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Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization
Formation of organ-specific vasculatures requires cross-talk between developing tissue and specialized endothelial cells. Here we show how developing zebrafish spinal cord neurons coordinate vessel growth through balancing of neuron-derived Vegfaa, with neuronal sFlt1 restricting Vegfaa-Kdrl mediate...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234075/ https://www.ncbi.nlm.nih.gov/pubmed/28071661 http://dx.doi.org/10.1038/ncomms13991 |
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author | Wild, Raphael Klems, Alina Takamiya, Masanari Hayashi, Yuya Strähle, Uwe Ando, Koji Mochizuki, Naoki van Impel, Andreas Schulte-Merker, Stefan Krueger, Janna Preau, Laetitia le Noble, Ferdinand |
author_facet | Wild, Raphael Klems, Alina Takamiya, Masanari Hayashi, Yuya Strähle, Uwe Ando, Koji Mochizuki, Naoki van Impel, Andreas Schulte-Merker, Stefan Krueger, Janna Preau, Laetitia le Noble, Ferdinand |
author_sort | Wild, Raphael |
collection | PubMed |
description | Formation of organ-specific vasculatures requires cross-talk between developing tissue and specialized endothelial cells. Here we show how developing zebrafish spinal cord neurons coordinate vessel growth through balancing of neuron-derived Vegfaa, with neuronal sFlt1 restricting Vegfaa-Kdrl mediated angiogenesis at the neurovascular interface. Neuron-specific loss of flt1 or increased neuronal vegfaa expression promotes angiogenesis and peri-neural tube vascular network formation. Combining loss of neuronal flt1 with gain of vegfaa promotes sprout invasion into the neural tube. On loss of neuronal flt1, ectopic sprouts emanate from veins involving special angiogenic cell behaviours including nuclear positioning and a molecular signature distinct from primary arterial or secondary venous sprouting. Manipulation of arteriovenous identity or Notch signalling established that ectopic sprouting in flt1 mutants requires venous endothelium. Conceptually, our data suggest that spinal cord vascularization proceeds from veins involving two-tiered regulation of neuronal sFlt1 and Vegfaa via a novel sprouting mode. |
format | Online Article Text |
id | pubmed-5234075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52340752017-01-24 Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization Wild, Raphael Klems, Alina Takamiya, Masanari Hayashi, Yuya Strähle, Uwe Ando, Koji Mochizuki, Naoki van Impel, Andreas Schulte-Merker, Stefan Krueger, Janna Preau, Laetitia le Noble, Ferdinand Nat Commun Article Formation of organ-specific vasculatures requires cross-talk between developing tissue and specialized endothelial cells. Here we show how developing zebrafish spinal cord neurons coordinate vessel growth through balancing of neuron-derived Vegfaa, with neuronal sFlt1 restricting Vegfaa-Kdrl mediated angiogenesis at the neurovascular interface. Neuron-specific loss of flt1 or increased neuronal vegfaa expression promotes angiogenesis and peri-neural tube vascular network formation. Combining loss of neuronal flt1 with gain of vegfaa promotes sprout invasion into the neural tube. On loss of neuronal flt1, ectopic sprouts emanate from veins involving special angiogenic cell behaviours including nuclear positioning and a molecular signature distinct from primary arterial or secondary venous sprouting. Manipulation of arteriovenous identity or Notch signalling established that ectopic sprouting in flt1 mutants requires venous endothelium. Conceptually, our data suggest that spinal cord vascularization proceeds from veins involving two-tiered regulation of neuronal sFlt1 and Vegfaa via a novel sprouting mode. Nature Publishing Group 2017-01-10 /pmc/articles/PMC5234075/ /pubmed/28071661 http://dx.doi.org/10.1038/ncomms13991 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wild, Raphael Klems, Alina Takamiya, Masanari Hayashi, Yuya Strähle, Uwe Ando, Koji Mochizuki, Naoki van Impel, Andreas Schulte-Merker, Stefan Krueger, Janna Preau, Laetitia le Noble, Ferdinand Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title_full | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title_fullStr | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title_full_unstemmed | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title_short | Neuronal sFlt1 and Vegfaa determine venous sprouting and spinal cord vascularization |
title_sort | neuronal sflt1 and vegfaa determine venous sprouting and spinal cord vascularization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5234075/ https://www.ncbi.nlm.nih.gov/pubmed/28071661 http://dx.doi.org/10.1038/ncomms13991 |
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