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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-...

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Autores principales: Zhou, Qi, Perovic, Tijana, Fechner, Ines, Edgar, Lowell T., Hoskins, Peter R., Gerhardt, Holger, Krüger, Timm, Bernabeu, Miguel O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2021
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.
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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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