Seasonal changes of plasma membrane H(+)-ATPase and endogenous ion current during cambial growth in poplar plants.
Identifieur interne : 004534 ( Main/Exploration ); précédent : 004533; suivant : 004535Seasonal changes of plasma membrane H(+)-ATPase and endogenous ion current during cambial growth in poplar plants.
Auteurs : Matthias Arend [Allemagne] ; Manfred H. Weisenseel ; Maria Brummer ; Wolfgang Osswald ; Jörg H. FrommSource :
- Plant physiology [ 0032-0889 ] ; 2002.
Descripteurs français
- KwdFr :
- Acide abscissique (métabolisme), Acides indolacétiques (métabolisme), Membrane cellulaire (métabolisme), Membrane cellulaire (ultrastructure), Microscopie de fluorescence (MeSH), Microscopie électronique (MeSH), Méristème (croissance et développement), Méristème (métabolisme), Méristème (ultrastructure), Potassium (métabolisme), Proton-Translocating ATPases (métabolisme), Saisons (MeSH), Salicaceae (croissance et développement), Salicaceae (métabolisme), Salicaceae (ultrastructure), Technique de Western (MeSH), Tiges de plante (croissance et développement), Tiges de plante (métabolisme), Tiges de plante (ultrastructure), Transport biologique (physiologie), Transport des ions (physiologie).
- MESH :
- croissance et développement : Méristème, Salicaceae, Tiges de plante.
- métabolisme : Acide abscissique, Acides indolacétiques, Membrane cellulaire, Méristème, Potassium, Proton-Translocating ATPases, Salicaceae, Tiges de plante.
- physiologie : Transport biologique, Transport des ions.
- ultrastructure : Membrane cellulaire, Microscopie de fluorescence, Microscopie électronique, Méristème, Saisons, Salicaceae, Technique de Western, Tiges de plante.
English descriptors
- KwdEn :
- Abscisic Acid (metabolism), Biological Transport (physiology), Blotting, Western (MeSH), Cell Membrane (metabolism), Cell Membrane (ultrastructure), Indoleacetic Acids (metabolism), Ion Transport (physiology), Meristem (growth & development), Meristem (metabolism), Meristem (ultrastructure), Microscopy, Electron (MeSH), Microscopy, Fluorescence (MeSH), Plant Stems (growth & development), Plant Stems (metabolism), Plant Stems (ultrastructure), Potassium (metabolism), Proton-Translocating ATPases (metabolism), Salicaceae (growth & development), Salicaceae (metabolism), Salicaceae (ultrastructure), Seasons (MeSH).
- MESH :
- chemical , metabolism : Abscisic Acid, Indoleacetic Acids, Potassium, Proton-Translocating ATPases.
- growth & development : Meristem, Plant Stems, Salicaceae.
- metabolism : Cell Membrane, Meristem, Plant Stems, Salicaceae.
- physiology : Biological Transport, Ion Transport.
- ultrastructure : Cell Membrane, Meristem, Plant Stems, Salicaceae.
- Blotting, Western, Microscopy, Electron, Microscopy, Fluorescence, Seasons.
Abstract
The plasma membrane H(+)-ATPase (PM H(+)-ATPase), potassium ions, and endogenous ion currents might play a fundamental role in the physiology of cambial growth. Seasonal changes of these parameters were studied in twigs of Populus nigra and Populus trichocarpa. Monoclonal and polyclonal antibodies against the PM H(+)-ATPase, x-ray analysis for K(+) localization and a vibrating electrode for measurement of endogenous ion currents were used as probes. In dormant plants during autumn and winter, only a slight immunoreactivity against the PM H(+)-ATPase was found in cross sections and tissue homogenates, K(+) was distributed evenly, and the density of endogenous current was low. In spring during cambial growth, strong immunoreactivity against a PM H(+)-ATPase was observed in cambial cells and expanding xylem cells using the monoclonal antibody 46 E5 B11 F6 for fluorescence microscopy and transmission electron microscopy. At the same time, K(+) accumulated in cells of the cambial region, and strong endogenous current was measured in the cambial and immature xylem zone. Addition of auxin to dormant twigs induced the formation of this PM H(+)-ATPase in the dormant cambial region within a few days and an increase in density of endogenous current in shoot cuttings within a few hours. The increase in PM H(+)-ATPase abundance and in current density by auxin indicates that auxin mediates a rise in number and activity of an H(+)-ATPase in the plasma membrane of cambial cells and their derivatives. This PM H(+)-ATPase generates the necessary H(+)-gradient (proton-motive force) for the uptake of K(+) and nutrients into cambial and expanding xylem cells.
