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Cell Calcium ; 35(4): 333-43, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15036950

RESUMO

A fluid stream induced by a concentration clamp system evokes in Xenopus oocytes a deformation of the membrane which results in transient chloride currents of high amplitude (stream-evoked inward current, I(i,st)) during calcium-activated chloride current oscillations. The involvement of cytoskeleton elements and of components of the phospholipase C-dependent signaling pathway on the generation of the I(i,st) were investigated. Incubation of the oocytes with cytoskeleton-disrupting agents exerted no effects on generation of the I(i,st), suggesting that the mechanotransduction is not mediated by these structures. The fluid stream induced an elevation of the submembraneous calcium concentration, as measured by an increase of Fluo-4-mediated fluorescence after the stimulus. Lowering the intracellular calcium concentration by injection of calcium chelators or depleting inositol 1,4,5-triphosphate (InsP(3))-sensitive calcium stores by blockers of the calcium pumps suppressed the generation of the I(i,st) in most cases. Furthermore, the phospholipase C inhibitor U73122 reversibly blocked the I(i,st). The results suggest that the fluid stream leads to a membrane stretch which modulates directly or indirectly the activity of a membrane-bound phospholipase C. The phospholipase C transiently elevates the InsP(3) concentration, in turn releasing calcium from InsP(3)-sensitive internal calcium stores, thus evoking an enhanced calcium-sensitive chloride current.


Assuntos
Cálcio/metabolismo , Citoesqueleto/fisiologia , Oócitos/fisiologia , Transdução de Sinais/fisiologia , Fosfolipases Tipo C/metabolismo , Animais , Bloqueadores dos Canais de Cálcio/farmacologia , Canais de Cálcio/fisiologia , Quelantes/farmacologia , Canais de Cloreto/efeitos dos fármacos , Canais de Cloreto/fisiologia , Inibidores Enzimáticos/farmacologia , Feminino , Inositol 1,4,5-Trifosfato/metabolismo , Líquido Intracelular/metabolismo , Potenciais da Membrana/fisiologia , Oócitos/efeitos dos fármacos , Fosfolipases Tipo C/antagonistas & inibidores , Xenopus laevis/metabolismo
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