Barbour Jayne Alexandra, Turner Nigel
Department of Pharmacology, School of Medical Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Int J Cell Biol. 2014;2014:156020. doi: 10.1155/2014/156020. Epub 2014 Jan 22.
Mitochondrial dysfunction has been implicated in the aetiology of many complex diseases, as well as the ageing process. Much of the research on mitochondrial dysfunction has focused on how mitochondrial damage may potentiate pathological phenotypes. The purpose of this review is to draw attention to the less well-studied mechanisms by which the cell adapts to mitochondrial perturbations. This involves communication of stress to the cell and successful induction of quality control responses, which include mitophagy, unfolded protein response, upregulation of antioxidant and DNA repair enzymes, morphological changes, and if all else fails apoptosis. The mitochondrion is an inherently stressful environment and we speculate that dysregulation of stress signaling or an inability to switch on these adaptations during times of mitochondrial stress may underpin mitochondrial dysfunction and hence amount to pathological states over time.
线粒体功能障碍与许多复杂疾病的病因以及衰老过程都有关联。关于线粒体功能障碍的许多研究都集中在线粒体损伤如何增强病理表型上。本综述的目的是提请人们关注细胞适应线粒体扰动的那些研究较少的机制。这涉及将应激传递给细胞并成功诱导质量控制反应,其中包括线粒体自噬、未折叠蛋白反应、抗氧化剂和DNA修复酶的上调、形态变化,以及在其他所有方法都失败时的细胞凋亡。线粒体本质上是一个充满应激的环境,我们推测应激信号失调或在面临线粒体应激时无法开启这些适应性反应可能是线粒体功能障碍的基础,进而随着时间的推移导致病理状态。