Sakharov D V, Nagelkerke J F, Rijken D C
Gaubius Laboratory, TNO-PG, Leiden, The Netherlands.
J Biol Chem. 1996 Jan 26;271(4):2133-8. doi: 10.1074/jbc.271.4.2133.
Binding of components of the fibrinolytic system to fibrin is important for the regulation of fibrinolysis. In this study, decomposition of the fibrin network and binding of plasminogen and plasminogen activators (PAs) to fibrin during lysis of a plasma clot were investigated with confocal microscopy using fluorescein-labeled preparations of fibrinogen, plasminogen, tissue-type PA (t-PA), and two-chain urokinase-type PA (tcu-PA). Lysis induced by PAs present throughout the plasma clot was accompanied by a gradual loss of fibrin content of fibers and by accumulation of plasminogen onto the fibers. Two sequential phases could be distinguished: a phase of prelysis, during which the fibrin network remained immobile, and a phase of final lysis, during which fibers moved with a tendency to shrink and eventually disappeared. The two phases occurred simultaneously but in different locations when lysis was induced by PAs present in the plasma surrounding the clot. The zone of final lysis was located within a 5-8 microns superficial layer, where fibers were mobile, a surface-associated fibrin agglomerates appeared. Plasminogen accumulated in these agglomerates up to 30-fold as compared with its concentration in the outer plasma. t-PA was also highly concentrated in the agglomerates, and tcu-PA bound to them slightly. The zone of prelysis, where plasminogen was moderately accumulated on the immobile fibers, was located deeper in the clot. This zone was much thinner in the case of t-PA-induced lysis than in the case of tcu-PA-induced lysis, reflecting the difference in penetration of the two PAs into the clot. We conclude that under conditions of diffusional transport of fibrinolytic enzymes from outside a plasma clot, extensive lysis is spatially restricted to a zone not exceeding 5-8 microns from the clot surface. In this zone the structure of the fibrin network undergoes significant changes, and strikingly high accumulation of fibrinolytic components takes place.
纤维蛋白溶解系统的成分与纤维蛋白的结合对于纤维蛋白溶解的调节至关重要。在本研究中,使用荧光素标记的纤维蛋白原、纤溶酶原、组织型纤溶酶原激活剂(t-PA)和双链尿激酶型纤溶酶原激活剂(tcu-PA)制剂,通过共聚焦显微镜研究了血浆凝块溶解过程中纤维蛋白网络的分解以及纤溶酶原和纤溶酶原激活剂与纤维蛋白的结合。整个血浆凝块中存在的纤溶酶原激活剂诱导的溶解伴随着纤维中纤维蛋白含量的逐渐减少以及纤溶酶原在纤维上的积累。可以区分出两个连续的阶段:预溶解阶段,在此期间纤维蛋白网络保持不动;最终溶解阶段,在此期间纤维移动并趋于收缩,最终消失。当凝块周围血浆中存在的纤溶酶原激活剂诱导溶解时,这两个阶段同时发生但位置不同。最终溶解区域位于5-8微米的表层内,此处纤维是可移动的,出现了与表面相关的纤维蛋白聚集体。与外层血浆中的浓度相比,纤溶酶原在这些聚集体中的积累高达30倍。t-PA也高度集中在聚集体中,而tcu-PA与它们的结合较弱。预溶解区域位于凝块更深的位置,在此区域纤溶酶原在不动的纤维上适度积累。在t-PA诱导溶解的情况下,该区域比tcu-PA诱导溶解的情况薄得多,这反映了两种纤溶酶原激活剂进入凝块的穿透能力差异。我们得出结论,在纤维蛋白溶解酶从血浆凝块外部进行扩散运输的条件下,广泛的溶解在空间上局限于距凝块表面不超过5-8微米的区域。在该区域,纤维蛋白网络的结构发生了显著变化,并且纤维蛋白溶解成分发生了惊人的高积累。