神经退行性疾病中的泛素-蛋白酶体系统

Journal of drug metabolism & toxicology Pub Date : 2015-01-01 Epub Date: 2015-08-13 DOI:10.4172/2157-7609.1000187
Geeta Rao, Brandon Croft, Chengwen Teng, Vibhudutta Awasthi
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引用次数: 0

摘要

细胞蛋白稳态是一个高度动态的过程,主要由泛素蛋白酶体系统(UPS)的降解工具完成。泛素-蛋白酶体系统功能异常会导致受损或折叠错误蛋白质的积累,从而形成细胞内和细胞外的聚集蛋白沉积,导致细胞功能障碍和/或死亡。异常蛋白聚集体的沉积和细胞无法清除这些聚集体与阿尔茨海默氏症和帕金森氏症等多种神经退行性疾病的发病机制有关。与肿瘤发生过程中蛋白酶体功能的上调以及将蛋白酶体抑制作为一种治疗策略相反,激活蛋白酶体功能将有助于达到治疗神经退行性疾病的目的。这篇综述介绍了目前对蛋白酶体在神经退行性疾病中作用的理解,以及蛋白酶体调节在其中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ubiquitin-Proteasome System in Neurodegenerative Disorders.

Ubiquitin-Proteasome System in Neurodegenerative Disorders.

Ubiquitin-Proteasome System in Neurodegenerative Disorders.

Ubiquitin-Proteasome System in Neurodegenerative Disorders.

Cellular proteostasis is a highly dynamic process and is primarily carried out by the degradation tools of ubiquitin-proteasome system (UPS). Abnormalities in UPS function result in the accumulation of damaged or misfolded proteins which can form intra- and extracellular aggregated proteinaceous deposits leading to cellular dysfunction and/or death. Deposition of abnormal protein aggregates and the cellular inability to clear them have been implicated in the pathogenesis of a number of neurodegenerative disorders such as Alzheimer's and Parkinson's. Contrary to the upregulation of proteasome function in oncogenesis and the use of proteasome inhibition as a therapeutic strategy, activation of proteasome function would serve therapeutic objectives of treatment of neurodegenerative diseases. This review describes the current understanding of the role of the proteasome in neurodegenerative disorders and potential utility of proteasomal modulation therein.

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