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miR-124 promotes the neuronal differentiation of mouse inner ear neural stem cells

机译:miR-124促进小鼠内耳神经干细胞的神经元分化

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摘要

MicroRNAs (miRNAs or miRs) act as key regulators in neuronal development, synaptic morphogenesis and plasticity. However, their role in the neuronal differentiation of inner ear neural stem cells (NSCs) remains unclear. In this study, 6 miRNAs were selected and their expression patterns during the neuronal differentiation of inner ear NSCs were examined by RT-qPCR. We demonstrated that the culture of spiral ganglion stem cells present in the inner ears of newborn mice gave rise to neurons in vitro. The expression patterns of miR-124, miR-132, miR-134, miR-20a, miR-17-5p and miR-30a-5p were examined during a 14-day neuronal differentiation period. We found that miR-124 promoted the neuronal differentiation of and neurite outgrowth in mouse inner ear NSCs, and that the changes in the expression of tropomyosin receptor kinase B (TrkB) and cell division control protein 42 homolog (Cdc42) during inner ear NSC differentiation were associated with miR-124 expression. Our findings indicate that miR-124 plays a role in the neuronal differentiation of inner ear NSCs. This finding may lead to the development of novel strategies for restoring hearing in neurodegenerative diseases.
机译:MicroRNA(miRNA或miR)在神经元发育,突触形态发生和可塑性中起关键调节剂的作用。但是,它们在内耳神经干细胞(NSC)的神经元分化中的作用仍不清楚。在这项研究中,选择了6个miRNA,并通过RT-qPCR检查了它们在内耳神经干细胞神经元分化过程中的表达模式。我们证明了新生小鼠内耳中存在的螺旋神经节干细胞的培养在体外产生了神经元。在14天的神经元分化期间检查了miR-124,miR-132,miR-134,miR-20a,miR-17-5p和miR-30a-5p的表达模式。我们发现miR-124促进小鼠内耳NSC的神经元分化和神经突生长,并且在内耳NSC分化过程中原肌球蛋白受体激酶B(TrkB)和细胞分裂控制蛋白42同源物(Cdc42)的表达变化与miR-124表达相关。我们的发现表明,miR-124在内耳NSC的神经元分化中起作用。这一发现可能导致开发新的策略来恢复神经退行性疾病的听力。

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