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JNK3是艾塞那肽4细胞保护作用所必需的。

JNK3 is required for the cytoprotective effect of exendin 4.

作者信息

Ezanno Hélène, Pawlowski Valérie, Abdelli Saida, Boutry Raphael, Gmyr Valery, Kerr-Conte Julie, Bonny Christophe, Pattou François, Abderrahmani Amar

机构信息

Lille 2 University, University of Lille Nord de France, European Genomic Institute for Diabetes, EGID FR 3508, UMR 8199, Lille, France.

Lille 2 University, University of Lille Nord de France, European Genomic Institute for Diabetes, EGID FR 3508, UMR 8199, Lille, France ; Department of Endocrine Surgery, Lille 2 University, University of Lille Nord de France, Lille University Hospital, INSERM UMR 859, Biotherapies for Diabetes, European Genomic Institute for Diabetes, Lille, France.

出版信息

J Diabetes Res. 2014;2014:814854. doi: 10.1155/2014/814854. Epub 2014 Jun 16.

Abstract

Preservation of beta cell against apoptosis is one of the therapeutic benefits of the glucagon-like peptide-1 (GLP1) antidiabetic mimetics for preserving the functional beta cell mass exposed to diabetogenic condition including proinflammatory cytokines. The mitogen activated protein kinase 10 also called c-jun amino-terminal kinase 3 (JNK3) plays a protective role in insulin-secreting cells against death caused by cytokines. In this study, we investigated whether the JNK3 expression is associated with the protective effect elicited by the GLP1 mimetic exendin 4. We found an increase in the abundance of JNK3 in isolated human islets and INS-1E cells cultured with exendin 4. Induction of JNK3 by exendin 4 was associated with an increased survival of INS-1E cells. Silencing of JNK3 prevented the cytoprotective effect of exendin 4 against apoptosis elicited by culture condition and cytokines. These results emphasize the requirement of JNK3 in the antiapoptotic effects of exendin 4.

摘要

保护β细胞免于凋亡是胰高血糖素样肽-1(GLP-1)抗糖尿病模拟物的治疗益处之一,这些模拟物可保护暴露于包括促炎细胞因子在内的致糖尿病条件下的功能性β细胞群。丝裂原活化蛋白激酶10也称为c-Jun氨基末端激酶3(JNK3),在胰岛素分泌细胞中对细胞因子引起的死亡起保护作用。在本研究中,我们调查了JNK3表达是否与GLP-1模拟物艾塞那肽4引发的保护作用相关。我们发现,在分离的人胰岛和用艾塞那肽4培养的INS-1E细胞中,JNK3的丰度增加。艾塞那肽4对JNK3的诱导与INS-1E细胞存活率增加相关。JNK3沉默可阻止艾塞那肽4对培养条件和细胞因子引发的凋亡的细胞保护作用。这些结果强调了JNK3在艾塞那肽4抗凋亡作用中的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd5b/4083605/6ef40f8c8d12/JDR2014-814854.001.jpg

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