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细胞追踪显示卵黄囊对成体造血的贡献。

Cell tracing shows the contribution of the yolk sac to adult haematopoiesis.

作者信息

Samokhvalov Igor M, Samokhvalova Natalia I, Nishikawa Shin-ichi

机构信息

Laboratory for Stem Cell Biology, Center for Developmental Biology, RIKEN Kobe, Kobe 650-0047, Japan.

出版信息

Nature. 2007 Apr 26;446(7139):1056-61. doi: 10.1038/nature05725. Epub 2007 Mar 21.

Abstract

The first haematopoietic stem cells (HSCs) appear in the aorta-gonad-mesonephros (AGM) region, major vitelline and umbilical vessels, and placenta; however, whether they arise locally or from immigrant yolk sac precursor cells remains unclear. This issue is best addressed by measuring cell-lineage relationships rather than cell potentials. To undertake long-term in vivo tracing of yolk sac cells, we designed a non-invasive pulse-labelling system based on Cre/loxP recombination. Here we show that in Runx1(+/-) (runt-related transcription factor 1) heterozygous mice, yolk sac cells expressing Runx1 at embryonic day 7.5 develop into fetal lymphoid progenitors and adult HSCs. During mid-gestation the labelled (embryonic day 7.5) yolk sac cells colonize the umbilical cord, the AGM region and subsequently the embryonic liver. This raises the possibility that some HSCs associated with major embryonic vasculature are derived from yolk sac precursors. We observed virtually no contribution of the labelled cells towards the yolk sac vasculature, indicating early segregation of endothelial and haematopoietic lineages.

摘要

首批造血干细胞(HSCs)出现在主动脉-性腺-中肾(AGM)区域、主要卵黄囊和脐血管以及胎盘中;然而,它们是在局部产生还是源自迁移的卵黄囊前体细胞仍不清楚。通过测量细胞谱系关系而非细胞潜能,能最好地解决这个问题。为了对卵黄囊细胞进行长期体内追踪,我们基于Cre/loxP重组设计了一种非侵入性脉冲标记系统。在此我们表明,在Runx1(+/-)( runt相关转录因子1)杂合小鼠中,在胚胎第7.5天表达Runx1的卵黄囊细胞发育为胎儿淋巴祖细胞和成年造血干细胞。在妊娠中期,标记的(胚胎第7.5天)卵黄囊细胞定植于脐带、AGM区域,随后定植于胚胎肝脏。这增加了一种可能性,即一些与主要胚胎血管相关的造血干细胞源自卵黄囊前体细胞。我们实际上观察到标记细胞对卵黄囊脉管系统几乎没有贡献,这表明内皮细胞和造血细胞谱系早期就发生了分离。

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