PoplarV1, Main, Exploration, bibRecord, 002A88

Extracellular ATP signaling is mediated by H₂O₂ and cytosolic Ca²⁺ in the salt response of Populus euphratica cells.

Identifieur interne : 002A88 ( Main/Exploration ); précédent : 002A87; suivant : 002A89

Extracellular ATP signaling is mediated by H₂O₂ and cytosolic Ca²⁺ in the salt response of Populus euphratica cells.

Auteurs : Jian Sun [République populaire de Chine] ; Xuan Zhang ; Shurong Deng ; Chunlan Zhang ; Meijuan Wang ; Mingquan Ding ; Rui Zhao ; Xin Shen ; Xiaoyang Zhou ; Cunfu Lu ; Shaoliang Chen

Source :

PloS one [ 1932-6203 ] ; 2012.

RBID : pubmed:23285259

Descripteurs français

KwdFr :
- Adaptation physiologique (effets des médicaments et des substances chimiques), Adaptation physiologique (physiologie), Adénosine triphosphate (métabolisme), Antioxydants (métabolisme), Calcium (métabolisme), Cellules cultivées (MeSH), Cellules végétales (effets des médicaments et des substances chimiques), Cellules végétales (métabolisme), Cellules végétales (ultrastructure), Chlorure de sodium (pharmacologie), Cytosol (effets des médicaments et des substances chimiques), Cytosol (métabolisme), Espace extracellulaire (effets des médicaments et des substances chimiques), Espace extracellulaire (métabolisme), Peroxyde d'hydrogène (pharmacologie), Populus (cytologie), Populus (effets des médicaments et des substances chimiques), Populus (métabolisme), Survie cellulaire (effets des médicaments et des substances chimiques), Tolérance au sel (effets des médicaments et des substances chimiques), Transduction du signal (effets des médicaments et des substances chimiques).
MESH :
- cytologie : Populus.
- effets des médicaments et des substances chimiques : Adaptation physiologique, Cellules végétales, Cytosol, Espace extracellulaire, Populus, Survie cellulaire, Tolérance au sel, Transduction du signal.
- métabolisme : Adénosine triphosphate, Antioxydants, Calcium, Cellules végétales, Cytosol, Espace extracellulaire, Populus.
- pharmacologie : Chlorure de sodium, Peroxyde d'hydrogène.
- physiologie : Adaptation physiologique.
- ultrastructure : Cellules cultivées, Cellules végétales.

English descriptors

KwdEn :
- Adaptation, Physiological (drug effects), Adaptation, Physiological (physiology), Adenosine Triphosphate (metabolism), Antioxidants (metabolism), Calcium (metabolism), Cell Survival (drug effects), Cells, Cultured (MeSH), Cytosol (drug effects), Cytosol (metabolism), Extracellular Space (drug effects), Extracellular Space (metabolism), Hydrogen Peroxide (pharmacology), Plant Cells (drug effects), Plant Cells (metabolism), Plant Cells (ultrastructure), Populus (cytology), Populus (drug effects), Populus (metabolism), Salt Tolerance (drug effects), Signal Transduction (drug effects), Sodium Chloride (pharmacology).
MESH :
- chemical , metabolism : Adenosine Triphosphate, Antioxidants, Calcium.
- cytology : Populus.
- drug effects : Adaptation, Physiological, Cell Survival, Cytosol, Extracellular Space, Plant Cells, Populus, Salt Tolerance, Signal Transduction.
- metabolism : Cytosol, Extracellular Space, Plant Cells, Populus.
- chemical , pharmacology : Hydrogen Peroxide, Sodium Chloride.
- physiology : Adaptation, Physiological.
- ultrastructure : Plant Cells.
- Cells, Cultured.

Abstract

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 Na⁺/H⁺ homeostasis and PM repair. Furthermore, we found that the eATP signaling was mediated by H₂O₂ and cytosolic Ca²⁺ 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 H₂O₂ and cytosolic Ca²⁺, which are required for the up-regulation of genes linked to Na⁺/H⁺ homeostasis and PM repair. Consequently, the viability of P. euphratica cells was maintained during a prolonged period of salt stress.

DOI: 10.1371/journal.pone.0053136
PubMed: 23285259
PubMed Central: PMC3532164

Affiliations:

Links toward previous steps (curation, corpus...)

