TY - JOUR
T1 - Microglia Heterogeneity in the Single-Cell Era
AU - Masuda, Takahiro
AU - Sankowski, Roman
AU - Staszewski, Ori
AU - Prinz, Marco
N1 - Funding Information:
T.M. was supported by the KANAE Foundation for the Promotion of Medical Science and the Japan Society for the Promotion of Science (JSPS) as the JSPS Postdoctoral Fellow for Research Abroad. M.P. is supported by the Sobek Foundation , the Ernst-Jung Foundation , the German Research Foundation ( SFB 992 , SFB1160 , Reinhart-Koselleck grant), the Ministry of Science, Research and Arts, Baden-Wuerttemberg (Sonderlinie “Neuroinflammation”), and the BMBF -funded competence network of multiple sclerosis (KKNMS). This study was supported by the German Research Foundation (DFG) under Germany’s Excellence Strategy ( CIBSS – EXC-2189 – project ID 390939984).
Publisher Copyright:
© 2020 The Author(s)
PY - 2020/2/4
Y1 - 2020/2/4
N2 - 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-cell techniques, such as cytometry by time-of-flight mass 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.
AB - 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-cell techniques, such as cytometry by time-of-flight mass 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.
UR - http://www.scopus.com/inward/record.url?scp=85078732878&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85078732878&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2020.01.010
DO - 10.1016/j.celrep.2020.01.010
M3 - Review article
C2 - 32023447
AN - SCOPUS:85078732878
SN - 2211-1247
VL - 30
SP - 1271
EP - 1281
JO - Cell Reports
JF - Cell Reports
IS - 5
ER -