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Probing Human Osteogenic Differentiation Using Double-Stranded Locked Nucleic Acid Biosensors

机译:双链锁定核酸生物传感器探测人骨质骨质分化

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Human mesenchymal stem cells (hMSCs) have great potential for tissue engineering and regenerative medicine due to their self-renewal and multi-differentiation properties. However, the cellular and molecular mechanisms that govern osteogenic differentiation are poorly understood due to a lack of effective tools to detect gene expression at single cell level. Here, we present a double-stranded locked nucleic acid biosensor to investigate gene expression analysis during hMSCs osteogenic differentiation. We first demonstrated this biosensor for gene expression analysis in single hMSCs. We next investigated the regulatory role of Notchl-D1l4 signaling in osteogenic differentiation. Our findings provide evidence that Notchl-D1l4 signaling is involved in hMSCs osteogenic differentiation. Inhibition of Notchl-D1l4 signaling significantly decreased osteogenic differentiation and D1l4 expression.
机译:由于其自我更新和多分化特性,人间充质干细胞(HMSCs)具有巨大的组织工程和再生医学潜力。 然而,由于缺乏缺乏有效工具以检测单细胞水平的基因表达,因此治理骨性发生分化的细胞和分子机制很差。 这里,我们介绍了一种双链锁定的核酸生物传感器,用于研究HMSCs osteogenic分化期间的基因表达分析。 我们首先在单次HMSCs中展示了这种生物传感器进行基因表达分析。 我们接下来研究了Notchl-D1L4信号传导在成骨分化中的调节作用。 我们的研究结果提供了证据表明Notchl-D1L4信号传导涉及HMSCs osteogenic分化。 抑制Notch1-D1L4信号传导显着降低了成骨分化和D1L4表达。

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