Aznar-Salatti J, Bastida E, Haas T A, Escolar G, Ordinas A, de Groot P H, Buchanan M R
Servicio de Hemoterapia y Hemostasia, Hospital Clinic i Provincial de Barcelona, Spain.
Arterioscler Thromb. 1991 Mar-Apr;11(2):436-42. doi: 10.1161/01.atv.11.2.436.
The relative thrombogenicity of extracellular matrixes (ECMs) produced by cultured human umbilical endothelial cells (ECs) was studied under flow conditions. ECMs were prepared using a number of physical and chemical methods, and their reactivity toward platelets was morphometrically evaluated. von Willebrand factor (vWF), fibronectin (FN), and 13-hydroxy-9-cis,11-trans-octadecadienoic acid (13-HODE) were also determined. We found that platelet adhesion to ECMs differed significantly, both quantitatively and qualitatively, with the method of ECM preparation. Mechanically prepared ECM exposed a less thrombogenic surface compared with ECM prepared by chemical methods (platelet-covered surface of 20% and 50%, respectively). Evaluation of the ECM components vWF, FN, and 13-HODE showed significant changes, both in their concentrations and distribution patterns, depending on the method of ECM preparation. The decrease measured in the levels of ECM-associated vWF (from 108 to 9.2 ng/10(4) cells) and the minor changes observed in the distribution pattern of subendothelial FN did not appear to be sufficient to explain the altered platelet adhesion observed in our model. This suggests that the amount of 13-HODE probably associated to the remaining ECs present in the mechanically exposed ECM could be one factor that specifically contributed to the nonthrombogenic state of these preparations. We conclude that the degree of ECM reactivity toward platelets is dependent on the method of ECM preparation and that this is related to the removal of specific EC/ECM components that modulate their thromboresistant/thrombogenic properties. This fact should be taken into account when ECMs produced by cultured ECs are used in platelet adhesion studies.
在流动条件下研究了培养的人脐内皮细胞(ECs)产生的细胞外基质(ECMs)的相对血栓形成性。使用多种物理和化学方法制备ECMs,并通过形态计量学评估它们对血小板的反应性。还测定了血管性血友病因子(vWF)、纤连蛋白(FN)和13-羟基-9-顺式,11-反式-十八碳二烯酸(13-HODE)。我们发现,血小板对ECMs的黏附在数量和质量上均因ECM制备方法的不同而有显著差异。与化学方法制备的ECM相比,机械制备的ECM暴露的血栓形成性表面较少(血小板覆盖表面分别为20%和50%)。对ECM成分vWF、FN和13-HODE的评估显示,根据ECM制备方法的不同,它们的浓度和分布模式均有显著变化。ECM相关vWF水平的降低(从108降至9.2 ng/10(4) 细胞)以及内皮下FN分布模式的微小变化似乎不足以解释我们模型中观察到的血小板黏附改变。这表明,与机械暴露的ECM中剩余的ECs可能相关的13-HODE量可能是导致这些制剂处于非血栓形成状态的一个特定因素。我们得出结论,ECM对血小板的反应程度取决于ECM的制备方法,这与去除调节其抗血栓/血栓形成特性的特定EC/ECM成分有关。在将培养的ECs产生的ECMs用于血小板黏附研究时,应考虑这一事实。