Kuwahara M, Sugimoto M, Tsuji S, Miyata S, Yoshioka A
Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan.
Blood. 1999 Aug 15;94(4):1149-55.
Recent flow studies indicated that platelets are transiently captured onto and then translocated along the surface through interaction of glycoprotein (GP) Ib with surface-immobilized von Willebrand factor (vWF). During translocation, platelets are assumed to be activated, thereafter becoming firmly adhered and cohered on the surface. In exploring the mechanisms by which platelets become activated during this process, we observed changes in platelet cytosolic calcium concentrations ([Ca(2+)]i) concomitantly with the real-time platelet adhesive and cohesive process on a vWF-coated surface under flow conditions. Reconstituted blood containing platelets loaded with the Ca(2+) indicators Fura Red and Calcium Green-1 was perfused over a vWF-coated glass surface in a flow chamber, and changes in [Ca(2+)]i were evaluated by fluorescence microscopy based on platelet color changes from red (low [Ca(2+)]i) to green (high [Ca(2+)]i) during the platelet adhesive and cohesive process. Under flow conditions with a shear rate of 1,500 s(-1), no change in [Ca(2+)]i was observed during translocation of platelets, but [Ca(2+)]i became elevated apparently after platelets firmly adhered to the surface. Platelets preincubated with anti-GP IIb-IIIa antibody c7E3 showed no firm adhesion and no [Ca(2+)]i elevation. The intracellular Ca(2+) chelator dimethyl BAPTA did not inhibit firm platelet adhesion but completely abolished platelet cohesion. Although both firm adhesion and cohesion of platelets have been thought to require activation of GP IIb-IIIa, our results indicate that [Ca(2+)]i elevation is a downstream phenomenon and not a prerequisite for firm platelet adhesion to a vWF-coated surface. After platelets firmly adhere to the surface, [Ca(2+)]i elevation might occur through the outside-in signaling from GP IIb-IIIa occupied by an adhesive ligand, thereby leading to platelet cohesion on the surface.
最近的血流研究表明,血小板通过糖蛋白(GP)Ib与表面固定的血管性血友病因子(vWF)相互作用,短暂地捕获到表面上,然后沿表面移位。在移位过程中,血小板被认为会被激活,随后在表面上牢固地粘附并凝聚。在探索血小板在此过程中被激活的机制时,我们观察到在流动条件下,血小板胞质钙浓度([Ca(2+)]i)的变化与血小板在vWF包被表面上的实时粘附和凝聚过程同时发生。将含有负载Ca(2+)指示剂Fura Red和Calcium Green-1的血小板的重组血液灌注到流动腔室中vWF包被的玻璃表面上,并基于血小板在粘附和凝聚过程中从红色(低[Ca(2+)]i)到绿色(高[Ca(2+)]i)的颜色变化,通过荧光显微镜评估[Ca(2+)]i的变化。在剪切速率为1500 s(-1)的流动条件下,血小板移位过程中未观察到[Ca(2+)]i的变化,但血小板牢固粘附到表面后,[Ca(2+)]i明显升高。用抗GP IIb-IIIa抗体c7E3预孵育的血小板未表现出牢固的粘附,也没有[Ca(2+)]i升高。细胞内Ca(2+)螯合剂二甲基BAPTA不抑制血小板的牢固粘附,但完全消除了血小板的凝聚。尽管血小板的牢固粘附和凝聚都被认为需要GP IIb-IIIa的激活,但我们的结果表明,[Ca(2+)]i升高是下游现象,而不是血小板牢固粘附到vWF包被表面的先决条件。血小板牢固粘附到表面后,[Ca(2+)]i升高可能通过被粘附配体占据的GP IIb-IIIa的外向内信号传导而发生,从而导致血小板在表面上凝聚。