首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The regulation of survival and differentiation of neural stem cells by miR-124 via modulating PAX3
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The regulation of survival and differentiation of neural stem cells by miR-124 via modulating PAX3

机译:miR-124通过调节pax3对神经干细胞的存活和分化的调节

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MicroRNAs (miRNAs) have crucial functions in the regulation of proliferation and differentiation of neural stem cells (NSCs). MiR-124 has been reported to be implicated in neurogenesis. However, the precise function and mechanism of miR-124 still need further verification. In this study, we identified paired box 3 (PAX3) as a potential target of miR-124 using bioinformatics approaches. Next, we found PAX3 had reversed expression pattern with miR-124 as well as TUBB3 and GFAP. Dual-luciferase assay showed that miR-124 could bind to the 3′-UTR of PAX3 mRNA and restrain its expression. It was demonstrated that overexpression and knocking down of miR-124 in NSCs could promote the survival and suppress the apoptosis of NSCs. Meanwhile, miR-124 enhanced the expression of TUBB3 and GFAP via impairing PAX3 expression. Mechanistic study revealed that augmented Akt-GSK3β signaling pathway was the driving-force for the regulatory functions of miR-124 in NSCs. In summary, this study for the first time uncovered that miR-124 could suppress PAX3 expression, which in turn regulated the differentiation of NSCs.
机译:MicroRNA(miRNA)在神经干细胞(NSCs)的增殖和分化调节中具有至关重要的功能。据报道,miR-124涉及神经发生。然而,MIR-124的精确功能和机制仍需要进一步验证。在本研究中,我们将配对盒3(PAX3)作为MIR-124的潜在目标识别使用生物信息学方法。接下来,我们发现PAX3具有与miR-124的反向表达模式以及径和GFAP。双荧光素酶测定表明miR-124可以结合PAX3 mRNA的3'-UTR并抑制其表达。据证明,NSC中的miR-124的过度表达和敲击可以促进生存率并抑制NSCs的凋亡。同时,MiR-124通过损害PAX3表达增强了TubB3和GFAP的表达。机械研究表明,增强AKT-GSK3β信号通路是MIR-124在NSCs中的调节功能的驱动力。总之,本研究首次揭示MIR-124可以抑制PAX3表达,这反过来调节NSC的分化。

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