Journal article
Testosterone Inhibits Adipogenic Differentiation in 3T3-L1 Cells: Nuclear Translocation of Androgen Receptor Complex with β-Catenin and T-Cell Factor 4 May Bypass Canonical Wnt Signaling to Down-Regulate Adipogenic Transcription Factors
Abstract
Testosterone supplementation in men decreases fat mass; however, the mechanisms by which it inhibits fat mass are unknown. We hypothesized that testosterone inhibits adipogenic differentiation of preadipocytes by activation of androgen receptor (AR)/beta-catenin interaction and subsequent translocation of this complex to the nucleus thereby bypassing canonical Wnt signaling. We tested this hypothesis in 3T3-L1 cells that differentiate to form …
Authors
Singh R; Artaza JN; Taylor WE; Braga M; Yuan X; Gonzalez-Cadavid NF; Bhasin S
Journal
Endocrinology, Vol. 147, No. 1, pp. 141–154
Publisher
The Endocrine Society
Publication Date
January 1, 2006
DOI
10.1210/en.2004-1649
ISSN
0013-7227
Fields of Research (FoR)
Medical Subject Headings (MeSH)
3T3 CellsAdipocytesAdipose TissueAnimalsCell DifferentiationCell NucleusGene Expression RegulationMiceProtein TransportRNA, MessengerReceptors, AndrogenReverse Transcriptase Polymerase Chain ReactionSignal TransductionTCF Transcription FactorsTestosteroneTranscription Factor 7-Like 2 ProteinTranscription FactorsTranscription, GeneticWnt Proteinsbeta Catenin