Wallace D C
Center for Molecular Medicine, Emory University, 1462 Clifton Road, Suite 420, Atlanta, GA 30322, USA.
Science. 1999 Mar 5;283(5407):1482-8. doi: 10.1126/science.283.5407.1482.
Over the past 10 years, mitochondrial defects have been implicated in a wide variety of degenerative diseases, aging, and cancer. Studies on patients with these diseases have revealed much about the complexities of mitochondrial genetics, which involves an interplay between mutations in the mitochondrial and nuclear genomes. However, the pathophysiology of mitochondrial diseases has remained perplexing. The essential role of mitochondrial oxidative phosphorylation in cellular energy production, the generation of reactive oxygen species, and the initiation of apoptosis has suggested a number of novel mechanisms for mitochondrial pathology. The importance and interrelationship of these functions are now being studied in mouse models of mitochondrial disease.
在过去十年中,线粒体缺陷与多种退行性疾病、衰老及癌症相关。对这些疾病患者的研究揭示了线粒体遗传学的诸多复杂性,线粒体遗传学涉及线粒体基因组与核基因组突变之间的相互作用。然而,线粒体疾病的病理生理学仍然令人困惑。线粒体氧化磷酸化在细胞能量产生、活性氧生成及细胞凋亡启动中的关键作用提示了一些线粒体病理学的新机制。目前正在线粒体疾病的小鼠模型中研究这些功能的重要性及相互关系。