Speiser W, Anders E, Preissner K T, Wagner O, Müller-Berghaus G
Blood. 1987 Mar;69(3):964-7.
Large vessel and microvascular endothelial cells were compared in their capacity to synthesize and secrete coagulant and fibrinolytic factors. Human omental tissue microvascular endothelial cells (HOTMEC) and human umbilical vein endothelial cells (HUVEC) were isolated, grown to confluency under identical conditions, and studied in primary cultures. After an incubation period of 12 hours in serum-free medium, the conditioned medium of confluent HOTMEC contained 100-fold higher levels of tissue plasminogen activator (tPA) antigen than that of HUVEC. The conditioned media as well as the lysates of both cell types did not contain any free tPA activity, but the free plasminogen activator inhibitor capacity was found intracellularly as well as extracellularly. Although von Willebrand factor was detected in both cell types by immunofluorescence, measurable amounts were only found in HUVEC using an enzyme-linked immunosorbent assay. The kinetics of protein C activation by thrombin on the surface of once-passaged cells were identical for HOTMEC and HUVEC. The present study indicates that cultivated HOTMEC produce larger quantities of tPA than HUVEC do, possess smaller amounts of von Willebrand factor than HUVEC do, and express thrombomodulin for protein C activation as effectively as HUVEC.
对大血管内皮细胞和微血管内皮细胞合成与分泌促凝因子和纤溶因子的能力进行了比较。分离出人网膜组织微血管内皮细胞(HOTMEC)和人脐静脉内皮细胞(HUVEC),在相同条件下培养至汇合状态,并在原代培养中进行研究。在无血清培养基中孵育12小时后,汇合的HOTMEC的条件培养基中组织纤溶酶原激活物(tPA)抗原水平比HUVEC的高100倍。两种细胞类型的条件培养基以及裂解物均未含有任何游离tPA活性,但在细胞内和细胞外均发现了游离纤溶酶原激活物抑制剂活性。尽管通过免疫荧光在两种细胞类型中均检测到血管性血友病因子,但使用酶联免疫吸附测定法仅在HUVEC中发现了可测量的量。对于HOTMEC和HUVEC,凝血酶在传代一次的细胞表面激活蛋白C的动力学是相同的。本研究表明,培养的HOTMEC比HUVEC产生更多的tPA,比HUVEC拥有更少的血管性血友病因子,并且在激活蛋白C方面表达血栓调节蛋白的效果与HUVEC相同。