AMPK and mTOR in Cellular Energy Homeostasis and Drug Targets

被引:651
作者
Inoki, Ken [1 ,2 ]
Kim, Joungmok [3 ,4 ]
Guan, Kun-Liang [3 ,4 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 52 | 2012年 / 52卷
关键词
rapamycin; TSC Rheb; Rag; ULK1; ribosome biogenesis; ACTIVATED PROTEIN-KINASE; TUBEROUS SCLEROSIS COMPLEX; MESSENGER-RNA TRANSLATION; NUTRIENT-SENSITIVE REGULATOR; TUMOR-SUPPRESSOR COMPLEX; ACETYL-COA CARBOXYLASE; MAMMALIAN TARGET; S6; KINASE; SKELETAL-MUSCLE; GENE-EXPRESSION;
D O I
10.1146/annurev-pharmtox-010611-134537
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The mammalian target of rapamycin (mTOR) is a central controller of cell growth and proliferation. mTOR forms two distinct complexes, mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). mTORC1 is regulated by multiple signals such as growth factors, amino acids, and cellular energy and regulates numerous essential cellular processes including translation, transcription, and autophagy. The AMP-activated protein kinase (AMPK) is a cellular energy sensor and signal transducer that is regulated by a wide array of metabolic stresses. These two pathways serve as a signaling nexus for regulating cellular metabolism, energy homeostasis, and cell growth, and dysregulation of each pathway may contribute to the development of metabolic disorders such as obesity, type 2 diabetes, and cancer. This review focuses on our current understanding of the relationship between AMPK and mTORC1 signaling and discusses their roles in cellular and organismal energy homeostasis.
引用
收藏
页码:381 / 400
页数:20
相关论文
共 149 条
[2]
BLENIS J, 1987, J BIOL CHEM, V262, P14373
[3]
AMP-activated protein kinase suppresses protein synthesis in rat skeletal muscle through down-regulated mammalian target of rapamycin (mTOR) signaling. [J].
Bolster, DR ;
Crozier, SJ ;
Kimball, SR ;
Jefferson, LS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (27) :23977-23980
[4]
MO25α/β interact with STRADα/β enhancing their ability to bind, activate and localize LKB1 in the cytoplasm [J].
Boudeau, J ;
Baas, AF ;
Deak, M ;
Morrice, NA ;
Kieloch, A ;
Schutkowski, M ;
Prescott, AR ;
Clevers, HC ;
Alessi, DR .
EMBO JOURNAL, 2003, 22 (19) :5102-5114
[5]
The regulation and function of mammalian AMPK-related kinases [J].
Bright, N. J. ;
Thornton, C. ;
Carling, D. .
ACTA PHYSIOLOGICA, 2009, 196 (01) :15-26
[6]
The TOR signaling cascade regulates gene expression in response to nutrients [J].
Cardenas, ME ;
Cutler, NS ;
Lorenz, MC ;
Di Como, CJ ;
Heitman, J .
GENES & DEVELOPMENT, 1999, 13 (24) :3271-3279
[7]
A YEAST GENE THAT IS ESSENTIAL FOR RELEASE FROM GLUCOSE REPRESSION ENCODES A PROTEIN-KINASE [J].
CELENZA, JL ;
CARLSON, M .
SCIENCE, 1986, 233 (4769) :1175-1180
[8]
mTORC1 Phosphorylates the ULK1-mAtg13-FIP200 Autophagy Regulatory Complex [J].
Chan, Edmond Y. .
SCIENCE SIGNALING, 2009, 2 (84)
[9]
Evolution of Atg1 function and regulation [J].
Chan, Edmond Y. ;
Tooze, Sharon A. .
AUTOPHAGY, 2009, 5 (06) :758-765
[10]
SiRNA screening of the kinome identifies ULK1 as a multidomain modulator of autophagy [J].
Chan, Edmond Y. W. ;
Kir, Serkan ;
Tooze, Sharon A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (35) :25464-25474