Information Science 274: 998-1001 (1996) Trends in Genetics 14: 1481-1483 (1997)

Information

http://www.arctur.com

Science 274: 998-1001 (1996) Trends in Genetics 14: 1481-1483 (1997)

The PixCell® II performs Laser Capture Microdissection (LCM) from heterogeneous ti

ssue samples simply, quickly and precisely. In minutes, you can locate a single cell o

r large groups of cells and, using a simple aim-and-shoot method, extract them for su

bsequent molecular analysis. LCM preserves the exact morphologies of both the capt

ured cells as well as the surrounding tissue. The PixCell II transfers cells from paraffi

n-embedded and frozen tissue samples, stained and immunolabelled slides. Monitor

and document the entire process, and store images in the archiving workstation. Micr

odissect fluorescently-stained cells with the optional fluorescence package.

The goal of LCMA rapid and accurate means of procuring homogenous cell populations of individual cells or cell clusters.

Type of laser used

A near infrared , solid state laser dipole.

The laser produces short , controlled burst of light that soften the thermoplastic film in localized areas.

No water or molecular dissociation absorption peaks associated with this wavelength.

The temperature of the thermoplastic film reaches 60-80°C at the site of the laser pulse.

The laser may not damage samples by destroying tissue or nucleic acids.

The time of laser last>1010 shots 5000 pulses/cap, 500cap/year, 400 years. 5000x5000x400=1x 1010

Laser beam diameter7.5 m, 15 m, 30 m

Objectives microscope 4X, 10X, 20X

  Spot Size Tissue Thickness

Small: < 7.5 microns < 10 microns

Medium: ~ 15 microns 5 to 15 microns

Large: ~ 30 microns 5 to 20 microns

How does LCM work?1. Cells are able to be microdissected through capture on th

ermoplastic film(ethylene vinyl acetate polymer, EVA).

2. A focused laser pulse activates the adhesiveness of the film localized to an area down to a resolution of 7.5m.

3 . Cells are captured and transferred to the film in the spot that the film was activated,then the cells are lifted off the section and placed directly into DNA, RNA or enzyme buffer for processing.

4. Cells are not directly impacted by the laser, only the transfer film is.

Method:1. Placing a thin transparent film (ethylene vinyl acetate po

lymer, EVA) over a tissue section, visualizing the tissue microscopically.

2. Selectively adhering the cells of interest to the film with a

fixed-position, short-duration, focused pulse from an infrared laser.

3. The film with the procured tissue is then removed from the section and placed directly into DNA, RNA or enzyme buffer for processing.

1. Prepare

• Follow routine protocols for preparing a tissue or smear on a standard microscope slide. Apply a Prep Strip™ to flatten the tissue and remove loose debris prior to LCM

2. Place

• Place a CapSure™ HS onto the tissue in the area of interest. The CapSure™ HS is custom designed to keep the transfer film out of contact with the tissue

3. Capture• Pulse the low power i

nfrared laser. The laser activates the transfer film which then expands down into contact with the tissue. The desired cell(s) adhere to the CapSure™ HS transfer film.

Puls

e

4. Microdissection• Lift the CapSure™ HS

film carrier, with the desired cell(s) attached to the film surface. The surrounding tissue remains intact

5.Extract

• Pipette the extraction buffer directly into the microcentrifuge tube and place the Capsure on the top of the tube.

6. Analyze

• Invert the microcentrifuge tube. After centrifuging, the lysate will be at the bottom of the tube. The cell contents, DNA, RNA or protein, are ready for subsequent molecular analysis.

Preparation of sample for LCM different from standard histology preparation

1. Frozen tissue Tissue MUST be frozen quickly after biopsy to prevent RNA , Protein

degradation. After sectioning, mount the section on a new slide, but DO NOT allow the tissue to thaw.

2. Paraffin embeded tissue: Paraffin sections MUST NOT be baked on the slides. Alcohol-based fixation and/or rapid perfusion fixation is preferred.

3. Use fresh reagents and solvents. Pipet a few drops of stain directly on the tissues.

4. Slides are NOT cover slipped.

5. Sample must be dehydrated fully with graded ethanols and xylenes.

6. Proper storage conditions must be observed. Slides may be stored in a desiccator with desiccant.

De-Paraffinization of Tissue Section for LCM

Section paraffin blocks at 5-10 microns. 5 microns is optimal for LCM, but the thickness should be dependant on the cell (nuclei) diameter that is being worked on.

Place ribbons into a water bath at 42° to smooth out and eliminate folds and wrinkles.

Mount sections on new, plain, uncharged, untreated glass slides. Air dry overnight at room temperature.

Dip the slide containing the tissue section in the following solutions for the specified times. 1. Xylene 15 minutes 2. Xylene 15 minutes 3. 100% Ethanol 5 minutes 4. 100% Ethanol 5 minutes 5. 90% Ethanol 5 minutes 6. 80% Ethanol 5 minutes 7. 70% Ethanol 5 minutes 8. 50% Ethanol 5 minutes 9. Water 1 minute

Hematoxylin and Eosin Staining for LCM Procedure 1. 70% ETOH 30 seconds 2. dH20 30 seconds 3. Hematoxylin 30 seconds 4. dH20 30 seconds 5. Eosin 30 seconds 6. 70% ETOH 30 seconds 7. 95% ETOH 30 seconds 8. 100% ETOH 30 seconds 9. 100% ETOH 30 seconds 10. Xylene 5 minutes 11. Xylene 5 minutes 12. Air Dry 20 minutes in a hood or vacuum desiccator   * molecular sieve treated 100% Ethanol.

