Kasirer-Friede A, Legrand C, Frojmovic M M
Dept of Experimental Medicine and Physiology, McGill University, Montreal, Canada.
Thromb Haemost. 2001 Aug;86(2):653-9.
We have evaluated the relative contribution of the adhesive ligands, von Willebrand factor (vWF), fibrinogen (Fg) and thrombospondin (TSP), all surface-expressed on washed platelets (WP) activated with a threshold thrombin concentration (approximately 0.04 U/ml), to platelet microaggregation (PA) at shear rates (G) from 300-2000 s(-1). In suspensions of thrombin-activated WP sheared immediately (tau0), all three ligands were required for optimal aggregation at all G, as shown by a 50-70% inhibition of capture efficiencies of PA (measured from initial rates of PA), by antibodies (Abs) directed against each protein. This aggregation involved both GPIb and GPIIbIIIa, as indicated by approximately 80% and 100% inhibition by Ab 6D1 and Ab 10E5, respectively. For WP preexposed to thrombin for 10 min to ensure maximal surface expression of secreted ligands and activated GPIIbIIIa (tau0), vWF was predominantly required at all G (63-75% inhibition by anti-vWF Ab), together with TSP (35-50% inhibition by anti-TSP Ab). Under these conditions, Fg was extensively converted to fibrin, so that fibrin, rather than Fg, could participate in microaggregation, with GPIb less required than GPIIbIIIa as indicated by a 30-60% inhibition by Ab 6D1 as compared to 100% inhibition by Ab 10E5. Our results show that interactions between multiple ligands and receptors favour microaggregation depending on shear and thrombin activation conditions.
我们评估了黏附配体、血管性血友病因子(vWF)、纤维蛋白原(Fg)和血小板反应蛋白(TSP)的相对贡献,这些配体均在经阈值凝血酶浓度(约0.04 U/ml)激活的洗涤血小板(WP)表面表达,研究了其在300 - 2000 s⁻¹的剪切速率(G)下对血小板微聚集(PA)的影响。在凝血酶激活的WP立即剪切的悬浮液(tau0)中,所有三种配体对于在所有G值下的最佳聚集都是必需的,针对每种蛋白质的抗体(Abs)可使PA的捕获效率抑制50 - 70%(根据PA的初始速率测量)。这种聚集涉及糖蛋白Ib(GPIb)和糖蛋白IIbIIIa(GPIIbIIIa),分别用抗体6D1和抗体10E5抑制约80%和100%可表明。对于预先暴露于凝血酶10分钟以确保分泌配体和活化的GPIIbIIIa最大程度表面表达的WP(tau0),在所有G值下主要需要vWF(抗vWF抗体抑制63 - 75%),以及TSP(抗TSP抗体抑制35 - 50%)。在这些条件下,Fg大量转化为纤维蛋白,因此纤维蛋白而非Fg可参与微聚集,与GPIIbIIIa相比,GPIb的需求较少,抗体6D1抑制30 - 60%,而抗体10E5抑制100%。我们的结果表明,多种配体与受体之间的相互作用有利于微聚集,这取决于剪切和凝血酶激活条件。