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早期命运决定小胶质细胞和非实质脑巨噬细胞的发育。

Early Fate Defines Microglia and Non-parenchymal Brain Macrophage Development.

机构信息

Institute of Experimental Immunology, University of Zurich, 8057 Zurich, Switzerland.

Singapore Immunology Network (SIgN), Agency for Science, Technology and Research (A∗STAR), 8A Biomedical Grove, Immunos Building, Levels 3 and 4, Singapore 138648, Singapore; Molecular Engineering Laboratory (MEL), Agency for Science, Technology and Research (A(∗)STAR), Singapore 138673, Singapore.

出版信息

Cell. 2020 Apr 30;181(3):557-573.e18. doi: 10.1016/j.cell.2020.03.021. Epub 2020 Apr 6.

Abstract

Central nervous system (CNS) macrophages comprise microglia and border-associated macrophages (BAMs) residing in the meninges, the choroid plexus, and the perivascular spaces. Most CNS macrophages emerge during development, with the exception of choroid plexus and dural macrophages, which are replaced by monocytes in adulthood. Whether microglia and BAMs share a developmental program or arise from separate lineages remains unknown. Here, we identified two phenotypically, transcriptionally, and locally distinct brain macrophages throughout development, giving rise to either microglia or BAMs. Two macrophage populations were already present in the yolk sac suggesting an early segregation. Fate-mapping models revealed that BAMs mostly derived from early erythro-myeloid progenitors in the yolk sac. The development of microglia was dependent on TGF-β, whereas the genesis of BAMs occurred independently of this cytokine. Collectively, our data show that developing parenchymal and non-parenchymal brain macrophages are separate entities in terms of ontogeny, gene signature, and requirement for TGF-β.

摘要

中枢神经系统 (CNS) 中的巨噬细胞包括小胶质细胞和存在于脑膜、脉络丛和血管周围间隙中的边缘相关巨噬细胞 (BAMs)。大多数 CNS 中的巨噬细胞是在发育过程中出现的,除了脉络丛和硬脑膜中的巨噬细胞,它们在成年后被单核细胞所取代。小胶质细胞和 BAMs 是否共享一个发育程序,或者是否来自不同的谱系,目前仍不清楚。在这里,我们在整个发育过程中鉴定出两种表型、转录和局部上不同的大脑巨噬细胞,它们分别产生小胶质细胞或 BAMs。两种巨噬细胞群体在蛋黄囊中已经存在,这表明它们在早期就已经分离。命运图谱模型表明,BAMs 主要来源于蛋黄囊中早期的红髓造血前体细胞。小胶质细胞的发育依赖于 TGF-β,而 BAMs 的产生则不依赖于这种细胞因子。总的来说,我们的数据表明,在发生、基因特征和对 TGF-β的需求方面,发育中的实质和非实质脑巨噬细胞是两个不同的实体。

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