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

نویسندگان

  • Chaoxun Wang
  • Xiaopan Chen
  • Xiaoying Ding
  • Yanju He
  • Chengying Gu
  • Ligang Zhou
چکیده

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.

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عنوان ژورنال:
  • Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

دوره 35 6  شماره 

صفحات  -

تاریخ انتشار 2015