Publikation:

One-way calcium spill-over during signal transduction in Parameciumcells : from the cell cortex into cilia, but not in the reverse direction

Lade...
Vorschaubild

Dateien

One_way_calcium.pdf
One_way_calcium.pdfGröße: 185.53 KBDownloads: 333

Datum

2004

Autor:innen

Husser, Marc R.
Hardt, Martin
Blanchard, Marie-Pierre
Klauke, Norbert

Herausgeber:innen

Kontakt

ISSN der Zeitschrift

Electronic ISSN

ISBN

Bibliografische Daten

Verlag

Schriftenreihe

Auflagebezeichnung

ArXiv-ID

Internationale Patentnummer

Angaben zur Forschungsförderung

Projekt

Open Access-Veröffentlichung
Open Access Green
Core Facility der Universität Konstanz

Gesperrt bis

Titel in einer weiteren Sprache

Publikationstyp
Zeitschriftenartikel
Publikationsstatus
Published

Erschienen in

Cell Calcium. 2004, 36(5), pp. 349-358. ISSN 0143-4160. Available under: doi: 10.1016/j.ceca.2004.02.003

Zusammenfassung

We asked to what extent Ca2+ signals in two different domains of Paramecium cells remain separated during different stimulations. Wild-type (7S) and pawn cells (strain d4-500r, without ciliary voltage-dependent Ca2+-channels) were stimulated for trichocyst exocytosis within 80 ms by quenched-flow preparation and analysed by energy-dispersive X-ray microanalysis (EDX), paralleled by fast confocal fluorochrome analysis. We also analysed depolarisation-dependent calcium signalling during ciliary beat rerversal, also by EDX, after 80-ms stimulation in the quenched-flow mode. EDX and fluorochrome analysis enable to register total and free intracellular calcium concentrations, [Ca] and [Ca2+], respectively. After exocytosis stimulation we find by both methods that the calcium signal sweeps into the basis of cilia, not only in 7S but also in pawn cells which then also perform ciliary reversal. After depolarisation we see an increase of [Ca] along cilia selectively in 7S, but not in pawn cells. Opposite to exocytosis stimulation, during depolarisation no calcium spill-over into the nearby cytosol and no exocytosis occurs. In sum, we conclude that cilia must contain a very potent Ca2+ buffering system and that ciliary reversal induction, much more than exocytosis stimulation, involves strict microdomain regulation of Ca2+ signals.

