An interactive resource of molecular signalling in the developing human haematopoietic stem cell niche

被引:2
|
作者
Crosse, Edie I. [1 ,4 ]
Binagui-Casas, Anahi [1 ]
Gordon-Keylock, Sabrina [1 ]
Rybtsov, Stanislav [1 ]
Tamagno, Sara [1 ]
Olofsson, Didrik [2 ]
Anderson, Richard A. [3 ]
Medvinsky, Alexander [1 ]
机构
[1] Univ Edinburgh, Ctr Regenerat Med, Edinburgh EH16 4UU, Scotland
[2] Omiqa Bioinformat GmbH, Altensteinstr 40, D-14195 Berlin, Germany
[3] Univ Edinburgh, MRC Ctr Reprod Hlth, Edinburgh EH16 4TJ, Scotland
[4] Fred Hutchinson Canc Ctr, 1100 Fairview Ave N, Seattle, WA 98109 USA
来源
DEVELOPMENT | 2023年 / 150卷 / 23期
基金
英国医学研究理事会;
关键词
Haematopoiesis; Human development; Spatial transcriptomics; Single cell RNA-seq; AGM region; EPITHELIAL-MESENCHYMAL TRANSITION; PROGENITOR CELLS; DEFINITIVE HEMATOPOIESIS; HEMOGENIC ENDOTHELIUM; MYB GENE; C-MYB; AORTA; DIFFERENTIATION; IDENTIFICATION; GENERATION;
D O I
10.1242/dev.201972
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The emergence of definitive human haematopoietic stem cells mesonephros (AGM) region is a tightly regulated process. Previously, we conducted spatial transcriptomic analysis of the human AGM region at the end of this period (CS16/CS17) and identified secreted factors involved in HSC development. Here, we extend our analysis to investigate the progression of dorso-ventral polarised signalling around the dorsal aorta over the entire period of HSC emergence. Our results reveal a dramatic increase in ventral signalling complexity from the CS13-CS14 transition, coinciding with the first appearance of definitive HSCs. We further observe stage-specific changes in signalling up to CS17, which may underpin the step-wise maturation of HSCs described in the mouse model. The data-rich resource is also presented in an online interface enabling in silico analysis of molecular interactions between spatially defined domains of the AGM region. This resource will be of particular interest for researchers as those developing in vitro methods for the generation of clinically relevant HSCs from pluripotent stem cells.
引用
收藏
页数:15
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