Factor IXa and von Willebrand factor modify the inactivation of factor VIII by activated protein C

J Lab Clin Med. 1990 Apr;115(4):415-21.

Abstract

Activated protein C inactivates factor VIII by proteolytic cleavage of the heavy chain of factor VIII. Protein S and calcium ions are cofactors in this reaction. We have examined the effects of several potential modulators of this reaction, including phospholipids, von Willebrand factor, and factor IXa, all of which bind factor VIII. Our results indicate that neither resting nor stimulated platelets nor phospholipid vesicles protect factor VIII from inactivation by activated protein C in either the presence or the absence of protein S. However, the addition of von Willebrand factor decreases the inactivation of factor VIII by activated protein C by 20% to 30%, and factor IXa, which is known to protect factor VIII from inactivation by activated protein C, confers additional protection with von Willebrand factor. The active site of factor IXa is necessary for the protective effect, because native factor IX and active site-inhibited factor IXa do not protect factor VIII from inactivation. Thus there is an additive protective effect when von Willebrand factor and factor IXa are present with factor VIII, leading to a decrease in the inactivation by activated protein C. These factors may be particularly important in stabilizing factor VIII in the circulation and during the early stages of coagulation.

Publication types

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

MeSH terms

  • Amino Acid Chloromethyl Ketones / pharmacology
  • Blood Platelets / metabolism
  • Cell Membrane / metabolism
  • Dansyl Compounds*
  • Factor IXa / pharmacology*
  • Factor VIII / metabolism*
  • Humans
  • Kinetics
  • Phospholipids / metabolism
  • Protein C / pharmacology*
  • von Willebrand Factor / pharmacology*

Substances

  • Amino Acid Chloromethyl Ketones
  • Dansyl Compounds
  • Phospholipids
  • Protein C
  • von Willebrand Factor
  • dansylglutamyl-glycyl-arginine chloromethyl ketone
  • Factor VIII
  • Factor IXa