Zusammenfassung in einer weiteren Sprache

Fachgebiet (DDC)
570 Biowissenschaften, Biologie

Schlagwörter

Ca2+, Calcium, Cilia, EDX, Paramecium, X-ray microanalysis

Konferenz

Rezension
undefined / . - undefined, undefined

Forschungsvorhaben

Organisationseinheiten

Zeitschriftenheft

Zugehörige Datensätze in KOPS

Zitieren

ISO 690HUSSER, Marc R., Martin HARDT, Marie-Pierre BLANCHARD, Joachim HENTSCHEL, Norbert KLAUKE, Helmut PLATTNER, 2004. One-way calcium spill-over during signal transduction in Parameciumcells : from the cell cortex into cilia, but not in the reverse direction. In: Cell Calcium. 2004, 36(5), pp. 349-358. ISSN 0143-4160. Available under: doi: 10.1016/j.ceca.2004.02.003
BibTex
@article{Husser2004Onewa-7701,
  year={2004},
  doi={10.1016/j.ceca.2004.02.003},
  title={One-way calcium spill-over during signal transduction in Parameciumcells : from the cell cortex into cilia, but not in the reverse direction},
  number={5},
  volume={36},
  issn={0143-4160},
  journal={Cell Calcium},
  pages={349--358},
  author={Husser, Marc R. and Hardt, Martin and Blanchard, Marie-Pierre and Hentschel, Joachim and Klauke, Norbert and Plattner, Helmut}
}
RDF
<rdf:RDF
    xmlns:dcterms="http://purl.org/dc/terms/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
    xmlns:bibo="http://purl.org/ontology/bibo/"
    xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
    xmlns:foaf="http://xmlns.com/foaf/0.1/"
    xmlns:void="http://rdfs.org/ns/void#"
    xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > 
  <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/7701">
    <dc:creator>Hardt, Martin</dc:creator>
    <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/7701/1/One_way_calcium.pdf"/>
    <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/7701/1/One_way_calcium.pdf"/>
    <dcterms:title>One-way calcium spill-over during signal transduction in Parameciumcells : from the cell cortex into cilia, but not in the reverse direction</dcterms:title>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:36:29Z</dc:date>
    <dc:contributor>Husser, Marc R.</dc:contributor>
    <dc:creator>Klauke, Norbert</dc:creator>
    <dcterms:rights rdf:resource="http://creativecommons.org/licenses/by-nc-nd/2.0/"/>
    <dcterms:abstract xml:lang="eng">We asked to what extent Ca2+ signals in two different domains of Paramecium cells remain separated during different stimulations. Wild-type (7S) and pawn cells (strain d4-500r, without ciliary voltage-dependent Ca2+-channels) were stimulated for trichocyst exocytosis within 80 ms by quenched-flow preparation and analysed by energy-dispersive X-ray microanalysis (EDX), paralleled by fast confocal fluorochrome analysis. We also analysed depolarisation-dependent calcium signalling during ciliary beat rerversal, also by EDX, after 80-ms stimulation in the quenched-flow mode. EDX and fluorochrome analysis enable to register total and free intracellular calcium concentrations, [Ca] and [Ca2+], respectively. After exocytosis stimulation we find by both methods that the calcium signal sweeps into the basis of cilia, not only in 7S but also in pawn cells which then also perform ciliary reversal. After depolarisation we see an increase of [Ca] along cilia selectively in 7S, but not in pawn cells. Opposite to exocytosis stimulation, during depolarisation no calcium spill-over into the nearby cytosol and no exocytosis occurs. In sum, we conclude that cilia must contain a very potent Ca2+ buffering system and that ciliary reversal induction, much more than exocytosis stimulation, involves strict microdomain regulation of Ca2+ signals.</dcterms:abstract>
    <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/7701"/>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-24T17:36:29Z</dcterms:available>
    <dc:creator>Husser, Marc R.</dc:creator>
    <dc:contributor>Hardt, Martin</dc:contributor>
    <dcterms:issued>2004</dcterms:issued>
    <dc:language>eng</dc:language>
    <dc:format>application/pdf</dc:format>
    <dc:creator>Plattner, Helmut</dc:creator>
    <dc:contributor>Blanchard, Marie-Pierre</dc:contributor>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dc:creator>Hentschel, Joachim</dc:creator>
    <dc:contributor>Plattner, Helmut</dc:contributor>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/28"/>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dc:contributor>Klauke, Norbert</dc:contributor>
    <dc:rights>Attribution-NonCommercial-NoDerivs 2.0 Generic</dc:rights>
    <dc:creator>Blanchard, Marie-Pierre</dc:creator>
    <dcterms:bibliographicCitation>First publ. in: Cell Calcium 36 (2004), pp. 349-358</dcterms:bibliographicCitation>
    <dc:contributor>Hentschel, Joachim</dc:contributor>
  </rdf:Description>
</rdf:RDF>

Interner Vermerk

xmlui.Submission.submit.DescribeStep.inputForms.label.kops_note_fromSubmitter

Kontakt
URL der Originalveröffentl.

Prüfdatum der URL

Prüfungsdatum der Dissertation

Finanzierungsart

Kommentar zur Publikation

Allianzlizenz
Corresponding Authors der Uni Konstanz vorhanden
Internationale Co-Autor:innen
Universitätsbibliographie
Ja
Begutachtet
Diese Publikation teilen