Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bonkhofer, Florian, Rispoli, Rossella, Pinheiro, Philip, Krecsmarik, Monika, Schneider-Swales, Janina, Tsang, Ingrid Ho Ching, de Bruijn, Marella, Monteiro, Rui, Peterkin, Tessa, Patient, Roger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783442769125048320
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
work_keys_str_mv AT bonkhoferflorian bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT rispolirossella bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT pinheirophilip bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT krecsmarikmonika bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT schneiderswalesjanina bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT tsangingridhoching bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT debruijnmarella bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT monteirorui bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT peterkintessa bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium
AT patientroger bloodstemcellforminghaemogenicendotheliuminzebrafishderivesfromarterialendothelium