A Non-random Mouse Model for Pharmacological Reactivation of Mecp2 on the Inactive X Chromosome

Summary

Here, we describe a protocol to generate a viable female murine model with non-random X chromosome inactivation, i.e., the maternally-inherited X chromosome is inactive in 100% of the cells. We also describe a protocol to test feasibility, tolerability, and safety of pharmacological reactivation of the inactive X chromosome in vivo.

Abstract

X chromosome inactivation (XCI) is the random silencing of one X chromosome in females to achieve gene dosage balance between the sexes. As a result, all females are heterozygous for X-linked gene expression. One of the key regulators of XCI is Xist, which is essential for the initiation and maintenance of XCI. Previous studies have identified 13 trans acting X chromosome inactivation factors (XCIFs) using a large-scale, loss-of-function genetic screen. Inhibition of XCIFs, such as ACVR1 and PDPK1, using short-hairpin RNA or small molecule inhibitors, reactivates X chromosome-linked genes in cultured cells. But the feasibility and tolerability of reactivating the inactive X chromosome in vivo remains to be determined. Towards this goal, a XistΔ:Mecp2/Xist:Mecp2-Gfp mouse model has been generated with non-random XCI due to deletion of Xist on one X chromosome. Using this model, the extent of inactive X reactivation was quantitated in the mouse brain following treatment with XCIF inhibitors. Recently published results show, for the first time, that pharmacological inhibition of XCIFs reactivates Mecp2 from the inactive X chromosome in cortical neurons of the living mouse brain.

Introduction

X chromosome inactivation (XCI) is a process of dosage compensation that balances X-linked gene expression by silencing one copy of the X chromosome in females¹. As a result, the inactive X chromosome (Xi) accumulates characteristic features of heterochromatin including DNA methylation and inhibitory histone modifications, such as histone H3-lysine 27 trimethylation (H3K27me3) and histone H2A ubiquitination (H2Aub)². The master regulator of X chromosome silencing is the X-inactivation center (Xic) region, around 100−500 kb, which controls the counting and pairing of the X chromosomes, the random choice of the X chromosome for inactivation, and the initiation and spreading of silencing along the X chromosome³. The process of X inactivation is initiated by X inactive specific transcript (Xist) that coats the Xi in cis to mediate chromosome-wide silencing and remodel the three-dimensional structure of the X chromosome⁴. Recently, several proteomic and genetic screens have identified additional regulators of XCI, such as Xist interacting proteins^{5,6,7,8,9,10,11,12}. For example, a previous study using an unbiased genome-wide RNA interference screen identified 13 trans-acting XCI factors (XCIFs)¹². Mechanistically, XCIFs regulate Xist expression and therefore, interfering with XCIFs function causes defective XCI¹². Together, recent advances in the field have provided important insights into the molecular machinery that is required to initiate and maintain XCI.

Identification of XCI regulators and understanding their mechanism in XCI is directly relevant to X-linked human diseases, such as Rett syndrome (RTT)^13,14. RTT is a rare neurodevelopmental disorder caused by a heterozygous mutation in the X-linked methyl-CpG binding protein 2 (MECP2) that affects predominantly girls¹⁵. Because MECP2 is located on the X chromosome, RTT girls are heterozygous for MECP2 deficiency with ~50% cells expressing wild-type and ~50% expressing mutant MECP2. Notably, RTT mutant cells harbor a dormant but wild-type copy of Mecp2 on the Xi, providing a source of the functional gene, which if reactivated, could potentially alleviate symptoms of the disease. In addition to RTT, there are several other X-linked human diseases, for which reactivation of Xi represents a potential therapeutic approach, such as DDX3X syndrome.

Inhibition of XCIFs, 3-phosphoinositide dependent protein kinase-1 (PDPK1), and activin A receptor type 1 (ACVR1), either by short hairpin RNA (shRNA) or small molecule inhibitors, reactivates Xi-linked genes¹². Pharmacological reactivation of Xi-linked genes is observed in various ex vivo models that include mouse fibroblast cell lines, adult mouse cortical neurons, mouse embryonic fibroblasts, and fibroblast cell lines derived from an RTT patient¹². However, whether pharmacological reactivation of Xi-linked genes is feasible in vivo remains to be demonstrated. One limiting factor is the lack of effective animal models to accurately measure the expression of genes from reactivated Xi. Towards this goal, a XistΔ:Mecp2/Xist:Mecp2-Gfp mouse model has been generated that carries a genetically labeled Mecp2 on Xi in all the cells due to heterozygous deletion in Xist on the maternal X chromosome¹⁶. Using this model, the expression of Mecp2 from Xi has been quantitated following treatment with XCIFs inhibitors in the brain of living mice. Here, the generation of the XistΔ:Mecp2/Xist:Mecp2-Gfp mouse model and methodology to quantitate Xi reactivation in cortical neurons using immunofluorescence-based assays is described.

