Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/7485
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSchmidt, C.en
dc.contributor.authorOhlemeyer, C.en
dc.contributor.authorLabrakakis, C.en
dc.contributor.authorWalter, T.en
dc.contributor.authorKettenmann, H.en
dc.contributor.authorSchnitzer, J.en
dc.date.accessioned2015-11-24T16:31:49Z-
dc.date.available2015-11-24T16:31:49Z-
dc.identifier.issn0894-1491-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/7485-
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectAnimals, Newbornen
dc.subjectBrain/*cytologyen
dc.subjectCell Movement/*physiologyen
dc.subjectCells, Cultureden
dc.subjectCerebellum/cytologyen
dc.subjectElectrophysiologyen
dc.subjectImmunohistochemistryen
dc.subjectLaminin/pharmacologyen
dc.subjectMembrane Potentialsen
dc.subjectOligodendroglia/*physiologyen
dc.subjectPatch-Clamp Techniquesen
dc.subjectRatsen
dc.subjectRen
dc.titleAnalysis of motile oligodendrocyte precursor cells in vitro and in brain slicesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/9262233-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/(SICI)1098-1136(199708)20:4<284::AID-GLIA2>3.0.CO;2-6/asset/2_ftp.pdf?v=1&t=hh1pvw2j&s=bf0629fde1a08611b8cdc88a24f711568128b287-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών και Τεχνολογιών. Τμήμα Βιολογικών Εφαρμογών και Τεχνολογιώνel
heal.publicationDate1997-
heal.abstractOligodendrocyte precursor cells are purported to migrate over long distances into the various brain regions where they differentiate into oligodendrocytes and fulfill their appropriate tasks, i.e., myelination of axons. Here we characterize motile oligodendrocyte precursor cells in detail. Video-time lapse analysis was performed on isolated precursor cells in single cell cultures, in co-culture with cerebellar microexplants, and in living brain slices. Motility analysis of individual cells was combined with electrophysiological, immunological, and morphological characterizations. Translocation of the cell bodies was not continuous but occurred in waves. All motile cells exhibited a simple morphology and most, but not all, of them expressed the A2B5 epitope in vitro. Patch clamp analysis of the motile cells confirmed that they belong to the O-2A lineage. The percentage of motile cells, as well as their velocities, were enhanced on substrate-coated laminin in comparison to poly-L-lysine. Motility was not influenced by the presence of cerebellar microexplants. O-2A progenitor cells did not migrate strictly along neurite fascicles which were projected from the microexplants. Glial progenitor cells in situ also did not strictly migrate along the main direction of the axonal fibers of the corpus callosum but rather traversed the fibers with an overall direction toward the cortex. After Lucifer Yellow filling of the motile progenitor cells in situ, we could demonstrate that they were dye-coupled to yet unidentified cells of the corpus callosum.en
heal.journalNameGliaen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

Files in This Item:
File Description SizeFormat 
Schmidt-1997-Analysis of motile o.pdf477.95 kBAdobe PDFView/Open    Request a copy


This item is licensed under a Creative Commons License Creative Commons