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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Selective loss of 20S proteasome alpha-subunits in the substantia nigra pars compacta in Parkinson's disease.
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Selective loss of 20S proteasome alpha-subunits in the substantia nigra pars compacta in Parkinson's disease.

机译:在帕金森氏病中,黑质致密部中20S蛋白酶体α亚基的选择性损失。

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摘要

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.
机译:在散发性帕金森氏病(PD)的黑质致密部(SNc)中,26 / 20S蛋白酶体的蛋白水解活性受到损害。在本研究中,我们通过确定通常共同构成26 / 20S蛋白酶体催化核心的β-和α-亚基的水平来检查蛋白酶体的结构完整性。 Western印迹分析和免疫组织化学染色显示,SNc的多巴胺能神经元中有大量选择性的α亚基丢失,而散发PD的其他脑区域则没有。已知该缺陷会导致蛋白酶体变得不稳定并阻止其组装,从而导致酶活性的损害。因此,散发性PD中SNc中26 / 20S蛋白酶体的结构和功能缺陷可能是蛋白质积累,蛋白质路易体形成和多巴胺能神经元死亡的基础。

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