EGF-Receptor phosphorylation and signaling are targeted by H2O2 redox stress

Am J Respir Cell Mol Biol. 1998 Nov;19(5):786-98. doi: 10.1165/ajrcmb.19.5.3249.


Inflammation of the respiratory tract is associated with the production of reactive oxygen species, such as hydrogen peroxide (H2O2) and superoxide (O2-), which contribute extensively to lung injury in diseases of the respiratory tract. The mechanisms and target molecules of these oxidants are mainly unknown but may involve modifications of growth-factor receptors. We have shown that H2O2 induces epidermal growth factor (EGF)-receptor tyrosine phosphorylation in intact cells as well as in membranes of A549 lung epithelial cells. On the whole, total phosphorylation of the EGF receptor induced by H2O2 was lower than that induced by the ligand EGF. Phosphorylation was confined to tyrosine residues and was inhibited by addition of genistein, indicating that it was due to the activation of protein tyrosine kinase (PTK). Phosphoamino acid analysis revealed that although the ligand, EGF, enhanced the phosphorylation of serine, threonine, and tyrosine residues, H2O2 preferentially enhanced tyrosine phosphorylation of the EGF receptor. Serine and threonine phosphorylation did not occur, and the turnover rate of the EGF receptor was slower after H2O2 exposure. Selective H2O2-mediated phosphorylation of tyrosine residues on the EGF receptor was sufficient to activate phosphorylation of an SH2-group-bearing substrate, phospholipase C-gamma (PLC-gamma), but did not increase mitogen-activated protein (MAP) kinase activity. Moreover, H2O2 exposure decreased protein kinase C (PKC)-alpha activity by causing translocation of PKC-alpha from the membrane to the cytoplasm. These studies provide novel insights into the capacity of a reactive oxidant, such as H2O2, to modulate EGF-receptor function and its downstream signaling. The H2O2-induced increase in tyrosine phosphorylation of the EGF receptor, and the receptor's slower rate of turnover and altered downstream phosphorylation signals may represent a mechanism by which EGF-receptor signaling can be modulated during inflammatory processes, thereby affecting cell proliferation and thus having implications in wound repair or tumor formation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • DNA / analysis
  • Diglycerides / metabolism
  • Enzyme Activation / drug effects
  • ErbB Receptors / metabolism*
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Isoenzymes / metabolism
  • Kinetics
  • Oxidation-Reduction
  • Phospholipase C gamma
  • Phosphorylation
  • Phosphotyrosine / analysis
  • Protein Kinase C / metabolism
  • Protein Kinase C-alpha
  • Signal Transduction / drug effects*
  • Stress, Physiological*
  • Tumor Cells, Cultured
  • Type C Phospholipases / metabolism
  • Tyrosine / metabolism


  • Diglycerides
  • Isoenzymes
  • Phosphotyrosine
  • Tyrosine
  • DNA
  • Hydrogen Peroxide
  • ErbB Receptors
  • PRKCA protein, human
  • Protein Kinase C
  • Protein Kinase C-alpha
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Type C Phospholipases
  • Phospholipase C gamma