纤维蛋白网络固有张力的生物力学起源。

Russell Spiewak, A. Gosselin, Danil Merinov, R. Litvinov, J. Weisel, Valerie Tutwiler, P. Purohit
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引用次数: 5

摘要

血管损伤部位会形成血块,以密封伤口并防止出血。凝块在发挥其生物功能并承受血液流动、血管壁波动、血管外肌肉收缩和其他力的流体动力时处于紧张状态。有几种机制会在血栓中产生张力,其中最著名的是活化血小板引起的收缩/回缩。在这里,我们通过实验和建模表明,血栓张力是由纤维蛋白的聚合产生的。我们的数学模型建立在这样一个假设之上,即具有双重对称性和离轴结合位点的纤维蛋白单体的形状最终是单个纤维和凝块中固有张力的来源。随着纤维直径在聚合过程中的增长,纤维蛋白单体必须经历轴向扭曲变形,以便它们保持对齐,以形成纤维蛋白原纤维的半交错排列特征。这种变形导致预应变,从而导致纤维和网络张力。我们对单个纤维蛋白纤维预应变的结果与通过切割纤维和测量其松弛长度来测量预应变的实验一致。我们使用聚合物弹性的8链模型将纤维的力学与网络的力学联系起来。通过将其与可膨胀弹性体的连续体模型相结合,我们可以计算受约束纤维蛋白凝胶中张力的演变。该模型预测的时间演变和拉伸应力与两个固定流变仪板之间聚合的纤维蛋白凝块固有张力的实验测量结果在质量上一致。这些实验还表明,增加凝血酶浓度会导致纤维蛋白网络中的内部张力增加。我们的模型可以扩展到解释在单个纤维中产生预应变并在三维蛋白质聚合物网络中引起张力的其他机制。
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Biomechanical origins of inherent tension in fibrin networks.
Blood clots form at the site of vascular injury to seal the wound and prevent bleeding. Clots are in tension as they perform their biological functions and withstand hydrodynamic forces of blood flow, vessel wall fluctuations, extravascular muscle contraction and other forces. There are several mechanisms that generate tension in a blood clot, of which the most well-known is the contraction/retraction caused by activated platelets. Here we show through experiments and modeling that clot tension is generated by the polymerization of fibrin. Our mathematical model is built on the hypothesis that the shape of fibrin monomers having two-fold symmetry and off-axis binding sites is ultimately the source of inherent tension in individual fibers and the clot. As the diameter of a fiber grows during polymerization the fibrin monomers must suffer axial twisting deformation so that they remain in register to form the half-staggered arrangement characteristic of fibrin protofibrils. This deformation results in a pre-strain that causes fiber and network tension. Our results for the pre-strain in single fibrin fibers is in agreement with experiments that measured it by cutting fibers and measuring their relaxed length. We connect the mechanics of a fiber to that of the network using the 8-chain model of polymer elasticity. By combining this with a continuum model of swellable elastomers we can compute the evolution of tension in a constrained fibrin gel. The temporal evolution and tensile stresses predicted by this model are in qualitative agreement with experimental measurements of the inherent tension of fibrin clots polymerized between two fixed rheometer plates. These experiments also revealed that increasing thrombin concentration leads to increasing internal tension in the fibrin network. Our model may be extended to account for other mechanisms that generate pre-strains in individual fibers and cause tension in three-dimensional proteinaceous polymeric networks.
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