E2Fs regulate adipocyte differentiation

被引:273
作者
Fajas, L
Landsberg, RL
Huss-Garcia, Y
Sardet, C
Lees, JA
Auwerx, J
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[2] CU Strasbourg, Strasbourg, France
[3] MIT, Ctr Canc Res, Cambridge, MA 02139 USA
[4] Inst Genet Mol, UMR 5535, F-34293 Montpellier, France
关键词
D O I
10.1016/S1534-5807(02)00190-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
When preadipocytes reenter the cell cycle, PPARgamma expression is induced, coincident with an increase in DNA synthesis, suggesting the involvement of the E2F family of cell cycle regulators. We show here that E2F1 induces PPAR transcription during clonal expansion, whereas E2F4 represses PPARgamma expression during terminal adipocyte differentiation. Using a combination of in vivo experiments with knockout and chimeric animals and in vitro experiments, we demonstrate that the absence of E2F1 impairs, whereas depletion of E2F4 stimulates, adipogenesis. E2Fs hence represent the link between proliferative signaling pathways, triggering clonal expansion, and terminal adipocyte differentiation through regulation of PPARgamma expression. This underscores the complex role of the E2F protein family in the control of both cell proliferation and differentiation.
引用
收藏
页码:39 / 49
页数:11
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