membrane of
the oval window, at which point the vibrations reach the inner ear (Bear et al., 2007; Bekesy
2017).
Figure 2: A view of the external and middle ear regions in the pathway of auditory mechanotransduction (Jones, 2017).
The fluid-filled, cochlea and the labyrinth comprise the inner ear; the former serves its
role predominantly in audition while the latter participates in the vestibular system, to maintain
equilibrium. The oval window resides at the base of the cochlea, and the round window is just
inferior. Within the cochlea are three chambers: the scala vestibuli, scala media, and scala
tympani, from superior to inferior (Figure 3a). Two membranes separate the regions: the
superior Reissner’s membrane and the inferior basilar membrane. Fluid waves advance through
the spiraled cochlea until they reach the apex of the basilar membrane, upon which rests the
Organ of Corti. The two fluids in this region include perilymph, an ionic fluid with low [K+]
(potassium) and high [Na+] (sodium; within the scala vestibuli and scala tympani), and
The Role of V-ATPase in Hair Cell Development 13
endolymph, with opposing high [K+] and low [Na+] (within the scala media). Due to active
transport, conductance, and concentration gradients in the scala media endothelium, an
endolymph electrical potential, or endocochlear potential, results that is about 80mV greater than
the potential of the perilymph fluid (Figure 4). Once vibrations reach the basilar membrane, the
mechanical stimuli shift to an electrochemical, or neural signal (Bear et al., 2007).
Figure 3 (left). a) cross-sectional diagram of human cochlea. b) cross-sectional diagram of Organ of Corti. (Pearson Education, 2004).
Figure 4 (right). Cross-sectional diagram of cochlea, featuring endolymph and perilymph electrical potentials (Treuting et al., 2018).
The aforementioned Organ of Corti consists of hair cell bundles, rods of Corti, and
supporting cells surrounding each hair cell bundle. Hair cells are the beginning of the neural
segment of mechanotransduction of sound in the inner ear, and have an estimate of 100
projections out of the apical surface, called stereocilia, which are made primarily of actin. (Bear
et al., 2007; Gillespie et al., 2005). There are two types of cochlear hair cells: inner and outer
hair cells (Figure 3b). The inner hair cells are afferent, or sensory, and send the signal to the
brain, while the outer hair cells are efferent, or motor, and aid in the cochlea’s ability to receive
The Role of V-ATPase in Hair Cell Development 14
frequencies by contracting the tectorial membrane (Purves et al., 2001). The incoming fluid
waves reach the stereocilia of inner hair cells and, if strong enough, will deflect the stereocilia
towards the single longest projecting cilia, known as the kinocilium, which is microtubule based
(Gillespie et al., 2005). All cilia are connected by tip links at the very end of their projections
(Figure 5). These tip links are connected to TRPA1 (transient receptor potential A1) channels on
either side that will open in response to stereocilia deflecting from the fluid wave, and allow
endolymph K+ ions to flow into the stereocilia and travel down towards the hair cell (Corey et al.,
2004). If this depolarization reaches the membrane threshold, then voltage-gated calcium
channels open, mobilizing neurotransmitter-containing vesicles to migrate to the basal end of the
hair cell (Xiong 2018). This is known as an action potential, in which the signal is propagated via
neurotransmitter release at the basal end of the hair cells and synapses with spiral ganglion cells
below the basilar membrane (Figure 3b). These neurons converge and synapse with the auditory
nerve, (i.e. auditory-vestibular nerve or Cranial Nerve VIII) which sends the signal to the
medullary cochlear nuclei (Bear et al., 2007), for later sound processing, conscious perception,
and response. Thus, hair cells are pivotal in the process of audition.
The Role of V-ATPase in Hair Cell Development 15
Figure 5. Apical surface of one hair cell with protruding stereocilia and kinocilia. Tip links appear across the top of each cilium, and are attached to a mechanical TRPA1 channel, not pictured (Gillespie et al., 2005).
Zebrafish as a Model System to Study Hearing
There are a few anatomical differences between human and zebrafish auditory-vestibular
system. The zebrafish lacks the outer and middle ear structures, specifically the auditory ossicles
featured in humans, and instead has two otolith organs, a saccular and a utricular otolith, that are
attached to a posterior and anterior macula, respectively, on either side (Baxendale et al., 2014;
Pais-Roldán et al., 2016). The otoliths are made of calcium carbonate and other otolithic
proteins, and are prefaced by the Weberian ossicles that aid in funneling sound towards the
otoliths (Baxendale et al., 2014; Stooke-Vaughan, et al., 2015). Hair cells appear in bundles in
the macula of the zebrafish inner ear, as opposed to an Organ of Corti within the inner ear
cochlea observed in humans. These otolith organs serve vestibular functions in the zebrafish, and
are equivalent to human otoconia within the otolithic membrane. Lastly, the zebrafish otoliths
respond to acceleration and sound waves moving through water and synapse at the macula hair
cells. The process of depolarization then propagates to the zebrafish brain (Pais-Roldán et al.,
2016).
