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

Yuwen Zhao, Rui Yang, Zoe Bousraou, Shue Wang
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引用次数: 3

Abstract

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.
利用双链锁定核酸生物传感器探测人类成骨分化
人间充质干细胞(hMSCs)具有自我更新和多向分化的特性,在组织工程和再生医学领域具有巨大的应用潜力。然而,由于缺乏有效的工具来检测单细胞水平的基因表达,控制成骨分化的细胞和分子机制尚不清楚。在这里,我们提出了一种双链锁定核酸生物传感器来研究hMSCs成骨分化过程中的基因表达分析。我们首先在单个hMSCs中展示了这种生物传感器的基因表达分析。接下来,我们研究了notchl - d1114信号在成骨分化中的调节作用。我们的发现提供了notchl - d1114信号参与hMSCs成骨分化的证据。抑制Notchl-D1l4信号可显著降低成骨分化和D1l4的表达。
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