Yin Z F, Huang Z F, Cui J, Fiehler R, Lasky N, Ginsburg D, Broze G J
Division of Hematology, Barnes-Jewish Hospital at Washington University School of Medicine, 216 South Kingshighway Boulevard, St. Louis, MO 63110, USA.
Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6734-8. doi: 10.1073/pnas.120081897.
Protein Z (PZ) is a vitamin K-dependent plasma protein whose function has been uncertain. The structure of PZ is very similar to that of the coagulation-related factors VII, IX, and X and PC, but PZ differs from these other proteins in that it is not the zymogen of a serine protease. We have shown recently that PZ forms a calcium ion-dependent complex with activated factor X at phospholipid surfaces and that this interaction leads to the inhibition of activated factor X activity through, in part, the action of a previously unidentified plasma protein named PZ-dependent protease inhibitor. Herein, we report that the presence of PZ dampens the coagulation response in human plasma and that concomitant PZ deficiency dramatically increases the severity of the prothrombotic phenotype of factor V(Leiden) mice. The results indicate that PZ plays a physiologically important role in the regulation of coagulation.
蛋白Z(PZ)是一种维生素K依赖的血浆蛋白,其功能尚不确定。PZ的结构与凝血相关因子VII、IX、X及蛋白C非常相似,但PZ与这些其他蛋白的不同之处在于它不是丝氨酸蛋白酶的酶原。我们最近发现,PZ在磷脂表面与活化的因子X形成钙离子依赖的复合物,并且这种相互作用部分通过一种先前未鉴定的名为PZ依赖蛋白酶抑制剂的血浆蛋白的作用导致活化因子X活性受到抑制。在此,我们报告PZ的存在会减弱人血浆中的凝血反应,并且PZ伴随缺乏会显著增加因子V(莱顿)小鼠血栓前表型的严重程度。结果表明,PZ在凝血调节中发挥着重要的生理作用。