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首页> 外文期刊>Cell stem cell >Notch-Induced miR-708 Antagonizes Satellite Cell Migration and Maintains Quiescence
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Notch-Induced miR-708 Antagonizes Satellite Cell Migration and Maintains Quiescence

机译:Notch诱导的miR-708拮抗卫星电池迁移并保持静止

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摘要

Critical features of stem cells include anchoring within a niche and activation upon injury. Notch signaling maintains skeletal muscle satellite (stem) cell quiescence by inhibiting differentiation and inducing expression of extracellular components of the niche. However, the complete spectrum of how Notch safeguards quiescence is not well understood. Here, we perform Notch ChIP-sequencing and small RNA sequencing in satellite cells and identify the Notch-induced microRNA-708, which is a mirtron that is highly expressed in quiescent cells and sharply downregulated in activated cells. We employ in vivo and ex vivo functional studies, in addition to live imaging, to show that miR-708 regulates quiescence and self-renewal by antagonizing cell migration through targeting the transcripts of the focal-adhesion-associated protein Tensin3. Therefore, this study identifies a Notch-miR708-Tensin3 axis and suggests that Notch signaling can regulate satellite cell quiescence and transition to the activation state through dynamic regulation of the migratory machinery.
机译:干细胞的关键特征包括锚固在利基内并在损伤时激活。 Notch信号传导通过抑制分化和诱导Niche的细胞外组分的表达来维持骨骼肌卫星(茎)细胞静脉。然而,Notch如何保护静止的完整频谱并不充分了解。在这里,我们在卫星细胞中进行凹口芯片测序和小RNA测序,并鉴定凹口诱导的微小RORNA-708,其是在静止细胞中高度表达并在活性细胞中急剧下降的麦克朗。除了实时成像之外,我们还雇用体内和离体功能研究,表明MIR-708通过靶向局灶性相关蛋白Tensin3的转录物来调节细胞迁移来调节静止和自我更新。因此,该研究识别出Notch-MiR708-Tensin3轴,并且表明陷波信令可以通过迁移机械的动态调节来调节卫星电池静态并过渡到激活状态。

著录项

  • 来源
    《Cell stem cell》 |2018年第6期|共15页
  • 作者单位

    Inst Pasteur Dept Dev &

    Stem Cell Biol Stem Cells &

    Dev F-75015 Paris France;

    Swiss Fed Inst Technol EPFL Sch Life Sci Bioimaging &

    Opt Platform BIOP Lausanne Switzerland;

    Inst Pasteur Dept Dev &

    Stem Cell Biol Stem Cells &

    Dev F-75015 Paris France;

    Inst Pasteur Dept Dev &

    Stem Cell Biol Stem Cells &

    Dev F-75015 Paris France;

    Inst Pasteur Dept Dev &

    Stem Cell Biol Stem Cells &

    Dev F-75015 Paris France;

    UPEC INSERM IMRB U955 E10 ENVA EFS F-94000 Creteil France;

    Univ Paris Saclay Univ Paris Sud Vectorol &

    Therapeut Anticancereuses UMR8203 CNRS Gustave;

    Inst Pasteur Dept Dev &

    Stem Cell Biol Stem Cells &

    Dev F-75015 Paris France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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