Bogáti Réka, Baráth Barbara, Pituk Dóra, Orbán-Kálmándi Rita, Szűcs Péter, Hegyi Zoltán, Bereczky Zsuzsanna, Bagoly Zsuzsa, Katona Éva
Division of Clinical Laboratory Science, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Kálmán Laki Doctoral School, University of Debrecen, 4032 Debrecen, Hungary.
Biomolecules. 2025 Aug 5;15(8):1127. doi: 10.3390/biom15081127.
Alpha2-plasmin inhibitor (α2PI) has a heterogeneous structure due to proteolytic cleavages in the circulation. The C-terminally cleaved form loses the plasminogen binding site and is, therefore, a slow plasmin inhibitor (NPB-α2PI). As FXIII primarily crosslinks the plasminogen-binding intact form (PB-α2PI) to fibrin, the effect of NPB-α2PI on fibrinolysis has been less studied. Herein, we investigated the effect of C-terminal truncation. Total-, PB-, and NPB-α2PI antigen levels and α2PI incorporation were measured by ELISAs from samples of 80 healthy individuals. Clot lysis parameters of the same subjects were investigated using an in vitro clot lysis assay. α2PI incorporation into the clot was demonstrated by Western blotting. Clot lysis and clot structure were also analyzed using an α2PI-deficient plasma substituted with recombinant PB- and NPB-α2PI. Both plasma and clot-bound levels of total- and NPB-α2PI showed a significant positive correlation with clot lysis parameters. NPB-α2PI was detected in the clot due to non-covalent binding. Regardless of the type of binding, both forms affected the clot structure by increasing the thickness of the fibrin fibers and reducing the pore size. In conclusion, we found that NPB-α2PI can bind non-covalently to fibrin, and this binding contributes to changes in clot structure and inhibition of fibrinolysis.
α2-纤溶酶抑制剂(α2PI)由于在循环中发生蛋白水解裂解而具有异质性结构。C末端裂解形式失去了纤溶酶原结合位点,因此是一种作用缓慢的纤溶酶抑制剂(NPB-α2PI)。由于因子XIII主要将纤溶酶原结合完整形式(PB-α2PI)交联到纤维蛋白上,因此对NPB-α2PI对纤维蛋白溶解的影响研究较少。在此,我们研究了C末端截短的影响。通过酶联免疫吸附测定法(ELISA)测定了80名健康个体样本中的总α2PI、PB-α2PI和NPB-α2PI抗原水平以及α2PI掺入量。使用体外凝块溶解试验研究了同一受试者的凝块溶解参数。通过蛋白质印迹法证实了α2PI掺入凝块中。还使用用重组PB-α2PI和NPB-α2PI替代的α2PI缺陷血浆分析了凝块溶解和凝块结构。总α2PI和NPB-α2PI的血浆水平和凝块结合水平均与凝块溶解参数呈显著正相关。由于非共价结合,在凝块中检测到了NPB-α2PI。无论结合类型如何,两种形式都通过增加纤维蛋白纤维的厚度和减小孔径来影响凝块结构。总之,我们发现NPB-α2PI可以与纤维蛋白非共价结合,这种结合有助于凝块结构的改变和纤维蛋白溶解的抑制。