Fukuyama M, Sakai K, Itagaki I, Kawano K, Murata M, Kawai Y, Watanabe K, Handa M, Ikeda Y
Department of Chemical Engineering, Waseda University, Tokyo, Japan.
Thromb Res. 1989 May 1;54(3):253-60. doi: 10.1016/0049-3848(89)90233-8.
A mechanical device for continuous recording of shear-induced platelet aggregation (SIPA) has been developed using a turbidometric technique. The device consists of three components: light source, a thermostated cone-plate streaming chamber and optical detection unit. There was a good correlation between platelet count and transmitted light intensity under the conditions in which no activation of platelets occurred. When platelets were exposed to shear stress at 37 degrees C, transmitted light intensity increased with time. Scanning electronmicroscopic examinations revealed that more prominent platelet aggregation was demonstrated when light intensity increased. Reproducible recording of SIPA was obtained when experiments were repeated using the same sample. No change in light intensity was observed when formalin-fixed platelets were sheared. Both PGE1, and anti-GPIIb/IIIa mouse monoclonal antibody, AP2, showed complete inhibition of SIPA. It is indicated that our device for continuous measurement of SIPA is an important new tool to study one aspect of platelet functions.
已利用比浊技术开发出一种用于连续记录剪切诱导血小板聚集(SIPA)的机械装置。该装置由三个部分组成:光源、恒温锥板流动腔和光学检测单元。在未发生血小板激活的条件下,血小板计数与透射光强度之间存在良好的相关性。当血小板在37℃下受到剪切应力作用时,透射光强度随时间增加。扫描电子显微镜检查显示,当光强度增加时,血小板聚集更为明显。使用相同样本重复实验时,可获得可重复的SIPA记录。当剪切福尔马林固定的血小板时,未观察到光强度变化。PGE1和抗GPIIb/IIIa小鼠单克隆抗体AP2均显示出对SIPA的完全抑制作用。表明我们用于连续测量SIPA的装置是研究血小板功能一个方面的重要新工具。