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成年小鼠海马背侧表面持续神经源性区域的鉴定及其受趋化因子SDF-1的调控

Identification of a sustained neurogenic zone at the dorsal surface of the adult mouse hippocampus and its regulation by the chemokine SDF-1.

作者信息

Belmadani Abdelhak, Ren Dongjun, Bhattacharyya Bula J, Rothwangl Katharina B, Hope Thomas J, Perlman Harris, Miller Richard J

机构信息

Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.

Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.

出版信息

Hippocampus. 2015 Nov;25(11):1224-41. doi: 10.1002/hipo.22428. Epub 2015 Mar 27.

Abstract

We identified a previously unknown neurogenic region at the dorsal surface of the hippocampus; (the "subhippocampal zone," SHZ) in the adult brain. Using a reporter mouse in which SHZ cells and their progeny could be traced through the expression of EGFP under the control of the CXCR4 chemokine receptor promoter we observed the presence of a pool of EGFP expressing cells migrating in direction of the dentate gyrus (DG), which is maintained throughout adulthood. This population appeared to originate from the SHZ where cells entered a caudal migratory stream (aCMS) that included the fimbria, the meninges and the DG. Deletion of CXCR4 from neural stem cells (NSCs) or neuroinflammation resulted in the appearance of neurons in the DG, which were the result of migration of NSCs from the SHZ. Some of these neurons were ectopically placed. Our observations indicate that the SHZ is a neurogenic zone in the adult brain through migration of NSCs in the aCMS. Regulation of CXCR4 signaling in these cells may be involved in repair of the DG and may also give rise to ectopic granule cells in the DG in the context of neuropathology.

摘要

我们在成年大脑海马体背侧表面发现了一个先前未知的神经源性区域;(“海马体下区”,SHZ)。利用一种报告基因小鼠,在CXCR4趋化因子受体启动子的控制下,通过绿色荧光蛋白(EGFP)的表达可以追踪SHZ细胞及其后代,我们观察到一群表达EGFP的细胞向齿状回(DG)方向迁移,这种现象在成年期一直存在。这群细胞似乎起源于SHZ,在那里细胞进入了一个尾侧迁移流(aCMS),该迁移流包括伞、脑膜和DG。从神经干细胞(NSCs)中删除CXCR4或神经炎症会导致DG中出现神经元,这是NSCs从SHZ迁移的结果。其中一些神经元位置异常。我们的观察表明,通过NSCs在aCMS中的迁移,SHZ是成年大脑中的一个神经源性区域。这些细胞中CXCR4信号的调节可能参与DG的修复,并且在神经病理学背景下也可能导致DG中出现异位颗粒细胞。

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