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EMBO J. 2008 May 7;27(9):1399-410. doi: 10.1038/emboj.2008.67. Epub 2008 Apr 3.

Akt- and Foxo1-interacting WD-repeat-FYVE protein promotes adipogenesis.

Author information

1
Institute of Medical Virology, University of Zurich, Zurich, Switzerland.

Abstract

We have previously identified a protein, consisting of seven WD-repeats, forming a putative beta-propeller, and an FYVE domain, ProF, which is highly expressed in 3T3-L1 cells, a cell line that can be differentiated into adipocytes. We recently found ProF to interact with the kinases Akt and protein kinase Czeta. Here we demonstrate that ProF is a positive regulator of adipogenesis. Knockdown of ProF by RNA interference leads to decreased adipocyte differentiation. This is shown by reduced lipid accumulation, decreased expression of the differentiation markers PPARgamma and C/EBPalpha, and reduced glucose uptake in differentiated cells. Furthermore, ProF overexpression leads to increased adipogenesis. ProF binds to the transcription factor Foxo1 (Forkhead box O1), a negative regulator of insulin action and adipogenesis, and facilitates the phosphorylation and thus inactivation of Foxo1 by Akt. Additionally, dominant-negative Foxo1 restores adipogenesis in ProF knockdown cells. Thus, ProF modulates Foxo1 phosphorylation by Akt, promoting adipocyte differentiation. Furthermore, ProF might be involved in metabolic disorders such as diabetes.

PMID:
18388859
PMCID:
PMC2374844
DOI:
10.1038/emboj.2008.67
[Indexed for MEDLINE]
Free PMC Article

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