Supercomputer simulations of platelet activation in blood plasma at multiple scales

Seetha Pothapragada
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引用次数: 2

Abstract

Thrombogenicity in cardiovascular devices and pathologies is associated with flow-induced shear stress activation of platelets resulting from pathological flow patterns. This platelet activation process poses a major modeling challenge as it covers disparate spatiotemporal scales, from flow down to cellular, to subcellular, and to molecular scales. This challenge can be resolved by implementing multiscale simulations feasible only on supercomputers. The simulation must couple the macroscopic effects of blood plasma flow and stresses to a microscopic platelet dynamics. In an attempt to model this complex and multiscale behavior we have first developed a phenomenological three-dimensional coarse-grained molecular dynamics (CGMD) particle-based model. This model depicts resting platelets and simulates their characteristic filopodia formation observed during activation. Simulations results are compared with in vitro measurements of activated platelet morphological changes, such as the core axes and filopodia thicknesses and lengths, after exposure to the prescribed flow-induced shear stresses. More recently, we extended this model by incorporating the platelet in Dissipative Particle Dynamics (DPD) blood plasma flow and developed a dynamic coupling scheme that allows the simulation of flow-induced shear stress platelet activation. This portion of research is in progress.
多尺度血浆中血小板活化的超级计算机模拟
心血管装置和病理中的血栓形成性与病理性血流模式引起的血流诱导的血小板剪切应力激活有关。这个血小板激活过程提出了一个主要的建模挑战,因为它涵盖了不同的时空尺度,从流动到细胞,到亚细胞,再到分子尺度。这一挑战可以通过在超级计算机上实现多尺度模拟来解决。模拟必须将血浆流动和应力的宏观影响与微观血小板动力学相结合。为了模拟这种复杂的多尺度行为,我们首先建立了一个基于粒子的现象学三维粗粒度分子动力学(CGMD)模型。该模型描述了静止血小板,并模拟了活化过程中观察到的丝状足形成的特征。模拟结果与体外活化血小板形态变化的测量结果进行了比较,如核心轴和丝状伪足的厚度和长度,暴露于规定的流动诱导剪切应力后。最近,我们通过将血小板纳入耗散粒子动力学(DPD)血浆流动扩展了该模型,并开发了一种动态耦合方案,可以模拟血流诱导的剪切应力血小板激活。这部分研究正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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