Johnson C M
Department of Pediatrics, Mayo Clinic/Foundation, Rochester, MN 55905.
J Lab Clin Med. 1993 May;121(5):675-82.
Binding of Staphylococcus aureus to vascular endothelial cells may be an initiating event in the pathogenesis of endovascular infection, particularly infective endocarditis. In this study a competition assay between labeled and unlabeled bacteria was used to identify potential S. aureus-binding determinants on the surface of cultured porcine aortic valve endothelial cells. Concanavalin A inhibited 30% to 40% of the specific binding of S. aureus to membrane-associated components. Concanavalin A affinity chromatography of radiolabeled cell-surface proteins, followed by isolation of S. aureus-binding proteins, identified a 130,000-molecular-weight cell surface protein that may function as an endothelial cell S. aureus receptor. These data suggest that specific binding of S. aureus to cardiac valve endothelial cells is mediated in part by a 130 kd mannose-containing glycoprotein.
金黄色葡萄球菌与血管内皮细胞的结合可能是血管内感染,尤其是感染性心内膜炎发病机制中的起始事件。在本研究中,采用标记菌与未标记菌之间的竞争试验来鉴定培养的猪主动脉瓣内皮细胞表面潜在的金黄色葡萄球菌结合决定簇。伴刀豆球蛋白A抑制了金黄色葡萄球菌与膜相关成分特异性结合的30%至40%。对放射性标记的细胞表面蛋白进行伴刀豆球蛋白A亲和层析,随后分离出金黄色葡萄球菌结合蛋白,鉴定出一种分子量为130,000的细胞表面蛋白,其可能作为内皮细胞金黄色葡萄球菌受体发挥作用。这些数据表明,金黄色葡萄球菌与心脏瓣膜内皮细胞的特异性结合部分是由一种130kd含甘露糖的糖蛋白介导的。