Involvement of putative glutamate receptors in plant defence signaling and NO production.
Identifieur interne : 001705 ( Main/Exploration ); précédent : 001704; suivant : 001706Involvement of putative glutamate receptors in plant defence signaling and NO production.
Auteurs : Parul Vatsa [France] ; Annick Chiltz ; Stéphane Bourque ; David Wendehenne ; Angela Garcia-Brugger ; Alain PuginSource :
- Biochimie [ 1638-6183 ] ; 2011.
Descripteurs français
- KwdFr :
- Acide glutamique (métabolisme), Acide glutamique (pharmacologie), Acide glutamique (physiologie), Agonistes des acides aminés excitateurs (pharmacologie), Antagonistes des acides aminés excitateurs (pharmacologie), Calcium (métabolisme), Immunité innée (MeSH), Monoxyde d'azote (métabolisme), Protéines d'algue (pharmacologie), Protéines fongiques (MeSH), Protéines végétales (métabolisme), Récepteurs au glutamate (métabolisme), Signalisation calcique (MeSH), Tabac (cytologie), Tabac (immunologie), Tabac (métabolisme), Techniques de culture cellulaire (MeSH).
- MESH :
- cytologie : Tabac.
- immunologie : Tabac.
- métabolisme : Acide glutamique, Calcium, Monoxyde d'azote, Protéines végétales, Récepteurs au glutamate, Tabac.
- pharmacologie : Acide glutamique, Agonistes des acides aminés excitateurs, Antagonistes des acides aminés excitateurs, Protéines d'algue.
- physiologie : Acide glutamique.
- Immunité innée, Protéines fongiques, Signalisation calcique, Techniques de culture cellulaire.
English descriptors
- KwdEn :
- Algal Proteins (pharmacology), Calcium (metabolism), Calcium Signaling (MeSH), Cell Culture Techniques (MeSH), Excitatory Amino Acid Agonists (pharmacology), Excitatory Amino Acid Antagonists (pharmacology), Fungal Proteins (MeSH), Glutamic Acid (metabolism), Glutamic Acid (pharmacology), Glutamic Acid (physiology), Immunity, Innate (MeSH), Nitric Oxide (metabolism), Plant Proteins (metabolism), Receptors, Glutamate (metabolism), Tobacco (cytology), Tobacco (immunology), Tobacco (metabolism).
- MESH :
- chemical , metabolism : Calcium, Glutamic Acid, Nitric Oxide, Plant Proteins, Receptors, Glutamate.
- chemical , pharmacology : Algal Proteins, Excitatory Amino Acid Agonists, Excitatory Amino Acid Antagonists, Glutamic Acid.
- chemical , physiology : Glutamic Acid.
- cytology : Tobacco.
- immunology : Tobacco.
- metabolism : Tobacco.
- Calcium Signaling, Cell Culture Techniques, Fungal Proteins, Immunity, Innate.
Abstract
Ionotropic glutamate receptors (iGluRs) are non-selective cation channels permeable to calcium, present in animals and plants. In mammals, glutamate is a well-known neurotransmitter and recently has been recognized as an immunomodulator. As animals and plants share common mechanisms that govern innate immunity with calcium playing a key role in plant defence activation, we have checked the involvement of putative iGluRs in plant defence signaling. Using tobacco cells, we first provide evidence supporting the activity of iGluRs as calcium channels and their involvement in NO production as reported in animals. Thereafter, iGluRs were shown to be activated in response to cryptogein, a well studied elicitor of defence response, and partly responsible for cryptogein-induced NO production. However, other cryptogein-induced calcium-dependent events including anion efflux, H(2)O(2) production, MAPK activation and hypersensitive response (HR) did not depend on iGluRs indicating that different calcium channels regulate different processes at the cell level. We have also demonstrated that cryptogein induces efflux of glutamate in the apoplast by exocytosis. Taken together, our results demonstrate for the first time, an involvement of a putative iGluR in plant defence signaling and NO production, by mechanisms that show homology with glutamate mode of action in mammals.
