Center for Theoretical Problems of Physicochemical Pharmacology, Moscow State University, Moscow, Russia.
Biophys J. 2011 Oct 19;101(8):1816-24. doi: 10.1016/j.bpj.2011.08.034.
Blood coagulation is triggered not only by surface tissue factor (TF) density but also by surface TF distribution. We investigated recognition of surface TF distribution patterns during blood coagulation and identified the underlying molecular mechanisms. For these investigations, we employed 1), an in vitro reaction-diffusion experimental model of coagulation; and 2), numerical simulations using a mathematical model of coagulation in a three-dimensional space. When TF was uniformly immobilized over the activating surface, the clotting initiation time in normal plasma increased from 4 min to >120 min, with a decrease in TF density from 100 to 0.7 pmol/m(2). In contrast, surface-immobilized fibroblasts initiated clotting within 3-7 min, independently of fibroblast quantity and despite a change in average surface TF density from 0.5 to 130 pmol/m(2). Experiments using factor V-, VII-, and VIII-deficient plasma and computer simulations demonstrated that different responses to these two TF distributions are caused by two positive feedback loops in the blood coagulation network: activation of the TF-VII complex by factor Xa, and activation of factor V by thrombin. This finding suggests a new role for these reactions: to supply sensitivity to local TF density during blood coagulation.
血液凝固不仅由表面组织因子 (TF) 密度触发,还由表面 TF 分布触发。我们研究了血液凝固过程中对表面 TF 分布模式的识别,并确定了潜在的分子机制。为此,我们采用了 1) 体外凝血反应-扩散实验模型;和 2) 使用三维空间凝血数学模型进行数值模拟。当 TF 在激活表面上均匀固定时,正常血浆中的凝血起始时间从 4 分钟延长至>120 分钟,而 TF 密度从 100 降低至 0.7 pmol/m(2)。相比之下,表面固定的成纤维细胞在 3-7 分钟内引发凝血,这与成纤维细胞数量无关,尽管平均表面 TF 密度从 0.5 增加至 130 pmol/m(2)。使用因子 V、VII 和 VIII 缺乏的血浆进行实验和计算机模拟表明,这两种 TF 分布的不同反应是由血液凝固网络中的两个正反馈环引起的:Xa 因子激活 TF-VII 复合物,以及凝血酶激活因子 V。这一发现提示了这些反应的新作用:在血液凝固过程中提供对局部 TF 密度的敏感性。