Kwon Young-Yon, Lee Sung-Keun, Lee Cheol-Koo
Department of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul 02841, Korea.
Department of Pharmacology, College of Medicine, Inha University, Incheon 22212, Korea.
Mol Cells. 2017 Apr;40(4):307-313. doi: 10.14348/molcells.2017.2279. Epub 2017 Apr 20.
Caloric restriction (CR) has been shown to extend lifespan and prevent cellular senescence in various species ranging from yeast to humans. Many effects of CR may contribute to extend lifespan. Specifically, CR prevents oxidative damage from reactive oxygen species (ROS) by enhancing mitochondrial function. In this study, we characterized 33 single electron transport chain (ETC) gene-deletion strains to identify CR-induced chronological lifespan (CLS) extension mechanisms. Interestingly, defects in 17 of these 33 ETC gene-deleted strains showed loss of both respiratory function and CR-induced CLS extension. On the contrary, the other 16 respiration-capable mutants showed increased CLS upon CR along with increased mitochondrial membrane potential (MMP) and intracellular adenosine triphosphate (ATP) levels, with decreased mitochondrial superoxide generation. We measured the same parameters in the 17 non-respiratory mutants upon CR. CR simultaneously increased MMP and mitochondrial superoxide generation without altering intracellular ATP levels. In conclusion, respiration is essential for CLS extension by CR and is important for balancing MMP, ROS, and ATP levels.
热量限制(CR)已被证明能延长从酵母到人类等各种物种的寿命,并防止细胞衰老。CR的许多作用可能有助于延长寿命。具体而言,CR通过增强线粒体功能来防止活性氧(ROS)造成的氧化损伤。在本研究中,我们对33个单电子转运链(ETC)基因缺失菌株进行了表征,以确定CR诱导的时序寿命(CLS)延长机制。有趣的是,这33个ETC基因缺失菌株中有17个存在缺陷,表现出呼吸功能丧失和CR诱导的CLS延长丧失。相反,其他16个具有呼吸能力的突变体在CR处理后CLS增加,同时线粒体膜电位(MMP)和细胞内三磷酸腺苷(ATP)水平升高,线粒体超氧化物生成减少。我们在CR处理后的17个非呼吸突变体中测量了相同的参数。CR同时增加了MMP和线粒体超氧化物生成,而不改变细胞内ATP水平。总之,呼吸对于CR延长CLS至关重要,并且对于平衡MMP、ROS和ATP水平很重要。