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机构地区:[1]山西医科大学口腔医学系,山西太原030001
出 处:《口腔医学研究》2017年第11期1181-1184,共4页Journal of Oral Science Research
基 金:山西省科技攻关项目(编号:20150313010-3);山西医科大学校科技创新基金项目(编号:02101313);山西医科大学博士启动基金项目(编号:03201321)
摘 要:目的:使用小干扰RNA(small interfering RNA,siRNA)沉默人牙周膜成纤维细胞(human periodontal ligament cell,hPDLC)肿瘤坏死因子受体相关因子6(tumor necrosis factor receptor associated factor 6,TRAF6)的基因,观察沉默TRAF6基因对LPS刺激的hPDLC成骨分化的影响。方法:实验分为空白对照组、转染试剂组、TRAF6siRNA组、control siRNA组,采用脂质体法将TRAF6siRNA、control siRNA分别瞬时转染入对应组中,设转染试剂组加入等量的转染试剂,空白对照组不做处理,再使用10 mg/L LPS刺激细胞,RT-PCR、Western blot检测转染后TRAF6的基因及蛋白表达水平,使用LPS+成骨诱导液培养细胞,碱性磷酸酶检测试剂盒检测碱性磷酸酶的活性,RT-PCR检测Runx-2和I型胶原蛋白(Col-I)基因表达情况。结果:TRAF6siRNA组的TRAF6mRNA和蛋白的表达显著降低(P<0.001);成骨诱导3d后,LPS刺激下各组ALP的表达量要显著低于对照组(P<0.05),TRAF6siRNA组的ALP表达量要高于空白对照、转染试剂组和control siRNA组(P<0.05),TRAF6siRNA的Runx-2和Col-I的mRNA表达均明显高于其余3组(P<0.05)。结论:沉默TRAF6基因能减轻LPS对hPDLC成骨分化的抑制作用,即沉默TRAF6基因能促进LPS刺激下的hPDLC成骨分化,推测TRAF6可能影响牙周炎的发生发展进程,是牙周炎潜在的治疗靶点。Objective:To observe the effect of tumor necrosis factor receptor-related factor 6(TRAF6)knockdown on osteogenic differentiation of human periodontal ligament cell(hPDLC)stimulated by LPS.Methods:The TRAF6 siRNA and control siRNA were transiently transfected into hPDLC.The cells were stimulated with 10μg/ml LPS.The silence efficiency of TRAF6 was detected by RT-PCR and Western blot.The expression of ALP was detected by alkaline phosphatase assay kit.The expression of Runx-2 and type I collagen(Col-I)gene was detected by RT-PCR.Results:The expression of TRAF6 mRNA and protein in TRAF6 siRNA group was significantly decreased(P0.001).The expression of ALP in LPS-stimulated group was significantly lower than that in nonLPS-stimulated group(P0.05).The expression of ALP,Runx-2,and Col-I mRNA in TRAF6 siRNA was significantly higher than that in the other three groups(P0.05).Conclusion:TRAF6 knockdown can alleviate the inhibitory effect of LPS on osteogenesis differentiation of hPDLC,which indicates that TRAF6 may affect the development of periodontitis and may be a potential therapeutic target for periodontitis.
关 键 词:肿瘤坏死因子受体相关因子6 RNA干扰 成骨分化 脂多糖
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