A recombinant murine meizothrombin precursor, prothrombin R157A/R268A, inhibits thrombosis in a model of acute carotid artery injury
| Autor: | Lisa A. Westfield, Kyuhwan Shim, J. Evan Sadler, Hongfa Zhu |
|---|---|
| Rok vydání: | 2004 |
| Předmět: |
Thrombomodulin
Immunology Kidney Fibrinogen Biochemistry Mice Thrombin Cricetinae medicine Animals Platelet Artery occlusion Platelet activation Cells Cultured Enzyme Precursors business.industry Thrombosis Biological activity Cell Biology Hematology Platelet Activation Molecular biology Mice Mutant Strains Recombinant Proteins Disease Models Animal Mutagenesis Acute Disease Prothrombin Carotid Artery Injuries business Protein C circulatory and respiratory physiology medicine.drug |
| Zdroj: | Blood. 104:415-419 |
| ISSN: | 1528-0020 0006-4971 |
| DOI: | 10.1182/blood-2004-02-0478 |
| Popis: | Mutations in human prothrombin that generate a stable form of meizothrombin or meizothrombin(desF1) cause dysprothrombinemia in both the homozygous and heterozygous state, suggesting that meizothrombin has dominant anticoagulant effects in vivo. The enzymatic characterization of recombinant mouse meizothrombin, meizothrombin(desF1), and thrombin indicates that all 3 enzymes have similar activity toward the chromogenic substrate S-2238, that meizothrombin and meizothrombin(desF1) have less than 10% of the fibrinogen-clotting activity of thrombin, and that meizothrombin is more active than thrombin or meizothrombin(desF1) for thrombomodulin-dependent protein C activation. Thus, activated mouse prothrombin R157A/R268A is similar to human meizothrombin in activity toward S-2238, fibrinogen, and protein C. The time to occlusion after FeCl3-induced carotid artery injury was delayed (11.8 ± 3.6 minutes, n = 5) in Cf2+/- mice infused with prothrombin R157A/R268A compared with control mice infused with wild-type prothrombin (5.3 ± 1.5 minutes, n = 3; P = .006). In this model, prothrombin R157A/R268A has anticoagulant activity that reflects its decreased fibrinogen-clotting activity and preserved protein C-activating activity and is consistent with dominant inhibition of fibrinogen clotting. (Blood. 2004;104:415-419) |
| Databáze: | OpenAIRE |
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