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α-突触核蛋白如何损害帕金森病神经元的线索。

Clues to how alpha-synuclein damages neurons in Parkinson's disease.

机构信息

Department of Neurology, Columbia University Medical School, New York State Psychiatric Institute, New York, New York 10032, USA.

出版信息

Mov Disord. 2010;25 Suppl 1:S27-31. doi: 10.1002/mds.22639.

Abstract

Alpha-synuclein (alpha-syn) appears to normally regulate neurotransmitter release, possibly via calcium-dependent binding and dissociation from lipid domains on secretory vesicles. The pathogenic effects of alpha-syn leading to Parkinson's disease (PD) appear to result from alternate toxic effects on lipid membrane. A variety of findings indicate that overexpression of wild-type alpha-syn, pathogenic mutations of alpha-syn, and dopamine-modified-alpha-syn promote toxic interaction between alpha-syn oligomers and lipids. These may disrupt transmembrane concentration gradients across secretory vesicles and other organelles and interfere with normal lysosomal or ubiqutin/proteasome mediated protein degradation or mitochondrial function. Additional causes of PD may interfere at other points with normal handling and degradation of alpha-syn, providing a variety of entry points to a converging neurodegenerative path underlying the disease.

摘要

阿尔法-突触核蛋白(alpha-syn)似乎可以正常调节神经递质的释放,可能是通过与分泌小泡上的脂质域的钙依赖性结合和解离来实现。导致帕金森病(PD)的 alpha-syn 的致病作用似乎是由于对脂质膜的替代毒性作用。各种研究结果表明,野生型 alpha-syn 的过表达、alpha-syn 的致病性突变以及多巴胺修饰的 alpha-syn 促进 alpha-syn 寡聚体与脂质之间的毒性相互作用。这可能会破坏分泌小泡和其他细胞器跨膜浓度梯度,并干扰正常的溶酶体或泛素/蛋白酶体介导的蛋白质降解或线粒体功能。PD 的其他原因可能会在其他方面干扰 alpha-syn 的正常处理和降解,为疾病背后的收敛性神经退行性途径提供了多种切入点。

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