Department of Physics, East Carolina University; 1000 E 5(th) St, Greenville, NC 27858, United States.
Medical Physics Graduate Program, Duke University; DUMC 2729, 2424 Erwin Rd Suite 101, Durham, NC 27705, USA.
Acta Biomater. 2020 Apr 15;107:164-177. doi: 10.1016/j.actbio.2020.02.025. Epub 2020 Feb 25.
Proper wound healing necessitates both coagulation (the formation of a blood clot) and fibrinolysis (the dissolution of a blood clot). A thrombus resistant to clot dissolution can obstruct blood flow, leading to vascular pathologies. This study seeks to understand the mechanisms by which individual fibrin fibers, the main structural component of blood clots, are cleared from a local volume during fibrinolysis. We observed 2-D fibrin networks during lysis by plasmin, recording the clearance of each individual fiber. We found that, in addition to transverse cleavage of fibers, there were multiple other pathways by which clot dissolution occurred, including fiber bundling, buckling, and collapsing. These processes are all influenced by the concentration of plasmin utilized in lysis. The network fiber density influenced the kinetics and distribution of these pathways. Individual cleavage events often resulted in large morphological changes in network structure, suggesting that the inherent tension in fibers played a role in fiber clearance. Using images before and after a cleavage event to measure fiber lengths, we estimated that fibers are strained ~23% beyond their equilibrium length during polymerization. To understand the role of fiber tension in fibrinolysis we modeled network clearance under differing amounts of fiber polymerized strain (prestrain). The comparison of experimental and model data indicated that fibrin tension enables 35% more network clearance due to network rearrangements after individual cleavage events than would occur if fibers polymerized in a non-tensed state. Our results highlight many characteristics and mechanisms of fibrin breakdown, which have implications on future fibrin studies, our understanding of the fibrinolytic process, and the development of thrombolytic therapies. STATEMENT OF SIGNIFICANCE: Fibrin fibers serve as the main structural element of blood clots. They polymerize under tension and have remarkable extensibility and elasticity. After the cessation of wound healing, fibrin must be cleared from the vasculature by the enzyme plasmin in order to resume normal blood flow: a process called fibrinolysis. In this study we investigate the mechanisms that regulate the clearance of individual fibrin fibers during fibrinolysis. We show that the inherent tension in fibers enhances the action of plasmin because every fiber cleavage event results in a redistribution of the network tension. This network re-equilibration causes fibers to buckle, bundle, and even collapse, leading to a more rapid fiber clearance than plasmin alone could provide.
适当的伤口愈合需要凝血(形成血栓)和纤维蛋白溶解(溶解血栓)。血栓对血栓溶解的抵抗力可能会阻塞血流,导致血管病变。本研究旨在了解单个纤维蛋白纤维(血栓的主要结构成分)在纤维蛋白溶解过程中从局部体积中清除的机制。我们在纤溶酶的作用下观察到 2-D 纤维网络,记录下每条纤维的清除情况。我们发现,除了纤维的横向切割外,还有多种其他途径可以发生血栓溶解,包括纤维束、弯曲和塌陷。这些过程都受到纤溶中使用的纤溶酶浓度的影响。网络纤维密度影响这些途径的动力学和分布。单个切割事件通常会导致网络结构的大形态变化,这表明纤维中的固有张力在纤维清除中起作用。使用切割事件前后的图像测量纤维长度,我们估计纤维在聚合过程中的应变比平衡长度大 23%。为了了解纤维张力在纤维蛋白溶解中的作用,我们在不同的纤维聚合应变(预应变)下对网络清除进行了建模。实验数据与模型数据的比较表明,由于单个切割事件后网络的重新排列,纤维张力使网络的清除率增加了 35%,而如果纤维在无张力状态下聚合,则不会发生这种情况。我们的结果突出了纤维蛋白降解的许多特性和机制,这对未来的纤维蛋白研究、我们对纤维蛋白溶解过程的理解以及溶栓治疗的发展都有影响。意义声明:纤维蛋白纤维是血栓的主要结构元素。它们在张力下聚合,具有显著的伸展性和弹性。在伤口愈合停止后,纤维必须通过酶纤溶酶从血管中清除,以恢复正常的血流:这个过程称为纤维蛋白溶解。在这项研究中,我们研究了调节纤维蛋白溶解过程中单个纤维蛋白纤维清除的机制。我们表明,纤维中的固有张力增强了纤溶酶的作用,因为每个纤维切割事件都会导致网络张力的重新分布。这种网络再平衡导致纤维弯曲、束状甚至塌陷,从而导致纤维清除速度比单独使用纤溶酶更快。