McCarroll D R, Levin E G, Montgomery R R
J Clin Invest. 1985 Apr;75(4):1089-95. doi: 10.1172/JCI111802.
von Willebrand antigen II (vW AgII) and von Willebrand factor (vWf) are immunochemically distinct proteins that are deficient in the plasma and platelets of patients with severe von Willebrand's disease. Normal human umbilical vein endothelial cells were cultured in the presence of [35S]methionine. Crossed immunoelectrophoresis of endothelial cell supernates and detergent-solubilized endothelial cells demonstrated specific incorporation of the [35S]methionine into vW AgII. Furthermore, when endothelial cells were lysed in the presence of proteolytic inhibitors, a second, less anodal peak was identified on crossed immunoelectrophoresis. This peak represented a complex of vW AgII and vWf and demonstrated a reaction of complete identity with the vW AgII immunoprecipitate. When plasma, serum, or platelets were evaluated by crossed immunoelectrophoresis, this "complex" peak was not present. When antibodies to vWf, fibronectin, or fibrinogen were present in the first dimension of crossed immunoelectrophoresis, only the antibodies to vWf removed the complex. Radioiodinated polyclonal and monoclonal antibodies to vWf also localized vWf to this complex. Under reducing conditions, sodium dodecyl sulfate-polyacrylamide gel electrophoresis of [35S]methionine-labeled immunoprecipitates indicated that the molecular weight of vW AgII is 98,000 and that vWf was present as two species of 220,000 and 260,000 mol wt, respectively. Immunofluorescent microscopy of endothelial cells demonstrated colocalization of vW AgII and vWf in endothelial cells with intense immunostaining of the same subcellular granules.
血管性血友病抗原II(vW AgII)和血管性血友病因子(vWf)是免疫化学上不同的蛋白质,在严重血管性血友病患者的血浆和血小板中缺乏。正常人脐静脉内皮细胞在[35S]甲硫氨酸存在的情况下进行培养。对内皮细胞上清液和去污剂溶解的内皮细胞进行交叉免疫电泳,结果表明[35S]甲硫氨酸特异性掺入vW AgII。此外,当在内皮细胞在蛋白水解抑制剂存在的情况下裂解时,在交叉免疫电泳中鉴定出第二个较不向阳极迁移的峰。这个峰代表vW AgII和vWf的复合物,并与vW AgII免疫沉淀物显示出完全相同的反应。当通过交叉免疫电泳评估血浆、血清或血小板时,不存在这个“复合物”峰。当在交叉免疫电泳的第一维中存在针对vWf、纤连蛋白或纤维蛋白原的抗体时,只有针对vWf的抗体能去除该复合物。针对vWf的放射性碘化多克隆和单克隆抗体也将vWf定位到这个复合物上。在还原条件下,对[35S]甲硫氨酸标记的免疫沉淀物进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳表明,vW AgII的分子量为98,000,vWf分别以分子量为220,000和260,000的两种形式存在。内皮细胞的免疫荧光显微镜检查显示,vW AgII和vWf在内皮细胞中共定位,同一亚细胞颗粒有强烈的免疫染色。