Porphyromonas gingivalis mediates the shedding and proteolysis of complement regulatory protein CD46 expressed by oral epithelial cells.

H Mahtout, F Chandad, J M Rojo, D Grenier
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引用次数: 29

Abstract

Introduction: Human cells express membrane-bound complement regulatory proteins to prevent complement-mediated autologous tissue damage. In this study, we hypothesized that Porphyromonas gingivalis, the major etiological agent of chronic periodontitis, causes the shedding or proteolysis of the complement regulatory protein CD46 expressed by oral epithelial cells.

Methods: Oral epithelial cells were treated with a culture of P. gingivalis before measurement of membrane-bound and shed CD46 by enzyme-linked immunosorbent assay (ELISA). The effect of soluble recombinant CD46 on secretion of interleukin-8 (IL-8) by epithelial cells was evaluated by ELISA. The susceptibility of soluble recombinant CD46 to proteolytic degradation by cells and purified Lys-gingipain of P. gingivalis was investigated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis/western immunoblotting analysis.

Results: Oral epithelial cells treated with a culture of P. gingivalis showed a lower reactivity with antibodies directed to CD46. ELISA revealed that such a treatment resulted in increased amounts of CD46 in the conditioned media suggesting that P. gingivalis caused the shedding of membrane-anchored CD46. Stimulation of epithelial cells with soluble recombinant CD46 induced IL-8 secretion in a dose-dependent manner. Whole cells and purified Lys-gingipain of P. gingivalis degraded recombinant CD46 in a dose-dependent manner.

Conclusion: This study showed the ability of P. gingivalis to induce the shedding/ proteolysis of CD46 from the surface of oral epithelial cells. This may render host cells susceptible to the complement system and contribute to tissue damage and the inflammatory process in periodontitis.

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牙龈卟啉单胞菌介导口腔上皮细胞表达的补体调节蛋白CD46的脱落和蛋白水解。
人类细胞表达膜结合补体调节蛋白以防止补体介导的自体组织损伤。在本研究中,我们假设慢性牙周炎的主要病原牙龈卟啉单胞菌引起口腔上皮细胞表达的补体调节蛋白CD46的脱落或蛋白水解。方法:用牙龈假单胞菌培养处理口腔上皮细胞,然后用酶联免疫吸附试验(ELISA)检测膜结合CD46和脱落CD46。ELISA法检测可溶性重组CD46对上皮细胞分泌白细胞介素-8 (IL-8)的影响。采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳/免疫印迹法研究了可溶性重组CD46对牙龈卟啉菌蛋白水解降解的敏感性。结果:牙龈假单胞菌培养的口腔上皮细胞对CD46抗体的反应性较低。ELISA结果显示,这种处理导致条件培养基中CD46的量增加,表明牙龈卟啉卟啉菌引起膜锚定CD46的脱落。可溶性重组CD46刺激上皮细胞以剂量依赖性方式诱导IL-8分泌。全细胞和纯化的ys-gingipain以剂量依赖的方式降解重组CD46。结论:本研究表明牙龈假单胞菌具有诱导口腔上皮细胞表面CD46脱落/蛋白水解的能力。这可能使宿主细胞易受补体系统的影响,并导致牙周炎的组织损伤和炎症过程。
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Distribution and hydrolytic enzyme characteristics of Candida albicans strains isolated from diabetic patients and their non-diabetic consorts. Automutanolysin disrupts clinical isolates of cariogenic streptococci in biofilms and planktonic cells. Scavenger receptor A is expressed by macrophages in response to Porphyromonas gingivalis, and participates in TNF-alpha expression. Helicobacter pylori in the oral cavity is associated with gastroesophageal disease. Progression of chronic periodontitis can be predicted by the levels of Porphyromonas gingivalis and Treponema denticola in subgingival plaque.
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