Sealey J E, Atlas S A, Laragh J H, Silverberg M, Kaplan A P
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5914-8. doi: 10.1073/pnas.76.11.5914.
Plasma prorenin is an inactive form of renin (EC 3.4.99.19) that can be converted to active renin in acid-treated plasma by an endogenous serine protease that is active at alkaline pH (alkaline phase activation). To identify this enzyme we first tested the ability of Hageman factor fragments, plasma kallikrein (EC 3.4.21.8), and plasmin (EC 3.4.21.7) to activate prorenin in acid-treated plasma. All three enzymes initiated prorenin activation; 50% activation was achieved with Hageman factor fragments at 1 microgram/ml, plasma kallikrein at 2-4 microgram/ml, or plasmin at 5-10 microgram/ml. We then showed that the alkaline phase of acid activation occurred normally in plasminogen-free plasma but was almost completely absent in plasmas deficient in either Hageman factor or prekallikrein; alkaline phase activation was restored to these latter plasmas when equal parts were mixed together. Therefore, both Hageman factor and prekallikrein were required for alkaline phase activation to occur. We then found that, although plasma kallikrein could activate prorenin in plasma deficient in either Hageman factor or prekallikrein, Hageman factor fragments were unable to activate prorenin in prekallikrein-deficient plasma. These studies demonstrate that alkaline phase prorenin activation is initiated by Hageman factor-dependent conversion of prekallikrein to kallikrein which, in turn, leads to activation of prorenin. In this fashion, we have revealed a possible link between the coagulation-kinin pathway and the renin-angiotensin system.
血浆肾素原是肾素(EC 3.4.99.19)的无活性形式,在酸性处理的血浆中可被一种在碱性pH下具有活性的内源性丝氨酸蛋白酶转化为活性肾素(碱性相激活)。为了鉴定这种酶,我们首先测试了Hageman因子片段、血浆激肽释放酶(EC 3.4.21.8)和纤溶酶(EC 3.4.21.7)在酸性处理的血浆中激活肾素原的能力。这三种酶均启动了肾素原的激活;当Hageman因子片段浓度为1微克/毫升、血浆激肽释放酶浓度为2 - 4微克/毫升或纤溶酶浓度为5 - 10微克/毫升时,可实现50%的激活。然后我们发现,酸性激活的碱性相在无纤溶酶原的血浆中正常发生,但在缺乏Hageman因子或前激肽释放酶的血浆中几乎完全不存在;当将等量的后两种血浆混合在一起时,碱性相激活恢复。因此,碱性相激活的发生需要Hageman因子和前激肽释放酶两者。然后我们发现,虽然血浆激肽释放酶可在缺乏Hageman因子或前激肽释放酶的血浆中激活肾素原,但Hageman因子片段在缺乏前激肽释放酶的血浆中无法激活肾素原。这些研究表明,碱性相肾素原激活是由Hageman因子依赖性地将前激肽释放酶转化为激肽释放酶引发的,进而导致肾素原的激活。通过这种方式,我们揭示了凝血 - 激肽途径与肾素 - 血管紧张素系统之间可能的联系。