Tyrosine phosphorylation of phospholipase C-gamma 2 is involved in the activation of phosphoinositide hydrolysis by Fc receptors in human neutrophils

Biochem Biophys Res Commun. 1994 Jun 30;201(3):1100-8. doi: 10.1006/bbrc.1994.1819.

Abstract

The stimulation of phosphoinositide hydrolysis by a number of agonists (phosphoinositide response) is a ubiquitous transmembrane signalling process for the regulation of several cell functions. Two mechanisms of activation have been identified that involve different phospholipases C: one regulated by G-proteins and another regulated by receptors having an intrinsic tyrosine kinase domain or that stimulate intracellular tyrosine kinase activity. This last mechanism is activated in several immunological cells, including lymphocytes, mastocytes, NK cells and monocytes, in response to agonists that bind antigen receptors, and receptors for IgE and IgG. In the present study, we have investigated the role of tyrosine phosphorylation in the stimulation of phosphoinositide hydrolysis mediated by Fc gamma Rs in human neutrophils. The results demonstrated that: 1) the activation of Fc gamma Rs with insoluble immune complexes (IIC) induced a tyrosine phosphorylation of several proteins that was dose-dependently inhibited by the tyrosine kinase inhibitor, genistein; 2) the activation of Fc gamma Rs caused a stimulation of phosphoinositide hydrolysis measured as [3H]inositol phosphates formation; 3) genistein depressed the activation of phosphoinositide hydrolysis; 4) among the several proteins that became tyrosine phosphorylated upon Fc gamma Rs activation by IIC, one 145 kDa protein was identified as PLC-gamma 2, using a specific antiserum. The phosphorylation of PLC-gamma 2 was completely inhibited by genistein. These results demonstrate that the phosphoinositide response to activation of Fc gamma Rs involves the tyrosine phosphorylation of PLC-gamma 2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genistein
  • Humans
  • Isoenzymes
  • Isoflavones / pharmacology
  • Neutrophils / physiology*
  • Phosphatidylinositols / metabolism*
  • Phosphoproteins / metabolism
  • Phosphotyrosine
  • Receptor Aggregation
  • Receptors, Fc / metabolism*
  • Signal Transduction
  • Time Factors
  • Type C Phospholipases / metabolism*
  • Tyrosine / analogs & derivatives*
  • Tyrosine / metabolism

Substances

  • Isoenzymes
  • Isoflavones
  • Phosphatidylinositols
  • Phosphoproteins
  • Receptors, Fc
  • Phosphotyrosine
  • Tyrosine
  • Genistein
  • Type C Phospholipases