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17β-雌二醇对人根尖牙乳头干细胞RANKL、OPG表达影响的研究 被引量:3

Effect of 17β-estrodial on the expression of RANKL and OPG in human stem cells from apical papillae
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摘要 目的:探讨17β-雌二醇对人根尖牙乳头干细胞(stem cells from apical papilla,SCAPs)核因子-κB受体活化因子配体(receptor activator for nuclear factor-κB ligand,RANKL)、骨保护素(osteoprotegerin,OPG)表达的影响。方法:通过酶消化法分离培养SCAPs,将SCAPs分别于对照组(普通培养基+10μmol/L无水乙醇)和含0.1μmol/L17β-雌二醇的培养基培养3d和7d后,实时荧光定量PCR法和蛋白质免疫印迹法分别检测RANKL、OPG mRNA和蛋白表达。结果:17β-雌二醇刺激3d和7d组,OPGmRNA和蛋白表达均较对照组升高(P<0.01),RANKL mRNA和蛋白表达均较对照组降低(P<0.01)。结论:17β-雌二醇可能通过调节RANKL/OPG系统,参与调节SCAPs成牙/骨及破牙/骨活性。 Objective:To evaluate the effects of 17β-estrodial on the expression of receptor activator of NF-κB ligand (RANKL) and osteoprotegerin (OPG) in human stem cells from apical papillae (SCAPs). Methods:SCAPs were cultured seperately by enzyme digestion. SCAPs cultured in L-MEM containing 10 μmol/L alcohol (control group) , L-MEM containing 0.1μmoL/L 17β-estrodial for 3 days and 7 days were respectively collected to evaluate the expression of RANKL and OPG at mRNA and protein levels by real-time RT-PCR and Western blotting. Results:For SCAPs cultured in 17 β-estrodial for 3 days and 7 days, expression of OPG at mRNA and protein levels was all higher than those in control group (P 〈 0.01 ),while expression of RANKL at mRNA and protein levels was all lower than those in control group (P 〈 0. 01 ). Conclusions:17β-estrodial may regulate the odonto/osteogenic and odonto/osteoclastic potential of SCAPs through RANKL/OPG system.
出处 《口腔生物医学》 2012年第4期185-188,共4页 Oral Biomedicine
基金 江苏省卫生厅医学重点人才项目(RC2011140) 江苏高校优势学科建设工程资助项目
关键词 17Β-雌二醇 人根尖牙乳头干细胞 核因子-ΚB受体活化因子配体 骨保护素 17β-estrodial Human stem cells from apical papilla Receptor activator of NF-κB ligand Osteoprotegerin
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