The role of gamma-carboxylation in the anti-apoptotic function of gas6

J Thromb Haemost. 2005 Dec;3(12):2790-7. doi: 10.1111/j.1538-7836.2005.01662.x.

Abstract

Gas6 is a novel member of the vitamin K-dependent family of gamma-carboxylated proteins and is a ligand for the receptor tyrosine kinase Axl. Gas6-Axl interactions have been shown to mediate cell survival in vascular endothelium. Although the receptor-binding portion of gas6 lies in the C-terminus, the significance of the N-terminal gamma-carboxylated residues (Gla domain) is not clear. To address this question, this study examines the role of the Gla domain in phospholipid binding as well as in the promotion of cell survival, especially in endothelial cells. The results show that carboxylated gas6 binds to phosphatidylserine-containing phospholipid membranes in an analogous manner to other gamma-carboxylated proteins whereas decarboxylated gas6 does not. The gamma-carboxylation inhibitor warfarin abrogates gas6-mediated protection of NIH3T3 fibroblasts from serum starvation-induced apoptosis. Furthermore, the role of gamma-carboxylation in gas6's survival effect on endothelium is demonstrated directly in that only carboxylated, but not decarboxylated, gas6 protects endothelial cells from serum starvation-induced apoptosis. gamma-carboxylation is also required for both Axl phosphorylation and PI3 kinase activation. Taken together, these findings demonstrate that gamma-carboxylation is necessary not only for gas6 binding to phospholipid membranes, but also for gas6-mediated endothelial cell survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Carboxyglutamic Acid*
  • Animals
  • Apoptosis*
  • Cells, Cultured
  • Endothelium, Vascular / cytology*
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Intercellular Signaling Peptides and Proteins / physiology
  • Mice
  • NIH 3T3 Cells
  • Oncogene Proteins / metabolism
  • Phospholipids / metabolism
  • Protein Processing, Post-Translational / physiology*
  • Proto-Oncogene Proteins
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Umbilical Veins / cytology
  • Warfarin / pharmacology

Substances

  • Intercellular Signaling Peptides and Proteins
  • Oncogene Proteins
  • Phospholipids
  • Proto-Oncogene Proteins
  • growth arrest-specific protein 6
  • 1-Carboxyglutamic Acid
  • Warfarin
  • Receptor Protein-Tyrosine Kinases
  • axl receptor tyrosine kinase