The plant defense elicitor cryptogein stimulates clathrin-mediated endocytosis correlated with reactive oxygen species production in bright yellow-2 tobacco cells.
Identifieur interne : 001C05 ( Main/Exploration ); précédent : 001C04; suivant : 001C06The plant defense elicitor cryptogein stimulates clathrin-mediated endocytosis correlated with reactive oxygen species production in bright yellow-2 tobacco cells.
Auteurs : Nathalie Leborgne-Castel [France] ; Jeannine Lherminier ; Christophe Der ; Jérôme Fromentin ; Valérie Houot ; Françoise Simon-PlasSource :
- Plant physiology [ 0032-0889 ] ; 2008.
Descripteurs français
- KwdFr :
- Colorants fluorescents (métabolisme), Composés d'ammonium quaternaire (métabolisme), Composés de pyridinium (métabolisme), Endocytose (physiologie), Espèces réactives de l'oxygène (métabolisme), Interactions hôte-pathogène (physiologie), Ligands (MeSH), Lignée cellulaire (MeSH), Membrane cellulaire (métabolisme), Microscopie électronique à transmission (MeSH), Protéines d'algue (physiologie), Protéines fongiques (MeSH), Spectrométrie de fluorescence (MeSH), Tabac (microbiologie), Tabac (physiologie), Tabac (ultrastructure), Transduction du signal (physiologie), Tyrphostines (MeSH), Vésicules tapissées de clathrine (métabolisme).
- MESH :
- microbiologie : Tabac.
- métabolisme : Colorants fluorescents, Composés d'ammonium quaternaire, Composés de pyridinium, Espèces réactives de l'oxygène, Membrane cellulaire, Vésicules tapissées de clathrine.
- physiologie : Endocytose, Interactions hôte-pathogène, Protéines d'algue, Tabac, Transduction du signal.
- ultrastructure : Ligands, Lignée cellulaire, Microscopie électronique à transmission, Protéines fongiques, Spectrométrie de fluorescence, Tabac, Tyrphostines.
English descriptors
- KwdEn :
- Algal Proteins (physiology), Cell Line (MeSH), Cell Membrane (metabolism), Clathrin-Coated Vesicles (metabolism), Endocytosis (physiology), Fluorescent Dyes (metabolism), Fungal Proteins (MeSH), Host-Pathogen Interactions (physiology), Ligands (MeSH), Microscopy, Electron, Transmission (MeSH), Pyridinium Compounds (metabolism), Quaternary Ammonium Compounds (metabolism), Reactive Oxygen Species (metabolism), Signal Transduction (physiology), Spectrometry, Fluorescence (MeSH), Tobacco (microbiology), Tobacco (physiology), Tobacco (ultrastructure), Tyrphostins (MeSH).
- MESH :
- chemical , metabolism : Fluorescent Dyes, Pyridinium Compounds, Quaternary Ammonium Compounds, Reactive Oxygen Species.
- chemical , physiology : Algal Proteins.
- metabolism : Cell Membrane, Clathrin-Coated Vesicles.
- microbiology : Tobacco.
- physiology : Endocytosis, Host-Pathogen Interactions, Signal Transduction, Tobacco.
- ultrastructure : Tobacco.
- Cell Line, Fungal Proteins, Ligands, Microscopy, Electron, Transmission, Spectrometry, Fluorescence, Tyrphostins.
Abstract
The plant defense elicitor cryptogein triggers well-known biochemical events of early signal transduction at the plasma membrane of tobacco (Nicotiana tabacum) cells, but microscopic observations of cell responses related to these early events were lacking. We determined that internalization of the lipophilic dye FM4-64, which is a marker of endocytosis, is stimulated a few minutes after addition of cryptogein to tobacco Bright Yellow-2 (BY-2) cells. This stimulation is specific to the signal transduction pathway elicited by cryptogein because a lipid transfer protein, which binds to the same receptor as cryptogein but without triggering signaling, does not increase endocytosis. To define the nature of the stimulated endocytosis, we quantified clathrin-coated pits (CCPs) forming on the plasma membrane of BY-2 cells. A transitory stimulation of this morphological event by cryptogein occurs within the first 15 min. In the presence of cryptogein, increases in both FM4-64 internalization and clathrin-mediated endocytosis are specifically blocked upon treatment with 5 microm tyrphostin A23, a receptor-mediated endocytosis inhibitor. The kinetics of the transient increase in CCPs at the plasma membrane coincides with that of transitory reactive oxygen species (ROS) production occurring within the first 15 min after elicitation. Moreover, in BY-2 cells expressing NtrbohD antisense cDNA, which are unable to produce ROS when treated with cryptogein, the CCP stimulation is inhibited. These results indicate that the very early endocytic process induced by cryptogein in tobacco is due, at least partly, to clathrin-mediated endocytosis and is dependent on ROS production by the NADPH oxidase NtrbohD.
