Editorial: progenitor diversity and neural cell specification in the central nervous system

Detalhes bibliográficos
Autor(a) principal: Rouaux, Caroline
Data de Publicação: 2015
Outros Autores: Hedin-Pereira, Cecília, Costa, Marcos Romualdo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/jspui/handle/123456789/23124
Resumo: The central nervous system (CNS) harbors an enormous diversity of neuronal and glial cell types, which can be identified according to morphological, chemical, and electrical properties. This variety of cell types is generated from progenitor cells located in different germinative niches, where distinct molecular signalings prompt distinctive transcription factors expression. In the last two decades, it has been acknowledged that such progenitor diversity is important for the generation of different subtypes of neurons, astrocytes and oligodendrocytes. Genetic fate-mapping studies have provided direct evidence for the contribution of separate cohorts of progenitor cells to generate individual subtypes of neurons and/or glial cells. Additionally, genetic deletions of single transcription factors and forced expression of ectopic transcription factor genes have pointed out the leading role of such molecules on the specification of different, individual cell types. However, other sources of data indicate that the environment plays important roles in cellular specification during CNS development, eventually overriding the influence of early transcription factors expression. These observations suggest that genetic determinants for both neuronal and glial specification would be changeable. However, the time-window during which neuronal and glial lineage genetic programs could be overwritten by external signals remains to be determined, along with exact signals that could perform such a fate modification. This research topic gathers a number of articles highlighting the role of a wide panel of intrinsic and extrinsic factors that contribute to the generation of such diversity.
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spelling Rouaux, CarolineHedin-Pereira, CecíliaCosta, Marcos Romualdo2017-05-26T16:33:10Z2017-05-26T16:33:10Z2015-09-09https://repositorio.ufrn.br/jspui/handle/123456789/2312410.3389/fncel.2015.00358engcentral nervous systemcellular diversityprogenitor cellsneuronsglial cellsfate specificationEditorial: progenitor diversity and neural cell specification in the central nervous systeminfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleThe central nervous system (CNS) harbors an enormous diversity of neuronal and glial cell types, which can be identified according to morphological, chemical, and electrical properties. This variety of cell types is generated from progenitor cells located in different germinative niches, where distinct molecular signalings prompt distinctive transcription factors expression. In the last two decades, it has been acknowledged that such progenitor diversity is important for the generation of different subtypes of neurons, astrocytes and oligodendrocytes. Genetic fate-mapping studies have provided direct evidence for the contribution of separate cohorts of progenitor cells to generate individual subtypes of neurons and/or glial cells. Additionally, genetic deletions of single transcription factors and forced expression of ectopic transcription factor genes have pointed out the leading role of such molecules on the specification of different, individual cell types. However, other sources of data indicate that the environment plays important roles in cellular specification during CNS development, eventually overriding the influence of early transcription factors expression. These observations suggest that genetic determinants for both neuronal and glial specification would be changeable. However, the time-window during which neuronal and glial lineage genetic programs could be overwritten by external signals remains to be determined, along with exact signals that could perform such a fate modification. This research topic gathers a number of articles highlighting the role of a wide panel of intrinsic and extrinsic factors that contribute to the generation of such diversity.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdfEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdfMarcosCosta_ICe_Progenitor diversity and neural cell specification_2015application/pdf186655https://repositorio.ufrn.br/bitstream/123456789/23124/1/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf2a6e57eb37d7f4896461b4dd27634caeMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.ufrn.br/bitstream/123456789/23124/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52TEXTEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdf.txtEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdf.txtExtracted texttext/plain11731https://repositorio.ufrn.br/bitstream/123456789/23124/5/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf.txt48a7d70037e97986b7ec18a901341946MD55THUMBNAILEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdf.jpgEditorial_Progenitor diversity and neural cell specification in the central nervous system.pdf.jpgIM Thumbnailimage/jpeg7783https://repositorio.ufrn.br/bitstream/123456789/23124/6/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf.jpgc6f4be8bb671da0986780a4a4ab7ecdcMD56123456789/231242021-07-09 17:40:01.172oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2021-07-09T20:40:01Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv Editorial: progenitor diversity and neural cell specification in the central nervous system
title Editorial: progenitor diversity and neural cell specification in the central nervous system
spellingShingle Editorial: progenitor diversity and neural cell specification in the central nervous system
Rouaux, Caroline
central nervous system
cellular diversity
progenitor cells
neurons
glial cells
fate specification
title_short Editorial: progenitor diversity and neural cell specification in the central nervous system
title_full Editorial: progenitor diversity and neural cell specification in the central nervous system
title_fullStr Editorial: progenitor diversity and neural cell specification in the central nervous system
title_full_unstemmed Editorial: progenitor diversity and neural cell specification in the central nervous system
title_sort Editorial: progenitor diversity and neural cell specification in the central nervous system
author Rouaux, Caroline
author_facet Rouaux, Caroline
Hedin-Pereira, Cecília
Costa, Marcos Romualdo
author_role author
author2 Hedin-Pereira, Cecília
Costa, Marcos Romualdo
author2_role author
author
dc.contributor.author.fl_str_mv Rouaux, Caroline
Hedin-Pereira, Cecília
Costa, Marcos Romualdo
dc.subject.por.fl_str_mv central nervous system
cellular diversity
progenitor cells
neurons
glial cells
fate specification
topic central nervous system
cellular diversity
progenitor cells
neurons
glial cells
fate specification
description The central nervous system (CNS) harbors an enormous diversity of neuronal and glial cell types, which can be identified according to morphological, chemical, and electrical properties. This variety of cell types is generated from progenitor cells located in different germinative niches, where distinct molecular signalings prompt distinctive transcription factors expression. In the last two decades, it has been acknowledged that such progenitor diversity is important for the generation of different subtypes of neurons, astrocytes and oligodendrocytes. Genetic fate-mapping studies have provided direct evidence for the contribution of separate cohorts of progenitor cells to generate individual subtypes of neurons and/or glial cells. Additionally, genetic deletions of single transcription factors and forced expression of ectopic transcription factor genes have pointed out the leading role of such molecules on the specification of different, individual cell types. However, other sources of data indicate that the environment plays important roles in cellular specification during CNS development, eventually overriding the influence of early transcription factors expression. These observations suggest that genetic determinants for both neuronal and glial specification would be changeable. However, the time-window during which neuronal and glial lineage genetic programs could be overwritten by external signals remains to be determined, along with exact signals that could perform such a fate modification. This research topic gathers a number of articles highlighting the role of a wide panel of intrinsic and extrinsic factors that contribute to the generation of such diversity.
publishDate 2015
dc.date.issued.fl_str_mv 2015-09-09
dc.date.accessioned.fl_str_mv 2017-05-26T16:33:10Z
dc.date.available.fl_str_mv 2017-05-26T16:33:10Z
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.uri.fl_str_mv https://repositorio.ufrn.br/jspui/handle/123456789/23124
dc.identifier.doi.none.fl_str_mv 10.3389/fncel.2015.00358
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identifier_str_mv 10.3389/fncel.2015.00358
dc.language.iso.fl_str_mv eng
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dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRN
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