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An RNA interference screen uncovers a new molecule in stem cell self-renewal and long-term regeneration

机译:RNA干扰筛查发现干细胞自我更新和长期再生中的新分子

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Adult stem cells sustain tissue maintenance and regeneration throughout the lifetime of an animal. These cells often reside in specific signalling niches that orchestrate the stem cell's balancing act between quiescence and cell-cycle re-entry based on the demand for tissue regeneration. How stem cells maintain their capacity to replenish themselves after tissue regeneration is poorly understood. Here we use RNA-interference-based loss-of-function screening as a powerful approach to uncover tran-scriptional regulators that govern the self-renewal capacity and regenerative potential of stem cells. Hair follicle stem cells provide an ideal model. These cells have been purified and characterized from their native niche in vivo and, in contrast to their rapidly dividing progeny, they can be maintained and passaged long-term in vitro. Focusing on the nuclear proteins and/or transcription factors that are enriched in stem cells compared with their progeny, we screened ~2,000 short hairpin RNAs for their effect on long-term, but not short-term, stem cell self-renewal in vitro. To address the physiological relevance of our findings, we selected one candidate that was uncovered in the screen: TBX1. This transcription factor is expressed in many tissues but has not been studied in the context of stem cell biology. By conditionally ablating Tbxl in vivo, we showed that during homeostasis, tissue regeneration occurs normally but is markedly delayed. We then devised an in vivo assay for stem cell replenishment and found that when challenged with repetitive rounds of regeneration, the Tbxl-deficient stem cell niche becomes progressively depleted. Addressing the mechanism of TBX1 action, we discovered that TBX1 acts as an intrinsic rheostat of BMP signalling: it is a gatekeeper that governs the transition between stem cell quiescence and proliferation in hair follicles. Our results validate the RNA interference screen and underscore its power in unearthing new molecules that govern stem cell self-renewal and tissue-regenerative potential.
机译:成年干细胞在动物的整个生命周期中都维持组织的维持和再生。这些细胞通常驻留在特定的信号传导壁ches中,这些壁ni根据组织再生的需求来协调干细胞在静止和细胞周期再进入之间的平衡作用。人们对干细胞如何在组织再生后如何维持自身的补充能力知之甚少。在这里,我们使用基于RNA干扰的功能丧失筛选作为发现转录调控因子的有力方法,该转录调控因子控制干细胞的自我更新能力和再生潜力。毛囊干细胞提供了理想的模型。这些细胞已在体内从其天然生态位中纯化并鉴定出来,与它们迅速分裂的后代相反,它们可以在体外长期维持和传代。针对与干细胞相比其后代中富含的核蛋白和/或转录因子,我们筛选了约2,000个短发夹RNA,以了解它们对长期(而非短期)干细胞自我更新的影响。为了解决我们发现的生理相关性,我们选择了屏幕中未发现的一个候选对象:TBX1。该转录因子在许多组织中表达,但尚未在干细胞生物学的背景下进行研究。通过在体内有条件地消融Tbxl,我们显示出体内稳态期间,组织再生正常发生,但明显延迟。然后,我们设计了一种用于干细胞补充的体内测定法,发现当受到重复的再生轮攻击时,Tbxl缺陷的干细胞生态位逐渐被消耗。在探讨TBX1作用的机制时,我们发现TBX1充当BMP信号传导的固有变阻器:它是控制干细胞静止和毛囊增殖之间过渡的守门人。我们的研究结果验证了RNA干扰筛查方法的有效性,并强调了其在挖掘控制干细胞自我更新和组织再生潜能的新分子中的作用。

著录项

  • 来源
    《Nature》 |2012年第7396期|p.104-108|共5页
  • 作者单位

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

    Howard Hughes Medical Institute, The Rockefeller University, New York, New York 10065, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 02:54:03

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