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

冲程(发动机) 神经保护 脑源性神经营养因子 医学 内科学 缺血性中风 缺血 神经营养素 神经学 星形胶质细胞 细胞生物学 胶质纤维酸性蛋白 小胶质细胞 神经生长因子 神经突 神经退行性变 脑缺血
作者
Zhe Zhang,Grace Y. Sun,Shinghua Ding
出处
期刊:Neurochemical Research [Springer Nature]
卷期号:46 (10): 2638-2650
标识
DOI:10.1007/s11064-021-03266-5
摘要

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.
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