Shimada T, Sugo T, Kato H, Iwanaga S
Adv Exp Med Biol. 1983;156:73-85.
We have shown that bovine HMW kininogen remarkably accelerates the activation of Factor XII and prekallikrein in the presence of kaolin, adsorbing on kaolin through the fragment 1.2 region and forming a complex with prekallikrein through the light chain region (Sugo et al., 1980; Ikari et al., 1981). The present study was undertaken to examine the role of HMW kininogen in the activation of Factor XII and prekallikrein with other negatively-charged surfaces. The activation system used here was as follows; (1) Activation of prekallikrein by Factor XII, (2) Activation of Factor XII by plasma kallikrein and (3) Activation of prekallikrein by Factor XIIa. Among a variety of foreign surfaces, amylose sulfate and sulfatide were the most efficient in the activation reaction of Factor XII and prekallikrein. Bovene HMW kininogen accelerated all the three reactions triggered by these surfaces. However, the accelerating effect of HMW kininogen on the activation of Factor XII by plasma kallikrein was very weak, when amylose sulfate or sulfatide was used as surface. The three reactions were highly dependent on the amounts of HMW kininogen and surfaces contained in the reaction mixtures. Excess amount of them inhibited these reactions. Among the various fragments, which were prepared from HMW kininogen digests with plasma and urinary kallikreins (Sugo et al., 1980), a large fragment consisting of fragment 1.2 and light chain accelerated the reactions. Thus both fragment 1.2 and the light chain region in HMW kininogen were essential for these activation reactions.
我们已经表明,牛高分子量激肽原在高岭土存在的情况下能显著加速因子XII和前激肽释放酶的激活,它通过1.2片段区域吸附在高岭土上,并通过轻链区域与前激肽释放酶形成复合物(须古等人,1980年;伊卡里等人,1981年)。本研究旨在探讨高分子量激肽原在因子XII和前激肽释放酶被其他带负电荷表面激活过程中的作用。这里使用的激活系统如下:(1)因子XII激活前激肽释放酶;(2)血浆激肽释放酶激活因子XII;(3)因子XIIa激活前激肽释放酶。在各种外来表面中,硫酸直链淀粉和硫苷脂在因子XII和前激肽释放酶的激活反应中效率最高。牛高分子量激肽原加速了由这些表面引发的所有三种反应。然而,当使用硫酸直链淀粉或硫苷脂作为表面时,高分子量激肽原对血浆激肽释放酶激活因子XII的加速作用非常弱。这三种反应高度依赖于反应混合物中高分子量激肽原和表面的量。它们的过量会抑制这些反应。在用血浆和尿激肽释放酶对高分子量激肽原进行消化制备的各种片段中(须古等人,1980年),一个由1.2片段和轻链组成的大片段加速了这些反应。因此,高分子量激肽原中的1.2片段和轻链区域对于这些激活反应都是必不可少的。