The multifaceted role of mTORC1 in the control of lipid metabolism

被引:208
作者
Ricoult, Stephane J. H. [1 ]
Manning, Brendan D. [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
adipocytes; Akt; insulin; liver; mTOR; ELEMENT-BINDING-PROTEIN; FATTY-ACID SYNTHESIS; MAMMALIAN TARGET; SKELETAL-MUSCLE; GENE-EXPRESSION; AMINO-ACID; ADIPOCYTE DIFFERENTIATION; LIPOPROTEIN-LIPASE; TSC1-TSC2; COMPLEX; TRANSGENIC MICE;
D O I
10.1038/embor.2013.5
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 mechanistic target of rapamycin is a protein kinase that, as part of the mechanistic target of rapamycin complex 1 (mTORC1), senses both local nutrients and, through insulin signalling, systemic nutrients to control a myriad of cellular processes. Although roles for mTORC1 in promoting protein synthesis and inhibiting autophagy in response to nutrients have been well established, it is emerging as a central regulator of lipid homeostasis. Here, we discuss the growing genetic and pharmacological evidence demonstrating the functional importance of its signalling in controlling mammalian lipid metabolism, including lipid synthesis, oxidation, transport, storage and lipolysis, as well as adipocyte differentiation and function. Defining the role of mTORC1 signalling in these metabolic processes is crucial to understanding the pathophysiology of obesity and its relationship-to complex diseases, including diabetes and cancer.
引用
收藏
页码:242 / 251
页数:10
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