MKP-1 mediates glucocorticoid-induced ERK1/2 dephosphorylation and reduction in pancreatic beta-cell proliferation in islets from early lactating mothers


Autoria(s): NICOLETTI-CARVALHO, Jose E.; LELLIS-SANTOS, Camilo; YAMANAKA, Tatiana S.; NOGUEIRA, Tatiane C.; CAPERUTO, Luciana C.; LEITE, Adriana R.; ANHE, Gabriel F.; BORDIN, Silvana
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Maternal pancreatic islets undergo a robust increase of mass and proliferation during pregnancy, which allows a compensation of gestational insulin resistance. Studies have described that this adaptation switches to a low proliferative status after the delivery. The mechanisms underlying this reversal are unknown, but the action of glucocorticoids (GCs) is believed to play an important role because GCs counteract the pregnancy-like effects of PRL on isolated pancreatic islets maintained in cell culture. Here, we demonstrate that ERK1/2 phosphorylation (phospho-ERK1/2) is increased in maternal rat islets isolated on the 19th day of pregnancy. Phospho-ERK1/2 status on the 3rd day after delivery (L3) rapidly turns to values lower than that found in virgin control rats (CTL). MKP-1, a protein phosphatase able to dephosphorylate ERK1/2, is increased in islets from L3 rats. Chromatin immunoprecipitation assay revealed that binding of glucocorticoid receptor (GR) to MKP-1 promoter is also increased in islets from L3 rats. In addition, dexamethasone (DEX) reduced phospho-ERK1/2 and increased MKP-1 expression in RINm5F and MIN-6 cells. Inhibition of transduction with cycloheximide and inhibition of phosphatases with orthovanadate efficiently blocked DEX-induced downregulation of phospho-ERK1/2. In addition, specific knockdown of MKP-1 with siRNA suppressed the downregulation of phosphoERK1/2 and the reduction of proliferation induced by DEX. Altogether, our results indicate that downregulation of phospho-ERK1/2 is associated with reduction in proliferation found in islets of early lactating mothers. This mechanism is probably mediated by GC-induced MKP-1 expression.

FAPESP Brazilian foundations Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

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

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq Conselho Nacional de Pesquisa

CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Identificador

AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, v.299, n.6, p.E1006-E1015, 2010

0193-1849

http://producao.usp.br/handle/BDPI/28004

10.1152/ajpendo.00341.2010

http://dx.doi.org/10.1152/ajpendo.00341.2010

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

Relação

American Journal of Physiology-endocrinology and Metabolism

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #mitogen-activated protein kinase phosphatase-1 #extracellular signal-regulated kinase 1/2 #dual-specificity phosphatases #pregnancy #lactation #PROTEIN-KINASE PHOSPHATASE-1 #PALMITATE-INDUCED APOPTOSIS #MAP KINASE #INSULIN-SECRETION #LACTOGENIC HORMONES #PREGNANT RATS #SMOOTH-MUSCLE #EXPRESSION #PROLACTIN #PATHWAY #Endocrinology & Metabolism #Physiology
Tipo

article

original article

publishedVersion