Editorial: progenitor diversity and neural cell specification in the central nervous system
Autor(a) principal: | |
---|---|
Data de Publicação: | 2015 |
Outros Autores: | , |
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. |
id |
UFRN_cdd7f01479fb3ff8572af7a0215d33ef |
---|---|
oai_identifier_str |
oai:https://repositorio.ufrn.br:123456789/23124 |
network_acronym_str |
UFRN |
network_name_str |
Repositório Institucional da UFRN |
repository_id_str |
|
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 |
format |
article |
status_str |
publishedVersion |
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 |
url |
https://repositorio.ufrn.br/jspui/handle/123456789/23124 |
identifier_str_mv |
10.3389/fncel.2015.00358 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRN instname:Universidade Federal do Rio Grande do Norte (UFRN) instacron:UFRN |
instname_str |
Universidade Federal do Rio Grande do Norte (UFRN) |
instacron_str |
UFRN |
institution |
UFRN |
reponame_str |
Repositório Institucional da UFRN |
collection |
Repositório Institucional da UFRN |
bitstream.url.fl_str_mv |
https://repositorio.ufrn.br/bitstream/123456789/23124/1/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf https://repositorio.ufrn.br/bitstream/123456789/23124/2/license.txt https://repositorio.ufrn.br/bitstream/123456789/23124/5/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf.txt https://repositorio.ufrn.br/bitstream/123456789/23124/6/Editorial_Progenitor%20diversity%20and%20neural%20cell%20specification%20in%20the%20central%20nervous%20system.pdf.jpg |
bitstream.checksum.fl_str_mv |
2a6e57eb37d7f4896461b4dd27634cae 8a4605be74aa9ea9d79846c1fba20a33 48a7d70037e97986b7ec18a901341946 c6f4be8bb671da0986780a4a4ab7ecdc |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN) |
repository.mail.fl_str_mv |
|
_version_ |
1814833043358089216 |