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myo-Inositol 1,4,5-trisphosphate stimulates protein phosphorylation in saponin-permeabilized human platelets.

In an attempt to establish a system with physiological substrates and phospholipid surfaces to investigate Ca2+- and 1,2-diacylglycerol-dependent protein kinase C activation, saponized platelets were used. Saponin, through interaction with plasma membrane cholesterol, makes cells permeable without m...

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Detalhes bibliográficos
Main Authors: Lapetina, E G, Watson, S P, Cuatrecasas, P
Formato: Artigo
Idioma:en
Publicado em: 1984
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC392160/
https://ncbi.nlm.nih.gov/pubmed/6438636
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Resumo:In an attempt to establish a system with physiological substrates and phospholipid surfaces to investigate Ca2+- and 1,2-diacylglycerol-dependent protein kinase C activation, saponized platelets were used. Saponin, through interaction with plasma membrane cholesterol, makes cells permeable without major disruption of organelles. Washed platelets, prelabeled with 32P, were treated with 1-50 micrograms of saponin per ml. Permeabilization was evident at a concentration of 10 micrograms of saponin per ml, as indicated by the action of extracellular Ca2+ on the phosphorylation of the 20,000- and 40,000-Da proteins. These proteins are, respectively, the substrates for myosin light chain kinase and protein kinase C. Activation of these enzymes occurred when the estimated free [Ca2+] was changed from approximately equal to 80 nM to 300 nM. The effect of Ca2+ on kinase C-induced phosphorylation was potentiated by 1,2-didecanoylglycerol (1 microM). myo-Inositol 1,4,5-trisphosphate (5-20 microM) increased phosphorylation of the 20,000- and 40,000-Da proteins. This action was time and concentration dependent. The effect of myo-inositol 1,4,5-trisphosphate on the activation of kinase C was additive with 1,2-didecanoylglycerol. The action of myo-inositol 1,4,5-trisphosphate could be due to mobilization of Ca2+ from platelet organelles and/or to a direct effect on protein kinases.