Hegde Ashok N, Upadhya Sudarshan C
Department of Neurology and Anatomy, Wake Forest University Health Sciences, Winston-Salem, NC 27157, USA.
Biochim Biophys Acta. 2011 Feb;1809(2):128-40. doi: 10.1016/j.bbagrm.2010.07.006. Epub 2010 Aug 3.
Proteolysis by the ubiquitin-proteasome pathway (UPP) is now widely recognized as a molecular mechanism controlling myriad normal functions in the nervous system. Also, this pathway is intimately linked to many diseases and disorders of the brain. Among the diseases connected to the UPP are neurodegenerative disorders such as Alzheimer's, Parkinson's and Huntington's diseases. Perturbation in the UPP is also believed to play a causative role in mental disorders such as Angelman syndrome. The pathology of neurodegenerative diseases is characterized by abnormal deposition of insoluble protein aggregates or inclusion bodies within neurons. The ubiquitinated protein aggregates are believed to result from dysfunction of the UPP or from structural changes in the protein substrates which prevent their recognition and degradation by the UPP. An early effect of abnormal UPP in diseases of the nervous system is likely to be impairment of synaptic function. Here we discuss the UPP and its physiological roles in the nervous system and how alterations in the UPP relate to development of nervous system diseases. This article is part of a Special Issue entitled The 26S Proteasome: When degradation is just not enough!
泛素-蛋白酶体途径(UPP)介导的蛋白质水解作用如今已被广泛认为是一种控制神经系统中无数正常功能的分子机制。此外,该途径与许多脑部疾病和功能紊乱密切相关。与UPP相关的疾病包括神经退行性疾病,如阿尔茨海默病、帕金森病和亨廷顿病。UPP的紊乱也被认为在诸如天使综合征等精神疾病中起致病作用。神经退行性疾病的病理学特征是神经元内出现不溶性蛋白质聚集体或包涵体的异常沉积。泛素化的蛋白质聚集体被认为是由UPP功能障碍或蛋白质底物的结构变化导致的,这些变化阻止了它们被UPP识别和降解。UPP异常在神经系统疾病中的早期影响可能是突触功能受损。在此,我们讨论UPP及其在神经系统中的生理作用,以及UPP的改变与神经系统疾病发展的关系。本文是名为“26S蛋白酶体:当降解远远不够时!”的特刊的一部分。