Lim Kah-Leong, Tan Jeanne M M
Neurodegeneration Research Laboratory, National Neuroscience Institute, Singapore.
BMC Biochem. 2007 Nov 22;8 Suppl 1(Suppl 1):S13. doi: 10.1186/1471-2091-8-S1-S13.
Parkinson's disease (PD) is the most common neurodegenerative movement disorder. Although a subject of intense research, the etiology of PD remains poorly understood. Recently, several lines of evidence have implicated an intimate link between aberrations in the ubiquitin proteasome system (UPS) and PD pathogenesis. Derangements of the UPS, which normally functions as a type of protein degradation machinery, lead to alterations in protein homeostasis that could conceivably promote the toxic accumulation of proteins detrimental to neuronal survival. Not surprisingly, various cellular and animal models of PD that are based on direct disruption of UPS function reproduce the most prominent features of PD. Although persuasive, new developments in the past few years have in fact raised serious questions about the link between the UPS and PD. Here I review current thoughts and controversies about their relationship and discuss whether strategies aimed at mitigating UPS dysfunction could represent rational ways to intervene in the disease. Publication history: Republished from Current BioData's Targeted Proteins database (TPdb; http://www.targetedproteinsdb.com).
帕金森病(PD)是最常见的神经退行性运动障碍。尽管是深入研究的课题,但PD的病因仍知之甚少。最近,几条证据链表明泛素蛋白酶体系统(UPS)异常与PD发病机制之间存在密切联系。UPS通常作为一种蛋白质降解机制发挥作用,其紊乱会导致蛋白质稳态改变,这可能会促进对神经元存活有害的蛋白质的毒性积累。毫不奇怪,基于直接破坏UPS功能的各种PD细胞和动物模型重现了PD最突出的特征。尽管有说服力,但过去几年的新进展实际上对UPS与PD之间的联系提出了严重质疑。在此,我回顾了关于它们关系的当前观点和争议,并讨论了旨在减轻UPS功能障碍的策略是否可能是干预该疾病的合理方法。出版历史:转载自Current BioData的靶向蛋白质数据库(TPdb;http://www.targetedproteinsdb.com)。