Functional properties of an endothelial cell cofactor for thrombin-catalyzed activation of protein C

J Biol Chem. 1981 Jun 10;256(11):5532-5.

Abstract

Thrombin-catalyzed activation of Protein C is accelerated by a human endothelial cell surface cofactor. The cofactor occurs also on mouse hemangioma cells (a transformed endothelial cell line), but not on cultured human smooth muscle cells or fibroblasts. The cofactor remains bound to the cell surface during Protein C activation. The cofactor is saturable with respect to both Protein C (Km = 0.72 +/- 0.07 microM) and thrombin (Km = 0.48 +/- 0.05 nM). Diisopropylphosphoryl-thrombin is a competitive inhibitor of the cofactor-dependent reaction with Ki = 0.56 +/- 0.1 nM. Prothrombin Fragment 1, the peptide derived from prothrombin that retains phospholipid binding capacity, does not inhibit activation of Protein C when present in a 7:1 molar excess over Protein C. Platelet Factor 4 (20 microgram/ml) also fails to inhibit Protein C activation. It is concluded that the endothelial cell provides a surface on which Protein C can be activated under physiological conditions.

Publication types

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

MeSH terms

  • Animals
  • Cell Line
  • Cells, Cultured
  • Endothelium / physiology
  • Enzyme Activation
  • Female
  • Glycoproteins / metabolism*
  • Humans
  • Kinetics
  • Mice
  • Organ Specificity
  • Pregnancy
  • Protein C
  • Thrombin / metabolism*
  • Umbilical Veins / physiology

Substances

  • Glycoproteins
  • Protein C
  • Thrombin