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Role of phosphatidylinositol 3-kinase in degranulation induced by IgE-dependent and -independent mechanisms in rat basophilic RBL-2H3 (ml) cells.
Hirasawa, N; Sato, Y; Yomogida, S; Mue, S; Ohuchi, K.
Afiliación
  • Hirasawa N; Department of Pathophysiological Biochemistry, Faculty of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan.
Cell Signal ; 9(3-4): 305-10, 1997.
Article en En | MEDLINE | ID: mdl-9218132
ABSTRACT
We have examined the role of phosphatidylinositol 3-kinase (P13-kinase) in the degranulation induced by the antigen, an IgE-dependent stimulant, and by carbachol and thapsigargin, IgE-independent stimulants, in the muscarine ml receptor-transfected mast cell line RBL-2h3 (ml) cells. These stimulants commonly increased P13-kinase activity in the anti-phosphotyrosine immunoprecipitate. The P13-kinase inhibitors wortmannin and LY294002 inhibited induced by these stimulants. The membrane ruffling induced by the antigen or carbachol was also inhibited by wortmannin. In contrast, thapsigargin induced by membrane ruffling but induced microspikes, which was not affected by wortmannin. In the permeabilized RBL-2H3 (ml) cells, wortmannin the GTP gamma S-induced membrane ruffling without inhibiting the GTP gamma S-induced degranulation. These findings suggest that P13-kinase is involved not only in IgE-dependent degranulation but also in IgE-independent degranulation, and that the GTP gamma S-sensitive protein at the downstream of P13-kinase is responsible for the degranulation but not for the membrane ruffling.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina E / Degranulación de la Célula / Fosfotransferasas (Aceptor de Grupo Alcohol) / Mastocitos Límite: Animals Idioma: En Revista: Cell Signal Año: 1997 Tipo del documento: Article País de afiliación: Japón
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Inmunoglobulina E / Degranulación de la Célula / Fosfotransferasas (Aceptor de Grupo Alcohol) / Mastocitos Límite: Animals Idioma: En Revista: Cell Signal Año: 1997 Tipo del documento: Article País de afiliación: Japón