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机构地区:[1]温州医学院附属口腔医院,浙江温州325027 [2]四川大学华西口腔医学院,四川成都610041
出 处:《牙体牙髓牙周病学杂志》2008年第8期425-428,共4页Chinese Journal of Conservative Dentistry
摘 要:目的:观察人甲状旁腺激素1-34(hum an Parathyroid hormone 1-34,hPTH1-34)对PTH-PTHrP(Parathyroid hormone-Parathyroid hormone related prote in)受体mRNA在体外培养的人牙髓细胞中表达的影响,探讨PTH影响牙本质形成和矿化的机制。方法:将培养的第4代牙髓细胞分为两组:实验组培养基加入含33.3 nmol/L hPTH1-34,在其培养的第5,10,15,20天提取总RNA,以RNA为模板在逆转录酶作用下合成cDNA,加入特异引物进行PCR扩增,同时扩增β-肌动蛋白的cDNA作为半定量RT-PCR的内参照,对PCR产物进行半定量分析。结果:在人牙髓细胞培养的5、10 d,对照组和实验组的PTH-PTHrP受体mRNA水平均较低,10 d以后PTH-PTHrP受体mRNA水平开始升高,实验组高于对照组,差异有统计学意义。结论:PTH-PTHrP受体的表达与牙髓细胞的分化密切相关;hPTH1-34可以促进PTH-PTHrP受体的表达,PTH可能通过促进PTH-PTHrP受体的表达或与PTH-PTHrP受体结合影响牙本质的形成和矿化。AIM: To study the change of expression of the PTH/PTHrP receptor in human dental pulp cells cultured in vitro. METHODS: The fourth passage of human dental pulp cells were cultured up to 5,10,15,20 days. The PTH group was cultured in the medium containing 33.3nmol/L hPTH1 - 34. PTH/PTHrP receptorg mRNA were enlarged by RT - PCR. The absorbence were measured and compared with β - actin. RESULTS: The mRNA of PTHrP receptor expressed lower when the cells were cultured in 5 and 10 days in both the experimental group and control group . But after 10 days, the expressions all increased with the cultured time. But the expression is higher in the experimental group than that in the control group. CONCLUSION: PTH is related with the differentiation Of pulp cells, hPTH1 -34 may promote the expression of PTH/PTHrP receptor. The formation and mineralization of dentin may be effected by parathyroid hormone itself or by combining with PTH/PTHrP receptor.
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