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主动脉-性腺-中肾区的分子图谱揭示BMPER是造血干细胞成熟的新型调节因子。

A molecular roadmap of the AGM region reveals BMPER as a novel regulator of HSC maturation.

作者信息

McGarvey Alison C, Rybtsov Stanislav, Souilhol Céline, Tamagno Sara, Rice Ritva, Hills David, Godwin Duncan, Rice David, Tomlinson Simon R, Medvinsky Alexander

机构信息

Stem Cell Bioinformatics Group, Institute for Stem Cell Research, Medical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, Scotland, UK.

Ontogeny of Haematopoietic Stem Cells Group, Institute for Stem Cell Research, Medical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, Scotland, UK.

出版信息

J Exp Med. 2017 Dec 4;214(12):3731-3751. doi: 10.1084/jem.20162012. Epub 2017 Nov 1.

DOI:10.1084/jem.20162012
PMID:29093060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5716029/
Abstract

In the developing embryo, hematopoietic stem cells (HSCs) emerge from the aorta-gonad-mesonephros (AGM) region, but the molecular regulation of this process is poorly understood. Recently, the progression from E9.5 to E10.5 and polarity along the dorso-ventral axis have been identified as clear demarcations of the supportive HSC niche. To identify novel secreted regulators of HSC maturation, we performed RNA sequencing over these spatiotemporal transitions in the AGM region and supportive OP9 cell line. Screening several proteins through an ex vivo reaggregate culture system, we identify BMPER as a novel positive regulator of HSC development. We demonstrate that BMPER is associated with BMP signaling inhibition, but is transcriptionally induced by BMP4, suggesting that BMPER contributes to the precise control of BMP activity within the AGM region, enabling the maturation of HSCs within a BMP-negative environment. These findings and the availability of our transcriptional data through an accessible interface should provide insight into the maintenance and potential derivation of HSCs in culture.

摘要

在发育中的胚胎中,造血干细胞(HSCs)源自主动脉-性腺-中肾(AGM)区域,但这一过程的分子调控机制尚不清楚。最近,从E9.5到E10.5的发育进程以及沿背腹轴的极性已被确定为支持性造血干细胞龛的明确界限。为了鉴定造血干细胞成熟的新型分泌调节因子,我们在AGM区域和支持性OP9细胞系的这些时空转变过程中进行了RNA测序。通过体外重聚集培养系统筛选了几种蛋白质,我们确定BMPER是造血干细胞发育的新型正向调节因子。我们证明BMPER与BMP信号抑制有关,但受BMP4转录诱导,这表明BMPER有助于精确控制AGM区域内的BMP活性,从而使造血干细胞在BMP阴性环境中成熟。这些发现以及我们通过可访问界面提供的转录数据应有助于深入了解培养中造血干细胞的维持和潜在来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/ffc2ee1e0375/JEM_20162012_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/b51920e4c9d2/JEM_20162012_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/4c2a90682b3c/JEM_20162012_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/9e2ea723dad7/JEM_20162012_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/90ed5f02af7b/JEM_20162012_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/2630247c2484/JEM_20162012_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/bf52dad551b7/JEM_20162012_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/ffc2ee1e0375/JEM_20162012_Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/b51920e4c9d2/JEM_20162012_Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/4c2a90682b3c/JEM_20162012_Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/9e2ea723dad7/JEM_20162012_Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/90ed5f02af7b/JEM_20162012_Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/2630247c2484/JEM_20162012_Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/bf52dad551b7/JEM_20162012_Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eae0/5716029/ffc2ee1e0375/JEM_20162012_Fig7.jpg

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