Wang Weiwei, Mody Nipa A, King Michael R
Department of Biomedical Engineering, Cornell University, NY 14853, USA.
J Comput Phys. 2013 Jul 1;244:223-235. doi: 10.1016/j.jcp.2012.08.014.
The tethering of platelets on the injured vessel surface mediated by glycoprotein Ibα (GPIbα) - Von Willebrand factor (vWF) bonds, as well as the interaction between flowing platelets and adherent platelets, are two key events that take place immediately following blood vessel injury. This early-stage platelet deposition and accumulation triggers the initiation of hemostasis, a self-defensive mechanism to prevent the body from excessive blood loss. To understand and predict this complex process, one must integrate experimentally determined information on the mechanics and biochemical kinetics of participating receptors over very small time frames (1-1000 µs) and length scales (10-100 nm), to collective phenomena occurring over seconds and tens of microns. In the present study, a unique three dimensional multiscale computational model, platelet adhesive dynamics (PAD), was applied to elucidate the unique physics of (i) a non-spherical, disk-shaped platelet interacting and tethering onto the damaged vessel wall followed by (ii) collisional interactions between a flowing platelet with a downstream adherent platelet. By analyzing numerous simulations under different physiological conditions, we conclude that the platelet's unique spheroid-shape provides heterogeneous, orientation-dependent translocation (rolling) behavior which enhances cell-wall interactions. We also conclude that platelet-platelet near field interactions are critical for cell-cell communication during the initiation of microthrombi. The PAD model described here helps to identify the physical factors that control the initial stages of platelet capture during this process.
由糖蛋白Ibα(GPIbα)-血管性血友病因子(vWF)键介导的血小板在受损血管表面的 tethering,以及流动血小板与黏附血小板之间的相互作用,是血管损伤后立即发生的两个关键事件。这种早期血小板沉积和聚集触发了止血的启动,这是一种防止身体过度失血的自我防御机制。为了理解和预测这个复杂的过程,必须将在非常短的时间框架(1 - 1000微秒)和长度尺度(10 - 100纳米)上关于参与受体的力学和生化动力学的实验确定信息,与在数秒和数十微米上发生的集体现象相结合。在本研究中,应用了一种独特的三维多尺度计算模型——血小板黏附动力学(PAD),以阐明(i)非球形盘状血小板与受损血管壁相互作用并 tethering,随后(ii)流动血小板与下游黏附血小板之间的碰撞相互作用的独特物理过程。通过分析不同生理条件下的大量模拟,我们得出结论,血小板独特的椭球体形状提供了异质的、依赖于取向的易位(滚动)行为,这增强了细胞 - 壁相互作用。我们还得出结论,血小板 - 血小板近场相互作用对于微血栓形成起始过程中的细胞 - 细胞通讯至关重要。这里描述的PAD模型有助于识别在此过程中控制血小板捕获初始阶段的物理因素。