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A computational approach for inferring the cell wall properties that govern guard cell dynamics
Guard cells dynamically adjust their shape in order to regulate photosynthetic gas exchange, respiration rates and defend against pathogen entry. Cell shape changes are determined by the interplay of cell wall material properties and turgor pressure. To investigate this relationship between turgor p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637902/ https://www.ncbi.nlm.nih.gov/pubmed/28741858 http://dx.doi.org/10.1111/tpj.13640 |
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author | Woolfenden, Hugh C. Bourdais, Gildas Kopischke, Michaela Miedes, Eva Molina, Antonio Robatzek, Silke Morris, Richard J. |
author_facet | Woolfenden, Hugh C. Bourdais, Gildas Kopischke, Michaela Miedes, Eva Molina, Antonio Robatzek, Silke Morris, Richard J. |
author_sort | Woolfenden, Hugh C. |
collection | PubMed |
description | Guard cells dynamically adjust their shape in order to regulate photosynthetic gas exchange, respiration rates and defend against pathogen entry. Cell shape changes are determined by the interplay of cell wall material properties and turgor pressure. To investigate this relationship between turgor pressure, cell wall properties and cell shape, we focused on kidney‐shaped stomata and developed a biomechanical model of a guard cell pair. Treating the cell wall as a composite of the pectin‐rich cell wall matrix embedded with cellulose microfibrils, we show that strong, circumferentially oriented fibres are critical for opening. We find that the opening dynamics are dictated by the mechanical stress response of the cell wall matrix, and as the turgor rises, the pectinaceous matrix stiffens. We validate these predictions with stomatal opening experiments in selected Arabidopsis cell wall mutants. Thus, using a computational framework that combines a 3D biomechanical model with parameter optimization, we demonstrate how to exploit subtle shape changes to infer cell wall material properties. Our findings reveal that proper stomatal dynamics are built on two key properties of the cell wall, namely anisotropy in the form of hoop reinforcement and strain stiffening. |
format | Online Article Text |
id | pubmed-5637902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56379022017-10-25 A computational approach for inferring the cell wall properties that govern guard cell dynamics Woolfenden, Hugh C. Bourdais, Gildas Kopischke, Michaela Miedes, Eva Molina, Antonio Robatzek, Silke Morris, Richard J. Plant J Original Articles Guard cells dynamically adjust their shape in order to regulate photosynthetic gas exchange, respiration rates and defend against pathogen entry. Cell shape changes are determined by the interplay of cell wall material properties and turgor pressure. To investigate this relationship between turgor pressure, cell wall properties and cell shape, we focused on kidney‐shaped stomata and developed a biomechanical model of a guard cell pair. Treating the cell wall as a composite of the pectin‐rich cell wall matrix embedded with cellulose microfibrils, we show that strong, circumferentially oriented fibres are critical for opening. We find that the opening dynamics are dictated by the mechanical stress response of the cell wall matrix, and as the turgor rises, the pectinaceous matrix stiffens. We validate these predictions with stomatal opening experiments in selected Arabidopsis cell wall mutants. Thus, using a computational framework that combines a 3D biomechanical model with parameter optimization, we demonstrate how to exploit subtle shape changes to infer cell wall material properties. Our findings reveal that proper stomatal dynamics are built on two key properties of the cell wall, namely anisotropy in the form of hoop reinforcement and strain stiffening. John Wiley and Sons Inc. 2017-08-23 2017-10 /pmc/articles/PMC5637902/ /pubmed/28741858 http://dx.doi.org/10.1111/tpj.13640 Text en © 2017 The Authors The Plant Journal © 2017 John Wiley & Sons Ltd and Society for Experimental Biology. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Woolfenden, Hugh C. Bourdais, Gildas Kopischke, Michaela Miedes, Eva Molina, Antonio Robatzek, Silke Morris, Richard J. A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title | A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title_full | A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title_fullStr | A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title_full_unstemmed | A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title_short | A computational approach for inferring the cell wall properties that govern guard cell dynamics |
title_sort | computational approach for inferring the cell wall properties that govern guard cell dynamics |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637902/ https://www.ncbi.nlm.nih.gov/pubmed/28741858 http://dx.doi.org/10.1111/tpj.13640 |
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