Shibeko Alexey M, Lobanova Ekaterina S, Panteleev Mikhail A, Ataullakhanov Fazoil I
National Research Center for Hematology, 4a Novyi Zykovskii pr, Moscow 125167, Russia.
BMC Syst Biol. 2010 Jan 26;4:5. doi: 10.1186/1752-0509-4-5.
Blood coagulation is a complex network of biochemical reactions, which is peculiar in that it is time- and space-dependent, and has to function in the presence of rapid flow. Recent experimental reports suggest that flow plays a significant role in its regulation. The objective of this study was to use systems biology techniques to investigate this regulation and to identify mechanisms creating a flow-dependent switch in the coagulation onset.
Using a detailed mechanism-driven model of tissue factor (TF)-initiated thrombus formation in a two-dimensional channel we demonstrate that blood flow can regulate clotting onset in the model in a threshold-like manner, in agreement with existing experimental evidence. Sensitivity analysis reveals that this is achieved due to a combination of the positive feedback of TF-bound factor VII activation by activated factor X (Xa) and effective removal of factor Xa by flow from the activating patch depriving the feedback of "ignition". The level of this trigger (i.e. coagulation sensitivity to flow) is controlled by the activity of tissue factor pathway inhibitor.
This mechanism explains the difference between red and white thrombi observed in vivo at different shear rates. It can be speculated that this is a special switch protecting vascular system from uncontrolled formation and spreading of active coagulation factors in vessels with rapidly flowing blood.
血液凝固是一个复杂的生化反应网络,其独特之处在于它具有时间和空间依赖性,并且必须在快速流动的情况下发挥作用。最近的实验报告表明,流动在其调节中起着重要作用。本研究的目的是使用系统生物学技术来研究这种调节,并确定在凝血起始过程中产生流动依赖性开关的机制。
使用二维通道中组织因子(TF)引发血栓形成的详细机制驱动模型,我们证明血流可以以阈值样方式调节模型中的凝血起始,这与现有实验证据一致。敏感性分析表明,这是由于活化因子X(Xa)对TF结合的因子VII激活的正反馈与血流从激活斑块有效去除Xa从而剥夺反馈“点火”的组合实现的。这种触发的水平(即凝血对流动的敏感性)由组织因子途径抑制剂的活性控制。
该机制解释了在体内不同剪切速率下观察到的红色和白色血栓之间的差异。可以推测,这是一种特殊的开关,可保护血管系统免受快速流动血液的血管中活性凝血因子不受控制的形成和扩散。