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Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks
Sprouting angiogenesis is an essential vascularization mechanism consisting of sprouting and remodelling. The remodelling phase is driven by rearrangements of endothelial cells (ECs) within the post-sprouting vascular plexus. Prior work has uncovered how ECs polarize and migrate in response to flow-...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220266/ https://www.ncbi.nlm.nih.gov/pubmed/34157895 http://dx.doi.org/10.1098/rsif.2021.0113 |
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author | Zhou, Qi Perovic, Tijana Fechner, Ines Edgar, Lowell T. Hoskins, Peter R. Gerhardt, Holger Krüger, Timm Bernabeu, Miguel O. |
author_facet | Zhou, Qi Perovic, Tijana Fechner, Ines Edgar, Lowell T. Hoskins, Peter R. Gerhardt, Holger Krüger, Timm Bernabeu, Miguel O. |
author_sort | Zhou, Qi |
collection | PubMed |
description | Sprouting angiogenesis is an essential vascularization mechanism consisting of sprouting and remodelling. The remodelling phase is driven by rearrangements of endothelial cells (ECs) within the post-sprouting vascular plexus. Prior work has uncovered how ECs polarize and migrate in response to flow-induced wall shear stress (WSS). However, the question of how the presence of erythrocytes (widely known as red blood cells (RBCs)) and their impact on haemodynamics affect vascular remodelling remains unanswered. Here, we devise a computational framework to model cellular blood flow in developmental mouse retina. We demonstrate a previously unreported highly heterogeneous distribution of RBCs in primitive vasculature. Furthermore, we report a strong association between vessel regression and RBC hypoperfusion, and identify plasma skimming as the driving mechanism. Live imaging in a developmental zebrafish model confirms this association. Taken together, our results indicate that RBC dynamics are fundamental to establishing the regional WSS differences driving vascular remodelling via their ability to modulate effective viscosity. |
format | Online Article Text |
id | pubmed-8220266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82202662021-06-23 Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks Zhou, Qi Perovic, Tijana Fechner, Ines Edgar, Lowell T. Hoskins, Peter R. Gerhardt, Holger Krüger, Timm Bernabeu, Miguel O. J R Soc Interface Life Sciences–Physics interface Sprouting angiogenesis is an essential vascularization mechanism consisting of sprouting and remodelling. The remodelling phase is driven by rearrangements of endothelial cells (ECs) within the post-sprouting vascular plexus. Prior work has uncovered how ECs polarize and migrate in response to flow-induced wall shear stress (WSS). However, the question of how the presence of erythrocytes (widely known as red blood cells (RBCs)) and their impact on haemodynamics affect vascular remodelling remains unanswered. Here, we devise a computational framework to model cellular blood flow in developmental mouse retina. We demonstrate a previously unreported highly heterogeneous distribution of RBCs in primitive vasculature. Furthermore, we report a strong association between vessel regression and RBC hypoperfusion, and identify plasma skimming as the driving mechanism. Live imaging in a developmental zebrafish model confirms this association. Taken together, our results indicate that RBC dynamics are fundamental to establishing the regional WSS differences driving vascular remodelling via their ability to modulate effective viscosity. The Royal Society 2021-06-23 /pmc/articles/PMC8220266/ /pubmed/34157895 http://dx.doi.org/10.1098/rsif.2021.0113 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Life Sciences–Physics interface Zhou, Qi Perovic, Tijana Fechner, Ines Edgar, Lowell T. Hoskins, Peter R. Gerhardt, Holger Krüger, Timm Bernabeu, Miguel O. Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title | Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title_full | Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title_fullStr | Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title_full_unstemmed | Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title_short | Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
title_sort | association between erythrocyte dynamics and vessel remodelling in developmental vascular networks |
topic | Life Sciences–Physics interface |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220266/ https://www.ncbi.nlm.nih.gov/pubmed/34157895 http://dx.doi.org/10.1098/rsif.2021.0113 |
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