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A novel electron emission-based cell culture device promotes cell proliferation and differentiation of pre-osteoblastic MC3T3-E1 cells

机译:一种新型的基于电子发射的细胞培养装置可促进成骨前MC3T3-E1细胞的增殖和分化

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摘要

In this report we demonstrate the effect of a novel electron emission-based cell culture device on the proliferation and differentiation of pre-osteoblastic MC3T3-E1 cells. Our device has an electron emission element that allows, for the first time, stable emission of electrons into an atmosphere. Atmospheric electrons react with gas molecules to generate radicals and negative ions, which induce a variety of biochemical reactions in the attached cell culture system. In this study, we demonstrated the effect of this new electron emission-based cell culture device on cell proliferation and differentiation using pre-osteoblastic MC3T3-E1 cells. Electron emission stimulation (EES) was applied directly to culture medium containing plated cells, after which the number of living cells, the mRNA levels of osteogenesis-related genes, and the alkaline phosphatase (ALP) activity were evaluated. The growth rate of EES-exposed cells increased by approximately 20% in comparison with unexposed control cells. We also found the mRNA levels of osteogenic specific genes such as collagen type I α-1, core-binding factor α-1, and osteocalcin to be up-regulated following EES. ALP activity, a marker for osteogenic activity, was significantly enhanced in EES-treated cells. Furthermore, reactive oxygen species generated by EES were measured to determine their effect on MC3T3-E1 cells. These results suggest that our new electron emission-based cell culture device, while providing a relatively weak stimulus in comparison with atmospheric plasma systems, promotes cell proliferation and differentiation. This system is expected to find application in regenerative medicine, specifically in relation to bone regeneration.
机译:在本报告中,我们证明了新型基于电子发射的细胞培养设备对成骨前成骨细胞MC3T3-E1细胞的增殖和分化的影响。我们的设备具有一个电子发射元件,首次使电子稳定地发射到大气中。大气电子与气体分子发生反应,产生自由基和负离子,从而在附着的细胞培养系统中引发各种生化反应。在这项研究中,我们证明了这种新的基于电子发射的细胞培养装置对使用成骨细胞前体MC3T3-E1细胞的细胞增殖和分化的影响。将电子发射刺激(EES)直接应用于含有平板细胞的培养基,然后评估活细胞的数量,成骨相关基因的mRNA水平和碱性磷酸酶(ALP)活性。与未暴露的对照细胞相比,暴露于EES的细胞的生长速率增加了约20%。我们还发现,在EES之后,成骨性特定基因(如I型胶原I-1,核心结合因子α-1和骨钙素)的mRNA水平被上调。在EES处理的细胞中,成骨活性的标志物ALP活性显着增强。此外,测量了EES产生的活性氧,以确定它们对MC3T3-E1细胞的影响。这些结果表明,与大气等离子系统相比,我们基于电子发射的新型细胞培养装置虽然提供了相对较弱的刺激,但可以促进细胞增殖和分化。该系统有望在再生医学中找到应用,特别是在骨再生方面。

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