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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

We provide a protocol for isolation of microglia from different dissected regions of an adult mouse brain hemisphere, followed by semi-automated library preparation for deep single-cell RNA sequencing of full-length transcriptomes. This method will help to elucidate functional heterogeneity of microglia in health and disease.

Abstract

As resident macrophages in the central nervous system, microglia actively control brain development and homeostasis, and their dysfunctions may drive human diseases. Considerable advances have been made to uncover the molecular signatures of homeostatic microglia as well as alterations of their gene expression in response to environmental stimuli. With the advent and maturation of single-cell genomic methodologies, it is increasingly recognized that heterogenous microglia may underlie the diverse roles they play in different developmental and pathological conditions. Further dissection of such heterogeneity can be achieved through efficient isolation of microglia from a given region of interest, followed by sensitive profiling of individual cells. Here, we provide a detailed protocol for the rapid isolation of microglia from different brain regions in a single adult mouse brain hemisphere. We also demonstrate how to use these sorted microglia for plate-based deep single-cell RNA sequencing. We discuss the adaptability of this method to other scenarios and provide guidelines for improving the system to accommodate large-scale studies.

Introduction

Microglia, representing 5%−10% of all neural cells, are resident macrophages scattered throughout the central nervous system (CNS)1. Protected behind blood-brain barrier, typical microglia in a healthy adult brain contain many fine processes that rapidly extend and retract to interact with neurons and other glial cells in the parenchyma. Microglia can also adopt the amoeboid morphology associated with increased phagocytic function during specific developmental stages or upon immune challenges in injury and disease1,2,3,

Protocol

All procedures involving rodents conformed to Stanford University guidelines, which comply with national and state laws and policies. All animal procedures were approved by Stanford University's Administrative Panel on Laboratory Animal Care.

NOTE: All solution and buffer compositions are provided in Table of Materials.

1. Preparation on the Day of Cell Isolation

  1. Prepare the following reagents and chill them on ice: medi.......

Representative Results

This protocol describes a method to isolate and sort microglia from different brain regions in one adult perfused brain hemisphere, followed by scRNA-seq. We use douncing to create single cell suspension and also as a first step to enrich microglia. Insufficient or over-douncing reduces the yield. In addition, adult mouse brains contain high levels of myelin, which can also reduce sorting efficiency and yield if not removed properly. Therefore, we examine the cell suspension under microscope by using trypan blue and a he.......

Discussion

Microglia actively interact with other cell types in the CNS, and they are very sensitive to environmental stimuli. In order to minimize inflammatory responses and aberrant changes in their gene expression during the isolation process, this protocol has been streamlined from a previously published method9, and it is now suitable to isolate microglia from multiple regions of a single mouse brain hemisphere in parallel. The tissues and reagents are kept at cold temperature and experiments are perfor.......

Acknowledgements

We thank Mariko L. Bennett, Liana Nicole Bonanno, and Spyros Darmanis for their help during the development of this protocol. We also thank the Stanford Shared FACS Facility, particularly Meredith Weglarz and Lisa Nichols; Yen Tran, Michael Eckart from Stanford Protein and Nucleic Acid Facility (PAN) for their great support for the filming. This work is funded by the JPB Foundation and Vincent J. Coates Foundation.

....

