| dc.contributor.author | Baron, Chloé S. | |
| dc.contributor.author | Kester, Lennart | |
| dc.contributor.author | Klaus, Anna | |
| dc.contributor.author | Boisset, Jean Charles | |
| dc.contributor.author | Thambyrajah, Roshana | |
| dc.contributor.author | Yvernogeau, Laurent | |
| dc.contributor.author | Kouskoff, Valérie | |
| dc.contributor.author | Lacaud, Georges | |
| dc.contributor.author | Van Oudenaarden, Alexander | |
| dc.contributor.author | Robin, Catherine | |
| dc.contributor.other | Universidad de Cantabria | es_ES |
| dc.date.accessioned | 2025-09-30T09:42:39Z | |
| dc.date.available | 2025-09-30T09:42:39Z | |
| dc.date.issued | 2018 | |
| dc.identifier.issn | 2041-1723 | |
| dc.identifier.uri | https://hdl.handle.net/10902/37550 | |
| dc.description.abstract | 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. | es_ES |
| dc.description.sponsorship | This work was supported in CR lab by a European Research Council
grant (ERC, project number 220-H75001EU/HSCOrigin-309361), a TOP8861-subsidy
from NWO/ZonMw (912.15.017), and the UMC Utrecht “Regenerative Medicine &
Stem Cells” priority research program, in G.L. and V.K. labs by the Medical Research
Council (MR/P000673/1), the Biotechnology and Biological Sciences Research Council
(BB/I001794/1), Bloodwise (12037), the European Union’s Horizon 2020 (GA6586250)
and Cancer Research UK (C5759/A20971), and in A. v O. lab by a TOP-subsidy NWO/
CW (714.016.001). | es_ES |
| dc.format.extent | 15 p. | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Nature Publishing Group | es_ES |
| dc.rights | © The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License. | es_ES |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.source | Nature Communications, 2012, 9(1), 2517 | es_ES |
| dc.title | Single-cell transcriptomics reveal the dynamic of haematopoietic stem cell production in the aorta | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publisherVersion | https://doi.org/10.1038/s41467-018-04893-3 | es_ES |
| dc.rights.accessRights | openAccess | es_ES |
| dc.identifier.DOI | 10.1038/s41467-018-04893-3 | |
| dc.type.version | publishedVersion | es_ES |