Institut für Immunologie und Transfusionsmedizin, Universitätsmedizin Greifswald, Greifswald, Germany.
Interfakultäres Institut für Genetik und Funktionelle Genomforschung, Abteilung Funktionelle Genomforschung, Universitätsmedizin Greifswald, Greifswald, Germany.
Thromb Haemost. 2019 Mar;119(3):407-420. doi: 10.1055/s-0039-1677875. Epub 2019 Feb 6.
Epidemiological studies found an association between increased platelet size and the risk for thrombotic complications, but functional differences of large and small platelets remain poorly understood due to a lack of standardized protocols separating platelets with different size. We designed a protocol to separate large and small platelets from 15 mL whole blood. Separated large and small platelet fractions differed in mean platelet volume: 12.1 fl (10.3-13.8 fl) versus 7.7 fl (6.8-9.5 fl, < 0.01), and forward scatter mean fluorescence intensity: 24.75 (19.9-30.9) versus 16.85 (11.3-20.6; < 0.01). Similar fold differences were observed in cell diameter and plateletcrit. Large platelets express 30 to 50% more glycoprotein (GP) Ia, GPIb, GPIIIa, GPVI and P2Y12 on their membranes compared with small ones. Single large platelets covered a 50% larger area on a collagen surface. Adhesion to collagen was faster in large platelets compared with small ones indicating enhanced outside-in signal transduction in large platelets via collagen receptors. In contrast, integrin activation was more pronounced in small platelets after ADP stimulation. Proteome analysis revealed that 80 of the 894 proteins quantified differed in abundance: ADP-ribosylation factor 1/3, guanosine triphosphate-binding protein SAR1a, Voltage-dependent anion-selective channel protein 3 and guanylate cyclase soluble sub-unit α-3 were higher abundant in large, whereas immunoglobulins, haptoglobin, hemopexin, α-1-antitrypsin, serotransferrin and vitronectin were more abundant in small platelets. We conclude that some functions and the protein composition of large and small platelets differ, which cannot only be explained by the size difference. Our data suggest different functional roles of large and small platelets.
流行病学研究发现血小板体积增大与血栓并发症风险增加之间存在关联,但由于缺乏分离不同大小血小板的标准化方案,大、小血小板的功能差异仍知之甚少。我们设计了一种从 15 毫升全血中分离大、小血小板的方案。分离的大、小血小板在平均血小板体积上存在差异:12.1 fl(10.3-13.8 fl)与 7.7 fl(6.8-9.5 fl,<0.01),前向散射平均荧光强度:24.75(19.9-30.9)与 16.85(11.3-20.6;<0.01)。细胞直径和血小板比容也观察到类似的倍数差异。与小血小板相比,大血小板在其膜上表达 30%至 50%更多的糖蛋白(GP)Ia、GPIb、GPIIIa、GPVI 和 P2Y12。单个大血小板在胶原表面覆盖的面积大 50%。与小血小板相比,大血小板在胶原上的粘附速度更快,表明大血小板通过胶原受体的外向信号转导增强。相比之下,ADP 刺激后小血小板中的整合素激活更为明显。蛋白质组分析显示,在定量的 894 种蛋白质中,有 80 种的丰度存在差异:ADP-核糖基化因子 1/3、鸟苷三磷酸结合蛋白 SAR1a、电压依赖性阴离子选择性通道蛋白 3 和鸟苷酸环化酶可溶性亚基α-3 在大血小板中含量较高,而免疫球蛋白、触珠蛋白、血红素结合蛋白、α-1-抗胰蛋白酶、转铁蛋白和玻连蛋白在小血小板中含量较高。我们得出结论,大、小血小板的某些功能和蛋白质组成存在差异,这不能仅用大小差异来解释。我们的数据表明大、小血小板具有不同的功能作用。