Ben Nasr A, Herwald H, Sjöbring U, Renné T, Müller-Esterl W, Björck L
Department of Cell and Molecular Biology, Section for Molecular Pathogenesis, Lund University, P.O. Box 94, S-221 00 Lund, Sweden.
Biochem J. 1997 Sep 15;326 ( Pt 3)(Pt 3):657-60.
H-kininogen (high-molecular-mass kininogen, HK) is the precursor of the vasoactive peptide hormone bradykinin (BK). Previous work has demonstrated that HK binds to Streptococcus pyogenes through M-proteins, fibrous surface proteins and important virulence factors of these bacteria. Here we find that M-protein-expressing bacteria absorb HK from human plasma. The HK bound to the bacteria was found to be cleaved, and analysis of the degradation pattern suggested that the cleavage of HK at the bacterial surface is associated with the release of BK. Moreover, addition of activated plasma prekallikrein to bacteria preincubated with human plasma, resulted in BK release. This mechanism, by which a potent vasoactive and proinflammatory peptide is generated at the site of infection, should influence the host-parasite relationship during S. pyogenes infections.
H-激肽原(高分子量激肽原,HK)是血管活性肽激素缓激肽(BK)的前体。先前的研究表明,HK通过M蛋白、纤维表面蛋白以及这些细菌的重要毒力因子与化脓性链球菌结合。在此我们发现,表达M蛋白的细菌会从人血浆中吸收HK。我们发现结合在细菌上的HK会被裂解,对降解模式的分析表明,HK在细菌表面的裂解与BK的释放有关。此外,向预先与人血浆孵育的细菌中添加活化的血浆前激肽释放酶会导致BK释放。在感染部位产生一种强效血管活性和促炎肽的这一机制,应该会在化脓性链球菌感染期间影响宿主与病原体的关系。