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帕金森病中突触小泡内吞功能障碍

Dysfunction of Synaptic Vesicle Endocytosis in Parkinson's Disease.

作者信息

Zou Li, Tian Ye, Zhang Zhentao

机构信息

Department of Neurology, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Front Integr Neurosci. 2021 May 20;15:619160. doi: 10.3389/fnint.2021.619160. eCollection 2021.

Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease. It is a chronic and progressive disorder estimated to affect at least 4 million people worldwide. Although the etiology of PD remains unclear, it has been found that the dysfunction of synaptic vesicle endocytosis (SVE) in neural terminal happens before the loss of dopaminergic neurons. Recently, accumulating evidence reveals that the PD-linked synaptic genes, including , , and , significantly contribute to the disruptions of SVE, which is vital for the pathogenesis of PD. In addition, the proteins encoded by other PD-associated genes such as , , , and also play key roles in the regulation of SVE. Here we present the facts about SVE-related genes and discussed their potential relevance to the pathogenesis of PD.

摘要

帕金森病(PD)是仅次于阿尔茨海默病的第二常见神经退行性疾病。它是一种慢性进行性疾病,据估计全球至少有400万人受其影响。尽管帕金森病的病因尚不清楚,但已发现神经末梢突触小泡内吞作用(SVE)功能障碍发生在多巴胺能神经元丧失之前。最近,越来越多的证据表明,与帕金森病相关的突触基因,包括[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]和[此处原文缺失具体基因名称],对SVE的破坏有显著影响,而SVE对帕金森病的发病机制至关重要。此外,其他与帕金森病相关基因如[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]、[此处原文缺失具体基因名称]和[此处原文缺失具体基因名称]所编码的蛋白质在SVE的调节中也起关键作用。在此,我们介绍了与SVE相关基因的相关事实,并讨论了它们与帕金森病发病机制的潜在相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faea/8172812/008a2a758286/fnint-15-619160-g001.jpg

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