Exendin-4 Promotes Beta Cell Proliferation via PI3k/Akt Signalling Pathway

Cell Physiol Biochem. 2015;35(6):2223-32. doi: 10.1159/000374027. Epub 2015 Apr 8.

Abstract

Background/aims: Prevention of diabetes requires maintenance of a functional beta-cell mass, the postnatal growth of which depends on beta cell proliferation. Past studies have shown evidence of an effect of an incretin analogue, Exendin-4, in promoting beta cell proliferation, whereas the underlying molecular mechanisms are not completely understood.

Methods: Here we studied the effects of Exendin-4 on beta cell proliferation in vitro and in vivo through analysing BrdU-incorporated beta cells. We also analysed the effects of Exendin-4 on beta cell mass in vivo, and on beta cell number in vitro. Then, we applied specific inhibitors of different signalling pathways and analysed their effects on Exendin-4-induced beta cell proliferation.

Results: Exendin-4 increased beta cell proliferation in vitro and in vivo, resulting in significant increases in beta cell mass and beta cell number, respectively. Inhibition of PI3K/Akt signalling, but not inhibition of either ERK/MAPK pathway, or JNK pathway, significantly abolished the effects of Exendin-4 in promoting beta cell proliferation.

Conclusion: Exendin-4 promotes beta cell proliferation via PI3k/Akt signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation / drug effects*
  • Exenatide
  • Female
  • Insulin-Secreting Cells / drug effects*
  • Insulin-Secreting Cells / metabolism
  • MAP Kinase Signaling System / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Peptides / pharmacology*
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction / drug effects*
  • Venoms / pharmacology*

Substances

  • Peptides
  • Venoms
  • Exenatide
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt