Retinoblastoma protein phosphorylation via PI 3-kinase and mTOR pathway regulates adipocyte differentiation

被引:24
|
作者
Usui, I [1 ]
Haruta, T [1 ]
Iwata, M [1 ]
Takano, A [1 ]
Uno, T [1 ]
Kawahara, J [1 ]
Ueno, E [1 ]
Sasaoka, T [1 ]
Kobayashi, M [1 ]
机构
[1] Toyama Med & Pharmaceut Univ, Dept Internal Med 1, Sugitani, Toyama 9300194, Japan
关键词
clonal expansion; adipocyte differentiation; retinoblastoma protein; mTOR; PI; 3-kinase; 3T3-L1; adipocyte; insulin;
D O I
10.1006/bbrc.2000.3201
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
In the early phase of adipocyte differentiation, transient increase of DNA synthesis, called clonal expansion, and transient hyperphosphorylation of retinoblastoma protein (Rb) are observed. We investigated the role of these phenomena in insulin-induced adipocyte differentiation of 3T3-L1 cells. Insulin-induced clonal expansion, Rb phosphorylation and adipocyte differentiation were all inhibited by the PI 3 kinase inhibitors and rapamycin, but not the MEK inhibitor, whereas the MEK inhibitor, but not PI 3-kinase inhibitors or rapamycin, decreased c-fos induction. We conclude that insulin induces hyperphosphorylation of Rb via PI 3-kinase and mTOR dependent pathway, which promotes clonal expansion and adipocyte differentiation of 3T3-L1 cells. (C) 2000 Academic Press.
引用
收藏
页码:115 / 120
页数:6
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