4.6 Article

Extracellular vesicles from amniotic fluid, milk, saliva, and urine expose complexes of tissue factor and activated factor VII

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 20, 期 10, 页码 2306-2312

出版社

WILEY
DOI: 10.1111/jth.15801

关键词

body fluids; coagulation factor VII; extracellular vesicles; extrinsic tenase complexes; tissue factor

资金

  1. China Scholarship Council [201708320341]
  2. International Society on Thrombosis and Haemostasis

向作者/读者索取更多资源

This study found that extracellular vesicles (EVs) in amniotic fluid, milk, saliva, and urine expose functional extrinsic tenase complexes that can trigger blood clotting. These EVs promote clotting in both normal plasma and FVII-deficient plasma, and their activity is inhibited by antibodies.
Background Tissue factor (TF) is expressed in the adventitia of the vessel wall and on extracellular vesicles (EVs) in body fluids. TF and activated coagulation factor (F) VII(a) together form the so-called extrinsic tenase complex, which initiates coagulation. Aim We investigated whether EVs in amniotic fluid, milk, saliva, and urine expose functional extrinsic tenase complexes that can trigger coagulation. Methods Milk, saliva, and urine were collected from healthy breastfeeding women (n = 6), and amniotic fluid was collected from healthy women undergoing routine amniocentesis (n = 7). EVs were isolated from body fluids by size exclusion chromatography (SEC) and clotting experiments were performed in the presence and absence of antibodies against TF and FVIIa in normal plasma and in FVII-deficient plasma. The ability of body fluids to generate FXa also was determined. Results Amniotic fluid, milk, saliva, and urine triggered clotting of normal plasma and of FVII-deficient plasma, which was almost completely inhibited by an anti-FVII antibody and to a lesser extent by an anti-TF antibody. Fractionation of body fluids by SEC showed that only the fractions containing EVs triggered clotting in normal plasma and FVII-deficient plasma and generated FXa, which again was almost completely inhibited by an anti-FVII antibody and partially by an anti-TF antibody. Conclusion Here we show that EVs from amniotic fluid, milk, saliva, and urine expose complexes of TF and FVIIa (i.e., extrinsic tenase complexes) that directly activate FX. Based on our present findings we propose that these EVs from normal body fluids provide hemostatic protection.

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