AI Article Synopsis

  • Microglia are key immune cells in the brain, acting as macrophages for the central nervous system (CNS) but their molecular diversity is not well understood due to limitations in traditional gene expression measurement methods.
  • Recent advancements like single-cell RNA sequencing (scRNAseq) allow researchers to study individual microglia, revealing subpopulations with unique molecular and functional traits.
  • Recent studies categorized these microglial subpopulations into three groups based on factors like age, location, and disease, and also compared findings across different research to identify similarities and differences.

Article Abstract

Microglia are macrophages present in the brain that function as the primary and most important source of immune response in the central nervous system (CNS). Regardless of their multitasking role, our knowledge regarding their molecular heterogeneity is limited; due to technical restrictions, it is only possible to measure gene expression in cell populations, not individual cells, with the results reflecting average mRNA levels. Therefore, recent scientific approaches have focused on single-cell techniques such as single-cell RNA sequencing (scRNAseq), a powerful technique that enables the delineation of transcriptomic cell-to-cell differences, revealing subpopulations with distinct molecular and functional characteristics. Here, we summarize recent studies that focused on transcriptomic microglial subpopulation clustering and classify them into three distinct groups based on age, spatial distribution, and disease. Additionally, we cross-compare populations from different studies to identify expressional and functional overlaps between them.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368511PMC
http://dx.doi.org/10.3390/cells11152383DOI Listing

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