Continuous live imaging of adult neural stem cell division and lineage progression in vitro

Detalhes bibliográficos
Autor(a) principal: Costa, Marcos Romualdo
Data de Publicação: 2011
Outros Autores: Ortega, Felipe, Brill, Monika S., Beckervordersandforth, Ruth, Petrone, Ciro, Schroeder, Timm, Götz, Magdalena, Berninger, Benedikt
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23066
Resumo: Little is known about the intrinsic specification of adult neural stem cells (NSCs) and to what extent they depend on their local niche. To observe adult NSC division and lineage progression independent of their niche, we isolated cells from the adult mouse subependymal zone (SEZ) and cultured them at low density without growth factors. We demonstrate here that SEZ cells in this culture system are primarily neurogenic and that adult NSCs progress through stereotypic lineage trees consisting of asymmetric stem cell divisions, symmetric transit-amplifying divisions and final symmetric neurogenic divisions. Stem cells, identified by their astro/radial glial identity and their slow-dividing nature, were observed to generate asymmetrically and fast-dividing cells that maintained an astro/radial glia identity. These, in turn, gave rise to symmetrically and fast-dividing cells that lost glial hallmarks, but had not yet acquired neuronal features. The number of amplifying divisions was limited to a maximum of five in this system. Moreover, we found that cell growth correlated with the number of subsequent divisions of SEZ cells, with slow-dividing astro/radial glia exhibiting the most substantial growth prior to division. The fact that in the absence both of exogenously supplied growth factors and of signals provided by the local niche neurogenic lineage progression takes place in such stereotypic fashion, suggests that lineage progression is, to a significant degree, cell intrinsic or pre-programmed at the beginning of the lineage.
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spelling Costa, Marcos RomualdoOrtega, FelipeBrill, Monika S.Beckervordersandforth, RuthPetrone, CiroSchroeder, TimmGötz, MagdalenaBerninger, Benedikt2017-05-24T16:54:20Z2017-05-24T16:54:20Z20110950-1991https://repositorio.ufrn.br/jspui/handle/123456789/2306610.1242/dev.061663engAsymmetric cell divisionAstrogliaNeurogenesisRadial gliaSubependymal zoneTime-lapse video microscopyMouseContinuous live imaging of adult neural stem cell division and lineage progression in vitroinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleLittle is known about the intrinsic specification of adult neural stem cells (NSCs) and to what extent they depend on their local niche. To observe adult NSC division and lineage progression independent of their niche, we isolated cells from the adult mouse subependymal zone (SEZ) and cultured them at low density without growth factors. We demonstrate here that SEZ cells in this culture system are primarily neurogenic and that adult NSCs progress through stereotypic lineage trees consisting of asymmetric stem cell divisions, symmetric transit-amplifying divisions and final symmetric neurogenic divisions. Stem cells, identified by their astro/radial glial identity and their slow-dividing nature, were observed to generate asymmetrically and fast-dividing cells that maintained an astro/radial glia identity. These, in turn, gave rise to symmetrically and fast-dividing cells that lost glial hallmarks, but had not yet acquired neuronal features. The number of amplifying divisions was limited to a maximum of five in this system. Moreover, we found that cell growth correlated with the number of subsequent divisions of SEZ cells, with slow-dividing astro/radial glia exhibiting the most substantial growth prior to division. 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dc.title.pt_BR.fl_str_mv Continuous live imaging of adult neural stem cell division and lineage progression in vitro
title Continuous live imaging of adult neural stem cell division and lineage progression in vitro
spellingShingle Continuous live imaging of adult neural stem cell division and lineage progression in vitro
Costa, Marcos Romualdo
Asymmetric cell division
Astroglia
Neurogenesis
Radial glia
Subependymal zone
Time-lapse video microscopy
Mouse
title_short Continuous live imaging of adult neural stem cell division and lineage progression in vitro
title_full Continuous live imaging of adult neural stem cell division and lineage progression in vitro
title_fullStr Continuous live imaging of adult neural stem cell division and lineage progression in vitro
title_full_unstemmed Continuous live imaging of adult neural stem cell division and lineage progression in vitro
title_sort Continuous live imaging of adult neural stem cell division and lineage progression in vitro
author Costa, Marcos Romualdo
author_facet Costa, Marcos Romualdo
Ortega, Felipe
Brill, Monika S.
Beckervordersandforth, Ruth
Petrone, Ciro
Schroeder, Timm
Götz, Magdalena
Berninger, Benedikt
author_role author
author2 Ortega, Felipe
Brill, Monika S.
Beckervordersandforth, Ruth
Petrone, Ciro
Schroeder, Timm
Götz, Magdalena
Berninger, Benedikt
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Costa, Marcos Romualdo
Ortega, Felipe
Brill, Monika S.
Beckervordersandforth, Ruth
Petrone, Ciro
Schroeder, Timm
Götz, Magdalena
Berninger, Benedikt
dc.subject.por.fl_str_mv Asymmetric cell division
Astroglia
Neurogenesis
Radial glia
Subependymal zone
Time-lapse video microscopy
Mouse
topic Asymmetric cell division
Astroglia
Neurogenesis
Radial glia
Subependymal zone
Time-lapse video microscopy
Mouse
description Little is known about the intrinsic specification of adult neural stem cells (NSCs) and to what extent they depend on their local niche. To observe adult NSC division and lineage progression independent of their niche, we isolated cells from the adult mouse subependymal zone (SEZ) and cultured them at low density without growth factors. We demonstrate here that SEZ cells in this culture system are primarily neurogenic and that adult NSCs progress through stereotypic lineage trees consisting of asymmetric stem cell divisions, symmetric transit-amplifying divisions and final symmetric neurogenic divisions. Stem cells, identified by their astro/radial glial identity and their slow-dividing nature, were observed to generate asymmetrically and fast-dividing cells that maintained an astro/radial glia identity. These, in turn, gave rise to symmetrically and fast-dividing cells that lost glial hallmarks, but had not yet acquired neuronal features. The number of amplifying divisions was limited to a maximum of five in this system. Moreover, we found that cell growth correlated with the number of subsequent divisions of SEZ cells, with slow-dividing astro/radial glia exhibiting the most substantial growth prior to division. The fact that in the absence both of exogenously supplied growth factors and of signals provided by the local niche neurogenic lineage progression takes place in such stereotypic fashion, suggests that lineage progression is, to a significant degree, cell intrinsic or pre-programmed at the beginning of the lineage.
publishDate 2011
dc.date.issued.fl_str_mv 2011
dc.date.accessioned.fl_str_mv 2017-05-24T16:54:20Z
dc.date.available.fl_str_mv 2017-05-24T16:54:20Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/23066
dc.identifier.issn.none.fl_str_mv 0950-1991
dc.identifier.doi.none.fl_str_mv 10.1242/dev.061663
identifier_str_mv 0950-1991
10.1242/dev.061663
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