| Literature DB >> 19254572 |
Ling Qi1, Maziyar Saberi, Erik Zmuda, Yiguo Wang, Judith Altarejos, Xinmin Zhang, Renaud Dentin, Susie Hedrick, Gautam Bandyopadhyay, Tsonwin Hai, Jerry Olefsky, Marc Montminy.
Abstract
Increases in adiposity trigger metabolic and inflammatory changes that interfere with insulin action in peripheral tissues, culminating in beta cell failure and overt diabetes. We found that the cAMP Response Element Binding protein (CREB) is activated in adipose cells under obese conditions, where it promotes insulin resistance by triggering expression of the transcriptional repressor ATF3 and thereby downregulating expression of the adipokine hormone adiponectin as well as the insulin-sensitive glucose transporter 4 (GLUT4). Transgenic mice expressing a dominant-negative CREB transgene in adipocytes displayed increased whole-body insulin sensitivity in the contexts of diet-induced and genetic obesity, and they were protected from the development of hepatic steatosis and adipose tissue inflammation. These results indicate that adipocyte CREB provides an early signal in the progression to type 2 diabetes.Entities:
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Year: 2009 PMID: 19254572 PMCID: PMC2730923 DOI: 10.1016/j.cmet.2009.01.006
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287