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From plasmodesma geometry to effective symplasmic permeability through biophysical modelling
Regulation of molecular transport via intercellular channels called plasmodesmata (PDs) is important for both coordinating developmental and environmental responses among neighbouring cells, and isolating (groups of) cells to execute distinct programs. Cell-to-cell mobility of fluorescent molecules...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994222/ https://www.ncbi.nlm.nih.gov/pubmed/31755863 http://dx.doi.org/10.7554/eLife.49000 |
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author | Deinum, Eva E Mulder, Bela M Benitez-Alfonso, Yoselin |
author_facet | Deinum, Eva E Mulder, Bela M Benitez-Alfonso, Yoselin |
author_sort | Deinum, Eva E |
collection | PubMed |
description | Regulation of molecular transport via intercellular channels called plasmodesmata (PDs) is important for both coordinating developmental and environmental responses among neighbouring cells, and isolating (groups of) cells to execute distinct programs. Cell-to-cell mobility of fluorescent molecules and PD dimensions (measured from electron micrographs) are both used as methods to predict PD transport capacity (i.e., effective symplasmic permeability), but often yield very different values. Here, we build a theoretical bridge between both experimental approaches by calculating the effective symplasmic permeability from a geometrical description of individual PDs and considering the flow towards them. We find that a dilated central region has the strongest impact in thick cell walls and that clustering of PDs into pit fields strongly reduces predicted permeabilities. Moreover, our open source multi-level model allows to predict PD dimensions matching measured permeabilities and add a functional interpretation to structural differences observed between PDs in different cell walls. |
format | Online Article Text |
id | pubmed-6994222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-69942222020-02-03 From plasmodesma geometry to effective symplasmic permeability through biophysical modelling Deinum, Eva E Mulder, Bela M Benitez-Alfonso, Yoselin eLife Cell Biology Regulation of molecular transport via intercellular channels called plasmodesmata (PDs) is important for both coordinating developmental and environmental responses among neighbouring cells, and isolating (groups of) cells to execute distinct programs. Cell-to-cell mobility of fluorescent molecules and PD dimensions (measured from electron micrographs) are both used as methods to predict PD transport capacity (i.e., effective symplasmic permeability), but often yield very different values. Here, we build a theoretical bridge between both experimental approaches by calculating the effective symplasmic permeability from a geometrical description of individual PDs and considering the flow towards them. We find that a dilated central region has the strongest impact in thick cell walls and that clustering of PDs into pit fields strongly reduces predicted permeabilities. Moreover, our open source multi-level model allows to predict PD dimensions matching measured permeabilities and add a functional interpretation to structural differences observed between PDs in different cell walls. eLife Sciences Publications, Ltd 2019-11-22 /pmc/articles/PMC6994222/ /pubmed/31755863 http://dx.doi.org/10.7554/eLife.49000 Text en © 2019, Deinum et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Deinum, Eva E Mulder, Bela M Benitez-Alfonso, Yoselin From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title | From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title_full | From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title_fullStr | From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title_full_unstemmed | From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title_short | From plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
title_sort | from plasmodesma geometry to effective symplasmic permeability through biophysical modelling |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994222/ https://www.ncbi.nlm.nih.gov/pubmed/31755863 http://dx.doi.org/10.7554/eLife.49000 |
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