Insulin signaling meets mitochondria in metabolism

被引:382
作者
Cheng, Zhiyong [1 ]
Tseng, Yolanda [1 ]
White, Morris F. [1 ]
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Childrens Hosp Boston,Div Endocrinol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
TYROSINE-PHOSPHATASE; 1B; TUBEROUS SCLEROSIS COMPLEX; HUMAN SKELETAL-MUSCLE; RECEPTOR SUBSTRATE 1; PHOSPHATIDYLINOSITOL; 3-KINASE; NUTRIENT HOMEOSTASIS; PLECKSTRIN HOMOLOGY; PROTEIN-SYNTHESIS; LIPID-METABOLISM; PHOSPHOINOSITIDE;
D O I
10.1016/j.tem.2010.06.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin controls nutrient and metabolic homeostasis via the IRS-PI3K-AKT signaling cascade that targets FOXO1 and mTOR. Mitochondria, as the prime metabolic platform, malfunction during insulin resistance in metabolic diseases. However, the molecular link between insulin resistance and mitochondrial dysfunction remains undefined. Here we review recent studies on insulin action and the mechanistic association with mitochondria! metabolism. These studies suggest that insulin signaling underpins mitochondrial electron transport chain integrity and activity by suppressing FOXO1/HMOX1 and maintaining the NAD(+)/NADH ratio, the mediator of the SIRT1/PGC1 alpha pathway for mitochondrial biogenesis and function. Mitochondria generate moderately reactive oxygen species (ROS) and enhance insulin sensitivity upon redox regulation of protein tyrosine phosphatase and insulin receptor. However, chronic exposure to high ROS levels could alter mitochondrial function and thereby cause insulin resistance.
引用
收藏
页码:589 / 598
页数:10
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