Vernier A, Diab M, Soell M, Haan-Archipoff G, Beretz A, Wachsmann D, Klein J P
Faculté de Pharmacie, Institut National de la Santé et de la Recherche Médicale Unité 392, Illkirch, France.
Infect Immun. 1996 Aug;64(8):3016-22. doi: 10.1128/iai.64.8.3016-3022.1996.
In order to examine the possible implication of human epithelial and endothelial cells in the pathogenesis of various diseases associated with oral viridans streptococci, we tested the immunomodulatory effects of 11 representative strains of oral viridans streptococci on human epithelial KB cells and endothelial cells. We then examined the possible role of two major adhesins from oral viridans streptococci, protein I/II and rhamnose-glucose polymers (RGPs), in this process. In this study we demonstrate that oral viridans streptococci are potent stimulators of interleukin-8 (IL-8) production from KB cells and of IL-6 and IL-8 production from endothelial cells. The ability of protein I/II and RGPs to contribute to these effects was then examined. Using biotinylated protein I/IIf and RGPs from Streptococcus mutans OMZ 175, we showed that these adhesins bind to KB and endothelial cells through specific interactions and that the binding of these molecules initiates the release of IL-8 from KB cells and of IL-6 and IL-8 from endothelial cells. These results suggest that protein I/IIf and RGPs play an important role in the interactions between bacteria and KB and endothelial cells in that similar cytokine profiles are obtained when cells are stimulated with bacteria or surface components. We also provide evidence that protein I/IIf binds to and stimulates KB and endothelial cells through lectin interactions and that N-acetyl neuraminic acid (NANA) and fucose present on cell surface glycoproteins may form the recognition site since binding and cytokine release can be inhibited by dispase and periodate treatment of cells and by NANA and fucose. These results demonstrate that oral viridans streptococci, probably by engaging two cell surface adhesins, exert immunomodulatory effects on human KB and endothelial cells.
为了研究人类上皮细胞和内皮细胞在与口腔草绿色链球菌相关的各种疾病发病机制中的潜在作用,我们测试了11种具有代表性的口腔草绿色链球菌菌株对人类上皮KB细胞和内皮细胞的免疫调节作用。然后,我们研究了口腔草绿色链球菌的两种主要黏附素,即蛋白I/II和鼠李糖 - 葡萄糖聚合物(RGPs)在此过程中的可能作用。在本研究中,我们证明口腔草绿色链球菌是KB细胞产生白细胞介素 - 8(IL - 8)以及内皮细胞产生IL - 6和IL - 8的强效刺激物。随后研究了蛋白I/II和RGPs促成这些作用的能力。使用来自变形链球菌OMZ 175的生物素化蛋白I/II和RGPs,我们表明这些黏附素通过特异性相互作用与KB细胞和内皮细胞结合,并且这些分子的结合引发了KB细胞释放IL - 8以及内皮细胞释放IL - 6和IL - 8。这些结果表明,蛋白I/II和RGPs在细菌与KB细胞和内皮细胞的相互作用中起重要作用,因为用细菌或表面成分刺激细胞时可获得相似的细胞因子谱。我们还提供证据表明,蛋白I/II通过凝集素相互作用与KB细胞和内皮细胞结合并刺激它们,并且细胞表面糖蛋白上存在的N - 乙酰神经氨酸(NANA)和岩藻糖可能形成识别位点,因为细胞经分散酶和高碘酸盐处理以及用NANA和岩藻糖处理后,结合和细胞因子释放可被抑制。这些结果表明,口腔草绿色链球菌可能通过结合两种细胞表面黏附素,对人类KB细胞和内皮细胞发挥免疫调节作用。