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Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion

Formation of a regularly branched blood vessel network is crucial in development and physiology. Here we show that the expression of the Notch ligand Dll4 fluctuates in individual endothelial cells within sprouting vessels in the mouse retina in vivo and in correlation with dynamic cell movement in...

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Autores principales: Ubezio, Benedetta, Blanco, Raquel Agudo, Geudens, Ilse, Stanchi, Fabio, Mathivet, Thomas, Jones, Martin L, Ragab, Anan, Bentley, Katie, Gerhardt, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894757/
https://www.ncbi.nlm.nih.gov/pubmed/27074663
http://dx.doi.org/10.7554/eLife.12167
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author Ubezio, Benedetta
Blanco, Raquel Agudo
Geudens, Ilse
Stanchi, Fabio
Mathivet, Thomas
Jones, Martin L
Ragab, Anan
Bentley, Katie
Gerhardt, Holger
author_facet Ubezio, Benedetta
Blanco, Raquel Agudo
Geudens, Ilse
Stanchi, Fabio
Mathivet, Thomas
Jones, Martin L
Ragab, Anan
Bentley, Katie
Gerhardt, Holger
author_sort Ubezio, Benedetta
collection PubMed
description Formation of a regularly branched blood vessel network is crucial in development and physiology. Here we show that the expression of the Notch ligand Dll4 fluctuates in individual endothelial cells within sprouting vessels in the mouse retina in vivo and in correlation with dynamic cell movement in mouse embryonic stem cell-derived sprouting assays. We also find that sprout elongation and branching associates with a highly differential phase pattern of Dll4 between endothelial cells. Stimulation with pathologically high levels of Vegf, or overexpression of Dll4, leads to Notch dependent synchronization of Dll4 fluctuations within clusters, both in vitro and in vivo. Our results demonstrate that the Vegf-Dll4/Notch feedback system normally operates to generate heterogeneity between endothelial cells driving branching, whilst synchronization drives vessel expansion. We propose that this sensitive phase transition in the behaviour of the Vegf-Dll4/Notch feedback loop underlies the morphogen function of Vegfa in vascular patterning. DOI: http://dx.doi.org/10.7554/eLife.12167.001
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spelling pubmed-48947572016-06-08 Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion Ubezio, Benedetta Blanco, Raquel Agudo Geudens, Ilse Stanchi, Fabio Mathivet, Thomas Jones, Martin L Ragab, Anan Bentley, Katie Gerhardt, Holger eLife Computational and Systems Biology Formation of a regularly branched blood vessel network is crucial in development and physiology. Here we show that the expression of the Notch ligand Dll4 fluctuates in individual endothelial cells within sprouting vessels in the mouse retina in vivo and in correlation with dynamic cell movement in mouse embryonic stem cell-derived sprouting assays. We also find that sprout elongation and branching associates with a highly differential phase pattern of Dll4 between endothelial cells. Stimulation with pathologically high levels of Vegf, or overexpression of Dll4, leads to Notch dependent synchronization of Dll4 fluctuations within clusters, both in vitro and in vivo. Our results demonstrate that the Vegf-Dll4/Notch feedback system normally operates to generate heterogeneity between endothelial cells driving branching, whilst synchronization drives vessel expansion. We propose that this sensitive phase transition in the behaviour of the Vegf-Dll4/Notch feedback loop underlies the morphogen function of Vegfa in vascular patterning. DOI: http://dx.doi.org/10.7554/eLife.12167.001 eLife Sciences Publications, Ltd 2016-04-13 /pmc/articles/PMC4894757/ /pubmed/27074663 http://dx.doi.org/10.7554/eLife.12167 Text en © 2016, Ubezio et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Ubezio, Benedetta
Blanco, Raquel Agudo
Geudens, Ilse
Stanchi, Fabio
Mathivet, Thomas
Jones, Martin L
Ragab, Anan
Bentley, Katie
Gerhardt, Holger
Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title_full Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title_fullStr Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title_full_unstemmed Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title_short Synchronization of endothelial Dll4-Notch dynamics switch blood vessels from branching to expansion
title_sort synchronization of endothelial dll4-notch dynamics switch blood vessels from branching to expansion
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894757/
https://www.ncbi.nlm.nih.gov/pubmed/27074663
http://dx.doi.org/10.7554/eLife.12167
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