Corash L, Tan H, Gralnick H R
Blood. 1977 Jan;49(1):71-87.
A quantitative high yield method utilizing isosmotic arabino-galactan (Stractan) solutions and isopycnic centrifugation was developed to isolate and to fractionate total human platelet populations into density-dependent subpopulations. Isolated platelets were free of factor VIII/von Willebrand factor and other plasma proteins. They responded to ADP, epinephrine, and collagen with a sensitivity equal to platelet-rich plasma platelets. The correlation of platelet density with volume and ultrastructure was examined for normal subjects. Recovery of total platelet populations averaged 92.76%+/-3.64% (SD). Normal individuals exhibited a narrow range of platelet buoyant density distribution. Computerized probability plot analysis of platelet volume distribution for 15 normal subjects' total platelet populations showed a mean volume of 5.17+/-0.46 cu mum (SD). Platelets with buoyant density less than or equal to 1.062 g/ml had a mean volume of 4.50+/-0.48 cu mum, while platelets with buoyant density greater than 1.071 g/ml, but less than or equal to 1.084 g/ml, had a mean volume of 5.32+/-0.63 cu mum (SD). The volume difference by paired t test was significant, p less than 0.001. Thin-section electron microscopy demonstrated a significant reduction of granule content in light platelets, as compared to heavy platelets, but an equal number of mitochondria for both groups. These differences of platelet volume and structure between light and heavy platelets suggested that aging may be a determinant of platelet heterogeneity.
开发了一种利用等渗阿拉伯半乳聚糖(Stractan)溶液和等密度离心的定量高产方法,以分离人血小板总群体并将其分级为密度依赖性亚群体。分离出的血小板不含因子VIII/血管性血友病因子和其他血浆蛋白。它们对ADP、肾上腺素和胶原的反应敏感性与富含血小板血浆中的血小板相同。对正常受试者检测了血小板密度与体积和超微结构的相关性。血小板总群体的回收率平均为92.76%±3.64%(标准差)。正常个体的血小板浮力密度分布范围较窄。对15名正常受试者的血小板总群体的体积分布进行计算机化概率图分析,显示平均体积为5.17±0.46立方微米(标准差)。浮力密度小于或等于1.062克/毫升的血小板平均体积为4.50±0.48立方微米,而浮力密度大于1.071克/毫升但小于或等于1.084克/毫升的血小板平均体积为5.32±0.63立方微米(标准差)。配对t检验显示体积差异具有显著性,p小于0.001。超薄切片电子显微镜显示,与重血小板相比,轻血小板中的颗粒含量显著减少,但两组的线粒体数量相同。轻、重血小板之间血小板体积和结构的这些差异表明,老化可能是血小板异质性的一个决定因素。