Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX.
Center for Translational Research on Inflammatory Diseases, Michael E. DeBakey Veterans Affairs Medical Center, Houston, TX.
Blood Adv. 2020 Apr 14;4(7):1340-1349. doi: 10.1182/bloodadvances.2020001500.
Systemic inflammation can lead to coagulopathy and disseminated intravascular coagulation (DIC). In prior studies, the recombinant A2 domain of human von Willebrand factor (VWF; A2 protein) attenuated DIC and decreased mortality in lipopolysaccharide (LPS)-treated mice. Here, we performed studies to dissect the mechanism by which the A2 protein moderates DIC. We used confocal microscopy to analyze the fibrin clot structure in plasma from healthy humans and endotoxemic mice, turbidity assays to examine fibrin polymerization, and a murine model for LPS-induced DIC and introduced a loss-of-function mutation into the A2 protein for fibrin. The mutation of the residue E1567 located in the α2 helix of the folded A2 domain of VWF inhibited binding activity for fibrin, possibly mapping a novel region containing a putative binding site for fibrin. The A2 protein increased the initial rate of change of fibrin polymerization, intercalated into the fibrin network, and modified the resultant clot structure in vitro. Furthermore, ex vivo experiments using plasma from mice with endotoxemia treated with the A2 protein revealed an increased rate of fibrin formation and an altered clot structure as compared with plasma from nontreated sick animals. Moreover, and in contrast to the A2 mutant, the A2 protein improved survival and reduced fibrin deposition and microvascular thrombosis in mice with endotoxemia-induced DIC. Importantly, in vivo and in vitro studies indicated that the A2 protein did not affect experimental thrombosis. Thus, we provide evidence for a novel treatment to attenuate systemic inflammation-induced coagulopathy/DIC via targeting fibrin formation, without an increased risk for bleeding.
全身性炎症可导致凝血功能障碍和弥散性血管内凝血(DIC)。在先前的研究中,人血管性血友病因子(VWF)的重组 A2 结构域(A2 蛋白)减轻了脂多糖(LPS)处理的小鼠的 DIC 并降低了死亡率。在这里,我们进行了研究以剖析 A2 蛋白调节 DIC 的机制。我们使用共焦显微镜分析了来自健康人类和内毒素血症小鼠的血浆中的纤维蛋白凝块结构,使用浊度测定法检查纤维蛋白聚合,并用 LPS 诱导的 DIC 小鼠模型引入了 A2 蛋白的功能丧失突变。位于 VWF 折叠 A2 结构域的α2 螺旋中的残基 E1567 的突变抑制了纤维蛋白的结合活性,可能映射出一个包含纤维蛋白的新结合位点的新区域。A2 蛋白增加了纤维蛋白聚合的初始变化率,插入纤维蛋白网络,并在体外改变了所得凝块结构。此外,用内毒素血症小鼠的血浆进行的离体实验表明,与未经治疗的患病动物的血浆相比,A2 蛋白增加了纤维蛋白的形成速度并改变了凝块结构。此外,与 A2 突变体相反,A2 蛋白改善了内毒素血症诱导的 DIC 小鼠的存活率,并减少了纤维蛋白沉积和微血管血栓形成。重要的是,体内和体外研究表明 A2 蛋白不会影响实验性血栓形成。因此,我们提供了通过靶向纤维蛋白形成来减轻全身性炎症引起的凝血功能障碍/DIC 的新治疗方法的证据,而不会增加出血的风险。