PhytophthoraV1, Main, Exploration, bibRecord, 001054

Modification of plasma membrane organization in tobacco cells elicited by cryptogein.

Identifieur interne : 001054 ( Main/Exploration ); précédent : 001053; suivant : 001055

Modification of plasma membrane organization in tobacco cells elicited by cryptogein.

Auteurs : Patricia Gerbeau-Pissot [France] ; Christophe Der ; Dominique Thomas ; Iulia-Andra Anca ; Kevin Grosjean ; Yann Roche ; Jean-Marie Perrier-Cornet ; Sébastien Mongrand ; Françoise Simon-Plas

Source :

Plant physiology [ 1532-2548 ] ; 2014.

RBID : pubmed:24235133

Descripteurs français

KwdFr :
- Biophysique (méthodes), Colorants fluorescents (métabolisme), Composés de pyridinium (métabolisme), Flagelline (métabolisme), Membrane cellulaire (effets des médicaments et des substances chimiques), Membrane cellulaire (métabolisme), Membrane cellulaire (ultrastructure), Microscopie confocale (méthodes), Photoblanchiment (MeSH), Protéines fongiques (métabolisme), Protéines fongiques (pharmacologie), Stérols (analyse), Tabac (cytologie), Transduction du signal (MeSH).
MESH :
- analyse : Stérols.
- cytologie : Tabac.
- effets des médicaments et des substances chimiques : Membrane cellulaire.
- métabolisme : Colorants fluorescents, Composés de pyridinium, Flagelline, Membrane cellulaire, Protéines fongiques.
- méthodes : Biophysique, Microscopie confocale.
- pharmacologie : Protéines fongiques.
- ultrastructure : Membrane cellulaire, Photoblanchiment, Transduction du signal.

English descriptors

KwdEn :
- Biophysics (methods), Cell Membrane (drug effects), Cell Membrane (metabolism), Cell Membrane (ultrastructure), Flagellin (metabolism), Fluorescent Dyes (metabolism), Fungal Proteins (metabolism), Fungal Proteins (pharmacology), Microscopy, Confocal (methods), Photobleaching (MeSH), Pyridinium Compounds (metabolism), Signal Transduction (MeSH), Sterols (analysis), Tobacco (cytology).
MESH :
- chemical , analysis : Sterols.
- chemical , metabolism : Flagellin, Fluorescent Dyes, Fungal Proteins, Pyridinium Compounds.
- cytology : Tobacco.
- drug effects : Cell Membrane.
- metabolism : Cell Membrane.
- methods : Biophysics, Microscopy, Confocal.
- chemical , pharmacology : Fungal Proteins.
- ultrastructure : Cell Membrane.
- Photobleaching, Signal Transduction.

Abstract

Lipid mixtures within artificial membranes undergo a separation into liquid-disordered and liquid-ordered phases. However, the existence of this segregation into microscopic liquid-ordered phases has been difficult to prove in living cells, and the precise organization of the plasma membrane into such phases has not been elucidated in plant cells. We developed a multispectral confocal microscopy approach to generate ratiometric images of the plasma membrane surface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment sensitive fluorescent probe. This allowed the in vivo characterization of the global level of order of this membrane, by which we could demonstrate that an increase in its proportion of ordered phases transiently occurred in the early steps of the signaling triggered by cryptogein and flagellin, two elicitors of plant defense reactions. The use of fluorescence recovery after photobleaching revealed an increase in plasma membrane fluidity induced by cryptogein, but not by flagellin. Moreover, we characterized the spatial distribution of liquid-ordered phases on the membrane of living plant cells and monitored their variations induced by cryptogein elicitation. We analyze these results in the context of plant defense signaling, discuss their meaning within the framework of the "membrane raft" hypothesis, and propose a new mechanism of signaling platform formation in response to elicitor treatment.

DOI: 10.1104/pp.113.225755
PubMed: 24235133
PubMed Central: PMC3875808

Affiliations:

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

to stream Main, to step Corpus: 001184
to stream Main, to step Curation: 001184

Le document en format XML

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<term>Flagellin (metabolism)</term>
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<term>Fungal Proteins (metabolism)</term>
<term>Fungal Proteins (pharmacology)</term>
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<term>Membrane cellulaire (ultrastructure)</term>
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<term>Signal Transduction</term>
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<front><div type="abstract" xml:lang="en">Lipid mixtures within artificial membranes undergo a separation into liquid-disordered and liquid-ordered phases. However, the existence of this segregation into microscopic liquid-ordered phases has been difficult to prove in living cells, and the precise organization of the plasma membrane into such phases has not been elucidated in plant cells. We developed a multispectral confocal microscopy approach to generate ratiometric images of the plasma membrane surface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment sensitive fluorescent probe. This allowed the in vivo characterization of the global level of order of this membrane, by which we could demonstrate that an increase in its proportion of ordered phases transiently occurred in the early steps of the signaling triggered by cryptogein and flagellin, two elicitors of plant defense reactions. The use of fluorescence recovery after photobleaching revealed an increase in plasma membrane fluidity induced by cryptogein, but not by flagellin. Moreover, we characterized the spatial distribution of liquid-ordered phases on the membrane of living plant cells and monitored their variations induced by cryptogein elicitation. We analyze these results in the context of plant defense signaling, discuss their meaning within the framework of the "membrane raft" hypothesis, and propose a new mechanism of signaling platform formation in response to elicitor treatment. </div>
</front>
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<Title>Plant physiology</Title>
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<ArticleTitle>Modification of plasma membrane organization in tobacco cells elicited by cryptogein.</ArticleTitle>
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<Abstract><AbstractText>Lipid mixtures within artificial membranes undergo a separation into liquid-disordered and liquid-ordered phases. However, the existence of this segregation into microscopic liquid-ordered phases has been difficult to prove in living cells, and the precise organization of the plasma membrane into such phases has not been elucidated in plant cells. We developed a multispectral confocal microscopy approach to generate ratiometric images of the plasma membrane surface of Bright Yellow 2 tobacco (Nicotiana tabacum) suspension cells labeled with an environment sensitive fluorescent probe. This allowed the in vivo characterization of the global level of order of this membrane, by which we could demonstrate that an increase in its proportion of ordered phases transiently occurred in the early steps of the signaling triggered by cryptogein and flagellin, two elicitors of plant defense reactions. The use of fluorescence recovery after photobleaching revealed an increase in plasma membrane fluidity induced by cryptogein, but not by flagellin. Moreover, we characterized the spatial distribution of liquid-ordered phases on the membrane of living plant cells and monitored their variations induced by cryptogein elicitation. We analyze these results in the context of plant defense signaling, discuss their meaning within the framework of the "membrane raft" hypothesis, and propose a new mechanism of signaling platform formation in response to elicitor treatment. </AbstractText>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gerbeau-Pissot</LastName>
<ForeName>Patricia</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Université de Bourgogne , Unité Mixte de Recherche 1347 Agroécologie, Equipe de Recherche Labelisée 6300 Centre National de la Recherche Scientifique, BP 86510, F-21000 Dijon, France.</Affiliation>
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<Author ValidYN="Y"><LastName>Anca</LastName>
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<Initials>Y</Initials>
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Modification of plasma membrane organization in tobacco cells elicited by cryptogein.

Modification of plasma membrane organization in tobacco cells elicited by cryptogein.

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