Phosphatidic acid and lipid-sensing by mTOR

被引:94
|
作者
Foster, David A. [1 ]
机构
[1] CUNY Hunter Coll, Dept Biol Sci, New York, NY 10065 USA
来源
基金
美国国家卫生研究院;
关键词
mTOR; phosphatidic acid; DG kinase; LPAAT; phospholipase D; CELL-CYCLE PROGRESSION; HUMAN CANCER-CELLS; PHOSPHOLIPASE-D; BREAST-CANCER; SURVIVAL SIGNALS; MAMMALIAN TARGET; PYRUVATE-KINASE; BINDING DOMAIN; GROWTH; METABOLISM;
D O I
10.1016/j.tem.2013.02.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mammalian target of rapamycin (mTOR) has been implicated as a sensor of nutrient sufficiency for dividing cells and is activated by essential amino acids and glucose. However, cells also require lipids for membrane biosynthesis. A central metabolite in the synthesis of membrane phospholipids is phosphatidic acid (PA), which is required for the stability and activity of mTOR complexes. Although PA is commonly generated by the phospholipase D-catalyzed hydrolysis of phosphatidylcholine, PA is also generated by diacylglycerol kinases and lysophosphatidic acid acyltransferases, which are at the center of phospholipid biosynthesis. It is proposed that the responsiveness of mTOR/TOR to PA evolved as a means for sensing lipid precursors for membrane biosynthesis prior to doubling the mass of a cell and dividing.
引用
收藏
页码:272 / 278
页数:7
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