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切变率梯度促进弱黏附蛋白(如纤维蛋白原)形成双相血栓,这种作用依赖于 vWF。

Shear rate gradients promote a bi-phasic thrombus formation on weak adhesive proteins, such as fibrinogen in a VWF-dependent manner.

机构信息

Université de Strasbourg, INSERM, EFS Grand-Est, BPPS UMR-S1255, FMTS, Strasbourg, France.

Faculty of Physics, Moscow State University, Moscow, Russia.

出版信息

Haematologica. 2020 Oct 1;105(10):2471-2483. doi: 10.3324/haematol.2019.235754.

Abstract

Blood flow profoundly varies throughout the vascular tree due to its pulsatile nature and to the complex vessel geometry. While thrombus formation has been extensively studied in vitro under steady flow, and in vivo under normal blood flow conditions, the impact of complex hemodynamics such as flow acceleration found in stenosed arteries has gained increased appreciation. We investigated the effect of flow acceleration, characterized by shear rate gradients, on the function of platelets adhering to fibrinogen, a plasma protein which plays a key role in hemostais and thrombosis. While we confirmed that under steady flow, fibrinogen only supports single platelet adhesion, we observed that under shear rate gradients, this surface becomes highly thrombogenic, supporting efficient platelet aggregation leading to occlusive thrombus formation. This shear rate gradient-driven thrombosis is biphasic with an initial step of slow platelet recruitment supported by direct plasma VWF adsorption to immobilized fibrinogen and followed by a second phase of explosive thrombosis initiated by VWF fiber formation on platelet monolayers. In vivo experiments confirmed that shear rate gradients accelerate thrombosis in a VWF-dependent manner. Together, this study characterizes a process of plasma VWF-dependent accelerated thrombosis on immobilized fibrinogen in the presence of shear rate gradients.

摘要

由于血流的脉动特性和复杂的血管几何形状,血流在整个脉管系统中变化很大。虽然血栓形成已经在体外的稳定流动和体内的正常血流条件下得到了广泛研究,但对狭窄动脉中发现的复杂血流动力学(如流速加速)的影响的认识也在不断增加。我们研究了流速加速(表现为剪切率梯度)对黏附于纤维蛋白原的血小板功能的影响,纤维蛋白原是一种在止血和血栓形成中起关键作用的血浆蛋白。虽然我们证实,在稳定的血流下,纤维蛋白原仅支持单个血小板黏附,但我们发现,在剪切率梯度下,这个表面会变得高度血栓形成,支持有效的血小板聚集,导致闭塞性血栓形成。这种剪切率梯度驱动的血栓形成是双相的,最初的缓慢血小板募集阶段是由直接的血浆 VWF 吸附到固定的纤维蛋白原上支持的,随后是由 VWF 纤维在血小板单层上形成引发的爆炸性血栓形成的第二阶段。体内实验证实,剪切率梯度以 VWF 依赖性的方式加速血栓形成。总之,这项研究描述了在存在剪切率梯度的情况下,血浆 VWF 依赖性加速血栓形成在固定纤维蛋白原上的过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f3a/7556676/0f760d215614/1052471.fig1.jpg

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