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Transport physics and biorheology in the setting of hemostasis and thrombosis.
- Source :
-
Journal of thrombosis and haemostasis : JTH [J Thromb Haemost] 2016 May; Vol. 14 (5), pp. 906-17. Date of Electronic Publication: 2016 Mar 30. - Publication Year :
- 2016
-
Abstract
- The biophysics of blood flow can dictate the function of molecules and cells in the vasculature with consequent effects on hemostasis, thrombosis, embolism, and fibrinolysis. Flow and transport dynamics are distinct for (i) hemostasis vs. thrombosis and (ii) venous vs. arterial episodes. Intraclot transport changes dramatically the moment hemostasis is achieved or the moment a thrombus becomes fully occlusive. With platelet concentrations that are 50- to 200-fold greater than platelet-rich plasma, clots formed under flow have a different composition and structure compared with blood clotted statically in a tube. The platelet-rich, core/shell architecture is a prominent feature of self-limiting hemostatic clots formed under flow. Importantly, a critical threshold concentration of surface tissue factor is required for fibrin generation under flow. Once initiated by wall-derived tissue factor, thrombin generation and its spatial propagation within a clot can be modulated by γ'-fibrinogen incorporated into fibrin, engageability of activated factor (FIXa)/activated FVIIIa tenase within the clot, platelet-derived polyphosphate, transclot permeation, and reduction of porosity via platelet retraction. Fibrin imparts tremendous strength to a thrombus to resist embolism up to wall shear stresses of 2400 dyne cm(-2) . Extreme flows, as found in severe vessel stenosis or in mechanical assist devices, can cause von Willebrand factor self-association into massive fibers along with shear-induced platelet activation. Pathological von Willebrand factor fibers are A Disintegrin And Metalloprotease with ThromboSpondin-1 domain 13 resistant but are a substrate for fibrin generation due to FXIIa capture. Recently, microfluidic technologies have enhanced the ability to interrogate blood in the context of stenotic flows, acquired von Willebrand disease, hemophilia, traumatic bleeding, and drug action.<br /> (© 2016 International Society on Thrombosis and Haemostasis.)
- Subjects :
- Animals
Blood Coagulation drug effects
Blood Flow Velocity
Blood Platelets drug effects
Constriction, Pathologic
Diffusion
Factor IXa chemistry
Factor VIIIa chemistry
Fibrin chemistry
Fibrinolysis
Humans
Mice
Platelet Activation drug effects
Platelet Adhesiveness drug effects
Platelet-Rich Plasma metabolism
Polyphosphates chemistry
Porosity
Stress, Mechanical
Thrombin pharmacology
Thromboplastin pharmacology
von Willebrand Factor chemistry
Hemostasis
Rheology
Thrombosis physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1538-7836
- Volume :
- 14
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal of thrombosis and haemostasis : JTH
- Publication Type :
- Academic Journal
- Accession number :
- 26848552
- Full Text :
- https://doi.org/10.1111/jth.13280