Resveratrol modulates the inflammatory response via an estrogen receptor-signal integration network
Abstract
Resveratrol has beneficial effects on aging, inflammation and metabolism, which are thought to result from activation of the lysine deacetylase, sirtuin 1 (SIRT1), the cAMP pathway, or AMP-activated protein kinase. Here we report that resveratrol acts as a pathway-selective estrogen receptor-α (ERα) ligand to modulate the inflammatory response but not cell proliferation. A crystal structure of the ERα ligand-binding domain (LBD) as a complex with resveratrol revealed a unique perturbation of the coactivator-binding surface, consistent with an altered coregulator recruitment profile. Gene expression analyses revealed significant overlap of TNFα genes modulated by resveratrol and estradiol. Furthermore, the ability of resveratrol to suppress interleukin-6 transcription was shown to require ERα and several ERα coregulators, suggesting that ERα functions as a primary conduit for resveratrol activity.
Article and author information
Author details
Reviewing Editor
- Leemor Joshua-Tor, Cold Spring Harbor Laboratory, United States
Version history
- Received: December 12, 2013
- Accepted: April 5, 2014
- Accepted Manuscript published: April 25, 2014 (version 1)
- Version of Record published: May 13, 2014 (version 2)
Copyright
© 2014, Nwachukwu et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
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