Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lipowczan, Marcin, Borowska-Wykręt, Dorota, Natonik-Białoń, Sandra, Kwiatkowska, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
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
_version_ 1783347691333353472
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
work_keys_str_mv AT lipowczanmarcin growingcellwallsshowagradientofelasticstrainacrosstheirlayers
AT borowskawykretdorota growingcellwallsshowagradientofelasticstrainacrosstheirlayers
AT natonikbiałonsandra growingcellwallsshowagradientofelasticstrainacrosstheirlayers
AT kwiatkowskadorota growingcellwallsshowagradientofelasticstrainacrosstheirlayers