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Growing cell walls show a gradient of elastic strain across their layers
The relatively thick primary walls of epidermal and collenchyma cells often form waviness on the surface that faces the protoplast when they are released from the tensile in-plane stress that operates in situ. This waviness is a manifestation of buckling that results from the heterogeneity of the el...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093493/ https://www.ncbi.nlm.nih.gov/pubmed/29945239 http://dx.doi.org/10.1093/jxb/ery237 |
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author | Lipowczan, Marcin Borowska-Wykręt, Dorota Natonik-Białoń, Sandra Kwiatkowska, Dorota |
author_facet | Lipowczan, Marcin Borowska-Wykręt, Dorota Natonik-Białoń, Sandra Kwiatkowska, Dorota |
author_sort | Lipowczan, Marcin |
collection | PubMed |
description | The relatively thick primary walls of epidermal and collenchyma cells often form waviness on the surface that faces the protoplast when they are released from the tensile in-plane stress that operates in situ. This waviness is a manifestation of buckling that results from the heterogeneity of the elastic strain across the wall. In this study, this heterogeneity was confirmed by the spontaneous bending of isolated wall fragments that were initially flat. We combined the empirical data on the formation of waviness in growing cell walls with computations of the buckled wall shapes. We chose cylindrical-shaped organs with a high degree of longitudinal tissue stress because in such organs the surface deformation that accompanies the removal of the stress is strongly anisotropic and leads to the formation of waviness in which wrinkles on the inner wall surface are always transverse to the organ axis. The computations showed that the strain heterogeneity results from individual or overlaid gradients of pre-stress and stiffness across the wall. The computed wall shapes depend on the assumed wall thickness and mechanical gradients. Thus, a quantitative analysis of the wall waviness that forms after stress removal can be used to assess the mechanical heterogeneity of the cell wall. |
format | Online Article Text |
id | pubmed-6093493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60934932018-08-22 Growing cell walls show a gradient of elastic strain across their layers Lipowczan, Marcin Borowska-Wykręt, Dorota Natonik-Białoń, Sandra Kwiatkowska, Dorota J Exp Bot Research Papers The relatively thick primary walls of epidermal and collenchyma cells often form waviness on the surface that faces the protoplast when they are released from the tensile in-plane stress that operates in situ. This waviness is a manifestation of buckling that results from the heterogeneity of the elastic strain across the wall. In this study, this heterogeneity was confirmed by the spontaneous bending of isolated wall fragments that were initially flat. We combined the empirical data on the formation of waviness in growing cell walls with computations of the buckled wall shapes. We chose cylindrical-shaped organs with a high degree of longitudinal tissue stress because in such organs the surface deformation that accompanies the removal of the stress is strongly anisotropic and leads to the formation of waviness in which wrinkles on the inner wall surface are always transverse to the organ axis. The computations showed that the strain heterogeneity results from individual or overlaid gradients of pre-stress and stiffness across the wall. The computed wall shapes depend on the assumed wall thickness and mechanical gradients. Thus, a quantitative analysis of the wall waviness that forms after stress removal can be used to assess the mechanical heterogeneity of the cell wall. Oxford University Press 2018-08-17 2018-06-26 /pmc/articles/PMC6093493/ /pubmed/29945239 http://dx.doi.org/10.1093/jxb/ery237 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Lipowczan, Marcin Borowska-Wykręt, Dorota Natonik-Białoń, Sandra Kwiatkowska, Dorota Growing cell walls show a gradient of elastic strain across their layers |
title | Growing cell walls show a gradient of elastic strain across their layers |
title_full | Growing cell walls show a gradient of elastic strain across their layers |
title_fullStr | Growing cell walls show a gradient of elastic strain across their layers |
title_full_unstemmed | Growing cell walls show a gradient of elastic strain across their layers |
title_short | Growing cell walls show a gradient of elastic strain across their layers |
title_sort | growing cell walls show a gradient of elastic strain across their layers |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093493/ https://www.ncbi.nlm.nih.gov/pubmed/29945239 http://dx.doi.org/10.1093/jxb/ery237 |
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