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April 14, 1998Proceedings of the National Academy of Sciences670 citationsOpen Access

ADD1/SREBP1 activates PPARγ through the production of endogenous ligand

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JKJae Bum KimHWHarold M. WrightMWMargaret E. Wright

Structured PICO

P
Population
Cell cultures (in vitro model) for studying adipose differentiation
I
Intervention
Expression of ADD1/SREBP1
C
Comparator
Control conditions without ADD1/SREBP1 expression
O
Outcome
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.

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.

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Cite This Study

Kim et al. (1998) studied this question.

synapsesocial.com/papers/69d77b6adb9d5e1bf4b8b037https://doi.org/10.1073/pnas.95.8.4333
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