Thrombin Flux and Wall Shear Rate Regulate Fibrin Fiber Deposition State during Polymerization under Flow

被引:105
作者
Neeves, K. B. [1 ]
Illing, D. A. R. [1 ]
Diamond, S. L. [2 ]
机构
[1] Colorado Sch Mines, Dept Chem Engn, Golden, CO 80401 USA
[2] Univ Penn, Dept Chem & Biomol Engn, Inst Med & Engn, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
CIRCULATING TISSUE FACTOR; BLOOD-COAGULATION; PLATELETS; VIVO; THROMBOGENESIS; PROFILES; DEVICE;
D O I
10.1016/j.bpj.2009.12.4275
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Thrombin is released as a soluble enzyme from the surface of platelets and tissue-factor-bearing cells to trigger fibrin polymerization during thrombosis under flow conditions. Although isotropic fibrin polymerization under static conditions involves protofibril extension and lateral aggregation leading to a gel, factors regulating fiber growth are poorly quantified under hemodynamic flow due to the difficulty of setting thrombin fluxes. A membrane microfluidic device allowed combined control of both thrombin wall flux (10(-13) to 10(-11) nmol/mu m(2) s) and the wall shear rate (10-100 s(-1)) of a flowing fibrinogen solution. At a thrombin flux of 10(-12) nmol/mu m(2) s, both fibrin deposition and fiber thickness decreased as the wall shear rate increased from 10 to 100 s(-1). Direct measurement and transport-reaction simulations at 12 different thrombin flux-wall shear rate conditions demonstrated that two dimensionless numbers, the Peclet number (Pe) and the Damkohler number (Da), defined a state diagram to predict fibrin morphology. For Da < 10, we only observed thin films at all Pe. For 10 < Da < 900, we observed either mat fibers or gels, depending on the Pe. For Da > 900 and Pe < 100, we observed three-dimensional gels. These results indicate that increases in wall shear rate quench first lateral aggregation and then protofibril extension.
引用
收藏
页码:1344 / 1352
页数:9
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