Neuromast and the Lateral Line
The lateral line is a facet of anatomy that is specific only to aquatic vertebrates and
amphibians (Thomas et al., 2014; Whitfield et al., 1996). Humans do not have a lateral line
system, but researching the effects of V-ATPase loss in this region allows further insight into the
The Role of V-ATPase in Hair Cell Development 16
overall qualities of both V-ATPase and hair cell development. Furthermore, other research has
suggested that there is an association between ideal pH and functionality of neuromast hair cells
(Lin et al., 2019), which also provides a basis to perform further experiments.
The lateral line (Figure 6) extends both anteriorly and posteriorly on the surfaces of the
zebrafish (Gompel et al., 2001), and is responsible for sensing changes in water flow and water
vibrations with a range of up to 300Hz (Thomas et al., 2014; Olt et al., 2016). Behaviorally, the
sensory information from the lateral line neuromasts influences the response of the organism- for
schooling, mating purposes, and prey and predator detection (Olt et al., 2016; Pujol-Martí et al.,
2013). Furthermore, the lateral line is somatotopically organized in the brain to allow complex
processing and timely responses to external stimuli (Pujol-Martí et al., 2013; Baxendale et al.,
2014). Very early in embryonic development, a cluster of cells known as the primordium
establishes multiple neuromasts along the lateral line (Thomas et al., 2014). Similar to the inner
ear, the hair cell bundles within each neuromast are also surrounded by support cells (Gompel et
al., 2014) and undergo mechanotransduction (Thomas et al., 2014). The apical ends of each hair
cell bundle face the water within an enclosed membrane known as the cupula (Stawicki et al.,
2014).
Research of this region from the past several years has suggested that hair cell bundles
within the neuromasts may have some ability to regenerate following damage, though this is
specific to the lateral line of aquatic and amphibians systems (Thomas et al., 2014).
The Role of V-ATPase in Hair Cell Development 17
Figure 6: Epifluorescence of neuromast locations.. Adapted from Whitfield et al., 1996, unpublished. (Zfin.org).
Experiment Overview
The goal of this project was to investigate the relationship between V-ATPase activity
and hair cell development. Previous results from our lab, particularly from Peu Santra, have
identified hair cell defects in neuromasts in V-ATPase mutant zebrafish. In atp6v1f mutants the
overall number of hair cells in the neuromasts is reduced. To determine whether this defect is
specific to hair cells in neuromasts or if it also includes the inner ear, I wanted to test the effect
of loss of V-ATPase function on hair cells in this region as well. In the first set of experiments, I
compared the number of inner ear hair cells in V-ATPase mutant and wild-type embryos.
Second, I measured the length of the stereocilia and quantified the amount of hair bundles in the
inner ear. Third, I tested the hypothesis that loss of V-ATPase activity alters cell proliferation by
utilizing the mitotic marker PH3B (phosphohistone 3B) to calculate the number of proliferating
cells.
The Role of V-ATPase in Hair Cell Development 18
Methods and Materials
Animal
All experiments were performed on Danio rerio, approved by the IACUC (Institutional
Animal Care and Use Committee). Adult fishes were raised in tanks supported by an automated
The Role of V-ATPase in Hair Cell Development 19
system that circulated UV treated water throughout the system. All the experiments utilized
embryos of 4 dpf unless stated otherwise.
Zebrafish, Danio rerio, are a well-known model organism used in developmental biology
research. They have a short breeding time, are externally fertilized, and develop rapidly (Pais-
Roldán et al., 2016), which tends to decrease the overall length of experiments. Their embryos
are transparent, making them very easy to observe in the first few day’s post-fertilization, which
is the timeline for all experiments conducted. Furthermore, they are easy to impose genetic and
chemical alterations on (Baxendale et al., 2014), allowing for a wide range of potential
experiments.
While mammalian systems contain bones that encapsulate the inner ear, making it more
difficult to study, zebrafish hair cell bundles do not have the same difficulty at either the inner
ear or neuromast regions; thus, they are relatively more accessible. In the first few day’s post-
fertilization, ossicles have not developed to obstruct any view or protocol (Olt et al., 2016;
Baxendale et al., 2014).
