Regulation of peroxisome proliferator-activated receptor gamma expression by adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1: implications for adipocyte differentiation and metabolism.

Détails

ID Serval
serval:BIB_06D5A6BEA7C9
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Regulation of peroxisome proliferator-activated receptor gamma expression by adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1: implications for adipocyte differentiation and metabolism.
Périodique
Molecular and Cellular Biology
Auteur⸱e⸱s
Fajas L., Schoonjans K., Gelman L., Kim J.B., Najib J., Martin G., Fruchart J.C., Briggs M., Spiegelman B.M., Auwerx J.
ISSN
0270-7306 (Print)
ISSN-L
0270-7306
Statut éditorial
Publié
Date de publication
1999
Volume
19
Numéro
8
Pages
5495-5503
Langue
anglais
Résumé
Peroxisome proliferator-activated receptor gamma (PPARgamma) is a nuclear receptor implicated in adipocyte differentiation and insulin sensitivity. We investigated whether PPARgamma expression is dependent on the activity of adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1 (ADD-1/SREBP-1), another transcription factor associated with both adipocyte differentiation and cholesterol homeostasis. Ectopic expression of ADD-1/SREBP-1 in 3T3-L1 and HepG2 cells induced endogenous PPARgamma mRNA levels. The related transcription factor SREBP-2 likewise induced PPARgamma expression. In addition, cholesterol depletion, a condition known to result in proteolytic activation of transcription factors of the SREBP family, induced PPARgamma expression and improved PPRE-driven transcription. The effect of the SREBPs on PPARgamma expression was mediated through the PPARgamma1 and -3 promoters. Both promoters contain a consensus E-box motif that mediates the regulation of the PPARgamma gene by ADD-1/SREBP-1 and SREBP-2. These results suggest that PPARgamma expression can be controlled by the SREBP family of transcription factors and demonstrate new interactions between transcription factors that can regulate different pathways of lipid metabolism.
Mots-clé
Adipocytes/cytology, Adipocytes/metabolism, CCAAT-Enhancer-Binding Proteins, Cell Differentiation/genetics, Cholesterol/metabolism, Cholesterol/pharmacology, Consensus Sequence, DNA-Binding Proteins/physiology, Fatty Acids/pharmacology, Gene Expression Regulation, Developmental/drug effects, Humans, Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology, Lipid Metabolism, Multigene Family, Nuclear Proteins/physiology, Peroxisome Proliferators/pharmacology, Promoter Regions, Genetic, Receptors, Cytoplasmic and Nuclear/biosynthesis, Receptors, Cytoplasmic and Nuclear/genetics, Simvastatin/pharmacology, Sterol Regulatory Element Binding Protein 1, Transcription Factors/biosynthesis, Transcription Factors/genetics
Pubmed
Web of science
Création de la notice
07/03/2013 17:10
Dernière modification de la notice
20/08/2019 13:29
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