University of Helsinki, Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, 00290 Helsinki, Finland.
Neuroscience Center, University of Helsinki, 00790 Helsinki, Finland.
Nat Rev Mol Cell Biol. 2018 Feb;19(2):77-92. doi: 10.1038/nrm.2017.66. Epub 2017 Aug 9.
Mitochondrial diseases affect one in 2,000 individuals; they can present at any age and they can manifest in any organ. How defects in mitochondria can cause such a diverse range of human diseases remains poorly understood. Insight into this diversity is emerging from recent research that investigated defects in mitochondrial protein synthesis and mitochondrial DNA maintenance, which showed that many cell-specific stress responses are induced in response to mitochondrial dysfunction. Studying the molecular regulation of these stress responses might increase our understanding of the pathogenesis and variability of human mitochondrial diseases.
线粒体疾病影响每 2000 人中的 1 人;它们可以在任何年龄出现,并可以在任何器官表现出来。线粒体缺陷如何导致如此多样化的人类疾病仍然知之甚少。最近的研究表明,对线粒体蛋白合成和线粒体 DNA 维持的缺陷进行研究,揭示了许多细胞特异性应激反应是由于线粒体功能障碍而引起的,这为这种多样性提供了一些认识。研究这些应激反应的分子调控可能会增加我们对人类线粒体疾病发病机制和变异性的理解。