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Expression and influence of BMP-4 in human dental pulp cells cultured in vitro

机译:BMP-4在体外培养人牙髓细胞中BMP-4的表达及影响

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Effects of bone morphogenetic protein (BMP)-4 on proliferation and differentiation capacities of dental pulp cells through BMP-4 acting on human dental pulp cells cultured in vitro were investigated. Dental pulp tissues of lesion-free teeth extracted from patients due to orthodontics were taken, and human dental pulp cells were cultured in vitro using the tissue explant method. Immunocytochemical staining was used for the identification of vimentin and keratin. The dental pulp cells were divided into groups A and B. A total of 100 ng/ml BMP-4 was added into group A, while no inducer was added into group B as the control group. The cell growth curves at day 1, 2, 3, 5 and 7 after culture were drawn. At day 7, the cell count, alkaline phosphatase (ALP) activity, number of calcified nodules, and expression levels of dentin sialophosphoprotein (DSPP), dentin matrix protein-1 (DMP-1) and each gene related to dentinogenesis in each group were detected, respectively. Human dental pulp cells were conformed to the biological characteristics of dental pulp cells according to the identification of vimentin and keratin via immunocytochemical staining. With the prolongation of culture time, the number of cells in both groups was gradually increased, reaching the peak at day 5 and began to decline at day 7. The number of cells in group A was significantly greater than that in group B (p0.05). According to the results of reverse transcription-quantitative polymerase chain reaction (RT-qPCR), the relative messenger ribonucleic acid (mRNA) expression levels of ALP, DSPP and DMP-1 in group A were significantly higher than those in group B (p0.05). BMP-4 can promote the growth of dental pulp cells and remarkably enhance the differentiation of dental pulp cells into odontoblasts.
机译:研究了骨形态发生蛋白(BMP)-4对通过BMP-4作用于体外培养的人牙髓细胞的牙髓细胞增殖和分化能力的影响。采用由正畸症提取的免病变牙齿的牙髓组织,并使用组织外消防方法在体外培养人牙髓细胞。免疫细胞化学染色用于鉴定Vimentin和角蛋白。将牙髓细胞分成A和B基团A和B.将总共100ng / ml BMP-4加入A组,同时将诱导剂加入B组作为对照组。在拉伸培养后第1,2,3,5和7天的细胞生长曲线。在第7天,细胞计数,碱性磷酸酶(ALP)活性,钙化结节数和牙本质唾液酸磷蛋白(DSPP),牙本质基质蛋白-1(DMP-1)的表达水平和与每组牙本发生有关的每个基因分别检测到。通过免疫细胞化学染色,人牙髓细胞符合牙髓细胞的生物学特性。随着培养时间的延长,两组细胞的数量逐渐增加,在第5天达到峰值,在第7天开始衰减。A组中的细胞数明显大于B组(P& 0.05)。根据逆转录定量聚合酶链反应(RT-QPCR)的结果,A ALP,A组中ALP,DSPP和DMP-1的相对信使核糖核酸(mRNA)表达水平明显高于B组(P< 0.05)。 BMP-4可以促进牙髓细胞的生长,并显着增强牙髓细胞的分化成牙卵细胞。

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