Deciphering microglia phenotypes in health and disease

被引:3
|
作者
Balak, Christopher [1 ,2 ]
Han, Claudia Z. [1 ]
Glass, Christopher K. [1 ,3 ]
机构
[1] Univ Calif San Diego, Dept Cellular & Mol Med, San Diego, CA 92093 USA
[2] Univ Calif San Diego, Biomed Sci Grad Program, San Diego, CA USA
[3] Univ Calif San Diego, Dept Med, San Diego, CA 92093 USA
关键词
IN-VIVO; BRAIN; MACROPHAGES; MOUSE; FATE; RISK; ONTOGENY; VARIANTS; DRIVES; SALL1;
D O I
10.1016/j.gde.2023.102146
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microglia are the major immune cells of the central nervous system (CNS) that perform numerous adaptive functions required for normal CNS development and homeostasis but are also linked to neurodegenerative and behavioral diseases. Microglia development and function are strongly influenced by brain environmental signals that are integrated at the level of transcriptional enhancers to drive specific programs of gene expression. Here, we describe a conceptual framework for how lineage-determining and signal-dependent transcription factors interact to select and regulate the ensembles of enhancers that determine microglia development and function. We then highlight recent findings that advance these concepts and conclude with a consideration of open questions that represent some of the major hurdles to be addressed in the future.
引用
收藏
页数:9
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