DOI: 10.1104/pp.107.111716
PubMed: 18184734
PubMed Central: PMC2259092
Affiliations:
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(metabolism)</term><term>Reactive Oxygen Species (metabolism)</term><term>Signal Transduction (physiology)</term><term>Spectrometry, Fluorescence (MeSH)</term><term>Tobacco (microbiology)</term><term>Tobacco (physiology)</term><term>Tobacco (ultrastructure)</term><term>Tyrphostins (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Colorants fluorescents (métabolisme)</term><term>Composés d'ammonium quaternaire (métabolisme)</term><term>Composés de pyridinium (métabolisme)</term><term>Endocytose (physiologie)</term><term>Espèces réactives de l'oxygène (métabolisme)</term><term>Interactions hôte-pathogène (physiologie)</term><term>Ligands (MeSH)</term><term>Lignée cellulaire (MeSH)</term><term>Membrane cellulaire (métabolisme)</term><term>Microscopie électronique à transmission (MeSH)</term><term>Protéines d'algue (physiologie)</term><term>Protéines fongiques (MeSH)</term><term>Spectrométrie de fluorescence (MeSH)</term><term>Tabac (microbiologie)</term><term>Tabac (physiologie)</term><term>Tabac (ultrastructure)</term><term>Transduction du signal (physiologie)</term><term>Tyrphostines (MeSH)</term><term>Vésicules tapissées de clathrine (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Fluorescent Dyes</term><term>Pyridinium Compounds</term><term>Quaternary Ammonium Compounds</term><term>Reactive Oxygen Species</term></keywords><keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Algal Proteins</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cell Membrane</term><term>Clathrin-Coated Vesicles</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Tabac</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Colorants fluorescents</term><term>Composés d'ammonium 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xml:lang="fr"><term>Ligands</term><term>Lignée cellulaire</term><term>Microscopie électronique à transmission</term><term>Protéines fongiques</term><term>Spectrométrie de fluorescence</term><term>Tabac</term><term>Tyrphostines</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The plant defense elicitor cryptogein triggers well-known biochemical events of early signal transduction at the plasma membrane of tobacco (Nicotiana tabacum) cells, but microscopic observations of cell responses related to these early events were lacking. We determined that internalization of the lipophilic dye FM4-64, which is a marker of endocytosis, is stimulated a few minutes after addition of cryptogein to tobacco Bright Yellow-2 (BY-2) cells. This stimulation is specific to the signal transduction pathway elicited by cryptogein because a lipid transfer protein, which binds to the same receptor as cryptogein but without triggering signaling, does not increase endocytosis. To define the nature of the stimulated endocytosis, we quantified clathrin-coated pits (CCPs) forming on the plasma membrane of BY-2 cells. A transitory stimulation of this morphological event by cryptogein occurs within the first 15 min. In the presence of cryptogein, increases in both FM4-64 internalization and clathrin-mediated endocytosis are specifically blocked upon treatment with 5 microm tyrphostin A23, a receptor-mediated endocytosis inhibitor. The kinetics of the transient increase in CCPs at the plasma membrane coincides with that of transitory reactive oxygen species (ROS) production occurring within the first 15 min after elicitation. Moreover, in BY-2 cells expressing NtrbohD antisense cDNA, which are unable to produce ROS when treated with cryptogein, the CCP stimulation is inhibited. These results indicate that the very early endocytic process induced by cryptogein in tobacco is due, at least partly, to clathrin-mediated endocytosis and is dependent on ROS production by the NADPH oxidase NtrbohD.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">18184734</PMID><DateCompleted><Year>2008</Year><Month>07</Month><Day>21</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0032-0889</ISSN><JournalIssue CitedMedium="Print"><Volume>146</Volume><Issue>3</Issue><PubDate><Year>2008</Year><Month>Mar</Month></PubDate></JournalIssue><Title>Plant physiology</Title><ISOAbbreviation>Plant Physiol</ISOAbbreviation></Journal><ArticleTitle>The plant defense elicitor cryptogein stimulates clathrin-mediated endocytosis correlated with reactive oxygen species production in bright yellow-2 tobacco cells.</ArticleTitle><Pagination><MedlinePgn>1255-66</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1104/pp.107.111716</ELocationID><Abstract><AbstractText>The plant defense elicitor cryptogein triggers well-known biochemical events of early signal transduction at the plasma membrane of tobacco (Nicotiana tabacum) cells, but microscopic observations of cell responses related to these early events were lacking. We determined that internalization of the lipophilic dye FM4-64, which is a marker of endocytosis, is stimulated a few minutes after addition of cryptogein to tobacco Bright Yellow-2 (BY-2) cells. This stimulation is specific to the signal transduction pathway elicited by cryptogein because a lipid transfer protein, which binds to the same receptor as cryptogein but without triggering signaling, does not increase endocytosis. To define the nature of the stimulated endocytosis, we quantified clathrin-coated pits (CCPs) forming on the