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Le document en format XML

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<term>Adaptation, Physiological (physiology)</term>
<term>Adenosine Triphosphate (metabolism)</term>
<term>Antioxidants (metabolism)</term>
<term>Calcium (metabolism)</term>
<term>Cell Survival (drug effects)</term>
<term>Cells, Cultured (MeSH)</term>
<term>Cytosol (drug effects)</term>
<term>Cytosol (metabolism)</term>
<term>Extracellular Space (drug effects)</term>
<term>Extracellular Space (metabolism)</term>
<term>Hydrogen Peroxide (pharmacology)</term>
<term>Plant Cells (drug effects)</term>
<term>Plant Cells (metabolism)</term>
<term>Plant Cells (ultrastructure)</term>
<term>Populus (cytology)</term>
<term>Populus (drug effects)</term>
<term>Populus (metabolism)</term>
<term>Salt Tolerance (drug effects)</term>
<term>Signal Transduction (drug effects)</term>
<term>Sodium Chloride (pharmacology)</term>
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<term>Adaptation physiologique (physiologie)</term>
<term>Adénosine triphosphate (métabolisme)</term>
<term>Antioxydants (métabolisme)</term>
<term>Calcium (métabolisme)</term>
<term>Cellules cultivées (MeSH)</term>
<term>Cellules végétales (effets des médicaments et des substances chimiques)</term>
<term>Cellules végétales (métabolisme)</term>
<term>Cellules végétales (ultrastructure)</term>
<term>Chlorure de sodium (pharmacologie)</term>
<term>Cytosol (effets des médicaments et des substances chimiques)</term>
<term>Cytosol (métabolisme)</term>
<term>Espace extracellulaire (effets des médicaments et des substances chimiques)</term>
<term>Espace extracellulaire (métabolisme)</term>
<term>Peroxyde d'hydrogène (pharmacologie)</term>
<term>Populus (cytologie)</term>
<term>Populus (effets des médicaments et des substances chimiques)</term>
<term>Populus (métabolisme)</term>
<term>Survie cellulaire (effets des médicaments et des substances chimiques)</term>
<term>Tolérance au sel (effets des médicaments et des substances chimiques)</term>
<term>Transduction du signal (effets des médicaments et des substances chimiques)</term>
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<term>Antioxidants</term>
<term>Calcium</term>
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<term>Extracellular Space</term>
<term>Plant Cells</term>
<term>Populus</term>
<term>Salt Tolerance</term>
<term>Signal Transduction</term>
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<keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Adaptation physiologique</term>
<term>Cellules végétales</term>
<term>Cytosol</term>
<term>Espace extracellulaire</term>
<term>Populus</term>
<term>Survie cellulaire</term>
<term>Tolérance au sel</term>
<term>Transduction du signal</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cytosol</term>
<term>Extracellular Space</term>
<term>Plant Cells</term>
<term>Populus</term>
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<term>Calcium</term>
<term>Cellules végétales</term>
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<term>Espace extracellulaire</term>
<term>Populus</term>
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<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Chlorure de sodium</term>
<term>Peroxyde d'hydrogène</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Hydrogen Peroxide</term>
<term>Sodium Chloride</term>
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<front><div type="abstract" xml:lang="en">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 Na⁺/H⁺ homeostasis and PM repair. Furthermore, we found that the eATP signaling was mediated by H₂O₂ and cytosolic Ca²⁺ 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 H₂O₂ and cytosolic Ca²⁺, which are required for the up-regulation of genes linked to Na⁺/H⁺ homeostasis and PM repair. Consequently, the viability of P. euphratica cells was maintained during a prolonged period of salt stress.</div>
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<Abstract><AbstractText>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 Na⁺/H⁺ homeostasis and PM repair. Furthermore, we found that the eATP signaling was mediated by H₂O₂ and cytosolic Ca²⁺ 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 H₂O₂ and cytosolic Ca²⁺, which are required for the up-regulation of genes linked to Na⁺/H⁺ homeostasis and PM repair. Consequently, the viability of P. euphratica cells was maintained during a prolonged period of salt stress.</AbstractText>
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<ForeName>Xuan</ForeName>
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<ForeName>Shurong</ForeName>
<Initials>S</Initials>
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<Author ValidYN="Y"><LastName>Zhang</LastName>
<ForeName>Chunlan</ForeName>
<Initials>C</Initials>
</Author>
<Author ValidYN="Y"><LastName>Wang</LastName>
<ForeName>Meijuan</ForeName>
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<Author ValidYN="Y"><LastName>Ding</LastName>
<ForeName>Mingquan</ForeName>
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</Author>
<Author ValidYN="Y"><LastName>Zhao</LastName>
<ForeName>Rui</ForeName>
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<Author ValidYN="Y"><LastName>Shen</LastName>
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<Initials>X</Initials>
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<Author ValidYN="Y"><LastName>Zhou</LastName>
<ForeName>Xiaoyang</ForeName>
<Initials>X</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lu</LastName>
<ForeName>Cunfu</ForeName>
<Initials>C</Initials>
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<Author ValidYN="Y"><LastName>Chen</LastName>
<ForeName>Shaoliang</ForeName>
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<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading><DescriptorName UI="D006861" MajorTopicYN="N">Hydrogen Peroxide</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
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<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
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<MeshHeading><DescriptorName UI="D032107" MajorTopicYN="Y">Populus</DescriptorName>
<QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading><DescriptorName UI="D055049" MajorTopicYN="N">Salt Tolerance</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012965" MajorTopicYN="N">Sodium Chloride</DescriptorName>
<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
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<Month>03</Month>
<Day>08</Day>
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<PubMedPubDate PubStatus="accepted"><Year>2012</Year>
<Month>11</Month>
<Day>27</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>2013</Year>
<Month>1</Month>
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Extracellular ATP signaling is mediated by H₂O₂ and cytosolic Ca²⁺ in the salt response of Populus euphratica cells.

Extracellular ATP signaling is mediated by H₂O₂ and cytosolic Ca²⁺ in the salt response of Populus euphratica cells.

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