DOI: 10.1104/pp.003905
PubMed: 12177478
PubMed Central: PMC166753
Affiliations:
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Seasonal changes of these parameters were studied in twigs of Populus nigra and Populus trichocarpa. Monoclonal and polyclonal antibodies against the PM H(+)-ATPase, x-ray analysis for K(+) localization and a vibrating electrode for measurement of endogenous ion currents were used as probes. In dormant plants during autumn and winter, only a slight immunoreactivity against the PM H(+)-ATPase was found in cross sections and tissue homogenates, K(+) was distributed evenly, and the density of endogenous current was low. In spring during cambial growth, strong immunoreactivity against a PM H(+)-ATPase was observed in cambial cells and expanding xylem cells using the monoclonal antibody 46 E5 B11 F6 for fluorescence microscopy and transmission electron microscopy. At the same time, K(+) accumulated in cells of the cambial region, and strong endogenous current was measured in the cambial and immature xylem zone. Addition of auxin to dormant twigs induced the formation of this PM H(+)-ATPase in the dormant cambial region within a few days and an increase in density of endogenous current in shoot cuttings within a few hours. The increase in PM H(+)-ATPase abundance and in current density by auxin indicates that auxin mediates a rise in number and activity of an H(+)-ATPase in the plasma membrane of cambial cells and their derivatives. This PM H(+)-ATPase generates the necessary H(+)-gradient (proton-motive force) for the uptake of K(+) and nutrients into cambial and expanding xylem cells.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">12177478</PMID><DateCompleted><Year>2002</Year><Month>12</Month><Day>03</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>30</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0032-0889</ISSN><JournalIssue CitedMedium="Print"><Volume>129</Volume><Issue>4</Issue><PubDate><Year>2002</Year><Month>Aug</Month></PubDate></JournalIssue><Title>Plant physiology</Title><ISOAbbreviation>Plant Physiol</ISOAbbreviation></Journal><ArticleTitle>Seasonal changes of plasma membrane H(+)-ATPase and endogenous ion current during cambial growth in poplar plants.</ArticleTitle><Pagination><MedlinePgn>1651-63</MedlinePgn></Pagination><Abstract><AbstractText>The plasma membrane H(+)-ATPase (PM H(+)-ATPase), potassium ions, and endogenous ion currents might play a fundamental role in the physiology of cambial growth. Seasonal changes of these parameters were studied in twigs of Populus nigra and Populus trichocarpa. Monoclonal and polyclonal antibodies against the PM H(+)-ATPase, x-ray analysis for K(+) localization and a vibrating electrode for measurement of endogenous ion currents were used as probes. In dormant plants during autumn and winter, only a slight immunoreactivity against the PM H(+)-ATPase was found in cross sections and tissue homogenates, K(+) was distributed evenly, and the density of endogenous current was low. In spring during cambial growth, strong immunoreactivity against a PM H(+)-ATPase was observed in cambial cells and expanding xylem cells using the monoclonal antibody 46 E5 B11 F6 for fluorescence microscopy and transmission electron microscopy. At the same time, K(+) accumulated in cells of the cambial region, and strong endogenous current was measured in the cambial and immature xylem zone. Addition of auxin to dormant twigs induced the formation of this PM H(+)-ATPase in the dormant cambial region within a few days and an increase in density of endogenous current in shoot cuttings within a few hours. The increase in PM H(+)-ATPase abundance and in current density by auxin indicates that auxin mediates a rise in number and activity of an H(+)-ATPase in the plasma membrane of cambial cells and their derivatives. This PM H(+)-ATPase generates the necessary H(+)-gradient (proton-motive force) for the uptake of K(+) and nutrients into cambial and expanding xylem cells.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Arend</LastName><ForeName>Matthias</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Fachgebeit Angewandte Holzbiologie, Technische Universität München, Munich, Germany. arend@holz.forst.tu-muenchen.de</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Weisenseel</LastName><ForeName>Manfred H</ForeName><Initials>MH</Initials></Author><Author ValidYN="Y"><LastName>Brummer</LastName><ForeName>Maria</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Osswald</LastName><ForeName>Wolfgang</ForeName><Initials>W</Initials></Author><Author ValidYN="Y"><LastName>Fromm</LastName><ForeName>Jörg H</ForeName><Initials>JH</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType 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UI="D011188">Potassium</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000040" MajorTopicYN="N">Abscisic Acid</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001692" MajorTopicYN="N">Biological Transport</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015153" MajorTopicYN="N">Blotting, Western</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002462" MajorTopicYN="N">Cell Membrane</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007210" MajorTopicYN="N">Indoleacetic Acids</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017136" MajorTopicYN="N">Ion Transport</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018519" MajorTopicYN="N">Meristem</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008854" MajorTopicYN="N">Microscopy, Electron</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008856" MajorTopicYN="N">Microscopy, Fluorescence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018547" MajorTopicYN="N">Plant Stems</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011188" MajorTopicYN="N">Potassium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006180" MajorTopicYN="N">Proton-Translocating ATPases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D031308" MajorTopicYN="N">Salicaceae</DescriptorName><QualifierName UI="Q000254" MajorTopicYN="Y">growth & development</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000648" MajorTopicYN="N">ultrastructure</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012621" MajorTopicYN="N">Seasons</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2002</Year><Month>8</Month><Day>15</Day><Hour>10</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2002</Year><Month>12</Month><Day>4</Day><Hour>4</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2002</Year><Month>8</Month><Day>15</Day><Hour>10</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">12177478</ArticleId><ArticleId IdType="doi">10.1104/pp.003905</ArticleId><ArticleId IdType="pmc">PMC166753</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Annu Rev Plant Physiol Plant Mol Biol. 2001 Jun;52:817-845</Citation><ArticleIdList><ArticleId IdType="pubmed">11337417</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1996 Aug;111(4):1199-1207</Citation><ArticleIdList><ArticleId IdType="pubmed">12226357</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 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Jorg H" uniqKey="Fromm J" first="Jörg H" last="Fromm">Jörg H. Fromm</name><name sortKey="Osswald, Wolfgang" sort="Osswald, Wolfgang" uniqKey="Osswald W" first="Wolfgang" last="Osswald">Wolfgang Osswald</name><name sortKey="Weisenseel, Manfred H" sort="Weisenseel, Manfred H" uniqKey="Weisenseel M" first="Manfred H" last="Weisenseel">Manfred H. Weisenseel</name></noCountry><country name="Allemagne"><region name="Bavière"><name sortKey="Arend, Matthias" sort="Arend, Matthias" uniqKey="Arend M" first="Matthias" last="Arend">Matthias Arend</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:12177478" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a PoplarV1
| This area was generated with Dilib version V0.6.37. |  |