In situ Patch-seq analysis of microglia reveals a lack of stress genes as found in FACS-isolated microglia.
Olga BakinaThomas ConradNina MiticRamon Oliveira VidalTessa ObrusnikSomesh SaiChristiane NolteMarcus SemtnerHelmut KettenmannPublished in: PloS one (2024)
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.
Keyphrases
- single cell
- inflammatory response
- genome wide
- rna seq
- neuropathic pain
- lipopolysaccharide induced
- high throughput
- dna methylation
- lps induced
- bioinformatics analysis
- genome wide identification
- spinal cord
- functional connectivity
- spinal cord injury
- poor prognosis
- genome wide analysis
- young adults
- cerebral ischemia
- resting state
- liver failure
- oxidative stress
- adipose tissue
- cell death
- skeletal muscle
- intensive care unit
- multiple sclerosis
- high resolution
- minimally invasive
- cognitive impairment
- drug induced
- cell proliferation
- artificial intelligence
- mass spectrometry