A role for G-proteins in the epidermal growth factor stimulation of phospholipase A2 in rat kidney mesangial cells

Biosci Rep. 1990 Aug;10(4):353-62. doi: 10.1007/BF01117235.

Abstract

We have previously demonstrated phospholipase C (PLC) independent activation of phospholipase A2(PLA2) by epidermal growth factor (EGF) in glomerular mesangial cells in culture. In the current study using glass beads to permeabilize [3H]- or [14C]-arachidonate labelled mesangial cells we demonstrate that guanine nucleotides modulate the EGF-mediated stimulation of arachidonic acid release (75% inhibition with 100 microM GDP beta S and 108% augmentation with 100 microM GTP gamma S). GTP gamma S alone stimulated both the release of free arachidonic acid and production of diacylglycerol (DAG), while EGF itself neither stimulated DAG nor augmented the DAG response to GTP gamma S. These findings suggest the intermediacy of a G-protein in PLC-independent stimulation of PLA2 by a growth factor, and provide a model system for determining the relationship between G-protein intermediacy and the intrinsic tyrosine kinase activity of the growth factor receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acids / metabolism
  • Calcium / pharmacology
  • Cells, Cultured
  • Epidermal Growth Factor / pharmacology*
  • GTP-Binding Proteins / metabolism*
  • Glomerular Mesangium / cytology
  • Glomerular Mesangium / enzymology*
  • Microscopy, Fluorescence
  • Phospholipases A / metabolism*
  • Phospholipases A2
  • Rats
  • Rats, Inbred Strains

Substances

  • Arachidonic Acids
  • Epidermal Growth Factor
  • Phospholipases A
  • Phospholipases A2
  • GTP-Binding Proteins
  • Calcium