Tijburg P N, van Heerde W L, Leenhouts H M, Hessing M, Bouma B N, de Groot P G
Department of Haematology, University Hospital Utrecht, The Netherlands.
J Biol Chem. 1991 Feb 25;266(6):4017-22.
Incubation of prothrombin on cultured human umbilical vein endothelial cells with factor Xa and calcium ions induced the activation of prothrombin. The mechanism of prothrombin activation was analyzed on sodium dodecyl sulfate gels using immuno- and amido-blotting techniques. It was demonstrated that meizothrombin was formed as an intermediate in prothrombin activation on the endothelial cell surface. In addition, considerable amounts of meizothrombin des-fragment-1 accumulated during prothrombin activation and were not further converted to thrombin. Although preincubation of the endothelial cells with thrombin did not influence the formation of meizothrombin, addition of hirudin to the prothrombin activation mixture inhibited the formation of meizothrombin and meizothrombin des-fragment-1 almost completely. This indicated that the activity of endogenously formed thrombin influenced the formation of meizothrombin via a feedback mechanism. The increased formation of meizothrombin and accumulation of meizothrombin des-fragment-1 in a latter phase of prothrombin activation points to a regulatory mechanism in hemostasis which subdues the formation of the procoagulant alpha-thrombin.
将凝血酶原与因子Xa及钙离子在培养的人脐静脉内皮细胞上孵育,可诱导凝血酶原激活。利用免疫印迹和酰胺印迹技术,在十二烷基硫酸钠凝胶上分析了凝血酶原激活机制。结果表明,在凝血酶原于内皮细胞表面激活过程中,中间产物凝血酶原中间体(meizothrombin)得以形成。此外,在凝血酶原激活过程中,大量的凝血酶原中间体去片段1(meizothrombin des-fragment-1)积累,且未进一步转化为凝血酶。尽管用凝血酶预孵育内皮细胞并不影响凝血酶原中间体的形成,但向凝血酶原激活混合物中加入水蛭素几乎完全抑制了凝血酶原中间体及凝血酶原中间体去片段1的形成。这表明内源性形成的凝血酶的活性通过反馈机制影响了凝血酶原中间体的形成。在凝血酶原激活后期,凝血酶原中间体形成增加及凝血酶原中间体去片段1积累,提示止血过程中存在一种调节机制,可抑制促凝血的α-凝血酶的形成。