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首页> 外文期刊>Cellular and Molecular Bioengineering >A Multiscale Model for Recruitment Aggregation of Platelets by Correlating with In Vitro Results
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A Multiscale Model for Recruitment Aggregation of Platelets by Correlating with In Vitro Results

机译:通过与体外结果相关性的血小板植入聚集的多尺度模型

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IntroductionWe developed a multiscale model to simulate the dynamics of platelet aggregation by recruitment of unactivated platelets flowing in viscous shear flows by an activated platelet deposited onto a blood vessel wall. This model uses coarse grained molecular dynamics for platelets at the microscale and dissipative particle dynamics for the shear flow at the macroscale. Under conditions of relatively low shear, aggregation is mediated by fibrinogen via alpha IIb beta 3 receptors.MethodsThe binding of alpha IIb beta 3 and fibrinogen is modeled by a molecular-level hybrid force field consisting of Morse potential and Hooke law for the nonbonded and bonded interactions, respectively. The force field, parametrized in two different interaction scales, is calculated by correlating with the platelet contact area measured in vitro and the detaching force between alpha IIb beta 3 and fibrinogen.ResultsUsing our model, we derived, the relationship between recruitment force and distance between the centers of mass of two platelets, by integrating the molecular-scale inter-platelet interactions during recruitment aggregation in shear flows. Our model indicates that assuming a rigid-platelet model, underestimates the contact area by 89% and the detaching force by 93% as compared to a model that takes into account the platelet deformability leading to a prediction of a significantly lower attachment during recruitment.ConclusionsThe molecular-level predictive capability of our model sheds a light on differences observed between transient and permanent platelet aggregation patterns. The model and simulation framework can be further adapted to simulate initial thrombus formation involving multiple flowing platelets as well as deposition and adhesion onto blood vessels.
机译:简介我们开发了一种多尺度模型来模拟血小板聚集的动态,通过募集在粘性剪切流动流动的未活化的血小板通过沉积在血管壁上的粘性剪切流动。该模型使用在Microscale和耗散粒子动力学的血小板的粗粒分子动力学,用于宏观上的剪切流。在相对低剪切的条件下,聚集通过αIIBβ3受体由纤维蛋白原介导。αIIBβ3和纤维蛋白原的方法由分子水平混合动力场建模,包括莫尔斯潜力和非粘结法的胡克法律。相互作用。通过与在体外测量的血小板接触面积和αIIBβ3和纤维蛋白原之间的分离力相关的血小板接触面积来计算力场。提供我们的模型,我们得出,招聘力与距离之间的关系通过将分子级间血小板相互作用整合在剪切流动期间的分子级间血小板相互作用。我们的模型表明,假设刚性血小板模型,与考虑到血小板可变形性的模型相比,在引起血小板可变形性的模型相比,将接触面积和分离力低于93%,导致招聘期间的附件显着降低的安装.C​​onclusionsthe我们模型的分子水平预测能力揭示了瞬态和永久性血小板聚集模式之间观察到的差异。该模型和仿真框架可以进一步适于模拟涉及多个流动血小板的初始血栓形成以及在血管上沉积和粘附。

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