Highly elevated plasma level of von Willebrand factor accelerates the formation of platelet thrombus under high shear stress in plasma with deficient ADAMTS13 activity
| Autor: | Yasuaki Shida, Yoshihiro Fujimura, Hideo Yagi, Naoko Yamaguchi, Kazuo Tubaki, Masanori Matsumoto, Mitsuhiko Sugimoto |
|---|---|
| Rok vydání: | 2017 |
| Předmět: |
Blood Platelets
0301 basic medicine Hemolytic anemia medicine.medical_specialty Thrombotic thrombocytopenic purpura ADAMTS13 Protein Context (language use) Mice 03 medical and health sciences Von Willebrand factor hemic and lymphatic diseases Internal medicine von Willebrand Factor medicine Animals Humans Platelet biology business.industry Antibodies Monoclonal Hematology Microangiopathic hemolytic anemia medicine.disease ADAMTS13 030104 developmental biology Endocrinology Immunology biology.protein Stress Mechanical Fresh frozen plasma business |
| Zdroj: | Thrombosis Research. 159:91-95 |
| ISSN: | 0049-3848 |
| DOI: | 10.1016/j.thromres.2017.10.007 |
| Popis: | Upshaw-Schulman syndrome (USS) is a thrombo-hemorrhagic disease caused by congenital deficiency of ADAMTS13 due to ADAMTS13 gene mutations. USS is characterized by repeated episodes of thrombocytopenia and microangiopathic hemolytic anemia that respond dramatically to infusions of fresh frozen plasma. There are two phenotypic expressions of USS: one is the early-onset type and the other, the late-onset type, is asymptomatic during childhood with the first bout of thrombotic thrombocytopenic purpura (TTP) developing after adolescence or during adulthood. We found that gravida with the latter phenotype developed thrombocytopenia and hemolytic anemia during the second or third trimesters, often followed by thrombotic microangiopathies (TMAs). These phenomena suggest that elevated plasma von Willebrand Factor (VWF) might be crucial because plasma levels of VWF antigen usually increase by 200-500% during this period of gestation. Here, we performed platelet function assays using a mixture of anti-coagulated blood from normal volunteers, human VWF, anti-ADAMTS13 monoclonal antibody A10, and purified plasma-derived ADAMTS13 to investigate the effect of plasma VWF levels on platelet thrombus formation in the context of deficient ADAMTS13. In vitro studies showed that mural thrombus formation and platelet aggregation under high shear stress were markedly augmented by increasing the amounts of exogenously added VWF when ADAMTS13 activity was deficient, as may be the case in the in vivo circulation of gravida with USS. These results suggest that highly elevated plasma VWF might accelerate platelet thrombus formation not only in the circulation but also on the surface of vascular endothelial cells in the setting of ADAMTS13 deficiency in USS. |
| Databáze: | OpenAIRE |
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