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首页> 外文期刊>Stem Cells >Linc1557 Linc1557 is critical for the initiation of embryonic stem cell differentiation by directly targeting the LIF/STAT3 signaling pathway
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Linc1557 Linc1557 is critical for the initiation of embryonic stem cell differentiation by directly targeting the LIF/STAT3 signaling pathway

机译:LINC1557 LINC1557对于通过直接瞄准LIF / Stat3信号传导途径来启动胚胎干细胞分化至关重要

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摘要

Abstract Embryonic stem cells (ESCs) have self‐renewal and multi‐lineage differentiation potential and perform critical functions in development and biomedicine. Several long noncoding RNAs (lncRNAs) have been reported as key regulators of stem cell pluripotency and differentiation. However, the function and regulatory mechanism of lncRNAs during the initiation of ESC differentiation remains unclear. Here, we found that linc1557 was highly expressed in mouse ESCs and required for the initiation of ESC differentiation. Knockdown of linc1557 increased the expression and phosphorylation levels of signal transducer and activator of transcription 3 (STAT3), a key factor in the leukemia inhibitory factor (LIF)/STAT3 signaling pathway. Furthermore, we found that linc1557 directly bound to Stat3 mRNA and affected its stability. The differentially expressed transcriptome after linc1557 knockdown in ESCs was involved primarily in multicellular organism development and cell differentiation as similar to that after Stat3 knockdown. Moreover, either knockdown of Stat3 or addition of a LIF/STAT3 signaling inhibitor rescued the suppressive effects of linc1557 knockdown on the initiation of mouse ESC differentiation. These findings not only elucidated the critical function of linc1557 in the initiation of mouse ESC differentiation but also clarified that its specific mechanism as directly affecting Stat3 mRNA stability, which enhanced the understanding of the lncRNA‐mediated regulatory mechanism for mRNA stability and key signaling pathways in ESC pluripotency and differentiation.
机译:摘要胚胎干细胞(ESC)具有自我更新和多谱系分化潜力,并在开发和生物医学中进行关键功能。已经报告了几种长期的NOODING RNA(LNCRNA)作为干细胞多能性和分化的关键调节剂。然而,在ESC分化开始期间LNCRNA的功能和调节机制仍不清楚。在这里,我们发现LINC1557在小鼠ESC中高度表达,并对ESC分化的开始所需。 LINC1557的敲低增加了转录3(Stat3)的信号传感器和活化剂的表达和磷酸化水平,是白血病抑制因子(LIF)/ Stat3信号通路的关键因素。此外,我们发现LINC1557直接与Stat3 mRNA结合并影响其稳定性。在ESC的LINC1557敲低后,差异表达的转录组主要涉及多细胞生物发育和细胞分化,与STAT3敲低后相似。此外,STAT3的敲低或加入LIF / Stat3信号抑制剂抢救了LINC1557敲低对小鼠ESC分化的抑制作用的抑制作用。这些发现不仅阐明了LINC1557在小鼠ESC分化的开始中的临界功能,而且还澄清了其直接影响STAT3 mRNA稳定性的特定机制,这提高了对mRNA稳定性和关键信号通路的LNCRNA介导的调节机制的理解ESC多能性和差异化。

著录项

  • 来源
    《Stem Cells 》 |2020年第3期| 共12页
  • 作者单位

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Department of Biostatistics and Computational Biology State Key Laboratory of Genetic Engineering;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

    Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物医学工程 ;
  • 关键词

    differentiation initiation; embryonic stem cells; Linc1557; mRNA stability; STAT3;

    机译:分化起始;胚胎干细胞;LINC1557;mRNA稳定;stat3;

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