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Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death

BACKGROUND: Ozone is a major secondary air pollutant often reaching high concentrations in urban areas under strong daylight, high temperature and stagnant high-pressure systems. Ozone in the troposphere is a pollutant that is harmful to the plant. PRINCIPAL FINDINGS: By exposing cells to a strong p...

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Autores principales: Kadono, Takashi, Tran, Daniel, Errakhi, Rafik, Hiramatsu, Takuya, Meimoun, Patrice, Briand, Joël, Iwaya-Inoue, Mari, Kawano, Tomonori, Bouteau, François
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954175/
https://www.ncbi.nlm.nih.gov/pubmed/20967217
http://dx.doi.org/10.1371/journal.pone.0013373
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author Kadono, Takashi
Tran, Daniel
Errakhi, Rafik
Hiramatsu, Takuya
Meimoun, Patrice
Briand, Joël
Iwaya-Inoue, Mari
Kawano, Tomonori
Bouteau, François
author_facet Kadono, Takashi
Tran, Daniel
Errakhi, Rafik
Hiramatsu, Takuya
Meimoun, Patrice
Briand, Joël
Iwaya-Inoue, Mari
Kawano, Tomonori
Bouteau, François
author_sort Kadono, Takashi
collection PubMed
description BACKGROUND: Ozone is a major secondary air pollutant often reaching high concentrations in urban areas under strong daylight, high temperature and stagnant high-pressure systems. Ozone in the troposphere is a pollutant that is harmful to the plant. PRINCIPAL FINDINGS: By exposing cells to a strong pulse of ozonized air, an acute cell death was observed in suspension cells of Arabidopsis thaliana used as a model. We demonstrated that O(3) treatment induced the activation of a plasma membrane anion channel that is an early prerequisite of O(3)-induced cell death in A. thaliana. Our data further suggest interplay of anion channel activation with well known plant responses to O(3), Ca(2+) influx and NADPH-oxidase generated reactive oxygen species (ROS) in mediating the oxidative cell death. This interplay might be fuelled by several mechanisms in addition to the direct ROS generation by O(3); namely, H(2)O(2) generation by salicylic and abscisic acids. Anion channel activation was also shown to promote the accumulation of transcripts encoding vacuolar processing enzymes, a family of proteases previously reported to contribute to the disruption of vacuole integrity observed during programmed cell death. SIGNIFICANCE: Collectively, our data indicate that anion efflux is an early key component of morphological and biochemical events leading to O(3)-induced programmed cell death. Because ion channels and more specifically anion channels assume a crucial position in cells, an understanding about the underlying role(s) for ion channels in the signalling pathway leading to programmed cell death is a subject that warrants future investigation.
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spelling pubmed-29541752010-10-21 Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death Kadono, Takashi Tran, Daniel Errakhi, Rafik Hiramatsu, Takuya Meimoun, Patrice Briand, Joël Iwaya-Inoue, Mari Kawano, Tomonori Bouteau, François PLoS One Research Article BACKGROUND: Ozone is a major secondary air pollutant often reaching high concentrations in urban areas under strong daylight, high temperature and stagnant high-pressure systems. Ozone in the troposphere is a pollutant that is harmful to the plant. PRINCIPAL FINDINGS: By exposing cells to a strong pulse of ozonized air, an acute cell death was observed in suspension cells of Arabidopsis thaliana used as a model. We demonstrated that O(3) treatment induced the activation of a plasma membrane anion channel that is an early prerequisite of O(3)-induced cell death in A. thaliana. Our data further suggest interplay of anion channel activation with well known plant responses to O(3), Ca(2+) influx and NADPH-oxidase generated reactive oxygen species (ROS) in mediating the oxidative cell death. This interplay might be fuelled by several mechanisms in addition to the direct ROS generation by O(3); namely, H(2)O(2) generation by salicylic and abscisic acids. Anion channel activation was also shown to promote the accumulation of transcripts encoding vacuolar processing enzymes, a family of proteases previously reported to contribute to the disruption of vacuole integrity observed during programmed cell death. SIGNIFICANCE: Collectively, our data indicate that anion efflux is an early key component of morphological and biochemical events leading to O(3)-induced programmed cell death. Because ion channels and more specifically anion channels assume a crucial position in cells, an understanding about the underlying role(s) for ion channels in the signalling pathway leading to programmed cell death is a subject that warrants future investigation. Public Library of Science 2010-10-13 /pmc/articles/PMC2954175/ /pubmed/20967217 http://dx.doi.org/10.1371/journal.pone.0013373 Text en Kadono et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kadono, Takashi
Tran, Daniel
Errakhi, Rafik
Hiramatsu, Takuya
Meimoun, Patrice
Briand, Joël
Iwaya-Inoue, Mari
Kawano, Tomonori
Bouteau, François
Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title_full Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title_fullStr Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title_full_unstemmed Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title_short Increased Anion Channel Activity Is an Unavoidable Event in Ozone-Induced Programmed Cell Death
title_sort increased anion channel activity is an unavoidable event in ozone-induced programmed cell death
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954175/
https://www.ncbi.nlm.nih.gov/pubmed/20967217
http://dx.doi.org/10.1371/journal.pone.0013373
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