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胶质细胞源性神经营养因子与局灶性缺血性脑卒中

Glial Cell Line-Derived Neurotrophic Factor and Focal Ischemic Stroke.

作者信息

Zhang Zhe, Sun Grace Y, Ding Shinghua

机构信息

Dalton Cardiovascular Research Center, University of Missouri-Columbia, Columbia, MO, 65211, USA.

Department of Biomedical, Biological and Chemical Engineering, University of Missouri-Columbia, Columbia, MO, 65211, USA.

出版信息

Neurochem Res. 2021 Oct;46(10):2638-2650. doi: 10.1007/s11064-021-03266-5. Epub 2021 Feb 16.

Abstract

Focal ischemic stroke (FIS) is a leading cause of human debilitation and death. Following the onset of a FIS, the brain experiences a series of spatiotemporal changes which are exemplified in different pathological processes. One prominent feature of FIS is the development of reactive astrogliosis and glial scar formation in the peri-infarct region (PIR). During the subacute phase, astrocytes in PIR are activated, referred to as reactive astrocytes (RAs), exhibit changes in morphology (hypotrophy), show an increased proliferation capacity, and altered gene expression profile, a phenomenon known as reactive astrogliosis. Subsequently, the morphology of RAs remains stable, and proliferation starts to decline together with the formation of glial scars. Reactive astrogliosis and glial scar formation eventually cause substantial tissue remodeling and changes in permanent structure around the PIR. Glial cell line-derived neurotrophic factor (GDNF) was originally isolated from a rat glioma cell-line and regarded as a potent survival neurotrophic factor. Under normal conditions, GDNF is expressed in neurons but is upregulated in RAs after FIS. This review briefly describes properties of GDNF, its receptor-mediated signaling pathways, as well as recent studies regarding the role of RAs-derived GDNF in neuronal protection and brain recovery. These results provide evidence suggesting an important role of RA-derived GDNF in intrinsic brain repair and recovery after FIS, and thus targeting GDNF in RAs may be effective for stroke therapy.

摘要

局灶性缺血性中风(FIS)是导致人类衰弱和死亡的主要原因。FIS发作后,大脑会经历一系列时空变化,这些变化在不同的病理过程中得以体现。FIS的一个突出特征是梗死周围区域(PIR)出现反应性星形胶质细胞增生和胶质瘢痕形成。在亚急性期,PIR中的星形胶质细胞被激活,称为反应性星形胶质细胞(RAs),其形态发生变化(萎缩),增殖能力增强,基因表达谱改变,这种现象称为反应性星形胶质细胞增生。随后,RAs的形态保持稳定,增殖开始下降,同时胶质瘢痕形成。反应性星形胶质细胞增生和胶质瘢痕形成最终导致PIR周围的大量组织重塑和永久结构变化。胶质细胞源性神经营养因子(GDNF)最初是从大鼠胶质瘤细胞系中分离出来的,被认为是一种强大的存活神经营养因子。在正常情况下,GDNF在神经元中表达,但在FIS后在RAs中上调。本文综述简要描述了GDNF的特性、其受体介导的信号通路,以及关于RAs来源的GDNF在神经元保护和脑恢复中的作用的最新研究。这些结果提供了证据,表明RAs来源的GDNF在FIS后的内源性脑修复和恢复中起重要作用,因此靶向RAs中的GDNF可能对中风治疗有效。

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