Ndfip1;
Pancreatic beta cells;
Cytokines;
Unfolded protein response;
JunB;
UBIQUITIN LIGASES;
ER STRESS;
INFLAMMATION;
EXPRESSION;
APOPTOSIS;
ITCH;
D O I:
10.1016/j.bbrc.2015.08.099
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
High-throughput siRNA screening was employed to identify novel genes that regulate cytokine-induced death of pancreatic beta-cells. One of the 'hits' was Nedd4 family interacting protein 1 (Ndfip1), an adaptor and activator of Nedd4-family ubiquitin ligases. Silencing of Ndfip1 inhibited cytokine-induced apoptosis of mouse and human pancreatic islets and promoted glucose-stimulated insulin secretion. These effects were associated with an increase in the cellular content of JunB, a potent inhibitor of ER stress and apoptosis. Silencing of Ndfip1 also increased the expression of ATF4, IRE-1 alpha, and the spliced form of XBP that govern the unfolded protein response (UPR) and relieve cytokine-induced ER stress, while overexpression of Ndfip1 exerted opposite effects. These findings implicate Ndfip1 in the degradation of JunB; inhibition of the UPR and insulin secretion; and promotion of cytokine-induced death of pancreatic beta-cells. (C) 2015 Elsevier Inc. All rights reserved.
机构:
Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3010, AustraliaUniv Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3010, Australia