Abstract
Adipose differentiation is an important part of the energy homeostasis system of higher organisms. Recent data have suggested that this process is controlled by an interplay of transcription factors including PPARgamma, the C/EBPs, and ADD1/SREBP1. Although these factors interact functionally to initiate the program of differentiation, there are no data concerning specific mechanisms of interaction. We show here that the expression of ADD1/SREBP1 specifically increases the activity of PPARgamma but not other isoforms, PPARalpha, or PPARdelta. This activation occurs through the ligand-binding domain of PPARgamma when it is fused to the DNA-binding domain of Gal4. The stimulation of PPARgamma by ADD1/SREBP1 does not require coexpression in the same cells; supernatants from cultures that express ADD1/SREBP1 augment the transcriptional activity of PPARgamma. Finally, we demonstrate directly that cells expressing ADD1/SREBP1 produce and secrete lipid molecule(s) that bind directly to PPARgamma, displacing the binding of radioactive thiazolidinedione ligands. These data establish that ADD1/SREBP1 can control the production of endogenous ligand(s) for PPARgamma and suggest a mechanism for coordinating the actions of these adipogenic factors.
MeSH Terms
3T3 Cells
Adipose Tissue/cytology,metabolism
Animals
Binding, Competitive
CCAAT-Enhancer-Binding Proteins
Cell Differentiation
DNA-Binding Proteins/biosynthesis,metabolism
Humans
Hypoglycemic Agents/metabolism
Kinetics
Ligands
Mice
Nuclear Proteins/biosynthesis,metabolism
Receptors, Cytoplasmic and Nuclear/metabolism
Recombinant Proteins/biosynthesis,metabolism
Rosiglitazone
Sterol Regulatory Element Binding Protein 1
Thiazoles/metabolism
Thiazolidinediones
Transcription Factors/metabolism
Transcription, Genetic
Transfection
Chemicals
CCAAT-Enhancer-Binding Proteins
DNA-Binding Proteins
Hypoglycemic Agents
Ligands
Nuclear Proteins
Receptors, Cytoplasmic and Nuclear
Recombinant Proteins
SREBF1 protein, human
Srebf1 protein, mouse
Sterol Regulatory Element Binding Protein 1
Thiazoles
Thiazolidinediones
Transcription Factors
Rosiglitazone
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kim J B
Dana-Farber Cancer Institute and the Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Wright H M
Wright M
Spiegelman B M
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