Minimizing the ex vivo confounds of cell-isolation techniques on transcriptomic profiles of purified microglia
Sarah R. OcañasiD, Kevin D. Pham, Harris E. BlankenshipiD, Adeline H. Machalinski, Ana J. Chucair‐ElliottiD, Willard M. FreemaniD
Abstract
Modern molecular neuroscience studies require analysis of specific cellular populations derived from brain tissue samples to disambiguate cell-type specific events. This is particularly true in the analysis of minority glial populations in the brain, such as microglia, which may be obscured in whole tissue analyses. Microglia have central functions in development, aging, and neurodegeneration and are a current focus of neuroscience research. A long-standing concern for glial biologists using in vivo models is whether cell isolation from CNS tissue could introduce ex vivo artifacts in microglia, which respond quickly to changes in the environment. Mouse microglia were purified by magnetic-activated cell sorting (MACS), as well as cytometer- and cartridge-based fluorescence-activated cell sorting (FACS) approaches to compare and contrast performance. The Cx3cr1-NuTRAP mouse model was used here to provide an endogenous fluorescent microglial marker and a microglial-specific translatome profile as a baseline comparison lacking cell isolation artifacts. All methods performed similarly for microglial purity with main differences being in cell yield and time of isolation. Ex vivo activation signatures occurred principally during the initial tissue dissociation and cell preparation and not the microglial cell sorting. Utilizing transcriptional and translational inhibitors during the cell preparation prevented the activational phenotype. These data demonstrate that a variety of microglial isolation approaches can be used, depending on experimental needs, and that inhibitor cocktails are effective at reducing cell preparation artifacts. Table of Contents Image O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=97 SRC="FIGDIR/small/452509v1_ufig1.gif" ALT="Figure 1"> View larger version (19K): org.highwire.dtl.DTLVardef@823562org.highwire.dtl.DTLVardef@7edb25org.highwire.dtl.DTLVardef@656feeorg.highwire.dtl.DTLVardef@197aae1_HPS_FORMAT_FIGEXP M_FIG C_FIG Main PointsMACS, cytometer-FACS, and cartridge-FACS give equivalent and sufficient yield/purity for microglial analyses. Ex vivo microglial activation is prevented by supplementation with transcription/translation inhibitors during cell preparation.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 8
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Translational Profiling Of Microglia Reveals Artifacts Of Cell Sorting
Silvia S. Kang, Kelsey E. Baker, … John Denis Fryer·bioRxiv·May 9, 2017
- A new method for obtaining bankable and expandable adult-like microglial cells
Min‐Jung You, Chan Rim, … Min‐Soo Kwon·Journal of NeuroinflammationPeer-reviewed·Dec 1, 2021
- A validated method for banking mixed glial cultures that yield responsive microglia
Annalise M. Sturno, James E. Hassell, … Kimberley D. Bruce·bioRxiv·Dec 20, 2025
- Protocol to isolate oligodendrocytes, microglia, endothelial cells, astrocytes, and neurons from a single mouse brain using magnetic-activated cell sorting
Samah Houmam, Dominika Siodłak, … Heather C. Rice·bioRxiv·Aug 8, 2025
- In situ Patch-seq analysis of microglia reveals a lack of stress genes as found in FACS-isolated microglia
O. Bakina, T. Conrad, … H. Kettenmann·bioRxiv·Mar 22, 2023
- PU.1-driven enrichment enables microglia profiling from frozen brain tissue using the high-throughput Smart-seq3xpress method
Dominika Dostalova, Pavel Abaffy, … Lukáš Valihrach·bioRxiv·Aug 11, 2025