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Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis

Salinity is one of the formidable environmental factors that affect plant growth and development and constrain agricultural productivity. Experimentally imposed short-term NaCl treatment triggers a transient increase in cytosolic free Ca(2+) concentration ([Ca(2+)](i)) via Ca(2+) influx across the p...

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Autores principales: Liu, Lulu, Jiang, Zhonghao, Zhang, Shu, Zhao, Hongyan, Yang, Weiguang, Siedow, James N., Pei, Zhen-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206402/
https://www.ncbi.nlm.nih.gov/pubmed/30405646
http://dx.doi.org/10.3389/fpls.2018.01390
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author Liu, Lulu
Jiang, Zhonghao
Zhang, Shu
Zhao, Hongyan
Yang, Weiguang
Siedow, James N.
Pei, Zhen-Ming
author_facet Liu, Lulu
Jiang, Zhonghao
Zhang, Shu
Zhao, Hongyan
Yang, Weiguang
Siedow, James N.
Pei, Zhen-Ming
author_sort Liu, Lulu
collection PubMed
description Salinity is one of the formidable environmental factors that affect plant growth and development and constrain agricultural productivity. Experimentally imposed short-term NaCl treatment triggers a transient increase in cytosolic free Ca(2+) concentration ([Ca(2+)](i)) via Ca(2+) influx across the plasma membrane. Salinity stress, as well as other stresses, induces the production of reactive oxygen species (ROS), such as H(2)O(2). It is well established that short-term H(2)O(2) treatment also triggers a transient increase in [Ca(2+)](i). However, whether and how long-term NaCl and H(2)O(2) treatments affect the basal levels of [Ca(2+)](i) as well as plant responses to additional NaCl and H(2)O(2) stresses remain poorly understood. Using an aequorin-based Ca(2+) imaging assay, we found that the long-term treatment of Arabidopsis seedlings with both moderate NaCl and H(2)O(2) in the growth media reduced the basal [Ca(2+)](i) levels. Interestingly, we found that the long-term treatment with NaCl, but not H(2)O(2,) affected the responses of plants to additional NaCl stress, and remarkably the roots displayed enhanced responses while the leaves showed reduced responses. These findings suggest that plants adapt to the long-term NaCl stress, while H(2)O(2) might be an integrator of many stresses.
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spelling pubmed-62064022018-11-07 Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis Liu, Lulu Jiang, Zhonghao Zhang, Shu Zhao, Hongyan Yang, Weiguang Siedow, James N. Pei, Zhen-Ming Front Plant Sci Plant Science Salinity is one of the formidable environmental factors that affect plant growth and development and constrain agricultural productivity. Experimentally imposed short-term NaCl treatment triggers a transient increase in cytosolic free Ca(2+) concentration ([Ca(2+)](i)) via Ca(2+) influx across the plasma membrane. Salinity stress, as well as other stresses, induces the production of reactive oxygen species (ROS), such as H(2)O(2). It is well established that short-term H(2)O(2) treatment also triggers a transient increase in [Ca(2+)](i). However, whether and how long-term NaCl and H(2)O(2) treatments affect the basal levels of [Ca(2+)](i) as well as plant responses to additional NaCl and H(2)O(2) stresses remain poorly understood. Using an aequorin-based Ca(2+) imaging assay, we found that the long-term treatment of Arabidopsis seedlings with both moderate NaCl and H(2)O(2) in the growth media reduced the basal [Ca(2+)](i) levels. Interestingly, we found that the long-term treatment with NaCl, but not H(2)O(2,) affected the responses of plants to additional NaCl stress, and remarkably the roots displayed enhanced responses while the leaves showed reduced responses. These findings suggest that plants adapt to the long-term NaCl stress, while H(2)O(2) might be an integrator of many stresses. Frontiers Media S.A. 2018-10-23 /pmc/articles/PMC6206402/ /pubmed/30405646 http://dx.doi.org/10.3389/fpls.2018.01390 Text en Copyright © 2018 Liu, Jiang, Zhang, Zhao, Yang, Siedow and Pei. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Liu, Lulu
Jiang, Zhonghao
Zhang, Shu
Zhao, Hongyan
Yang, Weiguang
Siedow, James N.
Pei, Zhen-Ming
Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title_full Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title_fullStr Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title_full_unstemmed Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title_short Both NaCl and H(2)O(2) Long-Term Stresses Affect Basal Cytosolic Ca(2+) Levels but Only NaCl Alters Cytosolic Ca(2+) Signatures in Arabidopsis
title_sort both nacl and h(2)o(2) long-term stresses affect basal cytosolic ca(2+) levels but only nacl alters cytosolic ca(2+) signatures in arabidopsis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206402/
https://www.ncbi.nlm.nih.gov/pubmed/30405646
http://dx.doi.org/10.3389/fpls.2018.01390
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