Single-cell transcriptomics reveal the dynamic of haematopoietic stem cell production in the aorta

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作者
Chloé S. Baron
Lennart Kester
Anna Klaus
Jean-Charles Boisset
Roshana Thambyrajah
Laurent Yvernogeau
Valérie Kouskoff
Georges Lacaud
Alexander van Oudenaarden
Catherine Robin
机构
[1] University Medical Center Utrecht,Hubrecht Institute
[2] The University of Manchester,KNAW
[3] The University of Manchester,CRUK Stem Cell Biology Group, Cancer Research UK Manchester Institute
[4] University Medical Center Utrecht,Division of Developmental Biology and Medicine
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Nature Communications | / 9卷
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摘要
Haematopoietic stem cells (HSCs) are generated from haemogenic endothelial (HE) cells via the formation of intra-aortic haematopoietic clusters (IAHCs) in vertebrate embryos. The molecular events controlling endothelial specification, endothelial-to-haematopoietic transition (EHT) and IAHC formation, as it occurs in vivo inside the aorta, are still poorly understood. To gain insight in these processes, we performed single-cell RNA-sequencing of non-HE cells, HE cells, cells undergoing EHT, IAHC cells, and whole IAHCs isolated from mouse embryo aortas. Our analysis identified the genes and transcription factor networks activated during the endothelial-to-haematopoietic switch and IAHC cell maturation toward an HSC fate. Our study provides an unprecedented complete resource to study in depth HSC generation in vivo. It will pave the way for improving HSC production in vitro to address the growing need for tailor-made HSCs to treat patients with blood-related disorders.
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