Microglia Heterogeneity in the Single-Cell Era

被引:437
|
作者
Masuda, Takahiro [1 ]
Sankowski, Roman [1 ,2 ]
Staszewski, Ori [1 ,2 ]
Prinz, Marco [1 ,3 ,4 ,5 ]
机构
[1] Univ Freiburg, Inst Neuropathol, Fac Med, Freiburg, Germany
[2] Univ Freiburg, Berta Ottenstein Programme Clinician Scientists, Fac Med, Freiburg, Germany
[3] Univ Freiburg, Signalling Res Ctr BIOSS, Freiburg, Germany
[4] Univ Freiburg, Signalling Res Ctr CIBSS, Freiburg, Germany
[5] Univ Freiburg, Ctr Basics NeuroModulat NeuroModulBasics, Fac Med, Freiburg, Germany
来源
CELL REPORTS | 2020年 / 30卷 / 05期
基金
日本学术振兴会;
关键词
CENTRAL-NERVOUS-SYSTEM; LANGERHANS CELLS; ADULT MICROGLIA; REVEALS; MACROPHAGES; MAINTENANCE; ACTIVATION; EXPRESSION; FATE; MYELINOGENESIS;
D O I
10.1016/j.celrep.2020.01.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:1271 / 1281
页数:11
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