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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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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 |
format | Online Article Text |
id | pubmed-4894757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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