首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Identification of a new intrinsically timed developmental checkpoint that reprograms key hematopoietic stem cell properties
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Identification of a new intrinsically timed developmental checkpoint that reprograms key hematopoietic stem cell properties

机译:识别新的内在定时发育检查点该检查点可重新编程关键的造血干细胞特性

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摘要

Hematopoietic stem cells (HSCs) execute self-renewal divisions throughout fetal and adult life, although some of their properties do alter. Here we analyzed the magnitude and timing of changes in the self-renewal properties and differentiated cell outputs of transplanted HSCs obtained from different sources during development. We also assessed the expression of several “stem cell” genes in corresponding populations of highly purified HSCs. Fetal and adult HSCs displayed marked differences in their self-renewal, differentiated cell output, and gene expression properties, with persistence of a fetal phenotype until 3 weeks after birth. Then, 1 week later, the HSCs became functionally indistinguishable from adult HSCs. The same schedule of changes in HSC properties occurred when HSCs from fetal or 3-week-old donors were transplanted into adult recipients. These findings point to the existence of a previously unrecognized, intrinsically regulated master switch that effects a developmental change in key HSC properties.
机译:造血干细胞(HSC)在整个胎儿和成年生活中都会进行自我更新分裂,尽管它们的某些特性确实会发生变化。在这里,我们分析了在发展过程中从不同来源获得的移植HSC的自我更新特性和分化细胞输出的变化幅度和时机。我们还评估了几个“干细胞”基因在相应的高纯度HSC群体中的表达。胎儿和成人HSC在自我更新,分化的细胞输出和基因表达特性方面显示出显着差异,并且胎儿的表型会持续到出生后3周。然后,在1周后,HSC与成人HSC在功能上无法区分开。当将来自胎儿或三周龄供体的HSC移植到成年受体中时,发生了HSC特性变化的相同时间表。这些发现表明,存在以前无法识别的,内在调节的主开关,该开关会影响关键HSC特性的发展变化。

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