Materials

NameCompanyCatalog NumberComments
5 M BetaineSigma-AldrichCat# B0300-5VL
10 mM dNTP mixThermo Fisher ScientificCat# R0192
0.5 M EDTA, pH 8.0Thermo Fisher ScientificCat# 15575020
10X Hanks' Balanced Salt SolutionThermo Fisher ScientificCat# 14185-052
1 M HEPESThermo Fisher ScientificCat# 15630080
1X KAPA HIFI Hotstart Master MixKapa BiosciencesCat# KK2602
5 mL Round Bottom Polystyrene Tube, with Cell Strainer CapCorningCat# 352235
AATI, High Sensitivity NGS Fragment Analysis Kit (1 bp – 6,000 bp)Advanced AnalyticalCat# DNF-474-1000
Bovine Serum AlbuminSigma AldrichCat# A8806
DNase IWorthingtonCat# LS002007Working solution: 12500 units/ml
DTT, Molecular GradePromegaCat# P1171
ERCC RNA Spike-In MixThermo Fisher ScientificCat# 4456740
Fetal Bovine SerumThermo Fisher ScientificCat# 10437-028
Illumina XT Index Kit v2 Set A (96 indexes)IlluminaCat# FC-131-2001
Illumina XT Index Kit v2 Set B (96 indexes)IlluminaCat# FC-131-2002
Illumina XT Index Kit v2 Set C (96 indexes)IlluminaCat# FC-131-2003
Illumina XT Index Kit v2 Set D (96 indexes)IlluminaCat# FC-131-2004
Lambda Exonuclease (5 U/μl)New England BioLabsCat# M0262S
Mouse Fc blockBD PharmingenCat# 553142
Myelin removal beadsMiltenyl BiotecCat# 130-096-433
Nextera XT DNA Sample Prep KitIlluminaCat# FC-131-1096
NextSeq 500/550 High Output Kit v2.5 (150 Cycles)IlluminaCat# 20024907
PBS (10X), pH 7.4Thermo Fisher ScientificCat# 70011044
PCRClean DX beadsAline BiosciencesCat# C-1003-50
Propidium IodideThermo Fisher ScientificCat# P3566Staining: 1:1000
Qubit dsDNA HS Assay KitThermal Fisher ScientificCat# Q32851
Rat monoclonal anti mouse/human CD11b, Brilliant Violet 421 (clone M1/70)BioLegendCat# 101236; RRID: AB_11203704Staining: 1:300
Rat monoclonal anti mouse CD45, PE/Cy7 (clone 30-F11)Thermo Fisher ScientificCat# 25-0451-82; RRID: AB_469625Staining: 1:300
Recombinant RNase InhibitorTakara BioCat# 2313B
SMARTScribe Reverse Transcriptase (100 U/μl)ClontechCat# 639538Containing 5x First strand buffer
Oligonucleotides
0.1 μM ISPCR Oligo: 5' - AAGCAGTGGTATCAA
CGCAGAGT-3'
(Picelli et al., 2014)
Oligo-dT30VN primer: 5' - AAGCAGTGGTATCAACGCA
GAGTACT 30 VN-3'
(Picelli et al., 2014)
TSO 5' - AAGCAGTGGTATCAACGCAGA
GTACATrGrG+G-3' ("r" is forribobases and "+" is for an LNA base)
(Picelli et al., 2014)
Solutions
FACS bufferRecipe: sterile-filtered 1% FBS, 2 mM EDTA, 25 mM HEPES in 1X PBS
MCS bufferRecipe: sterile-filtered 0.5% BSA, 2 mM EDTA in 1X PBS
Medium ARecipe: 15 mM HEPES, 0.5% glucose in 1X HBSS without phenol red
Plates
384-well Rigi-Plate PCR Microplates, Axygen ScientificVWR89005-556
Hard-shell 96-well PCR platesBio-RadHSP9631
Others
Dumont #55 forcepsFine Science Tools11295-51
Dounce homogenizer, 2 mlWheaton357422
Large depletion columnMiltenyi Biotec130-042-901
Large selection columnMiltenyi Biotec130-042-401
MACS MultiStandMiltenyi Biotec130-042-303
QuadroMACS SeparatorMiltenyi Biotec130-090-976
RNAzapThermo Fisher ScientificAM9780
Strainer (70 μm)Falcon352350
Equipment
BD FACSAria IIBD Bioscienceshttp://www.bdbiosciences.com/
BioanalyzerAgilent2100
Fragment AnalyzerAgilent5300
Mosquito HTS nanoliter pipetting robotTTP Labtechhttps://www.ttplabtech.com/
Qubit 4 FluorometerThermo Fisher ScientificQ33226

References

  1. Li, Q., Barres, B. A. Microglia and macrophages in brain homeostasis and disease. Nature Reviews Immunology. 18 (4), 225-242 (2018).
  2. Li, Q., et al. Developmental Heterogeneity of Microg....

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MicrogliaSingle cell RNA SequencingBrain RegionsTissue DissociationCell IsolationCell SeparationDounce HomogenizerMagnetic SeparationRNA ExtractionLibrary PreparationDeep Sequencing

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