氧化磷酸化
线粒体
糖酵解
内科学
内分泌学
高胰岛素血症
生物
能量稳态
细胞生物学
新陈代谢
化学
生物化学
肥胖
胰岛素抵抗
医学
作者
Liat Buzaglo-Azriel,Yael Kuperman,Michael Tsoory,Yehudit Zaltsman,Liat Shachnai,Smadar Levin Zaidman,Elad Bassat,Inbal Michailovici,Alona Sarver,Eldad Tzahor,Michal Haran,Cécile Vernochet,Atan Gross
出处
期刊:Cell Reports
[Cell Press]
日期:2016-02-01
卷期号:14 (7): 1602-1610
被引量:61
标识
DOI:10.1016/j.celrep.2016.01.046
摘要
Mitochondrial carrier homolog 2 (MTCH2) is a repressor of mitochondrial oxidative phosphorylation (OXPHOS), and its locus is associated with increased BMI in humans. Here, we demonstrate that mice deficient in muscle MTCH2 are protected from diet-induced obesity and hyperinsulinemia and that they demonstrate increased energy expenditure. Deletion of muscle MTCH2 also increases mitochondrial OXPHOS and mass, triggers conversion from glycolytic to oxidative fibers, increases capacity for endurance exercise, and increases heart function. Moreover, metabolic profiling of mice deficient in muscle MTCH2 reveals a preference for carbohydrate utilization and an increase in mitochondria and glycolytic flux in muscles. Thus, MTCH2 is a critical player in muscle biology, modulating metabolism and mitochondria mass as well as impacting whole-body energy homeostasis.
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