Adult Mouse DRG Dissociation for FACS of TrpV1PLAP nLacZ Mice (Version 1.0)
Version
1.0
Notice
This page is the corresponding protocol tomestone page generated as part of the ATLAS-D2K shutdown in July 2025. Many links on this page may be broken.
Authors
Janet Keast; Casey Smith-Anttila
Keywords
[‘ganglia’]
Subjects
[‘Isolation, purification and separation’]
Release Date
2017-08-07
Abstract
Adult Mouse DRG Dissociation for FACS of TrpV1PLAP nLacZ Mice protocol by the Keast Group
Procedure
Set up
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Turn on hood: UV for 15 mins, then laminar flow for 5 mins.
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Put all the reagents required on ice to thaw: collagenase, trypsin/EDTA.
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Put dissection instruments in 80% ethanol 10 mins then allow to dry
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Put 2.5ml 1X Tyrodes in 2 x 35mm petri dishes per mouse and put on ice.
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Put 3.5ml 1X Tyrodes in 2 x 15ml falcon tubes per mouse and put on ice.
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Add 320µl 1X Tyrodes to 750µl collagenase (per sample). Pre-warm the solution to 37°C.
Dissection
- Following the approved method for euthanizing the animal, dissect ganglia and place each in 1X Tyrodes in a 35mm petri dish on ice until the end of the dissection.
Dissociation
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Using forceps, transfer ganglia into a 15 ml tube containing 3.5 ml 1X Tyrodes. (Perform remaining steps in the laminar flow)
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Allow ganglia to settle and remove the 1X Tyrodes solution.
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Add pre-warmed collagenase/Tyrodes to the tube. Give the tube a gentle flick to mix and place in an incubator at 37°C for 1 hour.
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While this is incubating, pre-warm trypsin/EDTA solution to 37°C (320µl trypsin/EDTA + 750µl collagenase [per sample])
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Allow tissue to settle and remove collagenase/Tyrodes solution. Add collagenase/trypsin/EDTA solution and mix gently. Incubate at 37°C for 1 hour.
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Allow tissue to settle, remove supernatant and discard.
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Wash twice with 1ml Leibovitz’s L-15 medium (Life Technologies, Cat# 21083-027): i.e., with transfer pipette, add 1 ml L-15, allow tissue to settle and discard supernatant. Repeat.
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Triturate cells in 1ml L-15 medium. Do this by triturating 20 times with a 1000µl pipette.
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Centrifuge at 300x g for 8 mins at 4°C.
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Remove and discard supernatant using a pipette being careful not to disturb the cell pellet.
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Resuspend cells in 500 µl L-15 medium.
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Add 5µl of 1mM DDAOG (Molecular Probes, Cat# D-6488) in DMSO to the dissociated cells, mix gently and incubate on ice for 30 mins.
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Filter the dissociated cells through a 40µm pore size cell strainer and collect the cells into a FACS tube.
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Add 1µl of 100 µg/mL DAPI (200ng/ml final concentration) as a dead cell stain just prior to taking the samples for FACS.
FACS Sorting and RNA Extraction
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Take cells to the FACS facility for sorting. Keep the cells on ice.
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Sort cells directly into 1.5ml eppendorf tubes containing 500µl Qiagen RLT lysis buffer + 30µl 2M DTT. Keep tubes on ice after sorting.
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Homogenize cells by passing them through a 25 gauge needle 3 times. Proceed to RNA extraction immediately.
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Extract RNA using the Qiagen RNeasy Plus Micro kit according to the manufacturer’s instructions with the exception of adding 400 µl 70% ethanol per sample at Step 5 (long protocol)/ Step 3 (quick protocol).
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Store the RNA at -80°C.
Reagents
Tyrodes solution
10x stock
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Mix the following:
7.59 g NaCl
1.68 g NaHCO3
2.38 g HEPES
224 mg KCl (or 3 ml 1 M KCl)
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Make up to 100 ml with H2O and autoclave. Store at 4°C.
1x Tyrodes
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Mix the following:
500 µl antibiotic/antimycotic solution (0.5%)
1.2 ml 1 M glucose (filter sterilized)
400 µl 1 M CaCl2 (filter sterilized)
100 µl 1 M MgCl2 (filter sterilized)
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Add 87.8 ml autoclaved H2O and 10 ml of 10X stock.
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Store remaining solution at 4°C for < 1 month.
Antibiotic/antimycotic solution (Invitrogen, cat# 15240-062)
- Dispense into 500 µl aliquots, store at -20°C
Collagenase, type 1 (Supplier: Scima R, Manufacturer: Worthington, Cat# L5004196)
- 20 mg collagenase in 15 ml Tyrodes, filter sterilize, aliquot into 750 µl, store at -20°C.
Trypsin/EDTA (Gibco, Cat #25200056, 100 ml, 0.25% trypsin + 1 mM EDTA or Sigma T4049, 0.25% trypsin/EDTA)
- Dispense into 650 µl aliquots, store at -20°C.
Consortium
GenitoUrinary Development Molecular Anatomy Project (GUDMAP) Consortium