Citation

  • Authors: Garcia-Martinez, J. M., Chocarro-Calvo, A., De la Vieja, A., Garcia-Jimenez, C.
  • Year: 2014
  • Journal: Biochim Biophys Acta 1839 1141-50
  • Applications: in vitro / siRNA and DNA cotransfection / jetPRIME
  • Cell type: STC-1
    Description: Murine tumor intestinal enteroendocrine cell line

Abstract

Minutes after ingestion of fat or carbohydrates, vesicles stored in enteroendocrine cells release their content of incretin peptide hormones that, together with absorbed glucose, enhance insulin secretion by beta-pancreatic cells. Freshly-made incretins must therefore be packed into new vesicles in anticipation of the next meal with cells adjusting new incretin production to be proportional to the level of previous insulin release and absorbed blood glucose. Here we show that insulin stimulates the expression of the major human incretin, glucose-dependent insulinotropic peptide (GIP) in enteroendocrine cells but requires glucose to do it. Akt-dependent release of FoxO1 and glucose-dependent binding of LEF1/beta-catenin mediate induction of Gip expression while insulin-induced phosphorylation of beta-catenin does not alter its localization or transcriptional activity in enteroendocrine cells. Our results reveal a glucose-regulated feedback loop at the entero-insular axis, where glucose levels determine basal and insulin-induced Gip expression; GIP stimulation of insulin release, physiologically ensures a fine control of glucose homeostasis. How enteroendocrine cells adjust incretin production to replace incretin stores for future use is a key issue because GIP malfunction is linked to all forms of diabetes.

Pubmed