Suppr超能文献

Netrin-G1 调节轴突周围小胶质细胞的聚集,并支持出生后小鼠大脑中第 V 层神经元的存活。

Netrin-G1 Regulates Microglial Accumulation along Axons and Supports the Survival of Layer V Neurons in the Postnatal Mouse Brain.

机构信息

Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, 2-2, Yamadaoka, Suita, Osaka 565-0871, Japan; WPI Immunology Frontier Research Center, Osaka University, 3-1, Yamadaoka, Suita, Osaka 565-0871, Japan.

Department of Molecular Neuroscience, Graduate School of Medicine, Osaka University, 2-2, Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Cell Rep. 2020 Apr 28;31(4):107580. doi: 10.1016/j.celrep.2020.107580.

Abstract

Microglia, the resident immune cells of the central nervous system, accumulate along subcerebral projection axons and support neuronal survival during the early postnatal period. It remains unknown how microglia follow an axon-specific distribution pattern to maintain neural circuits. Here, we investigated the mechanisms of microglial accumulation along subcerebral projection axons that were necessary for microglial accumulation in the internal capsule. Screening of molecules involved in this accumulation of microglia to axons of layer V cortical neurons identified netrin-G1, a member of the netrin family of axon guidance molecules with a glycosyl-phosphatidylinositol anchor. Deletion or knockdown of the netrin-G1 gene Ntng1 reduced microglial accumulation and caused loss of cortical neurons. Netrin-G1 ligand-Ngl1 knockout-mice-derived microglia showed reduced accumulation along the axons compared with wild-type microglia. Thus, microglia accumulate around the subcerebral projection axons via NGL1-netrin-G1 signaling and support neuronal survival. Our observations unveil bidirectional neurotrophic interactions between neurons and microglia.

摘要

小胶质细胞是中枢神经系统的固有免疫细胞,它们沿着皮质下投射轴突聚集,并在出生后早期支持神经元的存活。目前尚不清楚小胶质细胞如何遵循特定的轴突分布模式来维持神经回路。在这里,我们研究了小胶质细胞沿皮质下投射轴突聚集的机制,这些机制对于小胶质细胞在内囊中的聚集是必要的。对参与小胶质细胞向 V 层皮质神经元轴突聚集的分子进行筛选,鉴定出了神经导向分子 netrin 家族的成员 netrin-G1,它带有糖基磷脂酰肌醇锚。netrin-G1 基因 Ntng1 的缺失或敲低减少了小胶质细胞的聚集,并导致皮质神经元的丧失。与野生型小胶质细胞相比,netrin-G1 配体 Ngl1 敲除小鼠来源的小胶质细胞沿轴突的聚集减少。因此,小胶质细胞通过 NGL1-netrin-G1 信号沿着皮质下投射轴突聚集,并支持神经元的存活。我们的观察结果揭示了神经元和小胶质细胞之间的双向神经营养相互作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验