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Synergistic cofactor function of factor V and protein S to activated protein C in the inactivation of the factor VIIIa - factor IXa complex -- species specific interactions of components of the protein C anticoagulant system.

Publication ,  Journal Article
Shen, L; He, X; Dahlbäck, B
Published in: Thromb Haemost
September 1997

Human factor V has been shown not only to be a precursor to procoagulant factor Va but also to express anticoagulant properties. Thus, factor V was recently found to potentiate the effect of protein S as cofactor to activated protein C (APC) in the inactivation of the factor VIIIa-factor IXa complex. The purpose of this study was to determine whether the APC-cofactor function of factor V was also expressed in the bovine protein C system and to elucidate the molecular background for the species specificity of APC. For this purpose, the effects of protein S and factor V on APC-mediated inactivation of factor VIIIa were studied using purified APC, protein S and factor V of human and bovine origin. The factor VIIIa investigated here was part of a Xase complex (i.e. factor IXa, factor VIIIa, phospholipid and calcium) and the APC-mediated inhibition of factor VIIIa was monitored by the ability of the Xase complex to activate factor X. Synergistic APC-cofactor function of factor V and protein S was demonstrated in the bovine system. The effect of bovine APC was potentiated by bovine protein S but not by human protein S, whereas both human or bovine protein S stimulated the function of human APC. Factor V did not express species specificity in its APC-cofactor activity even though bovine factor V was more potent than its human counterpart. Recombinant human/bovine protein S chimeras were used to demonstrate that the thrombin sensitive region and first epidermal growth factor-like module of protein S determine the species specificity of the APC-protein S interaction. In conclusion, both human and bovine factor V were found to express APC-cofactor activity which depends on the presence of protein S. The species specificity of APC was shown to be caused by the interaction between APC and protein S.

Duke Scholars

Published In

Thromb Haemost

ISSN

0340-6245

Publication Date

September 1997

Volume

78

Issue

3

Start / End Page

1030 / 1036

Location

Germany

Related Subject Headings

  • Species Specificity
  • Protein S
  • Protein C
  • Neoplasm Proteins
  • Humans
  • Factor VIIIa
  • Factor V
  • Factor IXa
  • Drug Synergism
  • Cysteine Endopeptidases
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Journal cover image

Published In

Thromb Haemost

ISSN

0340-6245

Publication Date

September 1997

Volume

78

Issue

3

Start / End Page

1030 / 1036

Location

Germany

Related Subject Headings

  • Species Specificity
  • Protein S
  • Protein C
  • Neoplasm Proteins
  • Humans
  • Factor VIIIa
  • Factor V
  • Factor IXa
  • Drug Synergism
  • Cysteine Endopeptidases