Protocol

Work involving mice was approved by the University of Virginia Institutional Animal Care and Use Committee (IACUC; #4112).

1. Generate a Non-random XCI Mouse Model with Genetically Labeled Mecp2 on Xi

NOTE: Mouse strains used in the study were as follows: Mecp2-Gfp/Mecp2-Gfp (Mecp2^tm3.1Bird, Table of Materials) and Xist/ΔXist (B6;129-Xist<tm5Sado>; provided by Antonio Bedalov, Fred Hutchinson Cancer Center, Seattle). Breeding strategies among the respective strains have been designed to expand the mouse colonies for each strain.

1. Perform PCR-genotyping on all mice strains and respective progenies obtained after breeding using gene specific primers listed in Table 1.

2. Design the Mouse Breeding Strategy to Generate XistΔ:Mecp2/Xist:Mecp2-Gfp

1. Set up a breeding pair by housing a Mecp2-Gfp/Y male and a XistΔ-Mecp2/Xist-Mecp2 female together (12 h/12 h: light / dark cycle)  (Figure 1A). Ideally, set up at least 5 breeding pairs at a time using viable and fertile mice. After the pregnant female gives birth, allow her to raise her first litter with the male.
   NOTE: Because paternal Xist knockout impairs imprinted XCI, dosage compensation, and differentiation pathways¹⁷, the use of XistΔ-Mecp2/Y mice in the breeding will fail to produce the female pups with required genotype.
2. After weaning the litter at post-natal day 21 (P21), identify and tag the XistΔ:Mecp2/Xist:Mecp2-Gfp female pups using a PCR-based genotyping assay (Figure 1B).
   NOTE: In terms of the number of animals needed per group, for the results reported below, 5 breeding pairs were set up which generated approximately 10 female XistΔ:Mecp2/Xist:Mecp2-Gfp mice.
3. Use female mouse models for all the proposed experiments.
   NOTE: Sex is an important biological variable for XCI studies, and the male model does not account for the confounding effects of random XCI.
4. To be consistent throughout the animal studies and rule out any effects of the animal age, perform all the experiments in 5−8-week-old female XistΔ:Mecp2/Xist:Mecp2-Gfp mice.

3. Isolate Female XistΔ:Mecp2/Xist:Mecp2-Gfp Mouse Embryonic Fibroblasts (MEFs)

1. Set up timed mating between the Mecp2-Gfp/Y male and XistΔ-Mecp2/Xist-Mecp2 female. Set up at least 3−4 mating cages to increase the likelihood of pregnancy.
2. After confirming the vaginal plug the morning after mating, separate the female and this day is considered embryonic day 0.5 (E0.5). Monitor the weight gain of the prospective pregnant female and visually inspect the abdomen of the mice to confirm pregnancy. On E14.5−15.5, euthanize the pregnant female mice via cervical dislocation.
3. Under a laminar hood, wipe the abdomen of the pregnant female with 70% ethanol. Using sterile scissors, dissect the abdominal cavity and remove the uterine horns containing the embryos. Using forceps, gently take out the embryos while cutting off the remaining abdominal tissue (6−12 embryos is usually expected).
4. Place the uterine horns containing the embryos in a 10 mm tissue-culture dish. Using sterile scissors and forceps, make an incision along the uterine horns to isolate individual sacs carrying an embryo. Carefully, place the uterine horns containing the rest of the embryos in 30 mL of sterile Hanks’ balanced salt solution (HBSS) on ice.
5. Gently cut open the sac and isolate the embryo using sterile scissors and forceps. Remove the placenta by cutting the umbilical cord.
6. Decapitate the embryo.
   NOTE: While the rest of the embryonic tissue will be further processed, the tissue from the embryo head will be used to isolate DNA for genotyping.
7. Open the abdomen by cutting the midline of the embryo using sterile scissors and forceps. Remove the visceral organs, such as the heart, liver, and lungs.
8. Transfer the remaining embryonic tissue into a sterile 60 mm tissue-culture plate and cut into small pieces using scissors or a razor blade. To break open the cell clumps, add 3 mL of trypsin-EDTA (0.05%) and incubate at 37 °C for 15 min.
9. Neutralize trypsin-EDTA by adding 5 mL of Dulbecco’s modified Eagle medium (DMEM) with 10% fetal bovine serum (FBS) and 10 µg/mL penicillin/streptomycin (pen/strep) to the plate and dissociate the tissue by repetitive pipetting (approximately 20−30 times).
10. Spin down cells at 300 x g for 5 min and re-suspend the cell pellet in 4 mL of DMEM with 10% FBS and 10 µg/mL pen/strep. Plate the cells on a 60 mm culture dish, and culture the cells at 37 °C in the presence of 5% CO₂.
11. Carry out steps 3.5−3.10 for each embryo.
12. Culture MEFs obtained in step 3.11 for at least 3−4 days.
    NOTE: At this stage, MEFs can also be cryopreserved for future experiments.
13. To determine the sex and genotype of each embryo, carry out genotyping-PCR using DNA isolated from the heads of the embryos using primers and PCR conditions listed in Table 1.

