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In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis
During embryogenesis, haematopoietic and endothelial lineages emerge closely in time and space. It is thought that the first blood and endothelium derive from a common clonal ancestor, the haemangioblast. However, investigation of candidate haemangioblasts in vitro revealed the capacity for mesenchy...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810727/ https://www.ncbi.nlm.nih.gov/pubmed/36596806 http://dx.doi.org/10.1038/s41467-022-35744-x |
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author | Biben, C. Weber, T. S. Potts, K. S. Choi, J. Miles, D. C. Carmagnac, A. Sargeant, T. de Graaf, C. A. Fennell, K. A. Farley, A. Stonehouse, O. J. Dawson, M. A. Hilton, D. J. Naik, S. H. Taoudi, S. |
author_facet | Biben, C. Weber, T. S. Potts, K. S. Choi, J. Miles, D. C. Carmagnac, A. Sargeant, T. de Graaf, C. A. Fennell, K. A. Farley, A. Stonehouse, O. J. Dawson, M. A. Hilton, D. J. Naik, S. H. Taoudi, S. |
author_sort | Biben, C. |
collection | PubMed |
description | During embryogenesis, haematopoietic and endothelial lineages emerge closely in time and space. It is thought that the first blood and endothelium derive from a common clonal ancestor, the haemangioblast. However, investigation of candidate haemangioblasts in vitro revealed the capacity for mesenchymal differentiation, a feature more compatible with an earlier mesodermal precursor. To date, no evidence for an in vivo haemangioblast has been discovered. Using single cell RNA-Sequencing and in vivo cellular barcoding, we have unravelled the ancestral relationships that give rise to the haematopoietic lineages of the yolk sac, the endothelium, and the mesenchyme. We show that the mesodermal derivatives of the yolk sac are produced by three distinct precursors with dual-lineage outcomes: the haemangioblast, the mesenchymoangioblast, and a previously undescribed cell type: the haematomesoblast. Between E5.5 and E7.5, this trio of precursors seeds haematopoietic, endothelial, and mesenchymal trajectories. |
format | Online Article Text |
id | pubmed-9810727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-98107272023-01-05 In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis Biben, C. Weber, T. S. Potts, K. S. Choi, J. Miles, D. C. Carmagnac, A. Sargeant, T. de Graaf, C. A. Fennell, K. A. Farley, A. Stonehouse, O. J. Dawson, M. A. Hilton, D. J. Naik, S. H. Taoudi, S. Nat Commun Article During embryogenesis, haematopoietic and endothelial lineages emerge closely in time and space. It is thought that the first blood and endothelium derive from a common clonal ancestor, the haemangioblast. However, investigation of candidate haemangioblasts in vitro revealed the capacity for mesenchymal differentiation, a feature more compatible with an earlier mesodermal precursor. To date, no evidence for an in vivo haemangioblast has been discovered. Using single cell RNA-Sequencing and in vivo cellular barcoding, we have unravelled the ancestral relationships that give rise to the haematopoietic lineages of the yolk sac, the endothelium, and the mesenchyme. We show that the mesodermal derivatives of the yolk sac are produced by three distinct precursors with dual-lineage outcomes: the haemangioblast, the mesenchymoangioblast, and a previously undescribed cell type: the haematomesoblast. Between E5.5 and E7.5, this trio of precursors seeds haematopoietic, endothelial, and mesenchymal trajectories. Nature Publishing Group UK 2023-01-03 /pmc/articles/PMC9810727/ /pubmed/36596806 http://dx.doi.org/10.1038/s41467-022-35744-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Biben, C. Weber, T. S. Potts, K. S. Choi, J. Miles, D. C. Carmagnac, A. Sargeant, T. de Graaf, C. A. Fennell, K. A. Farley, A. Stonehouse, O. J. Dawson, M. A. Hilton, D. J. Naik, S. H. Taoudi, S. In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title | In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title_full | In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title_fullStr | In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title_full_unstemmed | In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title_short | In vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
title_sort | in vivo clonal tracking reveals evidence of haemangioblast and haematomesoblast contribution to yolk sac haematopoiesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810727/ https://www.ncbi.nlm.nih.gov/pubmed/36596806 http://dx.doi.org/10.1038/s41467-022-35744-x |
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