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Hlf 标记造血干细胞的发育途径,但不标记红系-髓系祖细胞。

Hlf marks the developmental pathway for hematopoietic stem cells but not for erythro-myeloid progenitors.

机构信息

International Research Center for Medical Sciences, Kumamoto University, Kumamoto, Japan

Department of Hematology, Juntendo University Graduate School of Medicine, Tokyo, Japan.

出版信息

J Exp Med. 2019 Jul 1;216(7):1599-1614. doi: 10.1084/jem.20181399. Epub 2019 May 10.

Abstract

Before the emergence of hematopoietic stem cells (HSCs), lineage-restricted progenitors, such as erythro-myeloid progenitors (EMPs), are detected in the embryo or in pluripotent stem cell cultures in vitro. Although both HSCs and EMPs are derived from hemogenic endothelium, it remains unclear how and when these two developmental programs are segregated during ontogeny. Here, we show that hepatic leukemia factor (Hlf) expression specifically marks a developmental continuum between HSC precursors and HSCs. Using the -tdTomato reporter mouse, we found that is expressed in intra-aortic hematopoietic clusters and fetal liver HSCs. In contrast, EMPs and yolk sac hematopoietic clusters before embryonic day 9.5 do not express HSC specification, regulated by the Evi-1/Hlf axis, is activated only within Hlf nascent hematopoietic clusters. These results strongly suggest that HSCs and EMPs are generated from distinct cohorts of hemogenic endothelium. Selective induction of the Hlf lineage pathway may lead to the in vitro generation of HSCs from pluripotent stem cells.

摘要

在造血干细胞(HSCs)出现之前,在胚胎或体外多能干细胞培养物中可以检测到谱系受限的祖细胞,如红髓祖细胞(EMPs)。虽然 HSCs 和 EMPs 均来源于造血内皮,但尚不清楚这两个发育程序在个体发生过程中是如何以及何时分开的。在这里,我们表明肝白血病因子(Hlf)的表达特异性标记了 HSC 前体和 HSCs 之间的发育连续体。使用 -tdTomato 报告基因小鼠,我们发现 在主动脉造血簇和胎儿肝脏 HSCs 中表达。相比之下,EMP 和卵黄囊造血簇在胚胎第 9.5 天之前不表达 HSC 特异性,由 Evi-1/Hlf 轴调节,仅在 Hlf 新生造血簇中被激活。这些结果强烈表明 HSCs 和 EMP 是由不同的造血内皮群体产生的。选择性诱导 Hlf 谱系途径可能导致体外从多能干细胞生成 HSCs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/723c/6605751/e33ccfdaea7c/JEM_20181399_Fig1.jpg

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