FAK blunts adenosine-homocysteine-induced endothelial cell apoptosis: requirement for PI 3-kinase

Am J Physiol Lung Cell Mol Physiol. 2002 May;282(5):L1135-42. doi: 10.1152/ajplung.00174.2001.

Abstract

Treatment of cultured bovine pulmonary endothelial cells (BPAEC) with adenosine (Ado) alone or in combination with homocysteine (Hc) leads to disruption of focal adhesion complexes, caspase-dependent degradation of components of focal adhesion complexes, and subsequent apoptosis. Endothelial cells transiently overexpressing paxillin or p130(Cas) cDNAs underwent Ado-Hc-induced apoptosis to an extent similar to that of cells transfected with vector alone. However, overexpression of focal adhesion kinase (FAK) cDNA blunted Ado-Hc-induced apoptosis. FAK constructs lacking the central catalytic domain or containing a point mutation, rendering the catalytic domain enzymatically inactive, did not provide protection from apoptosis. Constructs containing a mutation in the major autophosphorylation site (tyrosine-397) similarly did not prevent cell death. A FAK mutant in amino acid 395, deficient in phosphatidylinositol 3-kinase (PI 3-kinase) binding, was not able to blunt apoptosis. Finally, overexpression of FAK did not provide protection from apoptosis in the presence of LY-294002, a PI 3-kinase inhibitor. Taken together, these data suggest that the survival signals mediated by overexpression of FAK in response to Ado-Hc-induced apoptosis require a PI 3-kinase-dependent pathway.

Publication types

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

MeSH terms

  • Adenosine / pharmacology
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Catalytic Domain
  • Cattle
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cells, Cultured
  • Crk-Associated Substrate Protein
  • Cytoskeletal Proteins / genetics
  • Cytoskeletal Proteins / metabolism
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / enzymology*
  • Focal Adhesion Protein-Tyrosine Kinases
  • Gene Expression Regulation, Enzymologic
  • Homocysteine / pharmacology
  • Paxillin
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism*
  • Proteins*
  • Pulmonary Artery / cytology
  • Pulmonary Artery / enzymology*
  • Retinoblastoma-Like Protein p130
  • Signal Transduction / physiology
  • Transfection

Substances

  • Crk-Associated Substrate Protein
  • Cytoskeletal Proteins
  • Paxillin
  • Phosphoproteins
  • Proteins
  • Retinoblastoma-Like Protein p130
  • Homocysteine
  • Phosphatidylinositol 3-Kinases
  • Protein-Tyrosine Kinases
  • Focal Adhesion Protein-Tyrosine Kinases
  • Adenosine