Chen S H
Zhonghua Yi Xue Za Zhi. 1989 Jul;69(7):382-4, 28.
A new platelet aggregating protein (PAP) was purified from the plasma of a patient with acute thrombotic thrombocytopenic purpura (TTP) using A1 (OH)3 adsorption, PEG fractionation, DEAE cellulose chromatography, lentil lectin Sepharose 4B chromatography and gel filtration HPLC. The M. W. of this PAP was estimated to be 59,000. It induced the aggregation of washed platelets from normal subjects and the same patient after recovery. The antigenic material was present in 2 out of 6 other TTP patients but was absent in 7 normal subjects, two patients with DIC and two patients with ITP. The aggregation of washed platelets by PAP was concentration dependent and required energy metabolism, Ca2+ and fibrinogen. PAP was present in the plasma of a subset of TTP patients and was likely the cause of platelet thrombi in the microvessels in these patients.
采用氢氧化铝吸附、聚乙二醇分级分离、二乙氨基乙基纤维素色谱法、扁豆凝集素琼脂糖4B色谱法和凝胶过滤高效液相色谱法,从一名急性血栓性血小板减少性紫癜(TTP)患者的血浆中纯化出一种新的血小板聚集蛋白(PAP)。该PAP的分子量估计为59,000。它能诱导正常受试者的洗涤血小板以及恢复后的同一患者的血小板发生聚集。6名其他TTP患者中有2名存在该抗原物质,但7名正常受试者、2名弥散性血管内凝血患者和2名免疫性血小板减少性紫癜患者中均未检测到。PAP诱导洗涤血小板聚集具有浓度依赖性,且需要能量代谢、钙离子和纤维蛋白原。PAP存在于一部分TTP患者的血浆中,可能是这些患者微血管中血小板血栓形成的原因。