Recessive Parkinson's disease

被引:24
作者
Kubo, Shin-ichiro
Hattori, Nobutaka
Mizuno, Yoshikuni
机构
[1] Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1138421, Japan
[2] Juntendo Univ, Sch Med, Res Inst Dis Old Age, Tokyo 113, Japan
关键词
parkin; PINK1; DJ-1; recessive Parkinson's disease; mitochondria; oxidative stress; ubiquitin-proteasome system;
D O I
10.1002/mds.20841
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease (PD) is a progressive neurodegenerative disease caused by loss of dopaminergic neurons in the substantia nigra pars compacta. Although the etiology of PD remains unclear, it is now clear that genetic factors contribute to the pathogenesis of the disease. Recently, several causative genes have been identified in monogenic forms of PD. Accumulating evidence indicates that their gene products play important roles in mitochondrial function, oxidative stress response, and the ubiquitin-proteasome system, which are also implicated in sporadic PD, suggesting that these gene products share a common pathway to nigral degeneration in both familial and sporadic PD. Here, we review recent advances in knowledge about genes associated with recessive PD, including parkin, PINK1, and DJ-1. (C) 2006 Movement Disorder Society.
引用
收藏
页码:885 / 893
页数:9
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