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dc.contributor.authorUggerud, Ida Margrethe
dc.contributor.authorKråkenes, Torbjørn
dc.contributor.authorHirai, Hirokazu
dc.contributor.authorVedeler, Christian Alexander
dc.contributor.authorSchubert, Manja
dc.date.accessioned2023-08-16T12:23:50Z
dc.date.available2023-08-16T12:23:50Z
dc.date.created2023-03-30T14:25:48Z
dc.date.issued2023
dc.identifier.issn1473-4222
dc.identifier.urihttps://hdl.handle.net/11250/3084404
dc.description.abstractElucidation of the mechanisms involved in neurodegenerative diseases of the cerebellum has been hampered by the lack of robust single cell models to study Purkinje neurons and replicate at the same time in vivo features. Cerebellar Purkinje neurons are difficult to grow in dispersed cell culture, and only limited work has been done using rat cells. We developed a refined protocol for growing rat Purkinje neurons from embryonic and postnatal tissue ex vivo that results in well-developed, mature, functional, and synaptically active neurons. The rat Purkinje neurons generated are responsive to paracrine factors and genetic manipulation, allowing great experimental flexibility at the single-cell level. This ex vivo model can be used to investigate disease mechanisms that disturb Purkinje neuron morphology, function, and communication in high- and low-throughput screening formats.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleDevelopment and Optimization of a Multilayer Rat Purkinje Neuron Cultureen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1007/s12311-022-01510-4
dc.identifier.cristin2138555
dc.source.journalCerebellumen_US
dc.identifier.citationCerebellum. 2023.en_US


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