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An unexpected role for IL-3 in the embryonic development of hematopoietic stem cells

机译:IL-3在造血干细胞胚胎发育中的意外作用

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摘要

Cytokines are important in adult hematopoiesis, yet their function in embryonic hematopoiesis has been largely unexplored. During development, hematopoietic stem cells (HSCs) are found in the aorta-gonad-mesonephros (AGM) region, yolk sac (YS), and placenta and require the Runx1 transcription factor for their normal generation. Since IL-3 is a Runx1 target and this cytokine acts on adult hematopoietic cells, we examined whether IL-3 affects HSCs in the mouse embryo. Using Runx1 haploinsufficient mice, we show that IL-3 amplifies HSCs from El 1 AGM, YS, and placenta. Moreover, we show that IL-3 mutant embryos are deficient in HSCs and that IL-3 reveals the presence of HSCs in the AGM and YS prior to the stage at which HSCs are normally detected. Thus, our studies support an unexpected role for IL-3 during development and strongly suggest that IL-3 functions as a proliferation and/or survival factor for the earliest HSCs in the embryo.
机译:细胞因子在成年造血细胞中很重要,但是在胚胎造血细胞中的功能尚未得到充分探索。在发育过程中,造血干细胞(HSC)被发现在主动脉-性腺-中肾(AGM),卵黄囊(YS)和胎盘中,并且需要Runx1转录因子才能正常生成。由于IL-3是Runx1靶标,并且该细胞因子作用于成年造血细胞,因此我们检查了IL-3是否会影响小鼠胚胎中的HSC。使用Runx1单倍体不足的小鼠,我们显示IL-3可从El 1 AGM,YS和胎盘中扩增HSC。此外,我们表明,IL-3突变体胚胎在HSC中缺乏,并且IL-3在正常检测到HSC的阶段之前揭示了AGM和YS中HSC的存在。因此,我们的研究支持IL-3在发育过程中的出乎意料的作用,并强烈建议IL-3充当胚胎中最早的HSC的增殖和/或存活因子。

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