c-Src interacts with and phosphorylates RelA/p65 to promote thrombin-induced ICAM-1 expression in endothelial cells

Am J Physiol Lung Cell Mol Physiol. 2007 Feb;292(2):L396-404. doi: 10.1152/ajplung.00163.2006. Epub 2006 Sep 29.

Abstract

The procoagulant thrombin promotes polymorphonuclear leukocyte (PMN) adhesion to endothelial cells by a mechanism involving expression of intercellular adhesion molecule-1 (ICAM-1) via an NF-kappaB-dependent pathway. We now provide evidence that activation of c-Src is crucial in signaling thrombin-induced ICAM-1 expression via tyrosine phosphorylation of RelA/p65. Stimulation of human umbilical vein endothelial cells with thrombin resulted in a time-dependent activation of c-Src, with maximal activation occurring at 30 min after thrombin challenge. Inhibition of c-Src by pharmacological and genetic approaches impaired thrombin-induced NF-kappaB-dependent reporter activity and ICAM-1 expression. Analysis of the NF-kappaB pathway revealed that the effect of c-Src inhibition occurred independently of IkappaBalpha degradation and NF-kappaB DNA binding function and was not associated with exchange of NF-kappaB dimers. Phosphorylation of RelA/p65 at Ser(536), an event mediating the transcriptional activity of DNA-bound RelA/p65, was also insensitive to c-Src inhibition. Interestingly, thrombin induced association of c-Src with RelA/p65, and inhibition of c-Src prevented this response, indicating that this interaction is contingent on activation of c-Src. We also observed that thrombin induced tyrosine phosphorylation of RelA/p65, and this phosphorylation was lost upon inhibition of c-Src, consistent with the requirement of activated c-Src for interaction with RelA/p65. These data implicate an important role of c-Src in phosphorylating RelA/p65 to promote the transcriptional activity of NF-kappaB and thereby ICAM-1 expression in endothelial cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • CSK Tyrosine-Protein Kinase
  • DNA / metabolism
  • Dimerization
  • Endothelial Cells / drug effects
  • Endothelial Cells / enzymology*
  • Gene Expression Regulation / drug effects
  • Humans
  • I-kappa B Proteins / metabolism
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism*
  • NF-KappaB Inhibitor alpha
  • Phosphorylation / drug effects
  • Phosphoserine / metabolism
  • Phosphotyrosine / metabolism
  • Protein Binding / drug effects
  • Protein Processing, Post-Translational / drug effects
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / deficiency
  • Protein-Tyrosine Kinases / metabolism*
  • Proto-Oncogene Proteins / antagonists & inhibitors
  • Proto-Oncogene Proteins / deficiency
  • Proto-Oncogene Proteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Thrombin / pharmacology*
  • Transcription Factor RelA / metabolism*
  • src-Family Kinases

Substances

  • I-kappa B Proteins
  • NFKBIA protein, human
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Transcription Factor RelA
  • Intercellular Adhesion Molecule-1
  • NF-KappaB Inhibitor alpha
  • Phosphoserine
  • Phosphotyrosine
  • DNA
  • Protein-Tyrosine Kinases
  • CSK Tyrosine-Protein Kinase
  • src-Family Kinases
  • CSK protein, human
  • Thrombin