Journal
CELL REPORTS
Volume 30, Issue 5, Pages 1271-1281Publisher
CELL PRESS
DOI: 10.1016/j.celrep.2020.01.010
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Funding
- KANAE Foundation for the Promotion of Medical Science
- Japan Society for the Promotion of Science (JSPS)
- Sobek Foundation
- Ernst-Jung Foundation
- German Research Foundation [SFB 992, SFB1160]
- Ministry of Science, Research and Arts, Baden-Wuerttemberg (Sonderlinie Neuroinflammation'')
- BMBF
- German Research Foundation (DFG) under Germany's Excellence Strategy [CIBSS -EXC-2189, 390939984]
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Microglia are resident immune cells in the central nervous system (CNS) that are capable of carrying out prominent and various functions during development and adulthood under both homeostatic and disease conditions.Although microglia are traditionally thought to be heterogeneous populations, which potentially allows them to achieve a wide range of responses to environmental changes for the maintenance of CNS homeostasis,a lack of unbiased and high-throughput methods to assess microglia heterogeneity has prevented the study of spatially and temporally distributed microglia subsets. The recent emergence of novel single-celltechniques, such as cytometry by time-of-flightmass spectrometry (CyTOF) and single-cell RNA sequencing,enabled scientists to overcome such limitations and reveal the surprising context-dependent heterogeneity of microglia. In this review, we summarize the current knowledge about the spatial, temporal, and functional diversity of microglia during development, homeostasis, and disease in mice and humans.
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