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Temporal modulation of collective cell behavior controls vascular network topology
Vascular network density determines the amount of oxygen and nutrients delivered to host tissues, but how the vast diversity of densities is generated is unknown. Reiterations of endothelial-tip-cell selection, sprout extension and anastomosis are the basis for vascular network generation, a process...
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/PMC4811760/ https://www.ncbi.nlm.nih.gov/pubmed/26910011 http://dx.doi.org/10.7554/eLife.13212 |
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author | Kur, Esther Kim, Jiha Tata, Aleksandra Comin, Cesar H Harrington, Kyle I Costa, Luciano da F Bentley, Katie Gu, Chenghua |
author_facet | Kur, Esther Kim, Jiha Tata, Aleksandra Comin, Cesar H Harrington, Kyle I Costa, Luciano da F Bentley, Katie Gu, Chenghua |
author_sort | Kur, Esther |
collection | PubMed |
description | Vascular network density determines the amount of oxygen and nutrients delivered to host tissues, but how the vast diversity of densities is generated is unknown. Reiterations of endothelial-tip-cell selection, sprout extension and anastomosis are the basis for vascular network generation, a process governed by the VEGF/Notch feedback loop. Here, we find that temporal regulation of this feedback loop, a previously unexplored dimension, is the key mechanism to determine vascular density. Iterating between computational modeling and in vivo live imaging, we demonstrate that the rate of tip-cell selection determines the length of linear sprout extension at the expense of branching, dictating network density. We provide the first example of a host tissue-derived signal (Semaphorin3E-Plexin-D1) that accelerates tip cell selection rate, yielding a dense network. We propose that temporal regulation of this critical, iterative aspect of network formation could be a general mechanism, and additional temporal regulators may exist to sculpt vascular topology. DOI: http://dx.doi.org/10.7554/eLife.13212.001 |
format | Online Article Text |
id | pubmed-4811760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-48117602016-04-04 Temporal modulation of collective cell behavior controls vascular network topology Kur, Esther Kim, Jiha Tata, Aleksandra Comin, Cesar H Harrington, Kyle I Costa, Luciano da F Bentley, Katie Gu, Chenghua eLife Computational and Systems Biology Vascular network density determines the amount of oxygen and nutrients delivered to host tissues, but how the vast diversity of densities is generated is unknown. Reiterations of endothelial-tip-cell selection, sprout extension and anastomosis are the basis for vascular network generation, a process governed by the VEGF/Notch feedback loop. Here, we find that temporal regulation of this feedback loop, a previously unexplored dimension, is the key mechanism to determine vascular density. Iterating between computational modeling and in vivo live imaging, we demonstrate that the rate of tip-cell selection determines the length of linear sprout extension at the expense of branching, dictating network density. We provide the first example of a host tissue-derived signal (Semaphorin3E-Plexin-D1) that accelerates tip cell selection rate, yielding a dense network. We propose that temporal regulation of this critical, iterative aspect of network formation could be a general mechanism, and additional temporal regulators may exist to sculpt vascular topology. DOI: http://dx.doi.org/10.7554/eLife.13212.001 eLife Sciences Publications, Ltd 2016-02-24 /pmc/articles/PMC4811760/ /pubmed/26910011 http://dx.doi.org/10.7554/eLife.13212 Text en © 2016, Kur 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 Kur, Esther Kim, Jiha Tata, Aleksandra Comin, Cesar H Harrington, Kyle I Costa, Luciano da F Bentley, Katie Gu, Chenghua Temporal modulation of collective cell behavior controls vascular network topology |
title | Temporal modulation of collective cell behavior controls vascular network topology |
title_full | Temporal modulation of collective cell behavior controls vascular network topology |
title_fullStr | Temporal modulation of collective cell behavior controls vascular network topology |
title_full_unstemmed | Temporal modulation of collective cell behavior controls vascular network topology |
title_short | Temporal modulation of collective cell behavior controls vascular network topology |
title_sort | temporal modulation of collective cell behavior controls vascular network topology |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811760/ https://www.ncbi.nlm.nih.gov/pubmed/26910011 http://dx.doi.org/10.7554/eLife.13212 |
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