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Voltage-dependent gating of SV channel TPC1 confers vacuole excitability

In contrast to the plasma membrane, the vacuole membrane has not yet been associated with electrical excitation of plants. Here, we show that mesophyll vacuoles from Arabidopsis sense and control the membrane potential essentially via the K(+)-permeable TPC1 and TPK channels. Electrical stimuli elic...

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Autores principales: Jaślan, Dawid, Dreyer, Ingo, Lu, Jinping, O’Malley, Ronan, Dindas, Julian, Marten, Irene, Hedrich, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572840/
https://www.ncbi.nlm.nih.gov/pubmed/31201323
http://dx.doi.org/10.1038/s41467-019-10599-x
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author Jaślan, Dawid
Dreyer, Ingo
Lu, Jinping
O’Malley, Ronan
Dindas, Julian
Marten, Irene
Hedrich, Rainer
author_facet Jaślan, Dawid
Dreyer, Ingo
Lu, Jinping
O’Malley, Ronan
Dindas, Julian
Marten, Irene
Hedrich, Rainer
author_sort Jaślan, Dawid
collection PubMed
description In contrast to the plasma membrane, the vacuole membrane has not yet been associated with electrical excitation of plants. Here, we show that mesophyll vacuoles from Arabidopsis sense and control the membrane potential essentially via the K(+)-permeable TPC1 and TPK channels. Electrical stimuli elicit transient depolarization of the vacuole membrane that can last for seconds. Electrical excitability is suppressed by increased vacuolar Ca(2+) levels. In comparison to wild type, vacuoles from the fou2 mutant, harboring TPC1 channels insensitive to luminal Ca(2+), can be excited fully by even weak electrical stimuli. The TPC1-loss-of-function mutant tpc1-2 does not respond to electrical stimulation at all, and the loss of TPK1/TPK3-mediated K(+) transport affects the duration of TPC1-dependent membrane depolarization. In combination with mathematical modeling, these results show that the vacuolar K(+)-conducting TPC1 and TPK1/TPK3 channels act in concert to provide for Ca(2+)- and voltage-induced electrical excitability to the central organelle of plant cells.
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spelling pubmed-65728402019-06-24 Voltage-dependent gating of SV channel TPC1 confers vacuole excitability Jaślan, Dawid Dreyer, Ingo Lu, Jinping O’Malley, Ronan Dindas, Julian Marten, Irene Hedrich, Rainer Nat Commun Article In contrast to the plasma membrane, the vacuole membrane has not yet been associated with electrical excitation of plants. Here, we show that mesophyll vacuoles from Arabidopsis sense and control the membrane potential essentially via the K(+)-permeable TPC1 and TPK channels. Electrical stimuli elicit transient depolarization of the vacuole membrane that can last for seconds. Electrical excitability is suppressed by increased vacuolar Ca(2+) levels. In comparison to wild type, vacuoles from the fou2 mutant, harboring TPC1 channels insensitive to luminal Ca(2+), can be excited fully by even weak electrical stimuli. The TPC1-loss-of-function mutant tpc1-2 does not respond to electrical stimulation at all, and the loss of TPK1/TPK3-mediated K(+) transport affects the duration of TPC1-dependent membrane depolarization. In combination with mathematical modeling, these results show that the vacuolar K(+)-conducting TPC1 and TPK1/TPK3 channels act in concert to provide for Ca(2+)- and voltage-induced electrical excitability to the central organelle of plant cells. Nature Publishing Group UK 2019-06-14 /pmc/articles/PMC6572840/ /pubmed/31201323 http://dx.doi.org/10.1038/s41467-019-10599-x 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
Jaślan, Dawid
Dreyer, Ingo
Lu, Jinping
O’Malley, Ronan
Dindas, Julian
Marten, Irene
Hedrich, Rainer
Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title_full Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title_fullStr Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title_full_unstemmed Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title_short Voltage-dependent gating of SV channel TPC1 confers vacuole excitability
title_sort voltage-dependent gating of sv channel tpc1 confers vacuole excitability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572840/
https://www.ncbi.nlm.nih.gov/pubmed/31201323
http://dx.doi.org/10.1038/s41467-019-10599-x
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