Distinct Features of Brain-Resident Macrophages: Microglia and Non-Parenchymal Brain Macrophages

被引:17
作者
Lee, Eunju [1 ]
Eo, Jun-Cheol [1 ]
Lee, Changjun [1 ]
Yu, Je-Wook [1 ]
机构
[1] Yonsei Univ, Brain Korea 21 Project Med Sci, Inst Immunol & Immunol Dis, Dept Microbiol & Immunol,Coll Med, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
system-associated macrophages; inflammasome; microglia; non-parenchymal brain macrophages; CENTRAL-NERVOUS-SYSTEM; ALZHEIMERS-DISEASE; IMMUNE PRIVILEGE; MYELOID SUBSETS; INFLAMMASOME; MONOCYTES; ONTOGENY; CELLS; MOUSE; FATE;
D O I
10.14348/molcells.2021.0060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tissue-resident macrophages play an important role in maintaining tissue homeostasis and innate immune defense against invading microbial pathogens. Brain-resident macrophages can be classified into microglia in the brain parenchyma and non-parenchymal brain macrophages, also known as central nervous system-associated or border associated macrophages, in the brain-circulation interface. Microglia and non-parenchymal brain macrophages, including meningeal, perivascular, and choroid plexus macrophages, are mostly produced during embryonic development, and maintained their population by self renewal. Microglia have gained much attention for their dual roles in the maintenance of brain homeostasis and the induction of neuroinflammation. In particular, diverse phenotypes of microglia have been increasingly identified under pathological conditions. Single-cell phenotypic analysis revealed that microglia are highly heterogenous and plastic, thus it is difficult to define the status of microglia as M1/M2 or resting/activated state due to complex nature of microglia. Meanwhile, physiological function of non-parenchymal brain macrophages remain to be fully demonstrated. In this review, we have summarized the origin and signatures of brain resident macrophages and discussed the unique features of microglia, particularly, their phenotypic polarization, diversity of subtypes, and inflammasome responses related to neurodegenerative diseases.
引用
收藏
页码:281 / 291
页数:11
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