Mitochondrial association of alpha-synuclein causes oxidative stress

被引:0
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作者
M. S. Parihar
A. Parihar
M. Fujita
M. Hashimoto
P. Ghafourifar
机构
[1] Ohio State University,Department of Surgery, Davis Heart and Lung Research Institute, and Institute of Mitochondrial Biology
[2] Tokyo Metropolitan Institute for Neuroscience,Laboratory for Chemistry and Metabolism
[3] Fuchu,undefined
来源
关键词
Alpha synuclein; mitochondria; nitric oxide; Parkinson’s disease; mitochondrial calcium; cytochrome c; mitochondrial nitric oxide synthase; oxidative stress;
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摘要
α-Synuclein is a neuron-specific protein that contributes to the pathology of Parkinson’s disease via mitochondria-related mechanisms. The present study investigated possible interaction of α-synuclein with mitochondria and consequences of such interaction. Using SHSY cells overexpressing α-synuclein A53T mutant or wild-type, as well as isolated rat brain mitochondria, the present study shows that α-synuclein localizes at the mitochondrial membrane. In both SHSY cells and isolated mitochondria, interaction of α-synuclein with mitochondria causes release of cytochrome c, increase of mitochondrial calcium and nitric oxide, and oxidative modification of mitochondrial components. These findings suggest a pivotal role for mitochondria in oxidative stress and apoptosis induced by α-synuclein.
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页码:1272 / 1284
页数:12
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