Inhibition of Adipogenesis by Wnt Signaling

Sarah E. Ross(University of Michigan), Nahid Hemati(Czech Academy of Sciences, Institute of Physiology), Kenneth Longo(Czech Academy of Sciences, Institute of Physiology), Christina N. Bennett(Czech Academy of Sciences, Institute of Physiology), Peter C. Lucas(University of Michigan), Robin L. Erickson(Czech Academy of Sciences, Institute of Physiology), Ormond A. MacDougald(Diabetes Australia)
Science
August 11, 2000
Cited by 1,881

Abstract

Wnts are secreted signaling proteins that regulate developmental processes. Here we show that Wnt signaling, likely mediated by Wnt-10b, is a molecular switch that governs adipogenesis. Wnt signaling maintains preadipocytes in an undifferentiated state through inhibition of the adipogenic transcription factors CCAAT/enhancer binding protein alpha (C/EBPalpha) and peroxisome proliferator- activated receptor gamma (PPARgamma). When Wnt signaling in preadipocytes is prevented by overexpression of Axin or dominant-negative TCF4, these cells differentiate into adipocytes. Disruption of Wnt signaling also causes transdifferentiation of myoblasts into adipocytes in vitro, highlighting the importance of this pathway not only in adipocyte differentiation but also in mesodermal cell fate determination.


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