The tissue sections are now ready for LCM. Store the samples in a desiccator when not in use.

DNA Extraction The following extraction method has been used for measuring loss of heterozygosity (LOH), dideoxy fingerprinting (DDF), clonality analysis (chromosome X inactivation) direct sequencing of PCR* products for single base mutational analysis.Extractions are typically performed on 500-1000captured cells.  Materials Proteinase K Digestion Buffer 1mg/ml Proteinase K 1% Tween 20 * in TE Buffer pH.8.0 *Detergent may interfere with amplification reactions with a small number of commercial DNA polymerases.  

Procedure 1. Pipet 50 ul of proteinase K digestion buffer into a microfuge tube. 2. Place the tube up-right in a humidified incubator at 37-42°C for 5 minutes to preheat. 3. Place the CapSure Transfer Film cap onto the microfuge tube with the insertion tool. 4. Invert the microfuge tube and flick down the digestion buffer until all the fluid is in contact with the surface of the cap containing the sample. 5. Incubate overnight in the humidified incubator at 37-42°C. 6. Centrifuge for 5 minutes at a maximum of 6400 rpm (2000xg) to collect the fluid and DNA. 7. Remove the transfer film cap and visually inspect under the microscope to verify that all cells have been digested (no cellular material remains on the transfer film areas of capture). 8. Inactivate the proteinase K by heating the microfuge tube at 95°C for 10 minutes. 9. Sample is now ready to go directly into amplifications or into other applications.

DNA Yield: 3000 transfer shots 1300ng2500 transfer shots 800ng1500 transfer shots 580ng750 transfer shots 300ng

  RNA Extraction (NIH Protocol) Materials GITC digestion buffer (final concentrations listed) · 5.25M GITC (guanidinium isothiocyanate) · 50mM Tris-HCl pH 6.4 · 20mM EDTA · 1% Triton X-100 · 0.1M -Mercaptoethanol (added fresh with each extraction) 2M Sodium Acetate (NaOAc, pH 4.5) Phenol - water saturated Chloroform-isoamyl alcohol Glycogen Isopropanol Ethanol DEPC water  

RNA Extraction (NIH Protocol)

Procedure 1. Place the cap in a reagent tube containing 200 ul RNA denaturing buffer(GITC) and 1.6 ul -mercaptoethanol. Invert several times over the course of 2 minutes to digest the tissue off of cap. 2. Remove the solution from the reagent tube and replace it in a 1.5 ml tube. 3. Add 20 ul (0.1X volume) 2M sodium acetate (pH 4.0). 4. Add 220 ul (1X volume) water saturated phenol (bottom layer). 5. Add 60 ul (0.3X volume) chloroform-isoamyl alcohol. 6. Vortex vigorously. 7. Put on wet ice for 15 minutes. 8. Centrifuge for 30 minutes at 4°C to separate the aqueous and organic phases. 9. Transfer upper aqueous layer to a new tube. 10. Add 1-2 ul glycogen (10 mg/ml). Glycogen is a carrier that is used if RNA quantities are less than 1 ug. It also facilitates visualization of the pellet. 11. Add 200 ul cold isopropanol. 12. Put in -80°C freezer for at least 30 minutes. It may be left overnight.

13. Centrifuge for 30 minutes at 4°C with cap hinges pointing outward so that the location of the pellet can be better predicted. 14. Remove the majority of the supernatant with a 1000 ul tip and then switch to smaller pipet to remove the rest of the supernatant. This minimizes disruption of the RNA pellet. 15. Wash with 400 ul cold 70% Ethanol. Add the alcohol and spin for 15 minutes. 16. Remove the supernatant as explained above. All of the supernatant should be removed at this point. 17. Let the pellet air dry on ice to remove any residual ethanol. Over drying prevents the pellet from resuspending easily. 18. Pellet can be stored at -80°C until use. 19. (optional) Resuspend pellet with DEPC water.

DNase Treatment (optional)

1. To RNA pellet, add 15 ul DEPC water, 0.5 ul of 40 units/ul rRNasin RNase inhibitor, 2 ul 5X DNase buffer ( 400 mM Tris-HCl pH 8.0 , 20 mM DDT, 100 mM MgCl2) and 2 ul 10 units/ul DNase. 2. Incubate at 37°C for 2 hours.

Re-extraction of RNA   1. 2 ul 2M NaOAc 2. 22 ul Phenol 3. 6 ul Chloroform-isoamyl alcohol 4. Place on ice for 15 minutes. 5. Centrifuge 10 minutes at 4°C. 6. Transfer upper layer to a new tube. 7. Continue with RNA extraction from step 10.

LCM has advantages over other cell microdissection

• Simple, no moving parts, no manual microdissection , one step transfer.• Retains its morphology, allowing microscopic verification of specificity of the capture material. • Able to microdissect cells from an area that was previously microdissected.• DNA, RNA and protein are all recoverable through LCM.

Applications utilizing LCMA valuable aid in cancer biology, neurobiology, genomics, experimental pathology, new drug discovery, and diagnostics.

Research Applications      Genomics           Differential Gene Profiling           Loss of Heterozygosity           Microsatellite Instability           Gene Quantification      Proteomics           Two-Dimensional Protein Gels           Western Blotting           Immuno-quantification of Proteins

Dissected cells on the cap

Before LCM After LCM