Journal
DIABETES
Volume 60, Issue 11, Pages 2892-2902Publisher
AMER DIABETES ASSOC
DOI: 10.2337/db11-0341
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Funding
- National Institutes of Health [DK-55267]
- Brehm Coalition
- Fondation pour la Recherche Medicale
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OBJECTIVE-Insulin receptor substrate-2 (IRS-2) plays an essential role in pancreatic islet beta-cells by promoting growth and survival. IRS-2 turnover is rapid in primary beta-cells, but its expression is highly regulated at the transcriptional level, especially by glucose. The aim was to investigate the molecular mechanism on how glucose regulates IRS-2 gene expression in beta-cells. RESEARCH DESIGN AND METHODS-Rat islets were exposed to inhibitors or subjected to adenoviral vector-mediated gene manipulations and then to glucose-induced IRS-2 expression analyzed by real-time PCR and immunoblotting. Transcription factor nuclear factor of activated T cells (NFAT) interaction with IRS-2 promoter was analyzed by chromatin immunoprecipitation assay and glucose-induced NFAT translocation by immunohistochemistry. RESULTS-Glucose-induced IRS-2 expression occurred in pancreatic islet beta-cells in vivo but not in liver. Modulating rat islet beta-cell Ca2+ influx with nifedipine or depolarization demonstrated that glucose-induced IRS-2 gene expression was dependent on a rise in intracellular calcium concentration derived from extracellular sources. Calcinernin inhibitors (FK506, cyclosporin A, and a peptide calcineurin inhibitor [CAIN]) abolished glucose-induced IRS-2 mRNA and protein levels, whereas expression of a constitutively active calcineurin increased them. Specific inhibition of NFAT with the peptide inhibitor VIVIT prevented a glucose-induced IRS-2 transcription. NFATc1 translocation to the nucleus in response to glucose and association of NFATc1 to conserved NFAT binding sites in the IRS-2 promoter were demonstrated. CONCLUSIONS-The mechanism behind glucose-induced transcriptional control of IRS-2 gene expression specific to the islet beta-cell is mediated by the Ca2+/calcineurin/NFAT pathway. This insight into the IRS-2 regulation could provide novel therapeutic means in type 2 diabetes to maintain an adequate functional mass. Diabetes 60:2892-2902, 2011
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