Lin Yi-Fan, Haynes Cole M
Cell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Cell Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; BCMB Allied Program, Weill Cornell Medical College, 1300 York Avenue, New York, NY 10065, USA.
Mol Cell. 2016 Mar 3;61(5):677-682. doi: 10.1016/j.molcel.2016.02.004.
During mitochondrial dysfunction or the accumulation of unfolded proteins within mitochondria, cells employ a transcriptional response known as the mitochondrial unfolded protein response (UPR(mt)) to promote cell survival along with the repair and recovery of defective mitochondria. Considerable progress has been made in understanding how cells monitor mitochondrial function and activate the response, as well as in identifying scenarios where the UPR(mt) plays a protective role, such as during bacterial infection, hematopoietic stem cell maintenance, or general aging. To date, much of the focus has been on the role of the UPR(mt) in maintaining or re-establishing protein homeostasis within mitochondria by transcriptionally inducing mitochondrial molecular chaperone and protease genes. In this review, we focus on the metabolic adaptations or rewiring mediated by the UPR(mt) and how this may contribute to the resolution of mitochondrial unfolded protein stress and cell-type-specific physiology.
在线粒体功能障碍或线粒体中未折叠蛋白积累期间,细胞会采用一种称为线粒体未折叠蛋白反应(UPR(mt))的转录反应,以促进细胞存活以及有缺陷线粒体的修复和恢复。在理解细胞如何监测线粒体功能并激活该反应,以及在确定UPR(mt)发挥保护作用的情况(如细菌感染、造血干细胞维持或一般衰老期间)方面已经取得了相当大的进展。迄今为止,大部分研究重点都放在了UPR(mt)通过转录诱导线粒体分子伴侣和蛋白酶基因来维持或重新建立线粒体内蛋白质稳态的作用上。在本综述中,我们重点关注由UPR(mt)介导的代谢适应或重塑,以及这如何有助于解决线粒体未折叠蛋白应激和细胞类型特异性生理学问题。