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Endothelial Notch signalling limits angiogenesis via control of artery formation
Angiogenic sprouting needs to be tightly controlled. It has been suggested that the Notch ligand dll4 expressed in leading tip cells restricts angiogenesis by activating Notch signalling in trailing stalk cells. Here, we show using live imaging in zebrafish that activation of Notch signalling is rat...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534340/ https://www.ncbi.nlm.nih.gov/pubmed/28714969 http://dx.doi.org/10.1038/ncb3574 |
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author | Hasan, Sana S. Tsaryk, Roman Lange, Martin Wisniewski, Laura Moore, John C. Lawson, Nathan D. Wojciechowska, Karolina Schnittler, Hans Siekmann, Arndt F. |
author_facet | Hasan, Sana S. Tsaryk, Roman Lange, Martin Wisniewski, Laura Moore, John C. Lawson, Nathan D. Wojciechowska, Karolina Schnittler, Hans Siekmann, Arndt F. |
author_sort | Hasan, Sana S. |
collection | PubMed |
description | Angiogenic sprouting needs to be tightly controlled. It has been suggested that the Notch ligand dll4 expressed in leading tip cells restricts angiogenesis by activating Notch signalling in trailing stalk cells. Here, we show using live imaging in zebrafish that activation of Notch signalling is rather required in tip cells. Notch activation initially triggers expression of the chemokine receptor cxcr4a. This allows for proper tip cell migration and connection to the pre-existing arterial circulation, ultimately establishing functional arterial-venous blood flow patterns. Subsequently, Notch signalling reduces cxcr4a expression, thereby preventing excessive blood vessel growth. Finally, we find that Notch signalling is dispensable for limiting blood vessel growth during venous plexus formation that does not generate arteries. Together, these findings link the role of Notch signalling in limiting angiogenesis to its role during artery formation and provide a framework for our understanding of the mechanisms underlying blood vessel network expansion and maturation. |
format | Online Article Text |
id | pubmed-5534340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-55343402018-01-17 Endothelial Notch signalling limits angiogenesis via control of artery formation Hasan, Sana S. Tsaryk, Roman Lange, Martin Wisniewski, Laura Moore, John C. Lawson, Nathan D. Wojciechowska, Karolina Schnittler, Hans Siekmann, Arndt F. Nat Cell Biol Article Angiogenic sprouting needs to be tightly controlled. It has been suggested that the Notch ligand dll4 expressed in leading tip cells restricts angiogenesis by activating Notch signalling in trailing stalk cells. Here, we show using live imaging in zebrafish that activation of Notch signalling is rather required in tip cells. Notch activation initially triggers expression of the chemokine receptor cxcr4a. This allows for proper tip cell migration and connection to the pre-existing arterial circulation, ultimately establishing functional arterial-venous blood flow patterns. Subsequently, Notch signalling reduces cxcr4a expression, thereby preventing excessive blood vessel growth. Finally, we find that Notch signalling is dispensable for limiting blood vessel growth during venous plexus formation that does not generate arteries. Together, these findings link the role of Notch signalling in limiting angiogenesis to its role during artery formation and provide a framework for our understanding of the mechanisms underlying blood vessel network expansion and maturation. 2017-07-17 2017-08 /pmc/articles/PMC5534340/ /pubmed/28714969 http://dx.doi.org/10.1038/ncb3574 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Hasan, Sana S. Tsaryk, Roman Lange, Martin Wisniewski, Laura Moore, John C. Lawson, Nathan D. Wojciechowska, Karolina Schnittler, Hans Siekmann, Arndt F. Endothelial Notch signalling limits angiogenesis via control of artery formation |
title | Endothelial Notch signalling limits angiogenesis via control of artery formation |
title_full | Endothelial Notch signalling limits angiogenesis via control of artery formation |
title_fullStr | Endothelial Notch signalling limits angiogenesis via control of artery formation |
title_full_unstemmed | Endothelial Notch signalling limits angiogenesis via control of artery formation |
title_short | Endothelial Notch signalling limits angiogenesis via control of artery formation |
title_sort | endothelial notch signalling limits angiogenesis via control of artery formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534340/ https://www.ncbi.nlm.nih.gov/pubmed/28714969 http://dx.doi.org/10.1038/ncb3574 |
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