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Interactions between Periodontal Bacteria and Human Oral Epithelial Cells: Fusobacterium nucleatum Adheres to and Invades Epithelial Cells

机译:牙周细菌和人类口腔上皮细胞之间的相互作用:核梭菌粘附并侵袭上皮细胞

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Bacteria are causative agents of periodontal diseases. Interactions between oral bacteria and gingival epithelial cells are essential aspects of periodontal infections. Using an in vitro tissue culture model, a selected group of gram-negative anaerobic bacteria frequently associated with periodontal diseases, includingBacteroides forsythus, Campylobacter curvus,Eikenella corrodens, Fusobacterium nucleatum,Porphyromonas gingivalis, and Prevotella intermedia, were examined for their ability to adhere to and invade primary cultures of human gingival epithelial cells (HGEC). The effects of these bacteria on the production of interleukin-8 (IL-8), a proinflammatory chemokine, were also measured. These studies provided an initial demonstration that F. nucleatum adhered to and invaded HGEC and that this was accompanied by high levels of IL-8 secretion from the epithelial cells. The attachment and invasion characteristics of F. nucleatumwere also tested using KB cells, an oral epithelial cell line. The invasion was verified by transmission electron microscopy and with metabolic inhibitors. Invasion appeared to occur via a “zipping” mechanism and required the involvement of actins, microtubules, signal transduction, protein synthesis, and energy metabolism of the epithelial cell, as well as protein synthesis by F. nucleatum. A spontaneous mutant, lam, of F. nucleatum, isolated as defective in autoagglutination, was unable to attach to or invade HGEC or KB cells, further indicating the requirement of bacterial components in these processes. Sugar inhibition assays indicated that lectin-like interactions were involved in the attachment of F. nucleatum to KB cells. Investigation of these new virulence phenotypes should improve our understanding of the role of F. nucleatum in periodontal infections.
机译:细菌是牙周疾病的病原体。口腔细菌和牙龈上皮细胞之间的相互作用是牙周感染的重要方面。使用体外组织培养模型,检查了一组与牙周疾病经常相关的革兰氏阴性厌氧细菌,包括连翘杆菌,弯曲杆菌,弯曲杆菌,核梭菌,牙龈卟啉单胞菌和中间普氏杆菌,它们的粘附能力并侵袭人类牙龈上皮细胞(HGEC)的原代培养。还测量了这些细菌对促炎性趋化因子白细胞介素8(IL-8)产生的影响。这些研究提供了最初的证明,即核镰刀菌粘附并侵袭了HGEC,并伴随着上皮细胞IL-8的高水平分泌。还使用KB细胞(一种口腔上皮细胞系)测试了核果镰刀菌的附着和侵袭特性。通过透射电子显微镜和代谢抑制剂验证了侵袭。入侵似乎是通过“拉锁”机制发生的,需要肌动蛋白,微管,信号转导,蛋白质合成和上皮细胞的能量代谢以及核镰刀菌的蛋白质合成参与。由于自凝集缺陷而分离出的自发核镰刀菌的自发突变体lam无法附着或侵袭HGEC或KB细胞,进一步表明在这些过程中需要细菌成分。糖抑制试验表明,凝集素样相互作用参与了F. nucleatum与KB细胞的附着。这些新的毒力表型的调查应增进我们对核仁镰刀菌在牙周感染中的作用的了解。

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