Insulin resistance, tissue inflammation, and adipose tissue dysfunction are features of obesity and Type 2 diabetes. We generated adipocyte-specific Nuclear Receptor Corepressor (NCoR) knockout (AKO) mice to investigate the function of NCoR in adipocyte biology, glucose and insulin homeostasis. Despite increased obesity, glucose tolerance was improved in AKO mice, and clamp studies demonstrated enhanced insulin sensitivity in liver, muscle, and fat. Adipose tissue macrophage infiltration and inflammation were also decreased. PPARĪ³ response genes were upregulated in adipose tissue from AKO mice and CDK5-mediated PPARĪ³ ser-273 phosphorylation was reduced, creating a constitutively active PPARĪ³ state. This identifies NCoR as an adaptor protein that enhances the ability of CDK5 to associate with and phosphorylate PPARĪ³. The dominant function of adipocyte NCoR is to transrepress PPARĪ³ and promote PPARĪ³ ser-273 phosphorylation, such that NCoR deletion leads to adipogenesis, reduced inflammation, and enhanced systemic insulin sensitivity, phenocopying the TZD-treated state.
WOS:000296902300015
2011
147
4
815
26
REVIEWED