Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes

Detalhes bibliográficos
Autor(a) principal: Chouchane, Malek
Data de Publicação: 2017
Outros Autores: Faria, Ana Raquel Melo de, Moura, Daniela Maria de Souza, Hilscher, Markus Michael, Schroder, Timm, Leão, Richardson Naves, Costa, Marcos Romualdo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23434
Resumo: Astroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in vivo. In this study we addressed these questions using two different astroglial populations isolated from the postnatal brain reprogrammed either with Neurogenin-2 (Neurog2) or Achaete scute homolog-1 (Ascl1). We show that cerebellum (CerebAstro) and cerebral cortex astroglia (CtxAstro) generates iNs with distinctive neurochemical and morphological properties. Both astroglial populations contribute iNs to the olfactory bulb following transplantation in the postnatal and adult mouse subventricular zone. However, only CtxAstro transfected with Neurog2 differentiate into pyramidal-like iNs after transplantation in the postnatal cerebral cortex. Altogether, our data indicate that the origin of the astroglial population and transcription factors used for reprogramming, as well as the region of integration, affect the fate of iNs.
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spelling Chouchane, MalekFaria, Ana Raquel Melo deMoura, Daniela Maria de SouzaHilscher, Markus MichaelSchroder, TimmLeão, Richardson NavesCosta, Marcos Romualdo2017-06-08T16:24:43Z2017-06-08T16:24:43Z2017-072213-6711https://repositorio.ufrn.br/jspui/handle/123456789/23434engAn error occurred getting the license - uri.info:eu-repo/semantics/openAccessLineage reprogrammingInduced neuronsProneural genesAstroglial cellsCerebral cortexCerebellumCell transplantationLineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleAstroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in vivo. In this study we addressed these questions using two different astroglial populations isolated from the postnatal brain reprogrammed either with Neurogenin-2 (Neurog2) or Achaete scute homolog-1 (Ascl1). We show that cerebellum (CerebAstro) and cerebral cortex astroglia (CtxAstro) generates iNs with distinctive neurochemical and morphological properties. Both astroglial populations contribute iNs to the olfactory bulb following transplantation in the postnatal and adult mouse subventricular zone. However, only CtxAstro transfected with Neurog2 differentiate into pyramidal-like iNs after transplantation in the postnatal cerebral cortex. 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dc.title.pt_BR.fl_str_mv Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
spellingShingle Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
Chouchane, Malek
Lineage reprogramming
Induced neurons
Proneural genes
Astroglial cells
Cerebral cortex
Cerebellum
Cell transplantation
title_short Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_full Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_fullStr Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_full_unstemmed Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
title_sort Lineage Reprogramming of Astroglial Cells from Different Origins into Distinct Neuronal Subtypes
author Chouchane, Malek
author_facet Chouchane, Malek
Faria, Ana Raquel Melo de
Moura, Daniela Maria de Souza
Hilscher, Markus Michael
Schroder, Timm
Leão, Richardson Naves
Costa, Marcos Romualdo
author_role author
author2 Faria, Ana Raquel Melo de
Moura, Daniela Maria de Souza
Hilscher, Markus Michael
Schroder, Timm
Leão, Richardson Naves
Costa, Marcos Romualdo
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Chouchane, Malek
Faria, Ana Raquel Melo de
Moura, Daniela Maria de Souza
Hilscher, Markus Michael
Schroder, Timm
Leão, Richardson Naves
Costa, Marcos Romualdo
dc.subject.por.fl_str_mv Lineage reprogramming
Induced neurons
Proneural genes
Astroglial cells
Cerebral cortex
Cerebellum
Cell transplantation
topic Lineage reprogramming
Induced neurons
Proneural genes
Astroglial cells
Cerebral cortex
Cerebellum
Cell transplantation
description Astroglial cells isolated from the rodent postnatal cerebral cortex are particularly susceptible to lineage reprogramming into neurons. However, it remains unknown whether other astroglial populations retain the same potential. Likewise, little is known about the fate of induced neurons (iNs) in vivo. In this study we addressed these questions using two different astroglial populations isolated from the postnatal brain reprogrammed either with Neurogenin-2 (Neurog2) or Achaete scute homolog-1 (Ascl1). We show that cerebellum (CerebAstro) and cerebral cortex astroglia (CtxAstro) generates iNs with distinctive neurochemical and morphological properties. Both astroglial populations contribute iNs to the olfactory bulb following transplantation in the postnatal and adult mouse subventricular zone. However, only CtxAstro transfected with Neurog2 differentiate into pyramidal-like iNs after transplantation in the postnatal cerebral cortex. Altogether, our data indicate that the origin of the astroglial population and transcription factors used for reprogramming, as well as the region of integration, affect the fate of iNs.
publishDate 2017
dc.date.accessioned.fl_str_mv 2017-06-08T16:24:43Z
dc.date.available.fl_str_mv 2017-06-08T16:24:43Z
dc.date.issued.fl_str_mv 2017-07
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.issn.none.fl_str_mv 2213-6711
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url https://repositorio.ufrn.br/jspui/handle/123456789/23434
dc.language.iso.fl_str_mv eng
language eng
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eu_rights_str_mv openAccess
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