DOI: 10.2337/db07-1538
Autocrine IGF-1 action in adipocytes controls systemic IGF-1 concentrations and growth
1Department of Medicine, University of Leipzig, Leipzig, Germany Objective: Insulin-like growth factor-1 (IGF-1) and the IGF-1 receptor (IGF-1R) have been implicated in the regulation of adipocyte differentiation and lipid accumulation in vitro. Research Design and Methods: To investigate the role of IGF-1 receptor in vivo, we have inactivated the IGF-1 receptor gene in adipose tissue (IGF-1RaP2Cre mice) using conditional gene targeting strategies. Results: Conditional IGF-1R inactivation resulted in increased adipose tissue mass with a predominantly increased lipid accumulation in epigonadal fat pads. However, insulin-stimulated glucose uptake into adipocytes was unaffected by the deletion of the IGF-1R. Surprisingly, IGF-1RaP2Cre mice exhibited markedly increased somatic growth in the presence of elevated IGF-1 serum concentrations and IGF-1 mRNA expression was significantly increased in liver and adipose tissue. IGF-1 stimulation of wild type adipocytes significantly decreased IGF-1 mRNA expression, while the opposite effect was obeserved in IGF-1R deficient adipocytes. Conclusions: IGF-1 receptor signaling in adipocytes does not appear to be crucial for the development and differentiation of adipose tissue in vivo, but we identified a negative IGF-1 receptor-mediated feedback mechanism of IGF-1 on its own gene expression in adipocytes, indicating an unexpected role for adipose tissue IGF-1 signaling in the regulation of IGF-1 serum concentrations in control of somatic growth.
Correspondence: jens.bruening{at}uni-koeln.de Correspondence: bluma{at}medizin.uni-leipzig.de
|
|
|
|||||||||||||||||||||||||||