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Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction

Phytotoxic potential of rosmarinic acid (RA), a caffeic acid ester largely found in aromatic species, was evaluated on Arabidopsis through metabolomic and microscopic approaches. In-vitro bioassays pointed out that RA affected root growth and morphology, causing ROS burst, ROS scavengers activity in...

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Autores principales: Araniti, Fabrizio, Costas-Gil, Aitana, Cabeiras-Freijanes, Luz, Lupini, Antonio, Sunseri, Francesco, Reigosa, Manuel J., Abenavoli, Maria Rosa, Sánchez-Moreiras, Adela M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306208/
https://www.ncbi.nlm.nih.gov/pubmed/30586368
http://dx.doi.org/10.1371/journal.pone.0208802
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author Araniti, Fabrizio
Costas-Gil, Aitana
Cabeiras-Freijanes, Luz
Lupini, Antonio
Sunseri, Francesco
Reigosa, Manuel J.
Abenavoli, Maria Rosa
Sánchez-Moreiras, Adela M.
author_facet Araniti, Fabrizio
Costas-Gil, Aitana
Cabeiras-Freijanes, Luz
Lupini, Antonio
Sunseri, Francesco
Reigosa, Manuel J.
Abenavoli, Maria Rosa
Sánchez-Moreiras, Adela M.
author_sort Araniti, Fabrizio
collection PubMed
description Phytotoxic potential of rosmarinic acid (RA), a caffeic acid ester largely found in aromatic species, was evaluated on Arabidopsis through metabolomic and microscopic approaches. In-vitro bioassays pointed out that RA affected root growth and morphology, causing ROS burst, ROS scavengers activity inhibition and consequently, an alteration on cells organization and ultrastructure. In particular, RA-treatment (175 μM) caused strong vacuolization, alteration of mitochondria structure and function and a consistent ROS-induced reduction of their transmembrane potential (ΔΨ(m)). These data suggested a cell energy deficit also confirmed by the metabolomic analysis, which highlighted a strong alteration of both TCA cycle and amino acids metabolism. Moreover, the increase in H(2)O(2) and O(2)(−) contents suggested that RA-treated meristems underwent oxidative stress, resulting in apoptotic bodies and necrotic cells. Taken together, these results suggest that RA inhibits two of the main ROS scavengers causing high ROS accumulation, responsible of the alterations on mitochondrial ultrastructure and activity through ΔΨ(m) dissipation, TCA-cycle alteration, cell starvation and consequently cell death on Arabidopsis seedlings. All these effects resulted in a strong inhibition on root growth and development, which convert RA in a promising molecule to be explored for further use in weed management.
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spelling pubmed-63062082019-01-08 Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction Araniti, Fabrizio Costas-Gil, Aitana Cabeiras-Freijanes, Luz Lupini, Antonio Sunseri, Francesco Reigosa, Manuel J. Abenavoli, Maria Rosa Sánchez-Moreiras, Adela M. PLoS One Research Article Phytotoxic potential of rosmarinic acid (RA), a caffeic acid ester largely found in aromatic species, was evaluated on Arabidopsis through metabolomic and microscopic approaches. In-vitro bioassays pointed out that RA affected root growth and morphology, causing ROS burst, ROS scavengers activity inhibition and consequently, an alteration on cells organization and ultrastructure. In particular, RA-treatment (175 μM) caused strong vacuolization, alteration of mitochondria structure and function and a consistent ROS-induced reduction of their transmembrane potential (ΔΨ(m)). These data suggested a cell energy deficit also confirmed by the metabolomic analysis, which highlighted a strong alteration of both TCA cycle and amino acids metabolism. Moreover, the increase in H(2)O(2) and O(2)(−) contents suggested that RA-treated meristems underwent oxidative stress, resulting in apoptotic bodies and necrotic cells. Taken together, these results suggest that RA inhibits two of the main ROS scavengers causing high ROS accumulation, responsible of the alterations on mitochondrial ultrastructure and activity through ΔΨ(m) dissipation, TCA-cycle alteration, cell starvation and consequently cell death on Arabidopsis seedlings. All these effects resulted in a strong inhibition on root growth and development, which convert RA in a promising molecule to be explored for further use in weed management. Public Library of Science 2018-12-26 /pmc/articles/PMC6306208/ /pubmed/30586368 http://dx.doi.org/10.1371/journal.pone.0208802 Text en © 2018 Araniti 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Araniti, Fabrizio
Costas-Gil, Aitana
Cabeiras-Freijanes, Luz
Lupini, Antonio
Sunseri, Francesco
Reigosa, Manuel J.
Abenavoli, Maria Rosa
Sánchez-Moreiras, Adela M.
Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title_full Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title_fullStr Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title_full_unstemmed Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title_short Rosmarinic acid induces programmed cell death in Arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
title_sort rosmarinic acid induces programmed cell death in arabidopsis seedlings through reactive oxygen species and mitochondrial dysfunction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306208/
https://www.ncbi.nlm.nih.gov/pubmed/30586368
http://dx.doi.org/10.1371/journal.pone.0208802
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