TNF-α增强牙龈卟啉单胞菌侵袭唐氏综合征牙龈成纤维细胞的作用

Kazukuni Ichikawa, Manabu Yaguchi, Yoko Tanaka
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引用次数: 0

摘要

众所周知,唐氏综合征(DS)的牙周病患病率很高。肿瘤坏死因子α (TNF-α)增加了牙龈卟啉单胞菌的侵袭。人牙龈上皮细胞中的牙龈病。我们检测了TNF-α对DS(DGF)患者牙龈成纤维细胞侵袭的影响,以及接种牙龈卟啉卟啉前TNF-α预处理DGF的细胞反应的影响。侵袭实验采用非ds (NGF)和DGF个体的牙龈成纤维细胞,在接种牙龈假单胞菌之前用TNF-α处理。实时荧光定量PCR法检测白细胞介素6(IL-6)和细胞间粘附分子1(ICAM-1) mRNA表达量。免疫印迹法检测接种前TNF-α预处理的NGF和DGF中TNF-α受体(TNFR)I和II蛋白表达、p65核清晰因子-κB(NF-κB)磷酸化和细胞外信号调节激酶(ERK)1/2磷酸化。TNF-α预处理的DGF组侵袭性牙龈假单胞菌数量多于NGF组。接种牙龈假单胞菌前用TNF-α预处理的DGF中IL-6和ICAM-1 mRNA的表达量显著高于NGF。tnf - I、磷酸化p-65 NF-κB和磷酸化ERK1/2的相对信号强度显著高于NGF。我们认为TNF-α预处理的DGF中TNF- I、phospho p65 NF-κB和phospho ERK1/2可能参与了ICMA-1 mRNA表达的增强和牙龈P.感染的发生。这些蛋白与牙龈卟啉卟啉菌的协同作用可能是退行性痴呆患者发生严重牙周病的关键因素。厌氧条件7天。计数菌落,测定侵袭性牙龈假单胞菌在成纤维细胞中的菌落形成单位(colony - forming units, cfu)数量。每个样品进行3次侵袭试验。
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The Effect of Porphyromonas gingivalis Augmented Invasion by TNF-α on Gingival Fibroblasts Derived from Down Syndrome
It is well known the high prevalence periodontal disease in Down syndrome(DS). Tumor necrosis factor alpha(TNF-α)augments invasion of Porphyromonas gingivalis(P. gingivalis)in human gingival epithelial cells. We examined the effect of TNF-α on invasion of P. gingivalis to gingival fibroblasts derived from individuals with DS(DGF)and the influence of the cellular response in DGF pretreated with TNF-α prior to inoculation of P. gingivalis. The invasion assay was performed using gingival fibroblasts derived from individuals with non-DS(NGF)and DGF treated with TNF-α prior to inoculation of P. gingivalis. The mRNA expression of interleukin 6(IL-6)and intercellular adhesion molecule 1(ICAM-1)were quantified using real time PCR. Furthermore, the protein expressions of TNF-α receptor(TNFR)I and II, and phosphorylation of p65 nu-clear factor-κB(NF-κB)and phosphorylation of extracellular signal-regulated kinase (ERK)1/2 were also performed in NGF and DGF pretreated with TNF-α prior to inoculation of P. gingivalis by Western blotting. The number of invasive P. gingivalis in TNF-α pretreated DGF was more than that in NGF. IL-6 and ICAM-1 mRNA expressions in DGF pretreated with TNF-α prior to inoculation of P. gingivalis were significantly higher than those in NGF. The relative signal intensity of TNFR I, phospho p-65 NF-κB, and phospho ERK1/2 were significantly higher than those in NGF. It was considered that TNFR I, phospho p65 NF-κB, and phospho ERK1/2 in DGF pretreated with TNF-α may contribute to enhancement of ICMA-1 mRNA expression and the infection of P. gingivalis. The collaboration of these protein and P. gingivalis may be a key factor for development of severe periodontal disease in DS. anaerobic conditions for 7 days. The colonies were count-ed to determine the number of colony - forming units (CFUs)of invasive P. gingivalis in fibroblast cells. Inva sion assays were performed 3 times for each sample.
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