4. Confirm the Lack of Green Fluorescent Protein (GFP) Expression in the Brain of XistΔ:Mecp2/Xist:Mecp2-Gfp Mice Using a Ffluorescence Activated Cell Sorting-based Assay

1. Using scissors, separate the cerebral cortex from the rest of the brain hemispheres, and place in 1 mL of ice-cold nuclei isolation media (NIM) buffer containing 250 mM sucrose, 25 mM potassium chloride (KCl), 5 mM magnesium chloride (MgCl₂), 10 mM Tris-Cl, supplemented with 2% paraformaldehyde (PFA), and 0.1% nonionic surfactant (Table of Materials).
2. Homogenize using an ice-cold glass homogenizer.
3. Spin down homogenized tissue at 600 x g, 4 °C for 5 min.
4. Remove supernatant and resuspend pellet in 1 mL of 25% iodixanol in NIM solution.
5. Add 1 mL of 29% lodixanol in NIM solution to a 4 mL ultracentrifuge tube (store on ice until samples are ready) and carefully layer 1 mL of sample (in 25% lodixanol).
6. Centrifuge at 9,000 x g, 4 °C for 10 min in an ultracentrifuge.
7. Aspirate supernatant and resuspend pellet in 500 μL of fluorescence activated cell sorting (FACS) buffer (phosphate-buffered saline [PBS] supplemented with 1 mM EDTA, 0.05% sodium azide, and 2% bovine serum albumin [BSA]).
   NOTE: Samples can be stored at 4 °C or up to 1 week.
8. Add 5 μL of 7-amino-actinomycin D (7-AAD; 50 mg/mL) for 5 min at room temperature to stain DNA.
9. Analyze samples for 7-AAD and green fluorescent protein (GFP) signal using flow cytometry.

5. Determine Feasibility of the XistΔ:Mecp2/Xist:Mecp2-Gfp Mouse Model for Xi Reactivation

1. Seed 1 x 10⁵ cells/mL female XistΔ:Mecp2/Xist:Mecp2-Gfp MEFs, Mecp2/Mecp2-Gfp and Xist-Mecp2/Y MEFs obtained in step 3.12 in a 6-well format and in chamber slides, in DMEM with 10% FBS and 10 µg/mL pen/strep, at 37 °C in the presence of 5% CO₂.
   NOTE: Mecp2/Mecp2-Gfp and Xist-Mecp2/Y MEFs are used as positive and negative controls in the experiments.
2. Add fresh medium to the cells after 24 h. For XistΔ:Mecp2/Xist:Mecp2-Gfp MEFs, add medium supplemented with XCIFs inhibitors (e.g., 0.5 μM LDN193189 and 2.5 μM GSK650394), or vehicle alone. Replace medium supplemented with fresh inhibitor or vehicle alone every 2 days. For Mecp2/Mecp2-Gfp and Xist-Mecp2/Y MEFs, add fresh medium every 2 days.
3. Post 1 week of inhibitor treatment, harvest MEFs either for RNA isolation (6-well plate) or fix cells for immunofluorescence (chamber slides). Use MEFs isolated from Mecp2/Mecp2-Gfp embryos as positive and Xist-Mecp2/Y embryos as negative controls respectively.
   1. For RNA isolation, isolate total RNA by guanidinium thiocyanate-based RNA extraction reagent, and reverse transcribe using reverse transcriptase. Measure Mecp2-Gfp expression by quantitative reverse transcriptase-PCR (qRT-PCR) using Mecp2-WT and Mecp2-GFP, and primers listed in Table 1, as described previously¹².
   2. For immunofluorescence, stain MEFs with an anti-GFP primary antibody (1:100), as described previously^12,16. Measure GFP intensity by quantitative immunofluorescence in drug treated XistΔ:Mecp2/Xist:Mecp2-Gfp MEFs, as described previously¹⁸.

