Rapamycin-sensitive phase of 3T3-L1 preadipocyte differentiation after clonal expansion

被引:67
作者
Gagnon, A
Lau, S
Sorisky, A
机构
[1] Univ Ottawa, Ottawa Hlth Res Inst, Ottawa Hosp, Dept Med, Ottawa, ON K1Y 4E9, Canada
[2] Univ Ottawa, Ottawa Hlth Res Inst, Ottawa Hosp, Dept Biochem, Ottawa, ON K1Y 4E9, Canada
[3] Univ Ottawa, Ottawa Hlth Res Inst, Ottawa Hosp, Dept Microbiol & Immunol, Ottawa, ON K1Y 4E9, Canada
关键词
D O I
10.1002/jcp.1132
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Inhibition of insulin-induced 3T3-L1 preadipocyte differentiation by rapamycin has been attributed to a blockade of the early critical clonal expansion phase of the adipogenic program. Rapamycin binds to, and inhibits, mTOR (mammalian target of rapamycin), leading to diminution of p70 S6 kinase activity and eukaryotic initiation factor 4E binding protein 1 (eIF4E-BP1) function. Our objective was to determine if rapamycin-sensitive pathways exist subsequent to the clonal expansion phase. We determined that the mitotic clonal expansion was complete by day 4 of the differentiation protocol, based on the response to Ara-C (cytosine beta -D-arabinofuranoside), which only inhibits differentiation when administered during this phase. Treatment of differentiating 3T3-L1 cells with rapamycin, starting on day 4, exerted potent negative effects on glycerol phosphate dehydrogenase activity, and triacylglycerol accumulation, as well as on the protein expression of adipogenic transcription factors, C/EBP alpha and PPAR gamma. Insulin-stimulated p70 S6 kinase activity, and its inhibition by rapamycin, were comparable in preadipocytes at day 0 vs. day 4 post-differentiation. We conclude that a component of the adipogenic program, operating after the completion of clonal expansion, is inhibited by rapamycin, suggesting an ongoing need for mTOR function in this process. J. Cell. Physiol. 189: 14-22, 2001. (C) 2001 Wiley-Liss, Inc.
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页码:14 / 22
页数:9
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