Using an adherent cell culture of the mouse subependymal zone to study the behavior of adult neural stem cells on a single-cell level

dc.contributor.authorOrtega, Felipe
dc.contributor.authorCosta, Marcos Romualdo
dc.contributor.authorSimon-Ebert, Tatiana
dc.contributor.authorSchroeder, Timm
dc.contributor.authorGötz, Magdalena
dc.date.accessioned2017-05-26T18:25:46Z
dc.date.available2017-05-26T18:25:46Z
dc.date.issued2011-11-03
dc.description.resumoA comprehensive understanding of the cell biology of adult neural stem cells (aNSCNSCNSCs) requires direct observation of aNSCNSCNSC division and lineage progression in the absence of niche-dependent signals. Here we describe a culture preparation of the adult mouse subependymal zone (SESEZ), which allows for continuous single-cell tracking of aNSCNSCNSC behavior. The protocol involves the isolation (~3 h) and culture of cells from the adult SESEZ at low density in the absence of mitogenic growth factors in chemically defined medium and subsequent live imaging using time-lapse video microscopy (5–7 d); these steps are followed by postimaging immunocytochemistry to identify progeny (~7 h). This protocol enables the observation of the progression from slow-dividing aNSCNSCNSCs of radial/astroglial identity up to the neuroblast stage, involving asymmetric and symmetric cell divisions of distinct fast-dividing precursors. This culture provides an experimental system for studying instructive or permissive effects of signal molecules on aNSCNSCNSC modes of cell division and lineage progression.pt_BR
dc.identifier.issn1754-2189
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/123456789/23135
dc.languageengpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectadult neural stem cellspt_BR
dc.subjectsingle-cell levelpt_BR
dc.subjectcell culturept_BR
dc.subjectmousept_BR
dc.titleUsing an adherent cell culture of the mouse subependymal zone to study the behavior of adult neural stem cells on a single-cell levelpt_BR
dc.typearticlept_BR

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