Iijima K, Murata M, Nakamura K, Kitaguchi T, Handa M, Watanabe K, Fujimura Y, Yoshioka A, Ikeda Y
Department of Physics and Engineering, Waseda University, Tokyo, Japan.
Biochem Biophys Res Commun. 1997 Apr 28;233(3):796-800. doi: 10.1006/bbrc.1997.6554.
High shear stress facilitates von Willebrand factor (vWF) binding to platelet glycoprotein (GP) Ib/IX, causing activation of GPIIb/IIIa to induce platelet aggregation. Here we report that activated GPIIb/IIIa, even occupied by ligands, is not sufficient to mediate platelet aggregation under high shear stress conditions when vWF binding to GPIb/IX is blocked. Platelet rich plasma or washed platelet suspension supplemented with purified human fibrinogen at a concentration of 2 mg/mL were treated with an anti-vWF monoclonal antibody NMC-4 which blocks the binding of vWF to GPIb/IX. After addition of 10 mumol/L ADP, aggregation was continuously monitored under various shear stress conditions (0-108 dyne/cm2) using a cone-plate type aggregometer previously described (Ikeda Y et al J Clin Invest 1991; 87:1234). The extent of maximal aggregation of agonist-stimulated platelets in the presence of NMC-4 correlated inversely with the level of shear stress applied, with the virtual absence of aggregation at 108 dyne/cm2. Once aggregated by 10 mumol/L ADP under low shear stress (12 dyne/cm2), platelets could be disaggregated, in part, by the application of high shear stress (108 dyne/cm2), and reaggregated when shear stress was returned to 12 dyne/cm2. Flow cytometric analysis revealed that platelets stimulated with 10 mumol/L ADP at 108 dyne/cm2 bound fluorescein isothiocyanate (FITC)-labeled fibrinogen, although aggregation was absent in this experimental condition. These results demonstrate the dual effect of shear stress on platelet functions; a pro-aggregating activity that induces vWF-GPIb/IX interaction leading to platelet activation, and an anti-aggregating force to prevent the growth of platelet thrombi. It is suggested that the efficacy of vWF blockade is greater under high shear than low shear stress conditions, and that a selective inhibition of platelet functions can be possible.
高剪切应力促进血管性血友病因子(vWF)与血小板糖蛋白(GP)Ib/IX结合,导致GPIIb/IIIa激活,进而诱导血小板聚集。在此我们报告,当vWF与GPIb/IX的结合被阻断时,即使被配体占据,活化的GPIIb/IIIa在高剪切应力条件下也不足以介导血小板聚集。用抗vWF单克隆抗体NMC-4处理富含血小板的血浆或补充有浓度为2 mg/mL的纯化人纤维蛋白原的洗涤血小板悬液,该抗体可阻断vWF与GPIb/IX的结合。加入10 μmol/L ADP后,使用先前描述的锥板式聚集仪(池田Y等人,《临床研究杂志》1991年;87:1234)在各种剪切应力条件(0 - 108达因/平方厘米)下连续监测聚集情况。在存在NMC-4的情况下,激动剂刺激的血小板的最大聚集程度与施加的剪切应力水平呈负相关,在108达因/平方厘米时几乎没有聚集。一旦在低剪切应力(12达因/平方厘米)下被10 μmol/L ADP聚集,血小板部分可通过施加高剪切应力(108达因/平方厘米)解聚,并在剪切应力恢复到12达因/平方厘米时重新聚集。流式细胞术分析显示,在108达因/平方厘米下用10 μmol/L ADP刺激的血小板结合了异硫氰酸荧光素(FITC)标记的纤维蛋白原,尽管在此实验条件下没有聚集。这些结果证明了剪切应力对血小板功能的双重作用;一种促聚集活性,诱导vWF - GPIb/IX相互作用导致血小板活化,以及一种抗聚集力,防止血小板血栓生长。提示vWF阻断在高剪切应力条件下比低剪切应力条件下更有效,并且可能实现对血小板功能的选择性抑制。