Abstrakt: |
Tumour‐promoting phorbol esters (phorbol‐12‐myristate‐13‐acetate, PMA; phorbol‐12,13‐dibutyrate, PDBu) but not 4β‐phorbol, activate protein kinase C. Using human platelets pre‐labelled with quin2 or 32PO4we examined the effects of these compounds on human platelet cytosolic free Ca2+([Ca2+]j) and on [32]phosphatidic acid ([32P]PtdOH). PMA and PDBu, but not 4β‐phorbol inhibited thrombin‐, PAF‐ and vasopressin‐induced elevation of [Ca2+], and [2+P]PtdOH formation. It is suggested that protein kinase C may act to terminate the transduction processes that link receptor occupancy to cellular activation. |