DOI: 10.1016/j.biochi.2011.04.006
PubMed: 21524679
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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glutamique</term><term>Agonistes des acides aminés excitateurs</term><term>Antagonistes des acides aminés excitateurs</term><term>Protéines d'algue</term></keywords><keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Acide glutamique</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Calcium Signaling</term><term>Cell Culture Techniques</term><term>Fungal Proteins</term><term>Immunity, Innate</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Immunité innée</term><term>Protéines fongiques</term><term>Signalisation calcique</term><term>Techniques de culture cellulaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Ionotropic glutamate receptors (iGluRs) are non-selective cation channels permeable to calcium, present in animals and plants. In mammals, glutamate is a well-known neurotransmitter and recently has been recognized as an immunomodulator. As animals and plants share common mechanisms that govern innate immunity with calcium playing a key role in plant defence activation, we have checked the involvement of putative iGluRs in plant defence signaling. Using tobacco cells, we first provide evidence supporting the activity of iGluRs as calcium channels and their involvement in NO production as reported in animals. Thereafter, iGluRs were shown to be activated in response to cryptogein, a well studied elicitor of defence response, and partly responsible for cryptogein-induced NO production. However, other cryptogein-induced calcium-dependent events including anion efflux, H(2)O(2) production, MAPK activation and hypersensitive response (HR) did not depend on iGluRs indicating that different calcium channels regulate different processes at the cell level. We have also demonstrated that cryptogein induces efflux of glutamate in the apoplast by exocytosis. Taken together, our results demonstrate for the first time, an involvement of a putative iGluR in plant defence signaling and NO production, by mechanisms that show homology with glutamate mode of action in mammals.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21524679</PMID><DateCompleted><Year>2012</Year><Month>02</Month><Day>24</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1638-6183</ISSN><JournalIssue CitedMedium="Internet"><Volume>93</Volume><Issue>12</Issue><PubDate><Year>2011</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Biochimie</Title><ISOAbbreviation>Biochimie</ISOAbbreviation></Journal><ArticleTitle>Involvement of putative glutamate receptors in plant defence signaling and NO production.</ArticleTitle><Pagination><MedlinePgn>2095-101</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.biochi.2011.04.006</ELocationID><Abstract><AbstractText>Ionotropic glutamate receptors (iGluRs) are non-selective cation channels permeable to calcium, present in animals and plants. In mammals, glutamate is a well-known neurotransmitter and recently has been recognized as an immunomodulator. As animals and plants share common mechanisms that govern innate immunity with calcium playing a key role in plant defence activation, we have checked the involvement of putative iGluRs in plant defence signaling. Using tobacco cells, we first provide evidence supporting the activity of iGluRs as calcium channels and their involvement in NO production as reported in animals. Thereafter, iGluRs were shown to be activated in response to cryptogein, a well studied elicitor of defence response, and partly responsible for cryptogein-induced NO production. However, other cryptogein-induced calcium-dependent events including anion efflux, H(2)O(2) production, MAPK activation and hypersensitive response (HR) did not depend on iGluRs indicating that different calcium channels regulate different processes at the cell level. We have also demonstrated that cryptogein induces efflux of glutamate in the apoplast by exocytosis. Taken together, our results demonstrate for the first time, an involvement of a putative iGluR in plant defence signaling and NO production, by mechanisms that show homology with glutamate mode of action in mammals.</AbstractText><CopyrightInformation>Copyright © 2011 Elsevier Masson SAS. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Vatsa</LastName><ForeName>Parul</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>UMR INRA 1088, CNRS 5184, Université de Bourgogne, Plante-Microbe-Environnement, 17 Rue Sully, Dijon, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chiltz</LastName><ForeName>Annick</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Bourque</LastName><ForeName>Stéphane</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Wendehenne</LastName><ForeName>David</ForeName><Initials>D</Initials></Author><Author ValidYN="Y"><LastName>Garcia-Brugger</LastName><ForeName>Angela</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Pugin</LastName><ForeName>Alain</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2011</Year><Month>04</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>France</Country><MedlineTA>Biochimie</MedlineTA><NlmUniqueID>1264604</NlmUniqueID><ISSNLinking>0300-9084</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020418">Algal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018690">Excitatory Amino Acid Agonists</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018691">Excitatory Amino Acid Antagonists</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017470">Receptors, Glutamate</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C061032">cryptogein protein, Phytophthora cryptogea</NameOfSubstance></Chemical><Chemical><RegistryNumber>31C4KY9ESH</RegistryNumber><NameOfSubstance UI="D009569">Nitric Oxide</NameOfSubstance></Chemical><Chemical><RegistryNumber>3KX376GY7L</RegistryNumber><NameOfSubstance UI="D018698">Glutamic Acid</NameOfSubstance></Chemical><Chemical><RegistryNumber>SY7Q814VUP</RegistryNumber><NameOfSubstance UI="D002118">Calcium</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D020418" MajorTopicYN="N">Algal Proteins</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002118" MajorTopicYN="N">Calcium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020013" MajorTopicYN="Y">Calcium Signaling</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018929" MajorTopicYN="N">Cell Culture Techniques</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018690" MajorTopicYN="N">Excitatory Amino Acid Agonists</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018691" MajorTopicYN="N">Excitatory Amino Acid Antagonists</DescriptorName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018698" MajorTopicYN="N">Glutamic Acid</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007113" MajorTopicYN="N">Immunity, Innate</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009569" MajorTopicYN="N">Nitric Oxide</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017470" MajorTopicYN="N">Receptors, Glutamate</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000166" 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IdType="pii">S0300-9084(11)00123-4</ArticleId><ArticleId IdType="doi">10.1016/j.biochi.2011.04.006</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>France</li></country><region><li>Bourgogne</li><li>Bourgogne-Franche-Comté</li></region><settlement><li>Dijon</li></settlement><orgName><li>Université de Bourgogne</li></orgName></list><tree><noCountry><name sortKey="Bourque, Stephane" sort="Bourque, Stephane" uniqKey="Bourque S" first="Stéphane" last="Bourque">Stéphane Bourque</name><name sortKey="Chiltz, Annick" sort="Chiltz, Annick" uniqKey="Chiltz A" first="Annick" last="Chiltz">Annick Chiltz</name><name sortKey="Garcia Brugger, Angela" sort="Garcia Brugger, Angela" uniqKey="Garcia Brugger A" first="Angela" last="Garcia-Brugger">Angela Garcia-Brugger</name><name sortKey="Pugin, Alain" sort="Pugin, Alain" uniqKey="Pugin A" first="Alain" last="Pugin">Alain Pugin</name><name sortKey="Wendehenne, David" sort="Wendehenne, David" uniqKey="Wendehenne D" first="David" last="Wendehenne">David Wendehenne</name></noCountry><country name="France"><region name="Bourgogne-Franche-Comté"><name sortKey="Vatsa, Parul" sort="Vatsa, Parul" uniqKey="Vatsa P" first="Parul" last="Vatsa">Parul Vatsa</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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