6. Demonstrate the Pharmacological Xi Reactivation in the Brain of the XistΔ:Mecp2/Xist:Mecp2-Gfp Mouse Model

1. Prepare drugs and vehicle control.
   1. Prepare a fresh, sterile solution of vehicle (0.9% NaCl, 0.5% methylcellulose, 4.5% dimethyl sulfoxide [DMSO]) for brain injections.
   2. Prepare chemical inhibitors including 1.5 mM LDN193189 (small molecule inhibitor of ACVR1) and 1.6 mM GSK650394 (small molecule inhibitor of SGK1, a downstream effector of PDPK1) re-suspended in vehicle (0.9% NaCl, 0.5% methylcellulose, 4.5% DMSO), or vehicle alone. The total volume of chemical inhibitors or vehicle injected is 10 µL per dose per animal.
2. Prepare animal for brain injections.
   1. Prepare the surgical area by wiping the bench and heating pad with disinfectant (10% sodium hypochlorite solution).
   2. Anesthetize the 4 week old mouse with an intraperitoneal injection of ketamine/xylazine mixture at a dose of 140 mg/kg and 10 mg/kg, respectively. Use the pedal withdrawal reflex to determine the level of anesthesia.
   3. Apply ophthalmic ointment to the eyes following induction of anesthesia to prevent corneal drying.
   4. Shave off the fur from the neck to the top of the head of the mouse.
   5. Position the mouse in the stereotactic platform by hooking the mouse’s incisor teeth in the bite bar of the snout restrainer and tightening the nose clamp over the snout while ensuring that the mouse’s head is on a level plane.
   6. Adjust the height of the ear bars, as necessary, to reach the caudal portion of the ear canal, securing them such that the mouse’s head is in a level plane and immobilized on finger touch.
   7. Disinfect the head of the mouse with alternating wipes of a topical antiseptic, such as povidone-iodine and 70% ethanol.
3. Administer drugs.
   1. Using a sterile scalpel, make a 0.75 cm horizontal incision in the mid-scalp.
   2. Using a 0.45 mm burr, drill two symmetrical holes above the right and left cortical hemispheres (2 mm from the sagittal suture and 2 mm from the lambdoid suture, approximately the middle of parietal bone).
   3. Attach a 10 μL syringe to the stereotactic platform firmly.
   4. Mix the solution of chemical inhibitors, and draw 10 μL of solution into the syringe. Avoid any air bubbles in the syringe.
   5. Advance the syringe needle into the burr hole maintaining the needle perpendicular (90°) to the skull. When the needle traverses the skull, zero out the coordinates on the stereotactic digital display and then advance the tip of the needle until it reaches a depth of 2.5 mm.
   6. Withdraw the needle 0.5 mm to the depth for 2 mm.
   7. Slowly inject 10 μL of solution (~1 min). After injection is complete, leave the needle in the brain for ~1 min and then withdraw the needle.
   8. Repeat the injection for the second hemisphere (vehicle only control).
   9. Using sutures or “skin glue” close the skin of the mouse (if wound is > 0.5cm both sutures and “skin glue” should be used).
   10. Loosen the ear bars and remove the mouse from the stereotactic apparatus.
   11. Administer analgesics (Buprenorphine SR 0.5 mg/kg IP) and place the mouse on a heating pad set to 37 °C until the animal regains consciousness.
   12. Once the mouse is alert and responsive, transfer the animal back to its original cage.
   13. Repeat the procedure every 2 days for 20 days. Repeat drilling of the area is not required for subsequent injections.
4. Isolate the mouse brain.
   1. Once the dose regimen is completed, euthanize the mouse in a CO₂ chamber.
   2. Immobilize the mouse on a surface using needles.
   3. Make a lateral incision through the integument and abdominal wall just beneath the rib cage using scissors and forceps. Carefully separate the liver from the diaphragm.
   4. Using scissors, cut the diaphragm and continue cutting along the entire length of the rib cage to expose the pleural cavity.
