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作 者:叶珊 方蛟[1] 李雪[1] 张一迪 丁鑫鑫 齐曼霖 王鹞 周延民[1] YE Shan;FANG Jiao;LI Xue;ZHANG Yi-di;DING Xin-xin;QI Man-lin;WANG Yao;ZHOU Yan-min(Department of Dental Implantology,Hospital of Stomatology,Jilin University&Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling,Changchun 130021,China)
机构地区:[1]吉林大学口腔医院口腔种植科,吉林省牙发育及颌骨重塑与再生重点实验室,吉林长春130021
出 处:《中国实用口腔科杂志》2020年第5期277-283,共7页Chinese Journal of Practical Stomatology
基 金:国家自然科学基金(81570983)。
摘 要:目的研究槲皮素对牙龈卟啉单胞菌脂多糖(Porphyromonas gingivalis lipopolysaccharide,P.g LPS)刺激的人牙龈成纤维细胞(human gingival fibroblasts,HGFs)生物学行为的影响。方法采用DNA片段凝胶电泳、CCK-8法、细胞划痕法观察不同浓度槲皮素(10、20、50、100μmol/L)对体外培养HGFs的毒性作用,以及对HGFs增殖与迁移的影响。采用P.g LPS刺激HGFs来建立体外炎症刺激模型,通过流式细胞术、细胞活性氧(reactive oxygen species,ROS)检测、酶联免疫吸附试验(ELISA)和实时荧光定量PCR(qRT-PCR)进一步观察槲皮素对HGFs凋亡、ROS的产生及肿瘤坏死因子-α(tumor necrosis factorα,TNF-α)和前列腺素E2(prostaglandin E2,PGE2)表达的影响。结果槲皮素对HGFs无毒性作用,且对HGFs的增殖无影响(P>0.05)。各组细胞迁移率总的比较,差异有统计学意义(F=9.973,P<0.05),在处理48 h后,20μmol/L槲皮素处理组细胞迁移率大于10、50μmol/L槲皮素处理组以及对照组,差异均有统计学意义(均P<0.05)。槲皮素对P.g LPS刺激的HGFs凋亡具有抑制作用,且其能够抑制并预防P.g LPS刺激的HGFs中ROS相对产生量增加现象(均P<0.05)。槲皮素处理显著抑制了P.g LPS诱导的TNF-α表达增加现象(P<0.05),而槲皮素处理组PGE2的表达水平与对照组比较,差异无统计学意义(P>0.05)。结论浓度为20μmol/L的槲皮素能够促进体外培养HGFs的迁移,且具有抗氧化、抗炎保护作用。Objective To study the effects of quercetin on the biological behavior of human gingival fibroblasts(HGFs)stimulated by Porphyromonas gingivalis lipopolysaccharide(P.g LPS).Methods DNA fragment electrophoresis,CCK-8 and wound healing method were used to observe the effect of different concentrations(10,20,50,100μmol/L)of quercetin on cell toxicity,cell proliferation,and cell migration of HGFs.Then we further stimulated HGFs with P.g LPS to create an in vitro inflammatory model;by applying flow cytometry,reactive oxygen species(ROS)test,enzyme-linked immunosorbent assay(ELISA)and realtime quantitative PCR(qRT-PCR),we tested the influence of quercetin on cell apoptosis and ROS production,as well as on TNF-αand PGE2 expression.Results No toxic effect or proliferation influence of quercetin was observed on HGFs(P>0.05).There was a significant difference in overall cell migration rate among each group(F=9.973,P<0.05).After 48 h of treatment,the group with quercetin at 20μmol/L showed higher cell migration rate than the 10,50μmol/L-quercetin treatment group and control group(P<0.05).Quercetin inhibited HGFs apoptosis stimulated by P.g LPS.Quercetin treatment could prevent and also inhibit the relative increase of ROS in HGFs induced by P.g LPS(P<0.05).Quercetin significantly inhibited the increased expression of TNF-αstimulated by P.g LPS(P<0.05);however,no significant difference in the expression of PGE2 was found between quercetin treatment group and control group(P>0.05).Conclusion Quercetin at 20μmol/L can promote in vitro HGFs cell migration and has anti-oxidative and anti-inflammatory protective effects.
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