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miR-375 Promotes Pancreatic Differentiation In Vitro by Affecting Different Target Genes at Different Stages

机译:miR-375通过影响不同阶段的不同靶基因促进体外胰腺分化

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Human embryonic stem cells (hESCs) possess the ability to differentiate into insulin-producing cells (IPCs), which can be used to treat type I diabetes. miR-375 is an essential transcriptional regulator in the development and maturation of the pancreas. In this study, we optimized a protocol to differentiate hESCs into IPCs and successfully obtained IPCs. Then, we performed overexpression and inhibition experiments of miR-375 on cells at different stages of differentiation and performed RNA-seq. The results showed that the expression of miR-375 fluctuated during hESC differentiation and was affected by miR-375 mimics and inhibitors. miR-375 influences global gene expression and the target genes of miR-375. The overexpression of miR-375 can cause changes in multiple signaling pathways during pancreatic development. miR-375 is a major participant in the differentiation of pancreatic β -cells through different target genes at different stages. This study provides new ideas for further investigation of how microRNAs affect cell fate and gene transcription.
机译:人胚胎干细胞(HESC)具有分化为胰岛素的细胞(IPC)的能力,可用于治疗I型糖尿病。 miR-375是胰腺发育和成熟的必要转录调节因子。在本研究中,我们优化了一个协议,将HESC区分为IPC,并成功获得了IPC。然后,我们在不同分化阶段的细胞上对miR-375进行过表达和抑制实验,并进行RNA-SEQ。结果表明,在HESC分化期间miR-375波动的表达,受MiR-375模拟和抑制剂的影响。 miR-375影响全球基因表达和miR-375的靶基因。 miR-375的过表达可能导致胰腺发育过程中多个信号通路的变化。 miR-375是通过不同阶段的不同靶基因分化胰腺β-cells的主要参与者。本研究提供了新的思路,以进一步调查MicroRNA如何影响细胞命运和基因转录。

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