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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...

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Detalles Bibliográficos
Autores principales: Deinum, Eva E, Mulder, Bela M, Benitez-Alfonso, Yoselin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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