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Low frequency mechanical stimulation inhibits adipogenic differentiation of C3H10T1/2 mesenchymal stem cells

机译:低频机械刺激抑制C3H10T1 / 2间充质干细胞成脂分化

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Oscillatory mechanical stimulation at relatively high frequencies (0.1. Hz) has been shown to inhibit adipogenic and promote osteogenic differentiation of mesenchymal stem cells. However, for physiological interpretations and ease of implementation it is of interest to know whether different rates of mechanical stimulation can produce similar results. We hypothesized that relatively low frequency mechanical stimulation (0.01. Hz) can inhibit adipogenic differentiation of C3H10T1/2 mouse mesenchymal stem cells, even in a potent adipogenic differentiation medium. C3H10T1/2 cells were cultured in adipogenic medium under control (non-mechanically stimulated) conditions and under oscillatory surface stretch with 10% amplitude and 0.01. Hz frequency for 6. h per day for up to 5 days. Cell population was assessed by counting and adipogenic differentiation was assessed by real-time quantitative PCR (qPCR) analysis of peroxisome proliferator-activated receptor gamma (PPARγ) and fatty acid binding protein 4 (FABP4) after 3 and 5 days. Involvement of the ERK signaling pathway was assessed by Western blot. Low frequency mechanical stimulation significantly decreased expression of PPARγ after 3 days and FABP4 after 3 and 5 days versus non-stimulated culture. ERK signaling was decreased in mechanically-stimulated culture, indicating a role in the inhibition of adipogenic differentiation. Application of this study: Low frequency mechanical stimulation may provide a technically simple means for control of mesenchymal stem cell differentiation in cell-based therapies, particularly for inhibition of differentiation toward undesired adipogenic lineages.
机译:相对较高的频率(0.1。Hz)的振荡机械刺激已显示出抑制成脂作用并促进间充质干细胞的成骨分化。然而,对于生理学解释和易于实施,感兴趣的是知道不同的机械刺激速率是否可以产生相似的结果。我们假设相对低频率的机械刺激(0.01。Hz)可以抑制C3H10T1 / 2小鼠间充质干细胞的成脂分化,即使在有效的成脂分化培养基中也是如此。 C3H10T1 / 2细胞在成脂培养基中(在非机械刺激下)控制条件下,在振荡表面拉伸下以10%的振幅和0.01的频率进行培养。每天6小时的Hz频率,最多5天。在第3天和第5天后,通过计数和过氧化物酶体增殖物激活受体γ(PPARγ)和脂肪酸结合蛋白4(FABP4)的实时定量PCR(qPCR)分析来评估细胞数量,并评估成脂分化。通过蛋白质印迹评估ERK信号传导途径的参与。与未刺激的培养相比,低频机械刺激在3天后显着降低了PPARγ的表达,在3和5天后显着降低了FABP4的表达。在机械刺激的文化中,ERK信号减少,表明在抑制成脂分化中的作用。这项研究的应用:低频机械刺激可能为控制基于细胞的疗法中的间充质干细胞分化提供技术上简单的方法,尤其是抑制向不良成脂谱系的分化。

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