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首页> 外文期刊>Cell Biochemistry and Biophysics >Influence of Novel Nano-Mesoporous Bioactive Glass on the Regulation of IGF-II Gene Expression in Osteoblasts
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Influence of Novel Nano-Mesoporous Bioactive Glass on the Regulation of IGF-II Gene Expression in Osteoblasts

机译:新型纳米介孔生物活性玻璃对成骨细胞IGF-II基因表达调控的影响

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To investigate whether the mesoporous bioactive glass (MBG) exerts any in vitro bioactivity on rat osteoblasts and the potential regulatory mechanism of this bioactivity. Rat osteoblasts were incubated in the presence and absence (control) of ionic dissolution product of MBG in minimal essential medium. The osteoblast proliferation and differentiation were measured using MTT and alkaline phosphatase methods. The IGF-II mRNA expression in osteoblasts was measured by RT-PCR. IGF-II protein and IGFBP were measured by ELISA. The level of alkaline phosphatase activity was increased to 125% of control. Expression of IGF-II mRNA was increased to 125% of control. There was a 175 and 237% increase in the concentration of unbound IGF-II protein and IGFBP, respectively, in the conditioned media of treated osteoblasts. The osteoblast proliferation was 92% of control. The ionic dissolution product of MBG was able to promote the differentiation of osteoblasts, probably by inducing IGF-II expression at both mRNA and protein level.
机译:要研究中孔生物活性玻璃(MBG)是否对大鼠成骨细胞发挥任何体外生物活性以及这种生物活性的潜在调控机制。在存在和不存在(对照)MBG离子溶解产物的情况下,在基本必需培养基中孵育大鼠成骨细胞。使用MTT和碱性磷酸酶方法测量成骨细胞的增殖和分化。通过RT-PCR测量成骨细胞中IGF-II mRNA的表达。通过ELISA测量IGF-II蛋白和IGFBP。碱性磷酸酶活性水平增加到对照的125%。 IGF-II mRNA的表达增加到对照的125%。在处理过的成骨细胞的条件培养基中,未结合的IGF-II蛋白和IGFBP的浓度分别增加了175%和237%。成骨细胞增殖为对照的92%。 MBG的离子溶出产物可能通过诱导mRNA和蛋白水平的IGF-II表达,从而促进成骨细胞的分化。

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