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Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells

Extracellular ATP (eATP) has been implicated in mediating plant growth and antioxidant defense; however, it is largely unknown whether eATP might mediate salinity tolerance. We used confocal microscopy, a non-invasive vibrating ion-selective microelectrode, and quantitative real time PCR analysis to...

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Autores principales: Sun, Jian, Zhang, Xuan, Deng, Shurong, Zhang, Chunlan, Wang, Meijuan, Ding, Mingquan, Zhao, Rui, Shen, Xin, Zhou, Xiaoyang, Lu, Cunfu, Chen, Shaoliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532164/
https://www.ncbi.nlm.nih.gov/pubmed/23285259
http://dx.doi.org/10.1371/journal.pone.0053136
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author Sun, Jian
Zhang, Xuan
Deng, Shurong
Zhang, Chunlan
Wang, Meijuan
Ding, Mingquan
Zhao, Rui
Shen, Xin
Zhou, Xiaoyang
Lu, Cunfu
Chen, Shaoliang
author_facet Sun, Jian
Zhang, Xuan
Deng, Shurong
Zhang, Chunlan
Wang, Meijuan
Ding, Mingquan
Zhao, Rui
Shen, Xin
Zhou, Xiaoyang
Lu, Cunfu
Chen, Shaoliang
author_sort Sun, Jian
collection PubMed
description Extracellular ATP (eATP) has been implicated in mediating plant growth and antioxidant defense; however, it is largely unknown whether eATP might mediate salinity tolerance. We used confocal microscopy, a non-invasive vibrating ion-selective microelectrode, and quantitative real time PCR analysis to evaluate the physiological significance of eATP in the salt resistance of cell cultures derived from a salt-tolerant woody species, Populus euphratica. Application of NaCl (200 mM) shock induced a transient elevation in [eATP]. We investigated the effects of eATP by blocking P2 receptors with suramin and PPADS and applying an ATP trap system of hexokinase-glucose. We found that eATP regulated a wide range of cellular processes required for salt adaptation, including vacuolar Na(+) compartmentation, Na(+)/H(+) exchange across the plasma membrane (PM), K(+) homeostasis, reactive oxygen species regulation, and salt-responsive expression of genes related to K(+)/Na(+) homeostasis and PM repair. Furthermore, we found that the eATP signaling was mediated by H(2)O(2) and cytosolic Ca(2+) released in response to high salt in P. euphratica cells. We concluded that salt-induced eATP was sensed by purinoceptors in the PM, and this led to the induction of downstream signals, like H(2)O(2) and cytosolic Ca(2+), which are required for the up-regulation of genes linked to K(+)/Na(+) homeostasis and PM repair. Consequently, the viability of P. euphratica cells was maintained during a prolonged period of salt stress.
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spelling pubmed-35321642013-01-02 Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells Sun, Jian Zhang, Xuan Deng, Shurong Zhang, Chunlan Wang, Meijuan Ding, Mingquan Zhao, Rui Shen, Xin Zhou, Xiaoyang Lu, Cunfu Chen, Shaoliang PLoS One Research Article Extracellular ATP (eATP) has been implicated in mediating plant growth and antioxidant defense; however, it is largely unknown whether eATP might mediate salinity tolerance. We used confocal microscopy, a non-invasive vibrating ion-selective microelectrode, and quantitative real time PCR analysis to evaluate the physiological significance of eATP in the salt resistance of cell cultures derived from a salt-tolerant woody species, Populus euphratica. Application of NaCl (200 mM) shock induced a transient elevation in [eATP]. We investigated the effects of eATP by blocking P2 receptors with suramin and PPADS and applying an ATP trap system of hexokinase-glucose. We found that eATP regulated a wide range of cellular processes required for salt adaptation, including vacuolar Na(+) compartmentation, Na(+)/H(+) exchange across the plasma membrane (PM), K(+) homeostasis, reactive oxygen species regulation, and salt-responsive expression of genes related to K(+)/Na(+) homeostasis and PM repair. Furthermore, we found that the eATP signaling was mediated by H(2)O(2) and cytosolic Ca(2+) released in response to high salt in P. euphratica cells. We concluded that salt-induced eATP was sensed by purinoceptors in the PM, and this led to the induction of downstream signals, like H(2)O(2) and cytosolic Ca(2+), which are required for the up-regulation of genes linked to K(+)/Na(+) homeostasis and PM repair. Consequently, the viability of P. euphratica cells was maintained during a prolonged period of salt stress. Public Library of Science 2012-12-28 /pmc/articles/PMC3532164/ /pubmed/23285259 http://dx.doi.org/10.1371/journal.pone.0053136 Text en © 2012 Sun 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
Sun, Jian
Zhang, Xuan
Deng, Shurong
Zhang, Chunlan
Wang, Meijuan
Ding, Mingquan
Zhao, Rui
Shen, Xin
Zhou, Xiaoyang
Lu, Cunfu
Chen, Shaoliang
Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title_full Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title_fullStr Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title_full_unstemmed Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title_short Extracellular ATP Signaling Is Mediated by H(2)O(2) and Cytosolic Ca(2+) in the Salt Response of Populus euphratica Cells
title_sort extracellular atp signaling is mediated by h(2)o(2) and cytosolic ca(2+) in the salt response of populus euphratica cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532164/
https://www.ncbi.nlm.nih.gov/pubmed/23285259
http://dx.doi.org/10.1371/journal.pone.0053136
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