Lastly, since hair cell structure and many of the genes influencing otic development and
hearing loss diseases are highly conserved between the two species, it is acceptable to use
zebrafish for these experiments since the results pertaining to the inner ear macula will be
generalizable to the theoretical results of the same experiments in humans (Baxendale et al.,
2014).
Genetic Knockout of V-ATPase
To create a comparison of hair cell development with and without functioning V-ATPase,
a genetic knockout was employed to characterize the effects. We used a zebrafish strain known
The Role of V-ATPase in Hair Cell Development 20
as atp6v1f, which denoted a mutation in the F subunit of the V1 region of V-ATPase, rendering
the entire pump dysfunctional. We crossed this line with the WT strain to yield our two testing
groups: homozygous WT and homozygous atp6v1f. At about 36hpf (hours post-fertilization),
hypopigmentation is visible to denote the mutants, as this is a marked defect also resulting from
V-ATPase inhibition (Duan et al., 2018). Since the v1f mutation is lethal, these embryos do not
survive past 5dpf (days post-fertilization).
Procedure
All offspring were raised in embryo water and incubated at 29.5 . Once the target ℃
incubation time for inner ear and neuromast development was reached (either 2dpf or 4dpf),
embryos were sorted into Eppendorf tubes depending on their genotype: WT or v1f. Following
this step, embryo water was removed and replaced with PFA1 (paraformaldehyde) to begin the
immunohistochemistry protocol (see next section).
For the first two experiments discussed, WT and v1f embryos were raised to 4dpf without
any further intervention. They were fixed with PFA and imaged following IHC. The third
experiment was the only one with embryos fixed at 2dpf, to provide a comparison between 2dpf
and 4dpf.
Once IHC for experiments was completed, embryos were imaged with a spinning disk
microscope and analyzed using the computer software Fiji to quantify cell types and/or measure
cilia length.
Immunohistochemistry Protocol
The Role of V-ATPase in Hair Cell Development 21
Immunohistochemistry, or IHC, is a very common application that allows researchers to tag a
specific cell or tissue type to track its appearance, movement, and/or disappearance over stages
of an experiment. IHC encompasses the strategic use of mono or polyclonal antibodies to label a
desired antigen (Kaliyappan et al., 2012). The specific location of antibody binding is observed
visually through the use of an immunofluorescent tag, that is seen at a specific wavelength under
the proper microscope. The following is the standard IHC protocol used for these experiments:
Day 1
1. Fix embryos with 4% PFA containing 1% Tween20 in PBS
Day 2
1. Remove fix by washing the embryos in PBS containing 1% Tween20,
2. Permeabilization in Acetone @ 20 for 8 minutes. ℃
3. Wash embryos once with PBS-1% Tween20 for 15 minutes at room temperature (RT).
4. Block with 10% BSA (bovine serum albumin) in 1X PBS at RT for an hour, ~200uL.
5. Add primary antibody/ies to the blocking solution at a 1:200uL ratio (10% BSA in 1X
PBS).
6. Incubate at 4 overnight. ℃
Day 3
1. Wash the embryos with PBS-1% Tween20, 8 times for 15 minutes each at RT.
2. Block with 10% BSA in 1X PBS for an hour at RT.
3. Add secondary antibody/ies and/or dyes, at a 1:200uL ratio.
4. Incubate at 4 overnight. ℃
Day 4
1. Wash the embryos with PBS-1% Tween20, 8 times for 15 minutes each at RT.
The Role of V-ATPase in Hair Cell Development 22
2. Image with spinning disk microscope, operating with three wavelengths for red, green,
and blue.
Antibodies and Dyes
Primary antibodies used:
1. Mouse anti acetylated tubulin (Sigma Aldrich-T7451) - 1:2002. Rabbit anti phosphohistone H3 (Cell signaling technology-9701) - 1:200
Secondary antibodies used:
1. Goat anti rabbit alexa fluor 488 (Abcam-ab150077) - 1:2002. Goat anti mouse alexa fluor 569 (ThermoFisher scientific-A11004) - 1:200
In the first two experiments, phalloidin was used specifically to stain F-actin based
stereocilia, while acetylated tubulin was used to bind to microtubule based kinocilia. In the third
experiment, acetylated tubulin and PH3B were used as primaries; acetylated tubulin was used to
tag microtubule-based structures and PH3B was used to label support cells that were actively
dividing at that stage in development, also known as mitotic.
Secondary antibodies used included Goat anti rabbit alexa fluor 488 and Goat anti mouse
alexa fluor 569 for all experiments. DAPI, a nuclear dye, was also added here to provide a view
of nuclei in both regions.
