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Bioimaging of microRNA124a-independent neuronal differentiation of human G2 neural stem cells

机译:人类G2神经干细胞的microRNA124a非依赖性神经元分化的生物成像

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Evaluation of the function of microRNAs (miRNAs or miRs) through miRNA expression profiles during neuronal differentiation plays a critical role not only in identifying unique miRNAs relevant to cellular development but also in understanding regulatory functions of the cell-specific miRNAs in living organisms. Here, we examined the microarray-based miRNA expression profiles of G2 cells (recently developed human neural stem cells) and monitored the expression pattern of known neuron-specific miR-9 and miR-124a during neuronal differentiation of G2 cells in vitro and in vivo. Of 500 miRNAs analyzed by microarray of G2 cells, the expression of 90 miRNAs was significantly increased during doxycycline-dependent neuronal differentiation of G2 cells and about 60 miRNAs showed a gradual enhancement of gene expression as neuronal differentiation progressed. Real-time PCR showed that expression of endogenous mature miR-9 was continuously and gradually increased in a pattern dependent on the period of neuronal differentiation of G2 cells while the increased expression of neuron-specific mature miR-124a was barely observed during neurogenesis. Our recently developed miRNA reporter imaging vectors (CMV/Gluc/3xPT
机译:在神经元分化过程中通过miRNA表达谱评估microRNA(miRNA或miR)的功能不仅在鉴定与细胞发育相关的独特miRNA方面而且在理解活生物体中特定于细胞的miRNA的调节功能中都起着至关重要的作用。在这里,我们检查了G2细胞(最近开发的人类神经干细胞)基于微阵列的miRNA表达谱,并监测了G2细胞在体外和体内神经元分化过程中已知神经元特异性miR-9和miR-124a的表达模式。 。通过G2细胞微阵列分析的500个miRNA中,在强力霉素依赖的G2细胞神经元分化过程中,90个miRNA的表达显着增加,随着神经元分化的进展,约60个miRNA显示出基因表达的逐渐增强。实时PCR显示,内源性成熟miR-9的表达以依赖于G2细胞神经元分化时期的方式连续且逐渐增加,而在神经发生过程中几乎未观察到神经元特异性成熟miR-124a的表达增加。我们最近开发的miRNA报告基因成像载体(CMV / Gluc / 3xPT

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