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帕金森病中黑质致密部20S蛋白酶体α亚基的选择性缺失。

Selective loss of 20S proteasome alpha-subunits in the substantia nigra pars compacta in Parkinson's disease.

作者信息

McNaught Kevin St P, Belizaire Roger, Jenner Peter, Olanow C Warren, Isacson Ole

机构信息

Department of Neurology, Mount Sinai School of Medicine, Annenberg 14-73, One Gustave L. Levy Place, New York, NY 10029, USA.

出版信息

Neurosci Lett. 2002 Jul 5;326(3):155-8. doi: 10.1016/s0304-3940(02)00296-3.

Abstract

The proteolytic activities of 26/20S proteasomes are impaired in the substantia nigra pars compacta (SNc) in sporadic Parkinson's disease (PD). In the present study, we examined the structural integrity of the proteasome by determining the levels of the beta- and alpha-subunits which together normally constitute the catalytic core of 26/20S proteasomes. Western blot analyzes and immunohistochemical staining revealed a major and selective loss of alpha-subunits in dopaminergic neurons of the SNc but not in other brain regions in sporadic PD. This defect is known to cause the proteasome to become unstable and prevents its assembly with resultant impairment of enzymatic activity. Thus, structural and function defects in 26/20S proteasomes may underlie protein accumulation, formation of proteinaceous Lewy bodies and dopaminergic neuronal death in the SNc in sporadic PD.

摘要

在散发性帕金森病(PD)中,黑质致密部(SNc)的26/20S蛋白酶体的蛋白水解活性受损。在本研究中,我们通过测定通常共同构成26/20S蛋白酶体催化核心的β亚基和α亚基的水平,来检测蛋白酶体的结构完整性。蛋白质印迹分析和免疫组织化学染色显示,散发性PD患者SNc的多巴胺能神经元中α亚基存在主要且选择性的缺失,而在其他脑区则没有。已知这种缺陷会导致蛋白酶体变得不稳定,并阻止其组装,从而导致酶活性受损。因此,26/20S蛋白酶体的结构和功能缺陷可能是散发性PD中SNc蛋白质积累、蛋白质路易小体形成和多巴胺能神经元死亡的基础。

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