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小胶质细胞通过 CXCL12/CXCR4 系统广泛地探测发育中的皮层,以帮助神经祖细胞获得分化特性。

Microglia extensively survey the developing cortex via the CXCL12/CXCR4 system to help neural progenitors to acquire differentiated properties.

机构信息

Department of Anatomy and Cell Biology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Japan Society for the Promotion of Science, Tokyo, Japan.

出版信息

Genes Cells. 2018 Oct;23(10):915-922. doi: 10.1111/gtc.12632. Epub 2018 Aug 24.

Abstract

Neocortical development proceeds through the formation of new zones in which neural-lineage cells are organized based on their differentiation status. Although microglia initially distribute homogeneously throughout the growing cerebral wall, they accumulate in the inner cytogenic zone, the ventricular zone (VZ) and the subventricular zone (SVZ) in the mid-embryonic stage. However, the roles of these cells remain to be elucidated. In this study, we found that microglia, despite being only a minor population of the cells that constitute the cerebral wall, promote the differentiation of neural progenitor cells by frequently moving throughout the cortex; their migration is mediated by the CXCL12/CXCR4 system. Pulse-chase experiments confirmed that microglia help Pax6 stem-like cells to differentiate into Tbr2 intermediate progenitors. Further, monitoring of microglia by live imaging showed that administration of AMD3100, an antagonist of CXCR4, dampened microglial movement and decreased microglial surveillance throughout the cortex. In particular, arrest of microglial motion led to a prominent decrease in the abundance of Tbr2 cells in the SVZ. Based on our findings, we propose that extensive surveillance by microglia contributes to the efficient functioning of these cells, thereby regulating the differentiation of neural stem-like cells.

摘要

新皮质的发育是通过形成新的区域来进行的,在这些区域中,神经谱系细胞根据其分化状态进行组织。尽管小胶质细胞最初在整个生长的脑壁中均匀分布,但它们在中胚层阶段会聚集在内细胞生区、脑室区(VZ)和侧脑室下区(SVZ)。然而,这些细胞的作用仍有待阐明。在这项研究中,我们发现小胶质细胞,尽管只占脑壁细胞的一小部分,通过在皮层中频繁移动来促进神经祖细胞的分化;它们的迁移是由 CXCL12/CXCR4 系统介导的。脉冲追踪实验证实,小胶质细胞有助于 Pax6 干细胞样细胞分化为 Tbr2 中间祖细胞。此外,通过活体成像监测小胶质细胞,我们发现施用 AMD3100(CXCR4 的拮抗剂)会抑制小胶质细胞的运动,并减少整个皮层中小胶质细胞的监测。特别是,小胶质细胞运动的停止导致 SVZ 中 Tbr2 细胞的丰度明显减少。基于我们的发现,我们提出小胶质细胞的广泛监测有助于这些细胞的有效功能,从而调节神经干细胞样细胞的分化。

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