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作 者:余姗姗[1] 蒋欣泉[1] 翁雨来[1] 花菲[1]
机构地区:[1]上海交通大学医学院附属第九人民医院口腔内科,上海市口腔医学重点实验室,上海市口腔医学研究所,上海200011
出 处:《口腔医学》2007年第7期347-350,共4页Stomatology
基 金:国家重点基础研究发展规划973项目(G1999054308)
摘 要:目的研究酸性成纤维细胞生长因子(aFGF)和转化生长因子(TGF)β1单独或联合应用后对猪牙乳头细胞(pDPCs)增殖的影响。方法通过体外细胞培养技术,用四甲基偶氮唑盐(MTT)比色法检测aFGF、TGFβ1不同浓度、不同时间单独及联合应用后对pDPCs增殖的影响,所得数据用单因素方差进行分析。结果aFGF在5~100ng/ml和8d范围内能促进pDPCs增殖,最强效应浓度为10ng/ml和25ng/ml,最强效应时间为8d;TGFβ1在5~50ng/ml和8d范围内能抑制pDPCs增殖,其中以5ng/ml和10ng/ml抑制作用较弱;以aFGF最强效应浓度与TGFβ1较弱抑制浓度交互联合后对pDPCs有显著的促进增殖作用,其中以aFGF25ng/ml+TGFβ110ng/ml的效果最明显。Objective To investigate the effects of acidic fibroblast growth factor and transforming growth factor-β1 on the proliferation of porcine dental papilla cells. Methods Isolated porcine dental papilla cells were cultured in DMEM/F12 supplemented with aFGF and TGF β1. MTF colorimetric method was used to assess dose-effect and time-effect of aFGF and TGF β1 on the proliferation of pDPCs. All statistical analyses were performed with one-way ANOVA. Results Within 8 days, aFGF could significantly promote the proliferation of pDPCs with the concentrations between 5 ng/ml and 100 ng/ml, especially with the concentration of 10 ng/ml and 25 ng/ml, while the proliferation effects of TGF β1 sharply decreased at the dose varying from 5 ng/ml to 50 ng/ml. The effect was the strongest for the proliferation of pDPCs with the combination of 25 ng/ml aFGF and 10 ng/ml TGF β1. Conclusion The results suggested that in certain conditions, aFGF enhanced the proliferation of pDPCs while TGF β1 inhibited the proliferation . However,the promotive effects were achieved when the growth factors were used in combination. Supported by National 973 Project ( G1999054308 ).
关 键 词:牙乳头细胞 酸性成纤维细胞生长因子 转化生长因子Β1
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