首页> 外文期刊>The Journal of Musculoskeletal and Neuronal Interactions >Effects of oncostatin M on cell proliferation and osteogenic differentiation in C3H10T1/2
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Effects of oncostatin M on cell proliferation and osteogenic differentiation in C3H10T1/2

机译:抑癌素M对C3H10T1 / 2细胞增殖和成骨分化的影响

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Objective: To explore the effects of protein factor Oncostatin M (OSM), a member of the Interleukin-6 (IL-6) family on cell proliferation, osteogenic differentiation and mineralization. Materials and methods: Basal nutrient solutions of different concentrations of OSM (0, 5, 10, 20, 40, 80 ng/ml) were used. In order to divide embryonic origin between mesenchymal stem cells C3H10T1/2 of in vitro cultured mice, and the effects of in vitro proliferation efficiencies of C3H10T1/2 cells of different concentrations of OSM, the C3H10T1/2 cells were divided into four groups: (1) Basal nutrient solution group (nega- tive control); (2) Osteogenesis induced liquid group (positive control); (3) OSM (20 ng/ml) group; (4) Experimental group (osteogenesis induced liquid + OSM (20 ng/ml)). The expressions levels of relevant osteogenesis and mineralization genes were detected. Results: OSM had several effects on promoting the proliferation of embryonic origin mesenchymal stem cells C3H10T1/2 with respect to time of exposure as well as concentrations. In the present study, it has been shown that when the concentration of OSM is 20 ng/ml, the effects of promoting proliferation are most obvious. OSM can induce osteogenic differentiation of C3H10T1/2, make the process of osteogenic differentiation in advance, and promote the formation of end- stage calcium deposits and mineralized nodule, and osteogenic differentiation of C3H10T1/2 is finally achieved. Conclusion: OSM can promote the proliferation of C3H10T1/2, and induce its osteogenic differentiation and end-stage mineralization.
机译:目的:探讨白介素6(IL-6)家族成员蛋白质因子癌抑素M(OSM)对细胞增殖,成骨分化和矿化的影响。材料和方法:使用不同浓度OSM(0、5、10、20、40、80 ng / ml)的基础营养液。为了在体外培养的小鼠的间充质干细胞C3H10T1 / 2之间划分胚胎来源,以及不同OSM浓度的C3H10T1 / 2细胞的体外增殖效率的影响,将C3H10T1 / 2细胞分为四组:( 1)基础营养液组(阴性对照); (2)成骨诱导液群(阳性对照); (3)OSM(20 ng / ml)组; (4)实验组(成骨诱导液+ OSM(20ng / ml))。检测相关成骨和矿化基因的表达水平。结果:就接触时间和浓度而言,OSM对促进胚胎来源的间充质干细胞C3H10T1 / 2的增殖具有多种作用。在本研究中,已经表明,当OSM浓度为20 ng / ml时,促进增殖的作用最为明显。 OSM可以诱导C3H10T1 / 2的成骨分化,提前进行成骨分化的过程,并促进终末期钙沉积物和矿化结节的形成,最终实现C3H10T1 / 2的成骨分化。结论:OSM可促进C3H10T1 / 2的增殖,并诱导其成骨分化和末期矿化。

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