Skip to content
2000
Volume 4, Issue 2
  • ISSN: 1871-5257
  • E-ISSN: 1875-6182

Abstract

Atherosclerosis remains a leading cause of morbidity and mortality worldwide. In addition to the deposition of cholesterol in the arterial wall, inflammation, cell proliferation and migration play important roles in the pathogenesis of atherosclerosis. Thrombomodulin (TM) is a cell surface-expressed glycoprotein which is predominantly synthesized by vascular endothelial cells and a critical cofactor for thrombin-mediated activation of protein C. Activated protein C is best known for its natural anticoagulant and anti-inflammatory properties. Recent evidence has revealed that TM also has protein C- and thrombin-independent physiological function. This review summarizes recent investigations of TM, giving an overview on the TM unique effects on cellular proliferation, adhesion and inflammation, all of which are important steps in atherosclerosis. The current evidence of TM in the pathogenesis of atherosclerosis will be reviewed, and the associations of TM gene polymorphisms with atherosclerosis are presented. Newly emerging data of the TM in mouse atherosclerosis model demonstrates that TM potentially may have therapeutic role in atherosclerosis.

Loading

Article metrics loading...

/content/journals/chamc/10.2174/187152506776369953
2006-04-01
2025-09-27
Loading full text...

Full text loading...

/content/journals/chamc/10.2174/187152506776369953
Loading

  • Article Type:
    Research Article
Keyword(s): adhesion; atherosclerosis; inflammation; polymorphism; proliferation; Thrombomodulin
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test