The Role of V-ATPase in Hair Cell Development 23
Imaging and Analysis
The embryos were mounted on 2% melting point agarose in a mattek dish and imaged
with 40X water objective using a Perkin Elmer Spinning disk confocal microscope. All images
were analyzed using Fiji/ImageJ. Statistical analyses were done and graphs were prepared using
Graphpad Prism. All experiments were tested for statistical significance using Student’s T-test
with Welch’s corrections, except experiment-3;fig.12 where we used One way ANOVA
Results
Experiment 1
In the first set of experiments, I tested the amount of hair cells in the neuromast and inner
ear, between WT and v1f lines. Since V-ATPase in the v1f lines is not functional, we expected
there to be a significant difference in HC quantity between the WT and v1f lines at both the IE
The Role of V-ATPase in Hair Cell Development 24
and NM regions; the v1f embryos would have fewer HCs than the WT. A decrease in HC
quantity would most likely poorly affect mechanotransduction, as there would be fewer cells to
receive the stimulus and convert it to a neuronal signal.
The results suggested that there was a significant difference in the NM, and the v1f line
had a lesser amount of HCs. Figure 7 shows a comparison of neuromast hair cells of WT (top
row) and v1f (bottom row). Using acetylated tubulin to stain for kinocilia, a notable difference is
observed between the WT and v1f (left column) kinocilia surrounding the center of the NM. The
center column also shows more HC nuclei between WT and v1f. Figure 8A quantitatively shows
a significant increase in pyknotic nuclei (PN) in the v1f line and Figure 8B shows a significant
decrease in HCs in the v1f line.
Using phalloidin and DAPI to stain the hair bundles and HC nuclei respectively, Figure 9
shows the images of hair bundle (left column) and hair cell nuclei (center column) between WT
and v1f. From the images, no significant qualitative data can be obtained to suggest differences
between the groups. Figure 10 also used PN as a potential marker for HC death; there was no
significant difference in the amount of PN between either group after 4dpf.
Overall, the results show that in the NM, significantly fewer HCs are surviving in the v1f
embryos than in the WT after 4dpf. PN data suggests that HCs appear to be developing in the
NM, but are dying more frequently in the mutants than in the WT. A rationale for this may be
that V-ATPase inhibition occurs at 4dpf in the mutants, leading to this outcome. PN data for the
IE was not significant, proposing that V-ATPase loss in HCs has a greater effect in the NM than
it does in the IE; it may not be highly important in this region for HC survival.
The Role of V-ATPase in Hair Cell Development 25
Figure 7. Images of neuromast acetylated-tubulin as a marker of hair cells. (Left column) Acetylated tubulin binding to kinocilia around the NM. (Center column) DAPI staining to HC nuclei of NM. (Right column) Combined image of left and center. Acetylated tubulin (pink) and DAPI (blue).
A B
The Role of V-ATPase in Hair Cell Development 26
Figure 8. (A) Results of pyknotic nuclei (PN) as a potential marker of hair cell death in the neuromast. The v1f line shows a significant increase in PN after 3 experiments. (B) Results show that the WT had significantly more HCs in the NM region than the mutant after 3 experiments. 4dpf.
Figure 9. (Left column) Images of hair bundles (white) via phalloidin staining of the IE in WT (top) and v1f (bottom). (Center column) Images of IE HC nuclei following DAPI staining. (Right column) Combined image of phalloidin stained hair bundles (pink) and DAPI stained HC nuclei (blue). 4dpf.
The Role of V-ATPase in Hair Cell Development 27
Figure 10. A measure of pyknotic nuclei in the IE after 2 experiments. There was no significant difference in PN proliferation between WT and v1f after 4dpf.
Experiment 2
In the second set of experiments I quantified both the amount and length of hair bundles
(i.e. stereocilia) in the IE. As mentioned, each hair cell has about 100 stereocilia protruding from
the apical side, denoted as a hair bundle. Thus, each hair bundle suggests one hair cell below it,
and becomes another marker to quantify HCs in the WT and v1f lines. The hypothesis was that
there would be a decreased amount of hair bundles in the mutant embryos as well as decreased
length, due to V-ATPase knockout. Both of these outcomes may adversely affect
mechanotransduction, and potentially result in the altered phenotype observed clinically.
Phalloidin and DAPI staining were used in Figure 11 to qualitatively depict the amount
of hair bundles (left column) and HC nuclei (center column), respectively. The images suggest
that there are more hair bundles and HC nuclei in the WT than in the v1f. Figure 12 confirms
The Role of V-ATPase in Hair Cell Development 28
these qualitative results; after quantitative analysis there were significantly fewer (Figure 12B)
and shorter (Figure 12A) hair bundles in v1f after 4dpf.
