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神经退行性疾病中的泛素蛋白酶体系统:罪魁祸首、帮凶还是受害者?

The ubiquitin proteasome system in neurodegenerative diseases: culprit, accomplice or victim?

机构信息

Department of Neuroscience, Faculty of Health Medicine and Life Sciences, Maastricht University, Universiteitssingel 50, P.O. Box 616, 6200 MD Maastricht, The Netherlands.

出版信息

Prog Neurobiol. 2012 Feb;96(2):190-207. doi: 10.1016/j.pneurobio.2012.01.003. Epub 2012 Jan 16.

Abstract

A shared hallmark for many neurodegenerative disorders is the accumulation of toxic protein species which is assumed to be the cause for these diseases. Since the ubiquitin proteasome system (UPS) is the most important pathway for selective protein degradation it is likely that it is involved in the aetiology neurodegenerative disorders. Indeed, impairment of the UPS has been reported to occur during neurodegeneration. Although accumulation of toxic protein species (amyloid β) are in turn known to impair the UPS the relationship is not necessarily causal. We provide an overview of the most recent insights in the roles the UPS plays in protein degradation and other processes. Additionally, we discuss the role of the UPS in clearance of the toxic proteins known to accumulate in the hallmarks of neurodegenerative diseases. The present paper will focus on critically reviewing the involvement of the UPS in specific neurodegenerative diseases and will discuss if UPS impairment is a cause, a consequence or both of the disease.

摘要

许多神经退行性疾病的一个共同特征是有毒蛋白质的积累,这被认为是这些疾病的原因。由于泛素蛋白酶体系统 (UPS) 是选择性蛋白质降解最重要的途径,因此它很可能参与了神经退行性疾病的发病机制。事实上,已有报道称 UPS 在神经退行性变过程中受到损害。尽管有毒蛋白质(淀粉样 β)的积累反过来已知会损害 UPS,但这种关系不一定具有因果关系。我们提供了 UPS 在蛋白质降解和其他过程中的作用的最新见解概述。此外,我们还讨论了 UPS 在清除神经退行性疾病特征中积累的有毒蛋白质中的作用。本文将重点批判性地审查 UPS 在特定神经退行性疾病中的参与情况,并讨论 UPS 损伤是疾病的原因、后果还是两者兼而有之。

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