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作 者:宋扬 秦青 高菊荣 王丽颖[2] 刘佳[2] 金作林
机构地区:[1]解放军323医院口腔科,主治医师陕西710054 [2]第四军医大学口腔医学院正畸科,博士陕西710032 [3]第四军医大学口腔医院正畸科,副主任医师教授陕西710032
出 处:《中华老年口腔医学杂志》2014年第2期80-84,共5页Chinese Journal of Geriatric Dentistry
基 金:国家自然科学基金资助项目(项目编号:30973358);陕西省自然科学基础研究计划(项目编号:2014JM4111)
摘 要:目的:联合应用BMP-2、bFGF和Dex诱导牙周膜细胞(PDLCs),观察其成骨分化能力。方法:体外培养犬PDLCs,将第4代PDLCs进行分组:(1)对照组增加矿化诱导液组(2)bFGF+Dex组、(3)BMP-2+bFGF组、(4)加BMP-2+Dex组、(5)bFGF+BMP-2+Dex组。MTT法观察BMP-2、bFGF和Dex联合应用对犬PDLCs增殖的影响;成骨分化实验观察BMP-2、bFGF、Dex联合应用对犬PDLCs分化的影响。结果:(1)PDLCs细胞呈典型的成纤维细胞样形态:长梭形、纺锤形、三角形等多形性。波形丝蛋白表达阳性,角蛋白表达阴性。(2)MTT增殖实验显示:bFGF+Dex、BMP-2+bFGF、BMP-2+Dex、bFGF+BMP-2+Dex组均促进犬PDLCs增殖,但各诱导组间无明显差异。(3)成骨诱导实验检测结果:bFGF+BMP-2+Dex组矿化结节染色深、面积较大、细胞密集而集中。结论:三种诱导因子两两结合均能增强犬PDLCs矿化结节形成能力,但三种因子联合应用成骨能力最强(P<0.05)。Objective: Osteogenic differentiation of periodontal ligament cells induced by BMP-2, bFGF and Dex in dogs. Methods: The fourth generation of PDLCs cultured in vitro were randomly divided into 5 groups: (1) the control group (with no inducible factors); (2) the group with 10p g/L bFGF and 200p g/L BMP-2 added; (3) the group with 200p g/L BMP-2 and 10-Smol/L Dex added; (4) the group with 10p g/L bFGF and 10-8mol/L Dex added; (5) the group with 200p g/LBMP-2, 10p g/L bFGF and 10-Smol/L Dex added. The effect of combined use ofBMP-2, bFGF and Dex on the proliferation of PDLCs in dogs were observed by MTT test, and osteogenic differentiation test assay. Results: (1) After 7, 14 days, the induced PDLCs differentiated into fibroblast-like cells with polygon in shape including triangle and fusiform. Vimentin expressed positive and keratin was negative; (2)MTT test demonstrated that all of the four experimental groups promoted the proliferation of PDLCs in dogs and the effect were time-dependent; (3) Osteogenesis induced by 31 d, bFGF+BMP-2+Dex mineralized nodule staining deep, larger cell density and concentrated. Conclusion: These results indicate that combined application BMP-2, bFGF and Dex can remarkably promote the osteogenic differentiation of PDLCs.
关 键 词:牙周膜细胞 骨形成蛋白-2 碱性成纤维细胞生长因子 地塞米松
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