These results show that V-ATPase plays a specific role in the development and survival
of hair bundles in the IE through 4dpf. For the mutant groups, there were a significantly fewer
number of hair cell bundles at 4dpf, allowing us to accept our hypothesis that V-ATPase is
necessary for stereocilia proliferation and development in the IE. This corroborates with existing
data that V-ATPase is needed for mechanotransduction, chiefly because it influences the
integrity of stereocilia during embryonic development.
Figure 11. ((Left column) Phalloidin staining stereocilia, to denote hair bundles(white) across the apical surface of HCs in the WT (top) and v1f (bottom) in IE.. (Center column) DAPI staining to show HC nuclei (white) in IE. (Right column) Merged image of hair bundles (pink) and hair cell nuclei (white). 4dpf,
The Role of V-ATPase in Hair Cell Development 29
Figure 12. Difference in amount of hair bundles and length of hair bundles in IE at 4dpf. A) A significant decrease in IE hair bundle length was observed in the mutant line after three experiments. B) A significant decrease in the amount of IE hair bundles was observed in the mutant line after 3 experiments. 4dpf.
Experiment 3
In this set of experiments, we used phosphohistone 3B (PH3B) to act as a marker for
mitotic (dividing) support cells in both the IE and NM at 2dpf and 4dpf. This experiment allowed
us to see if the amount of support cells in the IE and NM regions was influencing HC growth and
development. As mentioned earlier, support cells surround hair cell bundles and aid in their
development and regeneration. Support cells can mature into hair cells, for example, if the pre-
existing hair cells were damaged and needed to be replaced (Gompel et al., 2014). Thus, if they
were actively dividing during the time periods observed (2dpf and 4dpf), we can surmise that
there may have been an increased need for support cells, and potentially HCs at those times. This
would suggest that there was a loss of HCs with regards to V-ATPase inhibition in the mutant
embryos.That is, HCs developed, but died and needed to be replaced.
The Role of V-ATPase in Hair Cell Development 30
Figure 13 depicts the qualitative differences in the WT embryos at the IE and NM. In the
third column, PH3B was used to highlight mitotic cells; the results were such that only one
PH3B+ cell (grey) is seen in an IE WT embryo, and none were seen in a NM WT embryo.
Figure 14 depicts these differences in the v1f embryos at the IE and NM. In the third
panel, no PH3B+ cells were observed for these embryos.
Quantitative data from both the IE and NM (Figure 15) showed that the results were not
significant for either cell line. Overall, this experiment showed that V-ATPase loss on HCs does
not have any effect appreciable on support cell proliferation and differentiation.
Figure 13: (Far left) acetylated tubulin staining (grey) on any microtubule based cell types within WT embryos of IE (top) and NM (bottom). (Center left) DAPI staining to denote HC nuclei (grey) in WT of IE (top) and NM (bottom). (Center right) PH3B+ cells in either region. One was observed in the IE (grey), and none in the NM. (Far right) Merged image of all three panels; microtubule-based cells (pink), HC nuclei (blue), and PH3B+ cells (green).
The Role of V-ATPase in Hair Cell Development 31
Figure 14: (Far left) acetylated tubulin staining (grey) on any microtubule based cell types within WT embryos of IE (top) and NM (bottom). (Center left) DAPI staining to denote HC nuclei (grey) in WT of IE (top) and NM (bottom). (Center right) PH3B+ cells in either region. None were observed in the mutant lines in either region. (Far right) Merged image of all three panels; microtubule-based cells (pink), HC nuclei (blue), and PH3B+ cells (green).
Figure 15: Graphical analysis of PH3B+ cells in the NM (left) and IE (right). No statistical significance was observed for any group; n=1.
The Role of V-ATPase in Hair Cell Development 32
Discussion
Experiment 1
One major limitation of this experiment was that we were unable to obtain the HC
quantification for the IE. A next step would be to complete this analysis to fully establish the
results of this set of experiments. It is likely that the HCs in the IE will mimic the behavior of the
HCs in the NM since the prevalence of PN was not significantly increased in the mutant IE
embryos. If the results were the same as the NM, then V-ATPase presence is likely vital to HC
survival in the IE, suggesting that the morphology of both regions is similar and conserved. If the
results are the opposite, then it is possible that another variable is present in the IE at this time
period to protect the HCs from death, even without V-ATPase functionality.
