Leytin V, Shapiro H, Novikov I, Radnay J
Department of Hematology, Meir Hospital, Kfar-Saba, Israel.
Biochem Biophys Res Commun. 1996 Sep 4;226(1):94-100. doi: 10.1006/bbrc.1996.1316.
Large (L) activated platelets exhibit greater aggregability and express more activated glycoprotein IIb-IIIa (GPIIb-IIIa) per cell and per unit surface area than small (S) activated platelets. We studied the binding of CD61 monoclonal antibody to GPIIb-IIIa on resting platelets and developed a new method for determining platelet surface area by flow cytometry. Using this method, we found that resting L platelets contain two times more GPIIb-IIIa per cell than S platelets but the same amount of GPIIb-IIIa per unit surface area. The data suggest that the greater aggregability of L platelets is likely to be due to increased activation and/ or expression of GPIIb-IIIa rather than to elevated density of unactivated GPIIb-IIIa on resting L platelets.
与小(S)活化血小板相比,大(L)活化血小板表现出更强的聚集性,并且每个细胞和单位表面积表达更多的活化糖蛋白IIb-IIIa(GPIIb-IIIa)。我们研究了CD61单克隆抗体与静息血小板上GPIIb-IIIa的结合,并开发了一种通过流式细胞术测定血小板表面积的新方法。使用该方法,我们发现静息L血小板每个细胞所含的GPIIb-IIIa比S血小板多两倍,但单位表面积的GPIIb-IIIa量相同。数据表明,L血小板更强的聚集性可能是由于GPIIb-IIIa的活化和/或表达增加,而不是由于静息L血小板上未活化的GPIIb-IIIa密度升高。