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In situ Patch-seq analysis of microglia reveals a lack of stress genes as found in FACS-isolated microglia.


ABSTRACT: We applied the patch-seq technique to harvest transcripts from individual microglial cells from cortex, hippocampus and corpus callosum of acute brain slices from adult mice. After recording membrane currents with the patch-clamp technique, the cytoplasm was collected via the pipette and underwent adapted SMART-seq2 preparation with subsequent sequencing. On average, 4138 genes were detected in 113 cells from hippocampus, corpus callosum and cortex, including microglia markers such as Tmem119, P2ry12 and Siglec-H. Comparing our dataset to previously published single cell mRNA sequencing data from FACS-isolated microglia indicated that two clusters of cells were absent in our patch-seq dataset. Pathway analysis of marker genes in FACS-specific clusters revealed association with microglial activation and stress response. This indicates that under normal conditions microglia in situ lack transcripts associated with a stress-response, and that the microglia-isolation procedure by mechanical dissociation and FACS triggers the expression of genes related to activation and stress.

SUBMITTER: Bakina O 

PROVIDER: S-EPMC11239014 | biostudies-literature | 2024

REPOSITORIES: biostudies-literature

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In situ Patch-seq analysis of microglia reveals a lack of stress genes as found in FACS-isolated microglia.

Bakina Olga O   Conrad Thomas T   Mitic Nina N   Vidal Ramon Oliveira RO   Obrusnik Tessa T   Sai Somesh S   Nolte Christiane C   Semtner Marcus M   Kettenmann Helmut H  

PloS one 20240711 7


We applied the patch-seq technique to harvest transcripts from individual microglial cells from cortex, hippocampus and corpus callosum of acute brain slices from adult mice. After recording membrane currents with the patch-clamp technique, the cytoplasm was collected via the pipette and underwent adapted SMART-seq2 preparation with subsequent sequencing. On average, 4138 genes were detected in 113 cells from hippocampus, corpus callosum and cortex, including microglia markers such as Tmem119, P  ...[more]

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