| Literature DB >> 25766503 |
Margo P Emont1, Stelios Mantis1, Jonathan H Kahn1, Michael Landeche1, Xuan Han1, Robert M Sargis1, Ronald N Cohen2.
Abstract
Local modulation of glucocorticoid action in adipocytes regulates adiposity and systemic insulin sensitivity. However, the specific cofactors that mediate glucocorticoid receptor (GR) action in adipocytes remain unclear. Here we show that the silencing mediator of retinoid and thyroid hormone receptors (SMRT) is recruited to GR in adipocytes and regulates ligand-dependent GR function. Decreased SMRT expression in adipocytes in vivo increases expression of glucocorticoid-responsive genes. Moreover, adipocytes with decreased SMRT expression exhibit altered glucocorticoid regulation of lipolysis. We conclude that SMRT regulates the metabolic functions of GR in adipocytes in vivo. Modulation of GR-SMRT interactions in adipocytes represents a novel approach to control the local degree of glucocorticoid action and thus influence adipocyte metabolic function.Entities:
Keywords: Adipocyte; Corepressor; Glucocorticoid; Nuclear receptor
Mesh:
Substances:
Year: 2015 PMID: 25766503 PMCID: PMC4390535 DOI: 10.1016/j.mce.2015.03.002
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102