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Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium
Haematopoietic stem cells are generated from the haemogenic endothelium (HE) located in the floor of the dorsal aorta (DA). Despite being integral to arteries, it is controversial whether HE and arterial endothelium share a common lineage. Here, we present a transgenic zebrafish runx1 reporter line...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687740/ https://www.ncbi.nlm.nih.gov/pubmed/31395869 http://dx.doi.org/10.1038/s41467-019-11423-2 |
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author | Bonkhofer, Florian Rispoli, Rossella Pinheiro, Philip Krecsmarik, Monika Schneider-Swales, Janina Tsang, Ingrid Ho Ching de Bruijn, Marella Monteiro, Rui Peterkin, Tessa Patient, Roger |
author_facet | Bonkhofer, Florian Rispoli, Rossella Pinheiro, Philip Krecsmarik, Monika Schneider-Swales, Janina Tsang, Ingrid Ho Ching de Bruijn, Marella Monteiro, Rui Peterkin, Tessa Patient, Roger |
author_sort | Bonkhofer, Florian |
collection | PubMed |
description | Haematopoietic stem cells are generated from the haemogenic endothelium (HE) located in the floor of the dorsal aorta (DA). Despite being integral to arteries, it is controversial whether HE and arterial endothelium share a common lineage. Here, we present a transgenic zebrafish runx1 reporter line to isolate HE and aortic roof endothelium (ARE)s, excluding non-aortic endothelium. Transcriptomic analysis of these populations identifies Runx1-regulated genes and shows that HE initially expresses arterial markers at similar levels to ARE. Furthermore, runx1 expression depends on prior arterial programming by the Notch ligand dll4. Runx1(−/−) mutants fail to downregulate arterial genes in the HE, which remains integrated within the DA, suggesting that Runx1 represses the pre-existing arterial programme in HE to allow progression towards the haematopoietic fate. These findings strongly suggest that, in zebrafish, aortic endothelium is a precursor to HE, with potential implications for pluripotent stem cell differentiation protocols for the generation of transplantable HSCs. |
format | Online Article Text |
id | pubmed-6687740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66877402019-08-12 Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium Bonkhofer, Florian Rispoli, Rossella Pinheiro, Philip Krecsmarik, Monika Schneider-Swales, Janina Tsang, Ingrid Ho Ching de Bruijn, Marella Monteiro, Rui Peterkin, Tessa Patient, Roger Nat Commun Article Haematopoietic stem cells are generated from the haemogenic endothelium (HE) located in the floor of the dorsal aorta (DA). Despite being integral to arteries, it is controversial whether HE and arterial endothelium share a common lineage. Here, we present a transgenic zebrafish runx1 reporter line to isolate HE and aortic roof endothelium (ARE)s, excluding non-aortic endothelium. Transcriptomic analysis of these populations identifies Runx1-regulated genes and shows that HE initially expresses arterial markers at similar levels to ARE. Furthermore, runx1 expression depends on prior arterial programming by the Notch ligand dll4. Runx1(−/−) mutants fail to downregulate arterial genes in the HE, which remains integrated within the DA, suggesting that Runx1 represses the pre-existing arterial programme in HE to allow progression towards the haematopoietic fate. These findings strongly suggest that, in zebrafish, aortic endothelium is a precursor to HE, with potential implications for pluripotent stem cell differentiation protocols for the generation of transplantable HSCs. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687740/ /pubmed/31395869 http://dx.doi.org/10.1038/s41467-019-11423-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Bonkhofer, Florian Rispoli, Rossella Pinheiro, Philip Krecsmarik, Monika Schneider-Swales, Janina Tsang, Ingrid Ho Ching de Bruijn, Marella Monteiro, Rui Peterkin, Tessa Patient, Roger Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title_full | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title_fullStr | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title_full_unstemmed | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title_short | Blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
title_sort | blood stem cell-forming haemogenic endothelium in zebrafish derives from arterial endothelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687740/ https://www.ncbi.nlm.nih.gov/pubmed/31395869 http://dx.doi.org/10.1038/s41467-019-11423-2 |
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