首页> 美国卫生研究院文献>Biomolecules >Sub-Lethal 5-Fluorouracil Dose Challenges Planarian Stem Cells Promoting Transcriptional Profile Changes in the Pluripotent Sigma-Class Neoblasts
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Sub-Lethal 5-Fluorouracil Dose Challenges Planarian Stem Cells Promoting Transcriptional Profile Changes in the Pluripotent Sigma-Class Neoblasts

机译:亚致死的5-氟尿嘧啶剂量挑战平面症干细胞促进多能Σ-级新细胞的转录型材变化

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摘要

Under physiological conditions, the complex planarian neoblast system is a composite of hierarchically organized stem cell sub-populations with sigma-class neoblasts, including clonogenic neoblasts, endowed with larger self-renewal and differentiation capabilities, thus generating all the other sub-populations and dominating the regenerative process. This complex system responds to differentiated tissue demands, ensuring a continuous cell turnover in a way to replace aged specialized cells and maintain tissue functionality. Potency of the neoblast system can be appreciated under challenging conditions in which these stem cells are massively depleted and the few remaining repopulate the entire body, ensuring animal resilience. These challenging conditions offer the possibility to deepen the relationships among different neoblast sub-populations, allowing to expose uncanonical properties that are negligible under physiological conditions. In this paper, we employ short, sub-lethal 5-fluorouracil treatment to specifically affect proliferating cells passing through the S phase and demonstrate that S-phase slowdown triggers a shift in the transcriptional profile of sigma neoblasts, which reduces the expression of their hallmark sox-P1. Later, some cells reactivate sox-P1 expression, suggesting that some neoblasts in the earlier steps of commitment could modulate their expression profile, reacquiring a wider differentiative potential.
机译:在生理条件下,复杂的平面图是具有Sigma类新细胞的分层组织的干细胞群的复合物,包括克隆族新细胞,包括克隆族新细胞,赋予更大的自我更新和分化能力,从而产生所有其他子群和主导再生过程。这种复杂的系统响应分化的组织需求,确保替代老年专用细胞并维持组织功能的方式进行连续的细胞周转。在挑战条件下,可以理解新细胞系统的效力,其中这些干细胞大量耗尽,并且剩下的剩余少量储存整个身体,确保动物弹性。这些具有挑战性的条件提供了深化不同新布尔次级人群之间关系的可能性,允许暴露在生理条件下可忽略不计的无甘然属性。在本文中,我们采用短,亚致死的5-氟尿嘧啶处理,以特异性地影响通过S期的增殖细胞,并证明S相减速触发Sigma新细胞的转录轮廓,这减少了其标志的表达SOX-P1。后来,一些细胞重新激活SOX-P1表达,表明在较早的承诺的步骤中的一些新细胞可以调节它们的表达谱,重新探测更宽的差异​​潜力。

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