Factor viii

Author: Prof. Dr. med. Peter Altmeyer

All authors of this article

Last updated on: 29.10.2020

Dieser Artikel auf Deutsch

Synonym(s)

antihemophilic factor; Haemophilic globulin A; Plasmathromboplasmin Factor-A

Definition
This section has been translated automatically.

Factor VIII consists of two subunits connected by calcium:

  • the low molecular weight portion VIII C
  • and
  • the high-molecular F-VIII-associated protein, the FVII RvWF.

The coagulation active component is the F-VIII C.

Thrombin activates the F-VIII enzymatically by splitting off peptides. The molecular weight of F-VIII C is 268 kD, the plasma concentration is 0.15 mg/l.
Factor VIII C is a non-enzymatic cofactor of the complex of factor IXa, phospholipids and calcium. This complex is called tenase. Tenase catalyses the proteolytic activation of factor X and increases its activity many thousands of times over.

Factor VIII is synthesized in the liver. Factor VIII is encoded by the F-VIII gene located on the X chromosome. Deficient production or a functional disorder of factor V III C leads to "haemophilia A".
The high-molecular factor VIII forms a complex with the von Willebrand factor, which essentially causes the aggregation of the thrombocytes. It is known as the F-VIII-vWF complex. The synthesis takes place in the endothelium and in the thrombocytes. The molecular weight is over 1 million Dalton.

Subunits of the F-VIII are:

  • VIII C Cofactor of Tenase
  • VIII R:WF von Willebrand factor
  • VIII R:Rco Ristocetin cofactor activity (activity for the ristocetin-induced activity)
  • VIII R:Ag F-VIII-associated antigen I, reacts with antibodies against F-VIII
  • VIII AG I immunologically different from VIII R:Ag
  • VIII C:Ag reacts with homologous antibodies

Literature
This section has been translated automatically.

  1. HA Neumann (2014) The coagulation system. ABW-Wissenschaftsverlag GmbH Berlin S. 59f.

Outgoing links (1)

Von willebrand factor;

Authors

Last updated on: 29.10.2020