plasma membrane of BY-2 cells. A transitory stimulation of this morphological event by cryptogein occurs within the first 15 min. In the presence of cryptogein, increases in both FM4-64 internalization and clathrin-mediated endocytosis are specifically blocked upon treatment with 5 microm tyrphostin A23, a receptor-mediated endocytosis inhibitor. The kinetics of the transient increase in CCPs at the plasma membrane coincides with that of transitory reactive oxygen species (ROS) production occurring within the first 15 min after elicitation. Moreover, in BY-2 cells expressing NtrbohD antisense cDNA, which are unable to produce ROS when treated with cryptogein, the CCP stimulation is inhibited. These results indicate that the very early endocytic process induced by cryptogein in tobacco is due, at least partly, to clathrin-mediated endocytosis and is dependent on ROS production by the NADPH oxidase NtrbohD.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Leborgne-Castel</LastName><ForeName>Nathalie</ForeName><Initials>N</Initials><AffiliationInfo><Affiliation>UMR INRA 1088/CNRS 5184/Université de Bourgogne, Plante-Microbe-Environnement, Dijon, France. nathalie.leborgne-castel@dijon.inra.fr</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lherminier</LastName><ForeName>Jeannine</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Der</LastName><ForeName>Christophe</ForeName><Initials>C</Initials></Author><Author ValidYN="Y"><LastName>Fromentin</LastName><ForeName>Jérôme</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Houot</LastName><ForeName>Valérie</ForeName><Initials>V</Initials></Author><Author ValidYN="Y"><LastName>Simon-Plas</LastName><ForeName>Françoise</ForeName><Initials>F</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>2008</Year><Month>01</Month><Day>09</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Plant Physiol</MedlineTA><NlmUniqueID>0401224</NlmUniqueID><ISSNLinking>0032-0889</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020418">Algal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C092350">FM 4-64</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005456">Fluorescent Dyes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D005656">Fungal Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008024">Ligands</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011726">Pyridinium Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000644">Quaternary Ammonium Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D017382">Reactive Oxygen Species</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D020032">Tyrphostins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C061032">cryptogein protein, Phytophthora cryptogea</NameOfSubstance></Chemical><Chemical><RegistryNumber>RV0GCD31OJ</RegistryNumber><NameOfSubstance UI="C060641">tyrphostin A23</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D020418" MajorTopicYN="N">Algal Proteins</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002460" MajorTopicYN="N">Cell Line</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002462" MajorTopicYN="N">Cell Membrane</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D022163" MajorTopicYN="N">Clathrin-Coated Vesicles</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D004705" MajorTopicYN="N">Endocytosis</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005456" MajorTopicYN="N">Fluorescent Dyes</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005656" MajorTopicYN="N">Fungal Proteins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054884" MajorTopicYN="N">Host-Pathogen Interactions</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008024" MajorTopicYN="N">Ligands</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D046529" MajorTopicYN="N">Microscopy, Electron, Transmission</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011726" MajorTopicYN="N">Pyridinium Compounds</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000644" MajorTopicYN="N">Quaternary Ammonium Compounds</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017382" MajorTopicYN="N">Reactive Oxygen Species</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015398" MajorTopicYN="N">Signal Transduction</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013050" MajorTopicYN="N">Spectrometry, Fluorescence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020032" 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sort="Der, Christophe" uniqKey="Der C" first="Christophe" last="Der">Christophe Der</name><name sortKey="Fromentin, Jerome" sort="Fromentin, Jerome" uniqKey="Fromentin J" first="Jérôme" last="Fromentin">Jérôme Fromentin</name><name sortKey="Houot, Valerie" sort="Houot, Valerie" uniqKey="Houot V" first="Valérie" last="Houot">Valérie Houot</name><name sortKey="Lherminier, Jeannine" sort="Lherminier, Jeannine" uniqKey="Lherminier J" first="Jeannine" last="Lherminier">Jeannine Lherminier</name><name sortKey="Simon Plas, Francoise" sort="Simon Plas, Francoise" uniqKey="Simon Plas F" first="Françoise" last="Simon-Plas">Françoise Simon-Plas</name></noCountry><country name="France"><region name="Bourgogne-Franche-Comté"><name sortKey="Leborgne Castel, Nathalie" sort="Leborgne Castel, Nathalie" uniqKey="Leborgne Castel N" first="Nathalie" last="Leborgne-Castel">Nathalie Leborgne-Castel</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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