DefinitionThis section has been translated automatically.
Thrombomodulin is a protein that functions as a transmembrane receptor for thrombin in the endothelial cell. Thombomodulin regulates coagulation within the uninjured vessel.
Thrombomodulin plays a key role in inhibiting blood clotting (anticoagulation). It binds in activated form to its ligand thrombin formed during the clotting process. The trombomodulin-thrombin complex activates the protease protein C. In excess, the activated protein C forms a complex with protein S that deactivates the clotting factors factor V and factor VIII.
Note(s)This section has been translated automatically.
The role of thrombomodulin in thrombosis is controversial. Although there are several reports of THBD mutations in patients with venous thrombosis, clear functional evidence for the pathogenicity of these mutations is lacking.
In a review, Anastasiou et al (2012) noted that thrombomodulin plays an important role in capillary beds and that THBD variations may not be associated with thrombosis in large vessels. It is likely that genetic or environmental risk factors, in addition to the THBD mutant, are involved in the pathogenesis of venous thrombosis. However, a variation in the THBD gene may be associated with an increased risk of arterial thrombosis and myocardial infarction. This association may be due to the fact that thrombomodulin can modulate inflammatory processes, complement activity, and fibrinolysis.
LiteratureThis section has been translated automatically.
- Anastasiou G et al. (2012) Thrombomodulin as a regulator of the anticoagulant pathway: implication in the development of thrombosis. Blood Coagul Fibrinolysis 23: 1-10.
- Great Dane CJM et al (1998) A mutation in the thrombomodulin gene, 127G to A coding for ala25-to-thr, and the risk of myocardial infarction in men. Thromb Haemost 80: 743-748.
- Faioni EM et al (2002) Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia. Brit J Haemat 118: 595-599.
- Franchi F et al (2001) Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss. Brit J Haemat 114: 641-646.
- Kunz G et al (2000) Identification and characterization of a thrombomodulin gene mutation coding for an elongated protein with reduced expression in a kindred with myocardial infarction. Blood 95: 569-576.