To test for the effects of V-ATPase on HC proliferation, specifically to see if HCs had
developed at earlier stages, or at all, this same experiment should be conducted at earlier times
(i.e. 36hpf, 2dpf, and 3dpf). This would provide insight on the importance of V-ATPase before
4dpf.
Experiment 2
This experiment does not provide NM data unfortunately, and this is due to the anatomy
of the NM and analysis. During microscopy, the NM is viewed top down, while the IE is viewed
sagittally. A sagittal view allows us to observe all hair bundles and measure, but a top down view
at the NM makes this impossible. The next step with this experiment would be to apply other
methods of analysis that will allow an accurate view of NM stereocilia. This would provide
further insight on how conserved the V-ATPase physiology is between the two regions.
The Role of V-ATPase in Hair Cell Development 33
Experiment 3
Due to time constraints, the data here was only following one trial. To establish validity
of these results, they should be repeated. If there is still no significant relationship, then it can be
confidently deduced that V-ATPase loss has no effect on support cell proliferation and
differentiation. However, if V-ATPase loss significantly reduces HC proliferation, as seen in the
first set of experiments, then there should be a likely mechanism that signals the support cells to
increase their mitotic activity to replace the lost HCs. If this experiment continues to show no
relationship, then it is possible that another variable is present, preventing any communication
between HC death and support cell activity. A potential experiment could be to apply a
pharmacological drug that increases the amount of support cell mitotic activity and see if this
drug rescues the support cell mitotic activity in mutants.
This experiment could also be performed slightly earlier than 4dpf to see if V-ATPase
loss affects support cell mitotic activity during the initial development of HCs (At 3dpf, or
3.5dpf, for example). If this is true, then it would corroborate with the NM results from the first
set of experiments, and suggest that V-ATPase is affecting support cell activity at an earlier time;
another variable may be involved at 4dpf that is leading to the results presented here.
General Limitations
There are a few other limitations to address while acknowledging these results. The first
is that structurally, humans lack the lateral line system that aquatic vertebrate’s species entail.
Thus, the NM results are not directly generalizable to humans, but researching this area still
allows us further insight into overall V-ATPase functionality in the context of
mechanotransduction. Also, some results differed between the IE and NM, suggesting that
potentially another variable is present at one of these locations which is influencing our results.
The Role of V-ATPase in Hair Cell Development 34
Secondly, we had originally intended to provide results from several points in time: 2dpf,
3dpf, and 4dpf. This would allow us to confirm if hair cells, support cells, and/or ciliary groups
were developing initially and then died later due to V-ATPase loss, or if they had never appeared
at all during development. Due to time constraints and lost data, we were unable to provide this
comprehensive view.
Lastly, I had conducted a fourth, high-risk high-reward experiment solely on the NM hair
cells using pharmacological drugs, Neomycin and Concanamycin A (a known V-ATPase
inhibitor). Neomycin is an aminoglycoside that is commonly found in antibiotic creams to treat
infections, but has also caused loss of HCs (He et al., 2017), interestingly. Furthermore, previous
data from other experiments I completed showed that Concanamycin A had a beneficial effect on
HCs. I tested whether V-ATPase inhibition (from Concanamycin A) could protect hair cells from
damage imposed by Neomycin. Unfortunately, I was not able to obtain the results of this
experiment due to diminished lab access from unforeseen global circumstances. A next step
would be to analyze this data once lab access is allowed. If this experiment proved feasible in
zebrafish, and Concanamycin A did protect the HCs from damage, then repeating this work in
other animals may prove beneficial in working towards someday conducting tests clinically.
Conclusion
The Role of V-ATPase in Hair Cell Development 35
Our preliminary results suggest that genetic V-ATPase loss disrupts total hair cell bundle
proliferation in the NM, negatively affects total hair bundle length and quantity in the IE, and
does not significantly affect mitotic activity of the surrounding support cells in either region.
Altogether, we can support the hypothesis that V-ATPase is needed for the efficacy of
mechanotransduction in general, and it may specifically be the stereocilia and hair cells during
early embryonic development that are most reliant on V-ATPase presence for survival. V-
ATPase does not appear to greatly affect HC proliferation, as there are still HCs present in the
NM and IE at 4dpf, but experiments investigating earlier times are necessary to corroborate these
results. However, it does appear to affect stereocilia proliferation. Lastly, the results show that V-
ATPase does not greatly affect differentiation of HCs, leaving survival as the likely factor that
V-ATPase loss influences the most. Further experiments, including repetitions of some of the
ones included here, should be conducted to fully discern the relationship of V-ATPase on
survival. These data certainly contribute to our currently incomplete understanding of V-ATPase
functionality during zebrafish embryonic development and provide a foundation for further
research into the mechanisms of V-ATPase and chiefly, its role in HC survival.
