Regulation of the mTOR Complex 1 Pathway by Nutrients, Growth Factors, and Stress

被引:1011
作者
Sengupta, Shomit [1 ,2 ,3 ]
Peterson, Timothy R. [1 ,2 ,3 ]
Sabatini, David M. [1 ,2 ,3 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge Ctr 9, Cambridge, MA 02142 USA
[2] MIT, Howard Hughes Med Inst, Dept Biol, Cambridge, MA 02139 USA
[3] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
关键词
ACTIVATED PROTEIN-KINASE; TUBEROUS SCLEROSIS COMPLEX; DIET-INDUCED OBESITY; RICH AKT SUBSTRATE; 40 KDA PRAS40; MAMMALIAN TARGET; CELL-GROWTH; AMINO-ACID; S6; KINASE; SKELETAL-MUSCLE;
D O I
10.1016/j.molcel.2010.09.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The large serine/threonine protein kinase mTOR regulates cellular and organismal homeostasis by coordinating anabolic and catabolic processes with nutrient, energy, and oxygen availability and growth factor signaling. Cells and organisms experience a wide variety of insults that perturb the homeostatic systems governed by mTOR and therefore require appropriate stress responses to allow cells to continue to function. Stress can manifest from an excess or lack of upstream signals or as a result of genetic perturbations in upstream effectors of the pathway. mTOR nucleates two large protein complexes that are important nodes in the pathways that help buffer cells from stresses, and are implicated in the progression of stress-associated phenotypes and diseases, such as aging, tumorigenesis, and diabetes. This review focuses on the key components of the mTOR complex 1 pathway and on how various stresses impinge upon them.
引用
收藏
页码:310 / 322
页数:13
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