CA-2+ MOBILIZATION PRIMES PROTEIN KINASE-C IN HUMAN-PLATELETS - CA-2+ AND PHORBOL ESTERS STIMULATE PLATELET-AGGREGATION AND SECRETION SYNERGISTICALLY THROUGH PROTEIN KINASE-C

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  • 1 October 1988
    • journal article
    • research article
    • Vol. 255  (1) , 309-318
Abstract
Low concentrations of Ca2+-mobilizing agonists such as vasopressin, platelet-activating factor, ADP, the endoperoxide analogue U44069 and the Ca2+ ionophore A23187 enhance the binding of [3H]phorbol 12,13-dibutyrate (PdBu) to intact human platelets. This effect is prevented by preincubation of platelets with prostacyclin (except for A23187). Adrenaline, which does not increase Ca2+ in the platelt cytosol, does not enhance the binding of [3H]PdBu to platelets. In addition, all platelet agonsits except adrenaline potentiate the phosphorylation of the substrate of protein kinase C (40 kDa protein) induced by PdBu. Potentiation of protein kinase C activation is associated with increased platelet aggregation and secretion. Stimulus-induced myosin light-chain phosphorylation and shape change are not significantly affected, but formation of phosphatidic acid is decreased in the presence of PdBu. The results may indicate that low concentrations of agonists induce in intact platelets the translocation of protein kinase C to the plasma membrane by eliciting mobilization of Ca2+, and thereby place the enzyme in a strategic position for activation by phorbol ester. Such activation enhances platelet aggregation and secretion, but at the same time suppresses activation of phospholipase C. Therefore, at least part of the synergism evoked by Ca2+ and phorbol ester is mediated through a single pathway which involves protein kianse C. It is likely that the priming of protein kinase C by prior Ca2+ mobilization occurs physiologically in activated platelets.

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