List of Abbreviations
The Role of V-ATPase in Hair Cell Development 36
IE: Inner ear macula
NM: Lateral line neuromast
v1f: Mutant line
WT: Wild type
HC: Hair cell
Appendix
The Role of V-ATPase in Hair Cell Development 37
1PFA (paraformaldehyde) fix: 4% PFA in 1% PBST (500mL 16% PFA, 100ul of 10X Tween-
20) = 2mL PFA fix
References
The Role of V-ATPase in Hair Cell Development 38
Ballachanda, B. B., Miyamoto, R. T., Miyamoto, C., & Taylor, B. (2013). The human ear canal (2nd ed.). San Diego, CA: Plural Pub.
Baxendale, S., & Whitfield, T. T. (2014). Zebrafish inner ear development and function. () doi:10.1016/B978-0-12-408088-1.00003-8
Bear, M. F., Connors, B. W., & Paradiso, M. A. (2007). Neuroscience: Exploring the Brain (3rd ed.). Philadelphia, PA: Lippincott Williams & Wilkins.
Békésy, G. von. (2017). Sensory Inhibition. Princeton University Pres.
Békésy, G. V. (1974). Some Biophysical Experiments from Fifty Years Ago. Annual Review of Physiology, 36(1), 1–18. doi: 10.1146/annurev.ph.36.030174.000245
Chen, L., Wang, H.-L., Zhu, Y.-B., Jin, Z., Huang, J.-B., Lin, X.-F., … Fang, Z.-T. (2020). Screening and function discussion of a hereditary renal tubular acidosis family pathogenic gene. Cell Death & Disease, 11(3). doi: 10.1038/s41419-020-2354-y
Colacurcio, D. J., & Nixon, R. A. (2016, December). Disorders of lysosomal acidification-The emerging role of v-ATPase in aging and neurodegenerative disease. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112157/.
Corey, D., García-Añoveros, J., Holt, J., Kwan, K., Lin, S., Vollrath, M., Amalfitano, A., Cheung, E., Derfler, B., Duggan, A., Géléoc, G., Gray, P., Hoffman, M., Rehm, H., Tamasauskas, D. and Zhang, D., 2004. TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells. Nature, 432(7018), pp.723-730.
Duan, X., Yang, S., Zhang, L., & Yang, T. (2018). V-ATPases and osteoclasts: ambiguous future of V-ATPases inhibitors in osteoporosis. Theranostics, 8(19), 5379–5399. doi: 10.7150/thno.28391
Finbow, M. E., & Harrison, M. A. (1997). The vacuolar H -ATPase: a universal proton pump of eukaryotes. Biochemical Journal, 324(3), 697–712. doi: 10.1042/bj3240697
Geng, J., Zhao, Q., Zhang, T., & Xiao, B. (2017). In Touch With the Mechanosensitive Piezo Channels. Current Topics in Membranes Piezo Channels, 159–195. doi: 10.1016/bs.ctm.2016.11.006
Gillespie, Peter G., Dumont, Rachel A., Kachar, Bechara. “Have We Found the Tip Link, Transduction Channel, and Gating Spring of the Hair Cell?” Current Opinion in Neurobiology, vol. 15, no.4, 2005, pp. 389-396., doi:10.1016/j.conb.2005.06.007.
The Role of V-ATPase in Hair Cell Development 39
Gompel, N., Dambly-Chaudiere, C., & Ghysen, A. (2001). Neuronal differences prefigure somatotopy in the zebrafish lateral line. Development, 128(3), 387-93.
Horng, J.-L., Lin, L.-Y., Huang, C.-J., Katoh, F., Kaneko, T., & Hwang, P.-P. (2007). Knockdown of V-ATPase subunit A (atp6v1a) impairs acid secretion and ion balance in zebrafish (Danio rerio). American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 292(5). doi: 10.1152/ajpregu.00578.2006
Iskratsch, T., Wolfenson, H., & Sheetz, M. P. (2014). Appreciating force and shape — the rise of mechanotransduction in cell biology. Nature Reviews Molecular Cell Biology, 15(12), 825–833. doi: 10.1038/nrm3903
Jefferies, K. C., Cipriano, D. J., & Forgac, M. (2008, August 1). Function, structure and regulation of the vacuolar (H )-ATPases. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2543942/.
Jones, R. (2017). Audition (Hearing). Syracuse, NY. Syracuse University.
