| Texto completo | |
| Autor(es): Mostrar menos - |
Rajasekaran, Subu Surendran
;
Kim, Jaeyoon
;
Gaboardi, Gian-Carlo
;
Gromada, Jesper
;
Shears, Stephen B.
;
dos Santos, Karen Tiago
;
Nolasco, Eduardo Lima
;
Ferreira, Sabrina de Souza
;
Illies, Christopher
;
Kohler, Martin
;
Gu, Chunfang
;
Ryu, Sung Ho
;
Martins, Joilson O.
;
Dare, Elisabetta
;
Barker, Christopher J.
;
Berggren, Per-Olof
Número total de Autores: 16
|
| Tipo de documento: | Artigo Científico |
| Fonte: | CELLULAR SIGNALLING; v. 46, p. 9-pg., 2018-06-01. |
| Resumo | |
Diphosphoinositol pentakisphosphate (IP7) is critical for the exocytotic capacity of the pancreatic beta-cell, but its regulation by the primary instigator of beta-cell exocytosis, glucose, is unknown. The high K-m for ATP of the IP7-generating enzymes, the inositol hexakisphosphate kinases (IP6K1 and 2) suggests that these enzymes might serve as metabolic sensors in insulin secreting beta-cells and act as translators of disrupted metabolism in diabetes. We investigated this hypothesis and now show that glucose stimulation, which increases the ATP/ADP ratio, leads to an early rise in IP7 concentration in beta-cells. RNAi mediated knock down of the IP6K1 isoform inhibits both glucose-mediated increase in IP7 and first phase insulin secretion, demonstrating that IP6K1 integrates glucose metabolism and insulin exocytosis. In diabetic mouse islets the deranged ATP/ADP levels under both basal and glucose-stimulated conditions are mirrored in both disrupted IP7 generation and insulin release. Thus the unique metabolic sensing properties of IP6K1 guarantees appropriate concentrations of IP7 and thereby both correct basal insulin secretion and intact first phase insulin release. In addition, our data suggest that a specific cell signaling defect, namely, inappropriate IP7 generation may be an essential convergence point integrating multiple metabolic defects into the commonly observed phenotype in diabetes. (AU) | |
| Processo FAPESP: | 10/02272-0 - Efeito da insulina na inflamação pulmonar secundária a sepse, na imunidade inata, na ativação do seu gene (BGK) e seus receptores (IR-A e IR-B) |
| Beneficiário: | Joilson de Oliveira Martins |
| Modalidade de apoio: | Auxílio à Pesquisa - Jovens Pesquisadores |
| Processo FAPESP: | 17/11540-7 - Investigando o papel da insulina na vigência da inflamação alérgica pulmonar em camundongos diabéticos e sadios |
| Beneficiário: | Joilson de Oliveira Martins |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 14/05214-1 - Investigando o papel da insulina em diferentes infecções em animais diabéticos e sadios |
| Beneficiário: | Joilson de Oliveira Martins |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |