Cell cultures (in vitro model) for studying adipose differentiation
Expression of ADD1/SREBP1
Control conditions without ADD1/SREBP1 expression
Activation of PPARgamma and production of endogenous ligandsurrogate
ADD1/SREBP1 controls the production of endogenous ligands for PPARgamma, providing a mechanism for coordinating the actions of these adipogenic transcription factors.
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.
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Jae Bum Kim
Seoul National University
Harold M. Wright
Therapeutics Clinical Research
Margaret E. Wright
Illinois College
Proceedings of the National Academy of Sciences
Harvard University
Dana-Farber Cancer Institute
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Kim et al. (Tue,) studied this question.
synapsesocial.com/papers/69d77b6adb9d5e1bf4b8b037 — DOI: https://doi.org/10.1073/pnas.95.8.4333