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Transient CREB-mediated transcription is key in direct neuronal reprogramming

Combinations of neuronal determinants and/or small-molecules such as Forskolin (Fk) can be used to convert different cell types into neurons. As Fk is known to activate cAMP-dependent pathways including CREB-activity, we aimed here to determine the role of CREB in reprogramming – including its tempo...

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Detalles Bibliográficos
Autores principales: Gascón, Sergio, Ortega, Felipe, Götz, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345748/
https://www.ncbi.nlm.nih.gov/pubmed/28321434
http://dx.doi.org/10.1080/23262133.2017.1285383
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author Gascón, Sergio
Ortega, Felipe
Götz, Magdalena
author_facet Gascón, Sergio
Ortega, Felipe
Götz, Magdalena
author_sort Gascón, Sergio
collection PubMed
description Combinations of neuronal determinants and/or small-molecules such as Forskolin (Fk) can be used to convert different cell types into neurons. As Fk is known to activate cAMP-dependent pathways including CREB-activity, we aimed here to determine the role of CREB in reprogramming – including its temporal profile. We show that transient expression of the dominant-positive CREB-VP16 followed by its inactivation mediated by the dominant-negative ICER improves neuronal conversion of astrocytes mediated by the neurogenic determinant Ascl1. Contrarily, persistent over-activation by CREB-VP16 or persistent inhibition by ICER interferes with neuronal reprogramming, with the latter enhancing cell death. Taken together our work shows transient CREB activation as a key effector in neuronal reprogramming.
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spelling pubmed-53457482018-02-06 Transient CREB-mediated transcription is key in direct neuronal reprogramming Gascón, Sergio Ortega, Felipe Götz, Magdalena Neurogenesis (Austin) Brief Report Combinations of neuronal determinants and/or small-molecules such as Forskolin (Fk) can be used to convert different cell types into neurons. As Fk is known to activate cAMP-dependent pathways including CREB-activity, we aimed here to determine the role of CREB in reprogramming – including its temporal profile. We show that transient expression of the dominant-positive CREB-VP16 followed by its inactivation mediated by the dominant-negative ICER improves neuronal conversion of astrocytes mediated by the neurogenic determinant Ascl1. Contrarily, persistent over-activation by CREB-VP16 or persistent inhibition by ICER interferes with neuronal reprogramming, with the latter enhancing cell death. Taken together our work shows transient CREB activation as a key effector in neuronal reprogramming. Taylor & Francis 2017-02-06 /pmc/articles/PMC5345748/ /pubmed/28321434 http://dx.doi.org/10.1080/23262133.2017.1285383 Text en © 2017 The Author(s). Published with license by Taylor & Francis. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Brief Report
Gascón, Sergio
Ortega, Felipe
Götz, Magdalena
Transient CREB-mediated transcription is key in direct neuronal reprogramming
title Transient CREB-mediated transcription is key in direct neuronal reprogramming
title_full Transient CREB-mediated transcription is key in direct neuronal reprogramming
title_fullStr Transient CREB-mediated transcription is key in direct neuronal reprogramming
title_full_unstemmed Transient CREB-mediated transcription is key in direct neuronal reprogramming
title_short Transient CREB-mediated transcription is key in direct neuronal reprogramming
title_sort transient creb-mediated transcription is key in direct neuronal reprogramming
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345748/
https://www.ncbi.nlm.nih.gov/pubmed/28321434
http://dx.doi.org/10.1080/23262133.2017.1285383
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