Phosphatidic acid-mediated mitogenic activation of mTOR signaling

被引:863
作者
Fang, YM [1 ]
Vilella-Bach, M [1 ]
Bachmann, R [1 ]
Flanigan, A [1 ]
Chen, J [1 ]
机构
[1] Univ Illinois, Dept Cell & Struct Biol, Urbana, IL 61801 USA
关键词
D O I
10.1126/science.1066015
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mammalian target of rapamycin (mTOR) governs cell growth and proliferation by mediating the mitogen- and nutrient-dependent signal transduction that regulates messenger RNA translation. We identified phosphatidic acid (PA) as a critical component of mTOR signaling. In our study, mitogenic stimulation of mammalian cells led to a phospholipase D-dependent accumulation of cellular PA, which was required for activation of mTOR downstream effectors. PA directly interacted with the domain in mTOR that is targeted by rapamycin, and this interaction was positively correlated with mTOR's ability to activate downstream effectors. The involvement of PA in mTOR signaling reveals an important function of this lipid in signal transduction and protein synthesis, as well as a direct link between mTOR and mitogens. Furthermore, these studies suggest a potential mechanism for the in vivo actions of the immunosuppressant rapamycin.
引用
收藏
页码:1942 / 1945
页数:4
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