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Exendin-4 通过抑制 JNK 和 p38 磷酸化来保护胰岛β细胞免受雷帕霉素的细胞毒性作用。

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

机构信息

Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Horm Metab Res. 2010 May;42(5):311-7. doi: 10.1055/s-0030-1249035. Epub 2010 Mar 8.

Abstract

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.

摘要

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。

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