Exendin-4 protects pancreatic beta cells from the cytotoxic effect of rapamycin by inhibiting JNK and p38 phosphorylation.

نویسندگان

  • Y Kawasaki
  • S Harashima
  • M Sasaki
  • E Mukai
  • Y Nakamura
  • N Harada
  • K Toyoda
  • A Hamasaki
  • S Yamane
  • C Yamada
  • Y Yamada
  • Y Seino
  • N Inagaki
چکیده

It has been reported that the immunosuppressant rapamycin decreases the viability of pancreatic beta cells. In contrast, exendin-4, an analogue of glucagon-like peptide-1, has been found to inhibit beta cell death and to increase beta cell mass. We investigated the effects of exendin-4 on the cytotoxic effect of rapamycin in beta cells. Incubation with 10 nM rapamycin induced cell death in 12 h in murine beta cell line MIN6 cells and Wistar rat islets, but not when coincubated with 10 nM exendin-4. Rapamycin was found to increase phosphorylation of c-Jun amino-terminal kinase (JNK) and p38 in 30 minutes in MIN6 cells and Wistar rat islets while exendin-4 decreased their phosphorylation. Akt and extracellular signal-regulated kinase (ERK) were not involved in the cytoprotective effect of exendin-4. These results indicate that exendin-4 may exert its protective effect against rapamycin-induced cell death in pancreatic beta cells by inhibiting JNK and p38 signaling.

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عنوان ژورنال:
  • Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme

دوره 42 5  شماره 

صفحات  -

تاریخ انتشار 2010