共 32 条
The forkhead transcription factor Foxo1 regulates adipocyte differentiation
被引:661
作者:

Nakae, J
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA

Kitamura, T
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA

Kitamura, Y
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA

Biggs, WH
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA

Arden, KC
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA

Accili, D
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机构: Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
机构:
[1] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[2] Univ Calif San Diego, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
关键词:
D O I:
10.1016/S1534-5807(02)00401-X
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
An outstanding question in adipocyte biology is how hormonal cues are relayed to the nucleus to activate the transcriptional program that promotes adipogenesis. The forkhead transcription factor Foxo1 is regulated by insulin via Akt-dependent phosphorylation and nuclear exclusion. We show that Foxo1 is induced in the early stages of adipocyte differentiation but that its activation is delayed until the end of the clonal expansion phase. Constitutively active Foxo1 prevents the differentiation of preadipocytes, while dominant-negative Foxo1 restores adipocyte differentiation of fibroblasts from insulin receptor-deficient mice. Further, Foxo1 haploinsufficiency protects from diet-induced diabetes in mice. We propose that Foxo1 plays an important role in the integration of hormone-activated signaling pathways with the complex transcriptional cascade that promotes adipocyte differentiation.
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页码:119 / 129
页数:11
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