{"title":"Resolvin D1 Regulates Porphyromonas Gingivalis Lipopolysaccharide-induced Del-1 and Cytokine Expressions in Human Gingival Fibroblasts","authors":"S. Bozkurt, S. Hakki","doi":"10.30621/jbachs.1141356","DOIUrl":null,"url":null,"abstract":"Purpose: To detect the effect of Resolvin D1 (RvD1) on Developmental endothelial locus-1 (Del-1) and cytokine expressions of human gingival fibroblast cells exposed to Porphyromonas gingivalis lipopolysaccharide (P. gingivalis-LPS). \n \nMaterial and Methods: The effect of RvD1 on cell viability of human gingival fibroblasts exposed to P. gingivalis-LPS were determined by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Meanwhile, the effect of RvE1 on Del-1 and cytokine (IL-1β, IL-6, IL-8, IL-10, IL-17) expressions of human gingival fibroblasts exposed to P. gingivalis-LPS were studied by real-time PCR experiment, statistical analysis was performed using GraphPad Prism version 5 for Windows. \n \nResults: Cell viability assay results demonstrated that RvD1 concentrations upregulated cell number compared to control group at 24 and at 72 hours. While RvD1 reduced IL-6, IL-8, IL-17 mRNA expression, IL-10 and Del-1 mRNA expression increased as a time- and dose-dependent manner. Also, IL-1β was not affected by RvD1 treatments. \n \nConclusion: The increased expression of Del-1 and IL-10 by RvD1 down-regulated the pro-inflammatory cytokine expressions induced by P. gingivalis-LPS in gingival fibroblast. RvD1 displayed regulatory effects on gingival inflammation in P. gingivalis LPS-induced cell culture experiment. In particular, results of study display that Del-1 induced by RvD1 may have therapeutic potential to modulate periodontal inflammation.","PeriodicalId":40972,"journal":{"name":"Journal of Basic and Clinical Health Sciences","volume":" ","pages":""},"PeriodicalIF":0.3000,"publicationDate":"2023-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Basic and Clinical Health Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30621/jbachs.1141356","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: To detect the effect of Resolvin D1 (RvD1) on Developmental endothelial locus-1 (Del-1) and cytokine expressions of human gingival fibroblast cells exposed to Porphyromonas gingivalis lipopolysaccharide (P. gingivalis-LPS).
Material and Methods: The effect of RvD1 on cell viability of human gingival fibroblasts exposed to P. gingivalis-LPS were determined by MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay. Meanwhile, the effect of RvE1 on Del-1 and cytokine (IL-1β, IL-6, IL-8, IL-10, IL-17) expressions of human gingival fibroblasts exposed to P. gingivalis-LPS were studied by real-time PCR experiment, statistical analysis was performed using GraphPad Prism version 5 for Windows.
Results: Cell viability assay results demonstrated that RvD1 concentrations upregulated cell number compared to control group at 24 and at 72 hours. While RvD1 reduced IL-6, IL-8, IL-17 mRNA expression, IL-10 and Del-1 mRNA expression increased as a time- and dose-dependent manner. Also, IL-1β was not affected by RvD1 treatments.
Conclusion: The increased expression of Del-1 and IL-10 by RvD1 down-regulated the pro-inflammatory cytokine expressions induced by P. gingivalis-LPS in gingival fibroblast. RvD1 displayed regulatory effects on gingival inflammation in P. gingivalis LPS-induced cell culture experiment. In particular, results of study display that Del-1 induced by RvD1 may have therapeutic potential to modulate periodontal inflammation.
目的:检测溶溶蛋白D1(RvD1)对牙龈卟啉单胞菌脂多糖(P.gingivalis LPS)作用下人牙龈成纤维细胞发育内皮细胞-1(Del-1)和细胞因子表达的影响。材料和方法:采用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑啉)法测定RvD1对牙龈卟啉单胞菌LPS暴露的人牙龈成纤维细胞活力的影响。同时,通过实时PCR实验研究RvE1对暴露于牙龈卟啉单胞菌LPS的人牙龈成纤维细胞Del-1和细胞因子(IL-1β、IL-6、IL-8、IL-10、IL-17)表达的影响,并使用GraphPad Prism version 5 for Windows进行统计分析。结果:细胞活力测定结果表明,与对照组相比,RvD1浓度在24小时和72小时上调了细胞数量。RvD1降低IL-6、IL-8、IL-17mRNA表达,IL-10和Del-1mRNA表达呈时间和剂量依赖性增加。此外,IL-1β不受RvD1治疗的影响。结论:RvD1增加Del-1和IL-10的表达下调了牙龈卟啉单胞菌LPS诱导的牙龈成纤维细胞中促炎细胞因子的表达。在牙龈卟啉单胞菌LPS诱导的细胞培养实验中,RvD1对牙龈炎症具有调节作用。特别地,研究结果显示RvD1诱导的Del-1可能具有调节牙周炎症的治疗潜力。