Phenylarsine oxide inhibits tyrosine phosphorylation of phospholipase C gamma 2 in human platelets and phospholipase C gamma 1 in NIH-3T3 fibroblasts

FEBS Lett. 1995 Jul 17;368(2):377-80. doi: 10.1016/0014-5793(95)00670-5.

Abstract

The sulphydryl reagent phenylarsine oxide (PAO) (1 microM) inhibited completely formation of inositol phosphates in human platelets induced by collagen or by cross-linking of the platelet low affinity Fc receptor, F c gamma RIIA, but did not alter the response to the G protein receptor agonist thrombin. PAO also inhibited completely tyrosine phosphorylation of PLC gamma 2 in collagen and Fc gamma RIIA-stimulated cells, although tyrosine phosphorylation of other proteins including the tyrosine kinase syk was relatively unaffected. PAO (1 microM) also inhibited completely tyrosine phosphorylation of PLC gamma 1 induced by platelet derived growth factor (PDGF) in NIH-3T3 fibroblasts but only partially reduced phosphorylation of the PDGF receptor. These results provide further evidence that collagen and Fc gamma RIIA cross-linking activate platelets through a pathway distinct from that used by thrombin and suggest that PAO may be a selective inhibitor of PLC gamma relative to PLC beta isozymes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Antigens, CD*
  • Arsenicals / pharmacology*
  • Blood Platelets / drug effects*
  • Blood Platelets / enzymology
  • Collagen / pharmacology
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Inositol Phosphates / biosynthesis
  • Isoenzymes / metabolism*
  • Mice
  • Phospholipase C gamma
  • Phosphorylation / drug effects
  • Platelet Activation / drug effects*
  • Platelet-Derived Growth Factor / pharmacology
  • Receptors, IgG / metabolism
  • Type C Phospholipases / metabolism*
  • Tyrosine / metabolism

Substances

  • Antigens, CD
  • Arsenicals
  • Enzyme Inhibitors
  • Fc gamma receptor IIA
  • Inositol Phosphates
  • Isoenzymes
  • Platelet-Derived Growth Factor
  • Receptors, IgG
  • oxophenylarsine
  • Tyrosine
  • Collagen
  • Type C Phospholipases
  • Phospholipase C gamma