{"title":"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","authors":"Kazukuni Ichikawa, Manabu Yaguchi, Yoko Tanaka","doi":"10.5466/ijoms.20.87","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":14196,"journal":{"name":"International Journal of Oral-Medical Sciences","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Effect of Porphyromonas gingivalis Augmented Invasion by TNF-α on Gingival Fibroblasts Derived from Down Syndrome\",\"authors\":\"Kazukuni Ichikawa, Manabu Yaguchi, Yoko Tanaka\",\"doi\":\"10.5466/ijoms.20.87\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":14196,\"journal\":{\"name\":\"International Journal of Oral-Medical Sciences\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Oral-Medical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5466/ijoms.20.87\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Oral-Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5466/ijoms.20.87","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.