Mitochondrial stress signaling promotes cellular adaptations.

Q3 Biochemistry, Genetics and Molecular Biology International Journal of Cell Biology Pub Date : 2014-01-01 Epub Date: 2014-01-22 DOI:10.1155/2014/156020
Jayne Alexandra Barbour, Nigel Turner
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引用次数: 78

Abstract

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.

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线粒体应激信号促进细胞适应。
线粒体功能障碍与许多复杂疾病的病因学以及衰老过程有关。许多关于线粒体功能障碍的研究都集中在线粒体损伤如何增强病理表型上。这篇综述的目的是引起人们对细胞适应线粒体扰动的不太好的研究机制的关注。这包括向细胞传递压力和成功诱导质量控制反应,包括有丝分裂、未折叠蛋白反应、抗氧化和DNA修复酶的上调、形态变化,如果其他都失败,则凋亡。线粒体是一个固有的应激环境,我们推测应激信号的失调或在线粒体应激期间无法开启这些适应可能会支持线粒体功能障碍,从而随着时间的推移达到病理状态。
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来源期刊
International Journal of Cell Biology
International Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
3.30
自引率
0.00%
发文量
4
审稿时长
20 weeks
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