Islet neogenesis-associated protein signaling in neonatal pancreatic rat islets: involvement of the cholinergic pathway
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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Resumo |
Islet neogenesis associated protein (INGAP) increases islet mass and insulin secretion in neonatal and adult rat islets. lit the Present Study, we measured the short- and long-term effects of INGAP-PP (a pentadecapeptide having the 104-118 amino acid sequence of INGAP) upon islet protein expression and phosphorylation of components of the PI3K, MAPK and cholinergic pathways, and on insulin secretion. Short-term exposure of neonatal islets to INGAP-PP (90 s, 5, 15, and 30 min) significantly increased Akt1(-Ser473) and MAPK3/1(-Thr202/Tyr204) phosphorylation and INGAP-PP also acutely increased insulin secretion from islets perifused with 2 and 20 mM glucose. Islets cultured for 4 days in the presence of INGAP-PP showed an increased expression of Akt1, Frap1, and Mapk1 mRNAs as well as of the muscarinic M3 receptor subtype, and phospholipase C (PLC)-beta 2 proteins. These islets also showed increased Akt1 and MAPK3/1 protein phosphorylation. Brief exposure of INGAP-P-treated islets to carbachol (Cch) significantly increased P70S6K(-Thr389) and MAPK3/1 phosphorylation and these islets released more insulin when challenged with Cch that was prevented by the M3 receptor antagonist 4-DAMP in a concentration-dependent manner. In conclusion, these data indicate that short- and long-term exposure to INGAP-PP significantly affects the expression and the phosphorylation of proteins involved in islet PI3K and MAPK signaling pathways. The observations of INGAPP-PP-stimulated up-regulation of cholinergic M3 receptors and PLC-beta 2 proteins, enhanced P70S6K and MAIIK3/1 phosphorylation and Cch-induced insulin secretion suggest a participation of the cholinergic pathway in INGAP-PP-mediated effects. CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) CNPQ Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP UK Society for Endocrinology Small Grant Programme UK Society for Endocrinology Small Grant Programme |
Identificador |
JOURNAL OF ENDOCRINOLOGY, v.199, n.2, p.299-306, 2008 0022-0795 http://producao.usp.br/handle/BDPI/28602 10.1677/JOE-08-0309 |
Idioma(s) |
eng |
Publicador |
BIOSCIENTIFICA LTD |
Relação |
Journal of Endocrinology |
Direitos |
restrictedAccess Copyright BIOSCIENTIFICA LTD |
Palavras-Chave | #BETA-CELL MASS #1321N1 ASTROCYTOMA-CELLS #INSULIN-PRODUCING CELLS #PHOSPHOINOSITIDE 3-KINASE #MAP KINASE #DIFFERENTIATION #RECEPTOR #GLUCOSE #ACTIVATION #SECRETION #Endocrinology & Metabolism |
Tipo |
article original article publishedVersion |