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首页> 外文期刊>Journal of Otology >Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers
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Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers

机译:人牙髓干细胞中miR-124水平的升高改变了神经标志物的表达

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Auditory neuropathy is the particular form of deafness in humans which cannot be treated by replacement therapy. Human dental pulp stem cells (hDPSCs) are derived from an ectomesenchymal neural crest cell population. Therefore, they possess a promising capacity for neuronal differentiation and repair. miR-124, a key regulator of neuronal development in the inner ear, is expressed at high levels in auditory and vestibular neurons. Here, we evaluated the possible effect of miR-124 in alteration of neural protein markers expression. Using quantitative reverse transcription-PCR (qRT-PCR) analyses and immunofluorescence staining, we studied the expression patterns of neural progenitor markers (Nestin, NOTCH1, and SOX2) and neural markers (β-tubulin III, GATA-3, and peripherin) upon transfection of hDPSCs with miR-124. The qRT-PCR results showed that Nestin was upregulated 6?h post-transfection. In contrast, Nestin expression exhibited a decreasing trend 24?h and 48?h post-transfection. Higher levels of β-tubulin III, 6?h and 16?h post transfection in RNA level as compared with control cells, were determined in transfected DPSCs. However, β-tubulin-III expression decreased 48?h post-transfection. The immunoflourescence results indicated that transfection of hDPSCs with miR-124, only affected Nestin among the studied neural progenitor and neural marker expression in protein level.
机译:听觉神经病是人类耳聋的一种特殊形式,无法通过替代疗法治疗。人牙髓干细胞(hDPSCs)来源于外胚层神经c细胞群。因此,它们具有神经元分化和修复的有前途的能力。 miR-124是内耳神经元发育的关键调节因子,在听觉和前庭神经元中高水平表达。在这里,我们评估了miR-124改变神经蛋白质标记表达的可能作用。使用定量逆转录PCR(qRT-PCR)分析和免疫荧光染色,我们研究了神经祖细胞标记(Nestin,NOTCH1和SOX2)和神经标记(β-微管蛋白III,GATA-3和周围蛋白)的表达模式。用miR-124转染hDPSC。 qRT-PCR结果表明Nestin在转染后6小时被上调。相反,转染后24小时和48小时时,巢蛋白表达呈现下降趋势。在转染的DPSCs中,与对照细胞相比,在转染后的RNA水平分别为6?h和16?h的β-微管蛋白III水平更高。然而,转染后48小时,β-微管蛋白-III表达下降。免疫荧光结果表明,用miR-124转染hDPSCs仅影响所研究的神经祖细胞和蛋白质水平中神经标志物表达中的巢蛋白。

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