神经退行性变
线粒体
氧化应激
线粒体DNA
生物
程序性细胞死亡
氧化磷酸化
老化
细胞生物学
神经科学
疾病
遗传学
医学
生物信息学
基因
细胞凋亡
病理
生物化学
作者
Michael T. Lin,M. Flint Beal
出处
期刊:Nature
[Springer Nature]
日期:2006-10-01
卷期号:443 (7113): 787-795
被引量:5781
摘要
Many lines of evidence suggest that mitochondria have a central role in ageing-related neurodegenerative diseases. Mitochondria are critical regulators of cell death, a key feature of neurodegeneration. Mutations in mitochondrial DNA and oxidative stress both contribute to ageing, which is the greatest risk factor for neurodegenerative diseases. In all major examples of these diseases there is strong evidence that mitochondrial dysfunction occurs early and acts causally in disease pathogenesis. Moreover, an impressive number of disease-specific proteins interact with mitochondria. Thus, therapies targeting basic mitochondrial processes, such as energy metabolism or free-radical generation, or specific interactions of disease-related proteins with mitochondria, hold great promise.
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