Department of Chemical Engineering, University of Utah, Salt Lake City, UT 84112, USA.
Department of Mathematics, University of Utah, Salt Lake City, UT 84112, USA.
Colloids Surf B Biointerfaces. 2020 Sep;193:111118. doi: 10.1016/j.colsurfb.2020.111118. Epub 2020 May 12.
Transient exposure to elevated shear forces is known to prime platelets for enhanced downstream adhesion, but how far downstream these priming effects persist is not known. In the present study, the platelet capture regions, prepared by immobilizing fibrinogen, collagen, or von Willebrand factor, were placed at three different distances from the upstream stenotic region to vary the elapsed time of circulating platelets downstream. Platelet adhesion increased with the increase of upstream wall shear rates from 1620 s to 11,560 s for all three downstream proteins, but only the adhesion to fibrinogen increased significantly with the distance between the upstream stenotic region and the downstream capture region. In contrast, platelet adhesion to downstream collagen remained essentially independent on the distance and the adhesion to von Willebrand factor marginally increased with the distance after transient platelet exposure to upstream wall shear rates of 2145 s and 11,560 s. The results implied that the activation of fibrinogen receptor GPIIb/IIIa by transient exposure to high upstream wall shear rates progresses in a time-dependent manner during the downstream flow of platelets. The highly elevated upstream wall shear rate of 11,560 s altered the morphology of many platelets adhered to downstream fibrinogen from their native ellipsoidal to spread circular form. The platelet shape analysis showed that longer periods of post-stenotic flow increased the surface coverage fraction of ellipsoidal platelet population and decreased the surface coverage fraction of fully spread platelets on fibrinogen for both transiently elevated upstream wall shear rates.
短暂暴露于升高的剪切力已知可使血小板增强下游的黏附能力,但这些预激活作用能持续多久尚不清楚。在本研究中,将纤维蛋白原、胶原蛋白或血管性血友病因子固定化以制备血小板捕获区,将其放置在上游狭窄区域下游的三个不同距离处,以改变下游循环血小板的滞留时间。血小板黏附随上游壁剪切率从 1620 s 增加到 11560 s 而增加,对于所有三种下游蛋白均如此,但仅纤维蛋白原的黏附随上游狭窄区域和下游捕获区域之间的距离显著增加。相比之下,血小板对下游胶原蛋白的黏附基本不依赖于距离,并且在短暂暴露于上游壁剪切率 2145 s 和 11560 s 后,血小板对 von Willebrand 因子的黏附随距离的增加而略有增加。结果表明,血小板下游流动时,纤维蛋白原受体 GPIIb/IIIa 被短暂暴露于高上游壁剪切率激活是一个时间依赖性的过程。上游壁剪切率高达 11560 s 会改变许多黏附在下游纤维蛋白原上的血小板的形态,使其从原生的椭圆形变为扩展的圆形。血小板形态分析表明,短暂升高的上游壁剪切率会增加椭圆形血小板群体的表面覆盖率分数,并降低在纤维蛋白原上完全展开的血小板的表面覆盖率分数。