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神经退行性疾病中的线粒体质量控制

Mitochondrial quality control in neurodegenerative diseases.

作者信息

Dupuis Luc

机构信息

INSERM, U1118, Strasbourg F-67085, France; Université de Strasbourg, Fédération de Médecine Translationnelle (FMTS), UMRS1118, Strasbourg F-67085, France.

出版信息

Biochimie. 2014 May;100:177-83. doi: 10.1016/j.biochi.2013.07.033. Epub 2013 Aug 16.

DOI:10.1016/j.biochi.2013.07.033
PMID:23958438
Abstract

Mutations causing genetic forms of Parkinson's disease or hereditary neuropathies have been recently shown to affect key molecular players involved in the recycling of defective mitochondria, most notably PARKIN, PINK1, Mitofusin 2 or dynein heavy chain. Interestingly, the same pathways are also indirectly targeted by multiple other mutations involved in familial forms of amyotrophic lateral sclerosis, Huntington's disease or Alzheimer's disease. These recent genetic results strongly reinforce the notion that defective mitochondrial physiology might cause neurodegeneration. Mitochondrial dysfunction has however been observed in virtually every neurodegenerative disease and appears not restricted to the most vulnerable neuronal populations affected by a given disease. Thus, the mechanisms linking defective mitochondrial quality control to death of selective neuronal populations remain to be identified. This review provides an update on the most recent literature on mitochondrial quality control and its impairment during neurodegenerative diseases.

摘要

最近研究表明,导致帕金森病或遗传性神经病变的基因形式的突变会影响参与缺陷线粒体再循环的关键分子,最显著的是帕金森蛋白(PARKIN)、PTEN诱导激酶1(PINK1)、线粒体融合蛋白2(Mitofusin 2)或动力蛋白重链。有趣的是,参与肌萎缩侧索硬化症、亨廷顿舞蹈病或阿尔茨海默病家族形式的其他多种突变也间接靶向相同的信号通路。这些最新的遗传学研究结果有力地强化了缺陷线粒体生理学可能导致神经退行性变的观点。然而,几乎在每一种神经退行性疾病中都观察到了线粒体功能障碍,而且似乎并不局限于受特定疾病影响的最易受损的神经元群体。因此,将缺陷线粒体质量控制与选择性神经元群体死亡联系起来的机制仍有待确定。这篇综述提供了有关线粒体质量控制及其在神经退行性疾病中的损伤的最新文献的最新情况。

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