Scott C F, Schapira M, James H L, Cohen A B, Colman R W
J Clin Invest. 1982 Apr;69(4):844-52. doi: 10.1172/jci110524.
Factor XIa is a plasma protease that, by activating Factor IX, plays an important role in the early phase of the intrinsic pathway of blood coagulation. Four plasma protease inhibitors, alpha(1)-protease inhibitor, antithrombin III, C1-inhibitor, and alpha(2)-plasmin inhibitor, have been reported to inactivate human Factor XIa, but their quantitative contribution to the inactivation of Factor XIa in plasma has not been fully assessed. Using purified systems, we observed that the second-order rate constants for the reaction of Factor XIa with alpha(1)-protease inhibitor, antithrombin III, and CI-inhibitor were 4.08, 10, and 14.6 M(-1) min(-1) x 10(3), respectively. The pseudo-first-order rate constants, at plasma concentration of the inhibitors, were 1.86 x 10(-1), 4.68 x 10(-2), and 2.4 x 10(-2) min(-1), respectively. These kinetic data predict that alpha(1)-protease inhibitor should account for 68%, antithrombin III for 16%, and C1-inhibitor and the equipotent alpha(2)-plasmin inhibitor each for 8% of the total inhibitory activity of plasma against Factor XIa. The rate of inactivation of Factor XIa in various plasma samples specifically deficient in inhibitors was consistent with these predictions. Factor XI, the zymogen form of Factor XIa, circulates in plasma associated with the contact system cofactor, high molecular weight kininogen (HMW kininogen). Kinetic analysis indicated the existence of a reversible bimolecular Factor XIa-HMW kininogen complex with a dissociation constant (K(d)) = 0.17 muM. The light chain derived from HMW kininogen decreased the inactivation rate of Factor XIa by C1-inhibitor with a K(d) of 0.08 muM for a complex of Factor XIa and the light chain derived from HMW kininogen. The protective effect of HMW kininogen was confirmed by the finding that the inactivation rate of Factor XIa in kininogen-deficient plasma was increased over normal plasma. The present study confirms that alpha(1)-protease inhibitor is the major inhibitor of Factor XIa in plasma, and that the formation of a reversible complex between Factor XIa and HMW kininogen decreases the rate of inactivation of the enzyme by its inhibitors.
凝血因子 XIa 是一种血浆蛋白酶,通过激活凝血因子 IX,在血液凝固内源性途径的早期阶段发挥重要作用。据报道,四种血浆蛋白酶抑制剂,即α(1)-蛋白酶抑制剂、抗凝血酶 III、C1 抑制剂和α(2)-纤溶酶抑制剂,可使人类凝血因子 XIa 失活,但它们对血浆中凝血因子 XIa 失活的定量贡献尚未得到充分评估。使用纯化系统,我们观察到凝血因子 XIa 与α(1)-蛋白酶抑制剂、抗凝血酶 III 和 C1 抑制剂反应的二级速率常数分别为 4.08、10 和 14.6 M(-1) min(-1)×10(3)。在抑制剂的血浆浓度下,伪一级速率常数分别为 1.86×10(-1)、4.68×10(-2) 和 2.4×10(-2) min(-1)。这些动力学数据预测,α(1)-蛋白酶抑制剂应占血浆对凝血因子 XIa 总抑制活性的 68%,抗凝血酶 III 占 16%,C1 抑制剂和等效的α(2)-纤溶酶抑制剂各占 8%。在各种特异性缺乏抑制剂的血浆样本中,凝血因子 XIa 的失活速率与这些预测一致。凝血因子 XIa 的酶原形式凝血因子 XI 在血浆中与接触系统辅因子高分子量激肽原 (HMW 激肽原) 结合循环。动力学分析表明存在一种可逆的双分子凝血因子 XIa-HMW 激肽原复合物,其解离常数 (K(d)) = 0.17 μM。源自 HMW 激肽原的轻链降低了 C1 抑制剂对凝血因子 XIa 的失活速率,对于凝血因子 XIa 与源自 HMW 激肽原的轻链的复合物,其 K(d) 为 0.08 μM。激肽原缺乏血浆中凝血因子 XIa 的失活速率高于正常血浆,这一发现证实了 HMW 激肽原的保护作用。本研究证实,α(1)-蛋白酶抑制剂是血浆中凝血因子 XIa 的主要抑制剂,并且凝血因子 XIa 与 HMW 激肽原之间形成可逆复合物会降低其抑制剂对该酶的失活速率。