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作 者:王贵玲[1] 杨谛[1] 郭佳杰[1] 于雅琼[1] 仇丽鸿[1]
机构地区:[1]中国医科大学口腔医学院牙体牙髓病科,辽宁省口腔疾病重点实验室,辽宁沈阳110002
出 处:《口腔医学研究》2017年第11期1139-1142,共4页Journal of Oral Science Research
基 金:国家自然科学基金(编号:81500843);沈阳市科学技术项目计划(编号:F15-199-1-56)
摘 要:目的:探究microRNA 34a-5p(miR-34a-5p)对成骨细胞炎症反应及分化的调节作用,并初步探究其相关机制。方法:脂质体法瞬时转染人成骨样细胞系MG63使细胞中miR-34a-5p表达增强,同时设通用阴性对照(NC)组。牙髓卟啉单胞菌(Porphyromonas endodontalis,P.e)来源的不同浓度脂多糖(lipopolysaccharide,LPS)作用于MG63后,检测细胞内miR-34a-5p表达;取20mg/L P.e-LPS作用24h后,检测细胞内IL-6表达。成骨诱导48h后,检测细胞中成骨分化标志物以及Notch1受体的表达。结果:P.e-LPS作用于MG63细胞后,miR-34a-5p表达被抑制(P<0.05)。MiR-34a-5p转染细胞后,与NC组相比,细胞内IL-6表达减少(P<0.01);20mg/L P.e-LPS作用下,miR-34a-5p组IL-6表达较NC组下降更为明显(P<0.01)。成骨细胞诱导分化48h后,miR-34a-5p组中分化标志物表达较NC对照组均显著增加(P<0.05),而Notch1受体表达被抑制(P<0.05)。结论:MiR-34a-5p可能通过Notch1信号通路,发挥抑制成骨细胞炎症和促进成骨分化的作用。Objective:To investigate the effect of microRNA 34 a-5 p(miR-34 a-5 p)on the inflammation and differentiation of osteoblasts.Methods:MG63 was transfected with miR-34 a-5 p mimics to ensure a higher expression than general negative control(NC).Expression of miR-34 a-5 p was detected after MG63 was stimulated by different concentrations of lipopolysaccharide(LPS)from porphyromonas endodontalis(P.e).Transfected cells were stimulated by 20 mg/L P.e-LPS for 24 h,and expression of IL-6 was detected.Expressions of osteogenic differentiation markers and Notch1 were detected after osteogenic induction for 48 h.Results:Expression of miR-34 a-5 p in MG63 was down-regulated by P.e-LPS with different concentrations(P0.05).MiR-34 a-5 p inhibited the expression of IL-6 significantly both with and without the stimulation of P.e-LPS(P0.01).Osteogenic makers in MG63 were promoted by miR-34 a-5 p(P 0.05)and Notch1 was down-regulated(P0.05).Conclusion:MiR-34 a-5 p inhibits the inflammation and promotes the differentiation of osteoblast,and Notch1 may serve as a target during the process.
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