UPR-mediated TRIB3 expression correlates with reduced AKT phosphorylation and inability of interleukin 6 to overcome palmitate-induced apoptosis in RINm5F cells


Autoria(s): NICOLETTI-CARVALHO, Jose Edgar; NOGUEIRA, Tatiane C. Araujo; GORJAO, Renata; BROMATI, Carla Rodrigues; YAMANAKA, Tatiana S.; BOSCHERO, Antonio Carlos; VELLOSO, Licio Augusto; Curi, Rui; ANHE, Gabriel Forato; BORDIN, Silvana
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Unfolded protein response (UPR)-mediated pancreatic beta-cell death has been described as a common mechanism by which palmitate (PA) and pro-inflammatory cytokines contribute to the development of diabetes. There are evidences that interleukin 6 (IL6) has a protective action against beta-cell death induced by proinflammatory cytokines; the effects of IL6 on PA-induced apoptosis have not been investigated yet. In the present study, we have demonstrated that PA selectively disrupts IL6-induced RAC-alpha serine/threonine-protein kinase (AKT) activation without interfering with signal transducer and activator of transcription 3 phosphorylation in RINm5F cells. The inability of IL6 to activate AKT in the presence of PA correlated with an inefficient protection against PA-induced apoptosis. In contrast to PA, IL6 efficiently reduced apoptosis induced by pro-inflammatory cytokines. In addition, we have demonstrated that IL6 is unable to overcome PA-stimulated UPR, as assessed by activating transcription factor 4 (ATF4) andC/EBP homologous protein (CHOP) expression, X-box binding protein-1 gene mRNA splicing, and pancreatic eukaryotic initiation factor-2 alpha kinase phosphorylation, whereas no significant induction of UPR by pro-inflammatory cytokines was detected. This unconditional stimulation of UPR and apoptosis by PA was accompanied by the stimulation of CHOP and tribble3 (TRIB3) expression, irrespective of the presence of IL6. These findings suggest that IL6 is unable to protect pancreatic beta-cells from PA-induced apoptosis because it does not repress UPR activation. In this way, CHOP and ATF4 might mediate PA-induced TRIB3 expression and, by extension, the suppression of IL6 activation of pro-survival kinase AKT. Journal of Endocrinology (2010) 206, 183-193

FAPESP

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

CAPES

Identificador

JOURNAL OF ENDOCRINOLOGY, v.206, n.2, p.183-193, 2010

0022-0795

http://producao.usp.br/handle/BDPI/28018

10.1677/JOE-09-0356

http://dx.doi.org/10.1677/JOE-09-0356

Idioma(s)

eng

Publicador

BIOSCIENTIFICA LTD

Relação

Journal of Endocrinology

Direitos

restrictedAccess

Copyright BIOSCIENTIFICA LTD

Palavras-Chave #ENDOPLASMIC-RETICULUM STRESS #ACID-INDUCED APOPTOSIS #FREE FATTY-ACIDS #BETA-CELLS #INSULIN-SECRETION #ER STRESS #SURVIVAL #GLUCOSE #KINASE #CYTOKINES #Endocrinology & Metabolism
Tipo

article

original article

publishedVersion