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Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves

Differentiation into well-defined patterns and tissue growth are recognized as key processes in organismal development. However, it is unclear whether patterns are passively, homogeneously dilated by growth or whether they remodel during tissue expansion. Leaf vascular networks are well-fitted to in...

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Autores principales: Bar-Sinai, Yohai, Julien, Jean-Daniel, Sharon, Eran, Armon, Shahaf, Nakayama, Naomi, Adda-Bedia, Mokhtar, Boudaoud, Arezki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830508/
https://www.ncbi.nlm.nih.gov/pubmed/27074136
http://dx.doi.org/10.1371/journal.pcbi.1004819
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author Bar-Sinai, Yohai
Julien, Jean-Daniel
Sharon, Eran
Armon, Shahaf
Nakayama, Naomi
Adda-Bedia, Mokhtar
Boudaoud, Arezki
author_facet Bar-Sinai, Yohai
Julien, Jean-Daniel
Sharon, Eran
Armon, Shahaf
Nakayama, Naomi
Adda-Bedia, Mokhtar
Boudaoud, Arezki
author_sort Bar-Sinai, Yohai
collection PubMed
description Differentiation into well-defined patterns and tissue growth are recognized as key processes in organismal development. However, it is unclear whether patterns are passively, homogeneously dilated by growth or whether they remodel during tissue expansion. Leaf vascular networks are well-fitted to investigate this issue, since leaves are approximately two-dimensional and grow manyfold in size. Here we study experimentally and computationally how vein patterns affect growth. We first model the growing vasculature as a network of viscoelastic rods and consider its response to external mechanical stress. We use the so-called texture tensor to quantify the local network geometry and reveal that growth is heterogeneous, resembling non-affine deformations in composite materials. We then apply mechanical forces to growing leaves after veins have differentiated, which respond by anisotropic growth and reorientation of the network in the direction of external stress. External mechanical stress appears to make growth more homogeneous, in contrast with the model with viscoelastic rods. However, we reconcile the model with experimental data by incorporating randomness in rod thickness and a threshold in the rod growth law, making the rods viscoelastoplastic. Altogether, we show that the higher stiffness of veins leads to their reorientation along external forces, along with a reduction in growth heterogeneity. This process may lead to the reinforcement of leaves against mechanical stress. More generally, our work contributes to a framework whereby growth and patterns are coordinated through the differences in mechanical properties between cell types.
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spelling pubmed-48305082016-04-22 Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves Bar-Sinai, Yohai Julien, Jean-Daniel Sharon, Eran Armon, Shahaf Nakayama, Naomi Adda-Bedia, Mokhtar Boudaoud, Arezki PLoS Comput Biol Research Article Differentiation into well-defined patterns and tissue growth are recognized as key processes in organismal development. However, it is unclear whether patterns are passively, homogeneously dilated by growth or whether they remodel during tissue expansion. Leaf vascular networks are well-fitted to investigate this issue, since leaves are approximately two-dimensional and grow manyfold in size. Here we study experimentally and computationally how vein patterns affect growth. We first model the growing vasculature as a network of viscoelastic rods and consider its response to external mechanical stress. We use the so-called texture tensor to quantify the local network geometry and reveal that growth is heterogeneous, resembling non-affine deformations in composite materials. We then apply mechanical forces to growing leaves after veins have differentiated, which respond by anisotropic growth and reorientation of the network in the direction of external stress. External mechanical stress appears to make growth more homogeneous, in contrast with the model with viscoelastic rods. However, we reconcile the model with experimental data by incorporating randomness in rod thickness and a threshold in the rod growth law, making the rods viscoelastoplastic. Altogether, we show that the higher stiffness of veins leads to their reorientation along external forces, along with a reduction in growth heterogeneity. This process may lead to the reinforcement of leaves against mechanical stress. More generally, our work contributes to a framework whereby growth and patterns are coordinated through the differences in mechanical properties between cell types. Public Library of Science 2016-04-13 /pmc/articles/PMC4830508/ /pubmed/27074136 http://dx.doi.org/10.1371/journal.pcbi.1004819 Text en © 2016 Bar-Sinai et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bar-Sinai, Yohai
Julien, Jean-Daniel
Sharon, Eran
Armon, Shahaf
Nakayama, Naomi
Adda-Bedia, Mokhtar
Boudaoud, Arezki
Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title_full Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title_fullStr Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title_full_unstemmed Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title_short Mechanical Stress Induces Remodeling of Vascular Networks in Growing Leaves
title_sort mechanical stress induces remodeling of vascular networks in growing leaves
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830508/
https://www.ncbi.nlm.nih.gov/pubmed/27074136
http://dx.doi.org/10.1371/journal.pcbi.1004819
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