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剪切应力诱导血管性血友病因子与血小板结合。

Shear stress-induced binding of von Willebrand factor to platelets.

作者信息

Konstantopoulos K, Chow T W, Turner N A, Hellums J D, Moake J L

机构信息

Cox Lab for Biomedical Engineering, Rice University, Houston, Texas 77251-1892, USA.

出版信息

Biorheology. 1997 Jan-Feb;34(1):57-71. doi: 10.1016/S0006-355X(97)00004-8.

Abstract

Shear stress-induced platelet aggregation requires von Willebrand factor (vWF), platelet glycoprotein (GP) Ib, GPIIb-IIIa, Ca2+, and adenosine diphosphate (ADP). Recent reports using vWF labeled with either 125I or fluorescein isothiocyanate (FITC) have demonstrated that in shear-fields, vWF binds to both GPIb and GPIIb-IIIa. The sequence of the vWF finding to the two platelet receptors has not been precisely determined in these reports. In this study, a flow cytometry technique using a primary anti-vWF antibody and a secondary FITC IgG antibody was used to measure shear stress-induced vWF binding to platelets. Washed normal platelets suspended at 50,000/microliters with purified large vWF multimers were exposed to laminar shear stresses of 15 to 120 dynes/cm2 for 30 sec. At this low platelet count, little or no aggregation occurred in the shear fields. A significant increase in post-shear vWF-positive platelets was consistently observed. Experiments with platelets from normal and severe von Willebrand's disease (vWD) (which lack plasma and platelet alpha-granule vWF) demonstrated that exogenous vWF predominately contributed to the platelet-vWF binding. Blockade of platelet GPIb with the monoclonal anti-GPIb antibody, 6D1, completely inhibited shear stress-induced platelet-vWF attachment. In contrast, blockade of GPIIb-IIIa with monoclonal anti-GPIIb-IIIa antibodies, 10E5, or c7E3, or with the GPIIb-IIIa-blocking tetrapeptide, RGDS had little or no inhibitory effect on platelet-vWF binding. These data demonstrate that the binding of vWF to GPIb is likely to be the initial shear-induced platelet-ligand binding event.

摘要

剪切应力诱导的血小板聚集需要血管性血友病因子(vWF)、血小板糖蛋白(GP)Ib、GPIIb-IIIa、Ca2+和二磷酸腺苷(ADP)。最近使用用125I或异硫氰酸荧光素(FITC)标记的vWF的报告表明,在剪切场中,vWF与GPIb和GPIIb-IIIa都结合。在这些报告中,vWF与两种血小板受体结合的顺序尚未精确确定。在本研究中,使用一种使用抗vWF一抗和FITC IgG二抗的流式细胞术技术来测量剪切应力诱导的vWF与血小板的结合。将用纯化的大vWF多聚体悬浮在50,000/微升的洗涤正常血小板暴露于15至120达因/平方厘米的层流剪切应力下30秒。在这种低血小板计数下,在剪切场中几乎没有或没有发生聚集。始终观察到剪切后vWF阳性血小板显著增加。对来自正常和严重血管性血友病(vWD)(缺乏血浆和血小板α-颗粒vWF)的血小板进行的实验表明,外源性vWF主要促成血小板与vWF的结合。用单克隆抗GPIb抗体6D1阻断血小板GPIb完全抑制了剪切应力诱导的血小板与vWF的附着。相比之下,用单克隆抗GPIIb-IIIa抗体10E5或c7E3或用GPIIb-IIIa阻断四肽RGDS阻断GPIIb-IIIa对血小板与vWF的结合几乎没有抑制作用。这些数据表明,vWF与GPIb的结合可能是最初的剪切诱导的血小板-配体结合事件。

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