Department of Neurology, University of Kansas School of Medicine, Kansas City, KS 66160, USA.
J Alzheimers Dis. 2009;17(4):737-51. doi: 10.3233/JAD-2009-1095.
Mitochondria are physically or functionally altered in many neurodegenerative diseases. This is the case for very rare neurodegenerative disorders as well as extremely common age-related ones such as Alzheimer's disease and Parkinson's disease. In some disorders very specific patterns of altered mitochondrial function or systemic mitochondrial dysfunction are demonstrable. Some disorders arise from mitochondrial DNA mutation, some from nuclear gene mutation, and for some the etiology is not definitively known. This review classifies neurodegenerative diseases using mitochondrial dysfunction as a unifying feature, and in doing so defines a group of disorders called the neurodegenerative mitochondriopathies. It discusses what mitochondrial abnormalities have been identified in various neurodegenerative diseases, what is currently known about the mitochondria-neurodegeneration nexus, and speculates on the significance of mitochondrial function in some disorders not classically thought of as mitochondriopathies.
线粒体在许多神经退行性疾病中发生了物理或功能上的改变。这种情况不仅存在于非常罕见的神经退行性疾病中,也存在于极其常见的与年龄相关的疾病中,如阿尔茨海默病和帕金森病。在某些疾病中,可以证明存在非常特定的线粒体功能改变模式或系统性线粒体功能障碍。一些疾病是由线粒体 DNA 突变引起的,一些是由核基因突变引起的,而对于一些疾病,其病因尚不清楚。本综述将神经退行性疾病分类为以线粒体功能障碍为统一特征的疾病,并在此过程中定义了一组称为神经退行性线粒体病的疾病。它讨论了在各种神经退行性疾病中已经确定了哪些线粒体异常,目前关于线粒体-神经退行性变联系的了解程度,以及对一些通常不被认为是线粒体病的疾病中线粒体功能的意义进行推测。