   5. Using scissors, make an incision to the posterior end of the left ventricle.
   6. Immediately, start injecting the right heart chamber with ~15 mL of PBS over ~2 min. Liver color change from red to pale pink is indicative of good perfusion.
   7. Inject the right chamber of the mouse heart with ~10 mL of 4% paraformaldehyde in PBS over ~2 min.
   8. Decapitate the mouse, and use scissors to make a midline incision of the scalp to expose the skull.
   9. Place one tip of the scissors into the foramen magnum, and cut laterally into the skull toward the eye. Repeat for the other side. Try to keep the end of the scissors as superficial as possible to avoid injury of the brain.
   10. Use scissors to cut the region between the eyes and above the nose of the mouse.
   11. Use forceps to gently peel the cranial bones from the brain hemispheres.
   12. Lift the brain with a spatula, and use scissors to carefully dissect the cranial nerve fibers that fix it to the skull.
   13. Place the brain on a plastic dish, cut out the cerebellum and olfactory bulbs, and place the brain into a 15 mL tube filled with 4% PFA is PBS.
5. Cryo-section the mouse brain.
   1. Fix brain in 4% paraformaldehyde in PBS at 4 °C overnight.
   2. Rinse the brain with PBS at 4 °C at least 3x for 5 min each.
   3. Label the disposable molds for cryopreserving the tissues.
   4. Cut out the front of the brain using scissors and forceps (start making ~5 mm sections from injection sites).
   5. Transfer the brain to the cryomold with the front of the brain facing down to obtain coronal sections. Submerge the mold containing brain in the optimal cutting temperature compound (OCT).
   6. Pour liquid nitrogen into a 10 mm plastic petri dish and place the brain in the cryo-mold into the nitrogen.
      NOTE: It is important to orient the tissue as described in step 6.5.5 to guide the sectioning of the brain.
   7. When the OCT is solid white, place the frozen brain into an -80 °C freezer for storage.
   8. Equilibrate the brain to -20 °C for at least 30 min prior to sectioning with cryostat and cryosection (5−6 μm thickness) the brain, mounting 2−3 sections per slide. Slides can be stored at -80 °C for later use.
6. Determine Xi reactivation using an immunofluorescence-based approach.
   1. Before starting the staining procedure, dry the brain sections overnight at 4 °C.
   2. Immerse slides in antigen retrieval solution (0.1 M citric acid, 0.1 M Tris-base, pH = 6.0) on a 100 °C heat block for 5 min.
   3. Wash slides 4x with 1x PBS for 5 min each at room temperature.
   4. Immerse slides in blocking solution (0.1 M NH₄Cl/PBS/0.2% gelatin/0.05% nonionic surfactant) for 20 min at room temperature.
   5. Wash slides 3x with wash buffer (PBS/0.2% gelatin) at room temperature for 5 min each.
   6. Stain brain sections with anti-GFP-AlexaFluor647 (1:100) and anti-MAP2 (1:1,000) antibodies in incubation medium (PBS/0.2% gelatin/1% BSA) and incubate at 4 °C overnight.
   7. Collect primary antibodies (can be reused). Wash slides 4x with wash buffer for a total of 30 min at room temperature.
   8. Incubate brain sections with goat anti-chicken Fluorescein isothiocyanate (FITC)-labeled secondary antibody (1:1,000) in incubation medium and incubate 1−2 h at room temperature in the dark.
   9. Wash slides 4x with wash buffer for a total of 30 min at room temperature.
   10. Place a drop of mounting medium with 4′,6-diamidino-2-phenylindole (DAPI) on a 22 mm x 50 mm coverslip, then invert the coverslip onto a slide, covering all tissue sections.
   11. Image on a microscope and adjust images for contrast and brightness. Capture images and quantify the number of GFP-positive cells for both drug-treated and vehicle treated XistΔ:Mecp2/Xist:Mecp2-Gfp mouse brain hemispheres.

