JNK3 Is Required for the Cytoprotective Effect of Exendin 4.


Autoria(s): Ezanno H.; Pawlowski V.; Abdelli S.; Boutry R.; Gmyr V.; Kerr-Conte J.; Bonny C.; Pattou F.; Abderrahmani A.
Data(s)

2014

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_2BA4EFC99753

isbn:2314-6753 (Electronic)

pmid:25025079

doi:10.1155/2014/814854

isiid:000338060900001

http://my.unil.ch/serval/document/BIB_2BA4EFC99753.pdf

http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_2BA4EFC997535

Idioma(s)

en

Direitos

info:eu-repo/semantics/openAccess

Fonte

Journal of Diabetes Research, vol. 2014, pp. 814854

Tipo

info:eu-repo/semantics/article

article