Zhou Q, Chu X, Ruan C
Jiangsu Institute of Hematology, Thrombosis and Haemostasis Research Unit, Suzhou Medical College, China.
Thromb Haemost. 1994 Apr;71(4):507-10.
Cultured human umbilical vein endothelial cells were incubated with defibrotide at concentrations of 0, 5, 50 and 500 micrograms/ml for 4 and 24 h respectively. Thrombomodulin activity and molecules on the surface of the cells were determined by chromogenic assay and radioimmunoassay, thrombomodulin antigen in endothelial cells and in conditioned medium of the cells was measured by immunoradioassay. Thrombomodulin mRNA within the cells was analysed by slot blot. After 24 h of incubation, the activity and molecules of thrombomodulin on the surface of endothelial cells, as well as the antigen and mRNA of thrombomodulin in the cells were significantly increased in a dose dependent manner. However, the level of thrombomodulin antigen in conditioned medium was about equal to that of the control. Our data indicate that defibrotide stimulates expression of thrombomodulin in human endothelial cells. These beneficial effects may play a role in antithrombotic activity of defibrotide.
将培养的人脐静脉内皮细胞分别与浓度为0、5、50和500微克/毫升的去纤苷孵育4小时和24小时。通过显色测定法和放射免疫测定法测定细胞表面的血栓调节蛋白活性和分子,通过免疫放射测定法测量内皮细胞和细胞条件培养基中的血栓调节蛋白抗原。通过狭缝印迹分析细胞内的血栓调节蛋白mRNA。孵育24小时后,内皮细胞表面血栓调节蛋白的活性和分子以及细胞内血栓调节蛋白的抗原和mRNA均呈剂量依赖性显著增加。然而,条件培养基中血栓调节蛋白抗原的水平与对照组大致相当。我们的数据表明,去纤苷刺激人内皮细胞中血栓调节蛋白的表达。这些有益作用可能在去纤苷的抗血栓活性中发挥作用。