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作 者:刘景[1] 袁媛[1] LIU Jing;YUAN Yuan(Department of Stomatology,the Fifth Affiliated Hospital of Xinjiang Medical University,Urumqi 830011,China)
机构地区:[1]新疆医科大学第五附属医院口腔科,新疆乌鲁木齐830011
出 处:《口腔医学》2020年第3期198-203,共6页Stomatology
基 金:新疆维吾尔自治区自然科学基金(2016D01C229)。
摘 要:目的探讨柚皮苷(naringin,NRG)对脂多糖诱导的人牙周膜成纤维细胞增殖及炎症因子表达的影响。方法以脂多糖(lipopolysaccharide,LPS)(100μg/mL)诱导人牙周膜成纤维细胞(human periodontal ligament fibroblast,HPDLF)损伤,采用MTT法检测NRG对LPS诱导HPDLF损伤的保护作用,利用ELISA法和Western blotting法检测NRG对LPS诱导的HPDLF中白介素(interleukin,IL)-6、IL-8、IL-1β等炎症因子蛋白表达的影响,同时利用Real-time PCR方法检测NRG对LPS诱导的HPDLF组IL-6、IL-8、IL-1β等炎症因子基因表达的影响。结果经LPS(100μg/mL)刺激后,HPDLF增殖受到抑制,与CON组比较,LPS组细胞存活率显著降低,细胞周期进程受到抑制,差异具有统计学意义(P<0.05);不同浓度的NRG(40,20,10μg/mL)可显著抑制LPS诱导的HPDLF损伤,并可降低细胞内炎症因子表达;与LSP组比较,LPS+NRG 40μg/mL组、LPS+NRG 20μg/mL组、LPS+NRG 10μg/mL组HPDLF存活率显著提升,细胞周期进程加快,抑制IL-6、IL-8、IL-1β蛋白及基因表达水平均显著降低,差异具有统计学意义(P<0.05)。结论NRG对LPS诱导的HPDLF损伤具有保护作用,并可通过抑制LPS诱导的HPDLF中IL-6、IL-8、IL-1β的蛋白及基因表达水平,促进HPDLF增殖。Objective To investigate the effects of naringin(NRG)on the proliferation and expression of inflammatory factors of human periodontal ligament fibroblast(HPDLF)induced by lipopolysaccharide(LPS).Methods HPDLF was induced by lipopolysaccharide(LPS)(100μg/mL).The protective effect of NRG on LPS induced HPDLF injury was detected by MTT assay.The effects of NRG on the expression of IL-6,IL-8,IL-1βand other inflammatory factors in LPS-induced HPDLF were detected by ELISA and Western blotting.The effects of NRG on the expression of IL-6,IL-8 and IL-1βin LPS-induced HPDLF were also detected by Real-time PCR.Results The proliferation of HPDLF was inhibited after stimulation with LPS(100μg/mL).Compared with the CON group,the cell survival rate of LPS group significantly reduced,and the cell cycle process was inhibited.The difference was statistically significant(P<0.05).Different concentrations of NRG(40,20,10μg/mL)could significantly inhibit LPS-induced HPDLF injury and reduce the expression of inflammatory factors in cells(P<0.05).Compared with LSP group,the survival rates of HPDLF in LPS+NRG 40μg/mL group,LPS+NRG 20μg/mL group,LPS+NRG 10μg/mL group increased significantly,the cell cycle process accelerated,and the levels of inhibiting IL-6,IL-8,IL-1βprotein and gene expression decreased significantly.There was significant difference(P<0.05).Conclusion NRG has protective effect on LPS-induced HPDLF injury,and can promote the proliferation of HPDLF cells by inhibiting the expression levels of the protein and genes of IL-6,IL-8,IL-1βin LPS-induced HPDLF.
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