Simulation of platelet adhesion and aggregation regulated by fibrinogen and von Willebrand factor

被引:33
作者
Mori, Daisuke [1 ]
Yano, Koichiro [2 ]
Tsubota, Ken-ichi [3 ]
Ishikawa, Takuji [1 ]
Wada, Shigeo [4 ]
Yamaguchi, Takami [1 ]
机构
[1] Tohoku Univ, Dept Bioengn & Robot, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Toyota Motor Co Ltd, Toyota, Japan
[3] Chiba Univ, Dept Elect & Mech Engn, Chiba, Japan
[4] Osaka Univ, Dept Mech Sci & Bioengn, Suita, Osaka 565, Japan
关键词
computational simulation; glycoprotein receptors; thrombus; shear flow;
D O I
10.1160/TH07-08-0490
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We propose a method to analyze platelet adhesion and aggregation computationally, taking into account the distinct properties of two plasma proteins, von Willebrand factor (vWF) and fibrinogen (Fbg). In this method, the hydrodynamic interactions between platelet particles under simple shear flow were simulated using Stokesian dynamics based on the additivity of velocities. The binding force between particles mediated by vWF and Fbg was modeled using the Voigt model. Two Voigt models with different properties were introduced to consider the distinct behaviors of vWF and Fbg. Our results qualitatively agreed with the general observation of a previous in-vitro experiment, thus demonstrating that the significant development of thrombus formation in height requires not only vWF, but also Fbg. This agreement of simulation and experimental results qualitatively validates our model and suggests that consideration of the distinct roles of vWF and Fbg is essential to investigate the physiological and pathophysiological mechanisms of thrombus formation using a computational approach.
引用
收藏
页码:108 / 115
页数:8
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