Epinephrine and the Ca2+ ionophore A23187 synergistically induce platelet aggregation without protein kinase C activation

Aspirin‐pretreated, 32P‐prelabeled, washed human platelets resuspended in a buffer containing apyrase and 2% plasma were exposed to epinephrine and the Ca2+ ionophore A23187. Epinephrine potentiated platelet aggregation (not secretion), the production of [32P]phosphatidic acid and myosin light chain...

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Veröffentlicht in:FEBS letters 1989-01, Vol.243 (2), p.275-279
Hauptverfasser: Olbrich, Christine, Siess, Wolfgang
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Siess, Wolfgang
description Aspirin‐pretreated, 32P‐prelabeled, washed human platelets resuspended in a buffer containing apyrase and 2% plasma were exposed to epinephrine and the Ca2+ ionophore A23187. Epinephrine potentiated platelet aggregation (not secretion), the production of [32P]phosphatidic acid and myosin light chain phosphorylation induced by A23187. No phosphorylation of the 40 kDa protein, the substrate of protein kinase C, was observed. We conclude that G1‐protein activation evoked by epinephrine and Ca2+ mobilization caused by A23187 represents a novel synergism for platelet aggregation and that protein kinase C activation, under these conditions is not needed for platelet aggregation.
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subjects Biological and medical sciences
Blood coagulation. Blood cells
Ca2+ ionophore
Calcimycin - pharmacology
Drug Synergism
Enzyme Activation - drug effects
Epinephrine
Epinephrine - pharmacology
Fundamental and applied biological sciences. Psychology
Humans
Molecular and cellular biology
Phosphatidic acid
Phosphatidic Acids - biosynthesis
Phosphorylation
Platelet
Platelet aggregation
Platelet Aggregation - drug effects
Protein kinase C
Protein Kinase C - metabolism
Synergism
title Epinephrine and the Ca2+ ionophore A23187 synergistically induce platelet aggregation without protein kinase C activation
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