Tissue factor on the loose

Citation
Pla. Giesen et V. Nemerson, Tissue factor on the loose, SEM THROMB, 26(4), 2000, pp. 379-384
Citations number
51
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
SEMINARS IN THROMBOSIS AND HEMOSTASIS
ISSN journal
00946176 → ACNP
Volume
26
Issue
4
Year of publication
2000
Pages
379 - 384
Database
ISI
SICI code
0094-6176(2000)26:4<379:TFOTL>2.0.ZU;2-J
Abstract
The enzymatic complex of tissue factor (TF) and the blood coagulation facto r VIIa is generally considered to be the initiator of coagulation. Coagulat ion that occurs at the site of luminal injury to an artery is, along with p latelet deposition, the cause of arterial thrombosis, which is the leading cause of death in Western society. Under pathological conditions the intima , the neointima and the atherosclerotic plaque contain active TF. Therefore the initiation of thrombosis is believed to be due to TF present in the wa ll of the pathologically changed artery. This classical view of thrombosis has been challenged. In this article we review the evidence for the presenc e of TF activity in various tissues outside the vessel wall, in extracellul ar form, in encrypted form, and even in plasma. We found TF expression in a variety of cells in culture after growth factor or cytokine stimulation. T his TF was often also present in the extracellular matrix, and in addition we found latent TF on the outside of unbroken smooth muscle cells. Freeze-t hawing the cells or detergentlysis could activate this TF. We also found TF activity in native whole blood and in plasma. Inhibition of this circulati ng TF prevented formation of thrombi on collagen-coated glass slides in an ex vivo perfusion system. Furthermore, in a thrombosis model in which rat a orta was injured, TF was found on the intimal surface of the injured aorta. TF activity was measured in a flow chamber, and it was shown that all meas urable activity was extracellular. We conclude that blood-borne TF plays a major role in thrombosis. Encryption of TF present in circulation could be a mechanism that prevents thrombosis. Alternatively, circulating TF may be active but below the threshold required for the initiation of blood coagula tion.