Results

To demonstrate the feasibility of the XistΔ:Mecp2/Xist:Mecp2-Gfp mouse model for Xi reactivation studies, XCIF inhibitor-mediated reactivation of Xi-linked Mecp2-Gfp was tested in mouse embryonic fibroblasts (MEFs). Female MEFs were isolated from day 15.5 XistΔ:Mecp2/Xist:Mecp2-Gfp embryos as described in section 3 (Figure 1A). The genotypes of female XistΔ:Mecp2/Xist:Mecp2-Gfp MEFs were confirmed by genotyping-PCR, as de...

Discussion

Previously, XCIFs that are selectively required for silencing of Xi-linked genes in mammalian female cells were identified¹². We further optimized potent small molecule inhibitors to target XCIFs, such as ACVR1 and downstream effectors of PDPK1, which efficiently reactivate Xi-linked Mecp2 in mouse fibroblast cell lines, mouse cortical neurons, and a human fibroblast cell line derived from a RTT patient. These results suggest that Xi reactivation is a plausible therapeutic approach to res...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
MICE
Mecp2tm3.1Bird	The Jackson Laboratory	#014610
B6;129-Xist (tm5Sado)	provided by Antonio Bedalov, Fred Hutchinson Cancer Center, Seattle
REAGENTS
22x22 mm coverslip	FISHERfinest (Fisher Scientific)	125488
32% Paraformaldehyde	Electron Microscopy Sciences	15714-S
50 ml syringe	Medline Industries	NPMJD50LZ
60mm culture dish	CellStar	628160
7-AAD	BioLegend	420403
ammonium chloride (NH4Cl)	Fisher Chemical	A661-3
anti-GFP-AlexaFluor647	Invitrogen	A-31852
anti-MAP2	Aves Labs	MAP
BSA	Promega	R396D
Buprenorphine SR	Zoopharm
citric acid	Sigma	C-1857
DMSO	Fisher Bioreagents	BP231-100
Dulbecco's Modified Eagle Medium (DMEM)	Corning Cellgro	10-013-CV
Ethanol	Decon Labs	2701
fetal bovine serum (FBS)	VWR Life Science	89510-198
gelatin	Sigma-Aldrich	G9391
glass slides	Fisherbrand	22-034-486
goat anti-chicken FITC-labeled secondary antibody	Aves Labs	F-1005
GSK650394	ApexBio	B1051
hamilton 10μl syringe	Hamilton Sigma-Aldrich	28615-U
Hank's Balanced Salt Solution (HBSS)	Gibco	14025-092
Ketamine	Ketaset	NDC 0856-2013-01
Large blunt/blunt curved scissors	Fine Science Tools	14519-14
LDN193189	Cayman Chemicals	11802
lodixanol	Sigma	1343517
magnesium chloride (MgCl2)	Fisher Chemical	M35-212
Methylcelulose	Sigma	M0262-100G
mounting medium with DAPI	Vectashield	H-1200
Needle tip, 26 GA x 1.25"	PrecisionGlide	305111
ophthalmic ointment	Refresh Lacri-Lube	93468
optimal cutting temperature (O.C.T.)	ThermoFisher
PCR mix
Penicillin/Streptomycin (Pen/Strep)	Corning	30-002-Cl
Phosphate buffered saline pH 7.4 (PBS)	Corning Cellgro	46-103-CM
Potassium chloride (KCl)	Fisher Scientific	P330-500
scalpel blades
Shallow glass or plastic tray
skin glue/tissue adhesive	3M Vetbond	1469SB
sodium azide	Fisher Scientific	CAS 26628-22-8
Sodium chloride (NaCl)	Fisher Chemical	S642-212
standard hemostat forceps	Fine Science Tools	13013-14
Standard tweezers	Fine Science Tools	11027-12
Straight iris scissors	Fine Science Tools	14058-11
sucrose	Fisher Scientific	BP220-1
Tris-base	Fisher Bioreagents	BP152-5
Triton X-100	Fisher Bioreagents	BP151-500
Trypsin-EDTA	Gibco	15400-054
Xylazine	Akorn	NDC: 59399-111-50
EQUIPMENT
Zeiss AxioObserver Live-Cell microscope	Zeiss	Zeiss AxioObserver
0.45mm burr	IDEAL MicroDrill	67-1000
BD FACScalibur
centrifuge
glass homogenizer
cell culture incubator	Thermo Scientific HERACELL VIOS 160i	13-998-213
Leica 3050S research cryostat
stereotactic platform
thermocycler
Timer
ultracentrifuge	Beckman Coulter Optima L-100 XP
Water bath (37 ºC)	Fisher Scientific Isotemp 2239