Signal integration by mTORC1 coordinates nutrient input with biosynthetic output

被引:655
作者
Dibble, Christian C. [1 ,2 ]
Manning, Brendan D. [3 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Signal Transduct, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Syst Biol Dept, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02115 USA
关键词
TRANSFER-RNA SYNTHETASE; MAMMALIAN TARGET; TUBEROUS SCLEROSIS; CELL-GROWTH; AMINO-ACIDS; MESSENGER-RNA; RAG GTPASES; INSULIN-RESISTANCE; PHOSPHOLIPASE-D; REGULATES MTOR;
D O I
10.1038/ncb2763
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Flux through metabolic pathways is inherently sensitive to the levels of specific substrates and products, but cellular metabolism is also managed by integrated control mechanisms that sense the nutrient and energy status of a cell or organism. The mechanistic target of rapamycin complex 1 (mTORC1), a protein kinase complex ubiquitous to eukaryotic cells, has emerged as a critical signalling node that links nutrient sensing to the coordinated regulation of cellular metabolism. Here, we discuss the role of mTORC1 as a conduit between cellular growth conditions and the anabolic processes that promote cell growth. The emerging network of signalling pathways through which mTORC1 integrates systemic signals (secreted growth factors) with local signals (cellular nutrients - amino acids, glucose and oxygen - and energy, ATP) is detailed. Our expanding understanding of the regulatory network upstream of mTORC1 provides molecular insights into the integrated sensing mechanisms by which diverse cellular signals converge to control cell physiology.
引用
收藏
页码:555 / 564
页数:10
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