Ellegård K H, Christiansen K, Ingerslev J
Department of Clinical Immunology, University Hospital Skejby/Aarhus, Denmark.
Scand J Clin Lab Invest. 1992 Nov;52(7):731-9. doi: 10.3109/00365519209115519.
In plasma from healthy subjects a coupling was identified between von Willebrand factor (vWf), fibrinogen (fg), and fibronectin (fn) that was dependent of anticoagulants heparin, EDTA, and citrate. Binding was quantitated by ELISA methodologies, based on polyclonal antibodies directed against the proteins studied, in order to express the percentage of moles of fg or fn bound to moles vWf, C[fg/vWf] or C[fn/vWf] (mol/mol)%. The intra-assay coefficients of variation (CV%) for fg and fn bound to vWf were 10.6% and 7.4% (n = 10) respectively, and the inter-assay coefficients of variation were 24.4% and 22.2% (n = 10). The largest degree of coupling was found in heat-treated lyophilized heparin plasma, where C[fg/vWf] and C[fn/vWf] were 12.9 +/- 1.4 (mol/mol)% and 2.4 +/- 0.1 (mol/mol)% (mean +/- SD). Binding was further qualitatively demonstrated through experiments using gel filtration chromatography and agarose gel electrophoresis followed by immunoblotting. In all instances coupling of vWf with fg was higher than with fn. Lyophilisates of normal plasma that were subjected to dry heating (60 degrees C in 72 h) showed considerably increased coupling. Previous investigators, studying reconstituted factor VIII concentrates by means of gel filtration, pointed out that an association between vWf, fg and fn was present in such therapeutic material. This investigation signifies that a coupling between these proteins may be present even in the source plasma, and that 'dry heating' increases binding. Implications of these results are discussed.
在健康受试者的血浆中,发现血管性血友病因子(vWf)、纤维蛋白原(fg)和纤连蛋白(fn)之间存在一种依赖于抗凝剂肝素、乙二胺四乙酸(EDTA)和柠檬酸盐的偶联作用。结合情况通过酶联免疫吸附测定(ELISA)方法进行定量,该方法基于针对所研究蛋白质的多克隆抗体,以表达与vWf结合的fg或fn的摩尔数百分比,即C[fg/vWf]或C[fn/vWf](mol/mol)%。与vWf结合的fg和fn的批内变异系数(CV%)分别为10.6%和7.4%(n = 10),批间变异系数分别为24.4%和22.2%(n = 10)。在热处理的冻干肝素血浆中发现偶联程度最高,其中C[fg/vWf]和C[fn/vWf]分别为12.9±1.4(mol/mol)%和2.4±0.1(mol/mol)%(平均值±标准差)。通过使用凝胶过滤色谱和琼脂糖凝胶电泳然后进行免疫印迹的实验进一步定性证明了结合情况。在所有情况下,vWf与fg的偶联高于与fn的偶联。经过干热(72小时内60摄氏度)处理的正常血浆冻干物显示偶联显著增加。先前的研究人员通过凝胶过滤研究重组因子VIII浓缩物时指出,在这种治疗材料中存在vWf、fg和fn之间的关联。这项研究表明,即使在源血浆中这些蛋白质之间也可能存在偶联,并且“干热”会增加结合。讨论了这些结果的意义。