Kaliyappan, K., Palanisamy, M., Duraiyan, J. and Govindarajan, R., 2012. Applications of immunohistochemistry. Journal of Pharmacy and Bioallied Sciences, 4(6), p.307.
Lin, L.-Y., Hung, G.-Y., Yeh, Y.-H., Chen, S.-W., & Horng, J.-L. (2019). Acidified water impairs the lateral line system of zebrafish embryos. Aquatic Toxicology, 217, 105351. doi: 10.1016/j.aquatox.2019.105351
Olt, J., Johnson, S. L., & Marcotti, W. (2014, May 15). In vivo and in vitro biophysical properties of hair cells from the lateral line and inner ear of developing and adult zebrafish. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4027864/.
Olt, J., Ordoobadi, A., Marcotti, W., & Trapani, J. (2016). Physiological recordings from the zebrafish lateral line. Methods in Cell Biology The Zebrafish - Cellular and Developmental Biology, Part A Cellular Biology, 253–279. doi: 10.1016/bs.mcb.2016.02.004
The Role of V-ATPase in Hair Cell Development 40
Pais-Roldán, Patricia., Singh, Ajeet P., Schulz, Hildegard., Yu, Xin. “High Magnetic Field Induced Otolith Fusion in the Zebrafish Larvae.” Scientific Reports, vol. 6, no. 1, 2016, doi:10.1038/srep24151.
Paluch, E. K., Nelson, C. M., Biais, N., Fabry, B., Moeller, J., Pruitt, B. L., … Federle, W. (2015, July 4). Mechanotransduction: use the force(s). Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491211/.
Pichler, P., & Lagnado, L. (2020). Motor Behavior Selectively Inhibits Hair Cells Activated by Forward Motion in the Lateral Line of Zebrafish. Current Biology, 30(1). doi: 10.1016/j.cub.2019.11.020
Pujol-Martí, J., & López-Schier, H. (2013). Developmental and architectural principles of the lateral-line neural map. Frontiers in Neural Circuits, 7. doi: 10.3389/fncir.2013.00047
Purves D, Augustine GJ, Fitzpatrick D, et al., editors. Neuroscience. 2nd edition. Sunderland (MA): Sinauer Associates; 2001. Two Kinds of Hair Cells in the Cochlea. Available from: https://www.ncbi.nlm.nih.gov/books/NBK11122/
Ramaswamy, G., Bidez, M. W., & Misch, C. E. (2015). Bone Response to Mechanical Loads. Dental Implant Prosthetics, 107–125. doi: 10.1016/b978-0-323-07845-0.00006-3
Santra, Peu., (2018). IHC to visualize hair cells and supporting cells in zebrafish neuromast, adapted from Pinto-Teixeira et al., Inexhaustible hair-cell regeneration in young and aged zebrafish, (2015).
Stawicki, T. M., Owens, K. N., Linbo, T., Reinhart, K. E., Rubel, E. W., & Raible, D. W. (2014). The zebrafish merovingian mutant reveals a role for pH regulation in hair cell toxicity and function. Disease Models & Mechanisms, 7(7), 847–856. doi: 10.1242/dmm.016576
Stooke-Vaughan, G. A., Obholzer, N. D., Baxendale, S., Megason, S. G., & Whitfield, T. T. (2015). Otolith tethering in the zebrafish otic vesicle requires Otogelin and -Tectorin. Development, 142(6), 1137–1145. doi: 10.1242/dev.116632
Thomas, Eric D., et al. “There and Back Again: Development and Regeneration of the Zebrafish Lateral Line System.” Wiley Interdisciplinary Review:Developmental Biology, vol. 4, no. 1, 2014, pp. 1-16., doi:10.1002/wdev.160.
The Role of V-ATPase in Hair Cell Development 41
Toei, M., Saum, R., & Forgac, M. (2010). Regulation and Isoform Function of the V-ATPases. Biochemistry, 49(23), 4715–4723. doi: 10.1021/bi100397s
Treuting, P. M., Dintzis, S. M., & Montine, K. S. (2018;2017;). Comparative anatomy and histology: A mouse, rat, and human atlas (Second ed.). London: Elsevier/Academic Press.
Whitfield, T. T., Granato, M., Eeden, F. J. v., Schach, U., Brand, M., Furutani-Seiki, M., . . . Nusslein-Volhard, C. (1996). Mutations affecting development of the zebrafish inner ear and lateral line. Development, 123(1), 241.
Xiong, Wei. “Biophysical Properties of Mechanotransduction.” Mechanotransduction of the Hair Cell SpringerBriefs in Biochemistry and Molecular Biology, 2018, pp. 15-23., doi:10.1007/978-981-10-8557-4_3.