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Controlling intercellular flow through mechanosensitive plasmodesmata nanopores

In plants, plasmodesmata (PD) are nanopores that serve as channels for molecular cell-to-cell transport. Precise control of PD permeability is essential to regulate processes such as growth and tissue patterning, photoassimilate distribution and defense against pathogens. Callose deposition modulate...

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Autores principales: Park, Keunhwan, Knoblauch, Jan, Oparka, Karl, Jensen, Kaare H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687729/
https://www.ncbi.nlm.nih.gov/pubmed/31395861
http://dx.doi.org/10.1038/s41467-019-11201-0
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author Park, Keunhwan
Knoblauch, Jan
Oparka, Karl
Jensen, Kaare H.
author_facet Park, Keunhwan
Knoblauch, Jan
Oparka, Karl
Jensen, Kaare H.
author_sort Park, Keunhwan
collection PubMed
description In plants, plasmodesmata (PD) are nanopores that serve as channels for molecular cell-to-cell transport. Precise control of PD permeability is essential to regulate processes such as growth and tissue patterning, photoassimilate distribution and defense against pathogens. Callose deposition modulates PD transport but little is known of the rapid events that lead to PD closure in response to tissue damage or osmotic shock. We propose a mechanism of PD closure as a result of mechanosensing. Pressure forces acting on the dumbbell-shaped ER-desmotubule complex cause it to be displaced from its equilibrium position, thus closing the PD aperture. The filamentous protein tethers that link the plasma membrane to the ER-desmotubule complex play a key role in determining the selectivity of the PD pore. This model of PD control compares favorably with experimental data on the pressure-generated closure of PD.
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spelling pubmed-66877292019-08-12 Controlling intercellular flow through mechanosensitive plasmodesmata nanopores Park, Keunhwan Knoblauch, Jan Oparka, Karl Jensen, Kaare H. Nat Commun Article In plants, plasmodesmata (PD) are nanopores that serve as channels for molecular cell-to-cell transport. Precise control of PD permeability is essential to regulate processes such as growth and tissue patterning, photoassimilate distribution and defense against pathogens. Callose deposition modulates PD transport but little is known of the rapid events that lead to PD closure in response to tissue damage or osmotic shock. We propose a mechanism of PD closure as a result of mechanosensing. Pressure forces acting on the dumbbell-shaped ER-desmotubule complex cause it to be displaced from its equilibrium position, thus closing the PD aperture. The filamentous protein tethers that link the plasma membrane to the ER-desmotubule complex play a key role in determining the selectivity of the PD pore. This model of PD control compares favorably with experimental data on the pressure-generated closure of PD. Nature Publishing Group UK 2019-08-08 /pmc/articles/PMC6687729/ /pubmed/31395861 http://dx.doi.org/10.1038/s41467-019-11201-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Park, Keunhwan
Knoblauch, Jan
Oparka, Karl
Jensen, Kaare H.
Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title_full Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title_fullStr Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title_full_unstemmed Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title_short Controlling intercellular flow through mechanosensitive plasmodesmata nanopores
title_sort controlling intercellular flow through mechanosensitive plasmodesmata nanopores
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687729/
https://www.ncbi.nlm.nih.gov/pubmed/31395861
http://dx.doi.org/10.1038/s41467-019-11201-0
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