Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Horm Metab Res. 2010 May;42(5):311-7. doi: 10.1055/s-0030-1249035. Epub 2010 Mar 8.
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.
据报道,免疫抑制剂雷帕霉素降低了胰腺β细胞的活力。相反,胰高血糖素样肽-1 的类似物 exendin-4 已被发现可抑制β细胞死亡并增加β细胞数量。我们研究了 exendin-4 对雷帕霉素在β细胞中细胞毒性作用的影响。在 MIN6 细胞和 Wistar 大鼠胰岛中,10 nM 雷帕霉素孵育 12 小时可诱导细胞死亡,但与 10 nM exendin-4 共孵育时则不会。雷帕霉素在 30 分钟内在 MIN6 细胞和 Wistar 大鼠胰岛中增加 c-Jun 氨基末端激酶(JNK)和 p38 的磷酸化,而 exendin-4 则降低其磷酸化。Akt 和细胞外信号调节激酶(ERK)不参与 exendin-4 的细胞保护作用。这些结果表明,exendin-4 可能通过抑制 JNK 和 p38 信号通路发挥其对雷帕霉素诱导的胰腺β细胞死亡的保护作用。