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Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity

Strategies for promoting neural regeneration are hindered by the difficulty of manipulating desired neural fates in the brain without complex genetic methods. The subventricular zone (SVZ) is the largest germinal zone of the forebrain and is responsible for the lifelong generation of interneuron sub...

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Autores principales: Azim, Kasum, Angonin, Diane, Marcy, Guillaume, Pieropan, Francesca, Rivera, Andrea, Donega, Vanessa, Cantù, Claudio, Williams, Gareth, Berninger, Benedikt, Butt, Arthur M., Raineteau, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370089/
https://www.ncbi.nlm.nih.gov/pubmed/28350803
http://dx.doi.org/10.1371/journal.pbio.2000698
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author Azim, Kasum
Angonin, Diane
Marcy, Guillaume
Pieropan, Francesca
Rivera, Andrea
Donega, Vanessa
Cantù, Claudio
Williams, Gareth
Berninger, Benedikt
Butt, Arthur M.
Raineteau, Olivier
author_facet Azim, Kasum
Angonin, Diane
Marcy, Guillaume
Pieropan, Francesca
Rivera, Andrea
Donega, Vanessa
Cantù, Claudio
Williams, Gareth
Berninger, Benedikt
Butt, Arthur M.
Raineteau, Olivier
author_sort Azim, Kasum
collection PubMed
description Strategies for promoting neural regeneration are hindered by the difficulty of manipulating desired neural fates in the brain without complex genetic methods. The subventricular zone (SVZ) is the largest germinal zone of the forebrain and is responsible for the lifelong generation of interneuron subtypes and oligodendrocytes. Here, we have performed a bioinformatics analysis of the transcriptome of dorsal and lateral SVZ in early postnatal mice, including neural stem cells (NSCs) and their immediate progenies, which generate distinct neural lineages. We identified multiple signaling pathways that trigger distinct downstream transcriptional networks to regulate the diversity of neural cells originating from the SVZ. Next, we used a novel in silico genomic analysis, searchable platform-independent expression database/connectivity map (SPIED/CMAP), to generate a catalogue of small molecules that can be used to manipulate SVZ microdomain-specific lineages. Finally, we demonstrate that compounds identified in this analysis promote the generation of specific cell lineages from NSCs in vivo, during postnatal life and adulthood, as well as in regenerative contexts. This study unravels new strategies for using small bioactive molecules to direct germinal activity in the SVZ, which has therapeutic potential in neurodegenerative diseases.
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spelling pubmed-53700892017-04-06 Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity Azim, Kasum Angonin, Diane Marcy, Guillaume Pieropan, Francesca Rivera, Andrea Donega, Vanessa Cantù, Claudio Williams, Gareth Berninger, Benedikt Butt, Arthur M. Raineteau, Olivier PLoS Biol Research Article Strategies for promoting neural regeneration are hindered by the difficulty of manipulating desired neural fates in the brain without complex genetic methods. The subventricular zone (SVZ) is the largest germinal zone of the forebrain and is responsible for the lifelong generation of interneuron subtypes and oligodendrocytes. Here, we have performed a bioinformatics analysis of the transcriptome of dorsal and lateral SVZ in early postnatal mice, including neural stem cells (NSCs) and their immediate progenies, which generate distinct neural lineages. We identified multiple signaling pathways that trigger distinct downstream transcriptional networks to regulate the diversity of neural cells originating from the SVZ. Next, we used a novel in silico genomic analysis, searchable platform-independent expression database/connectivity map (SPIED/CMAP), to generate a catalogue of small molecules that can be used to manipulate SVZ microdomain-specific lineages. Finally, we demonstrate that compounds identified in this analysis promote the generation of specific cell lineages from NSCs in vivo, during postnatal life and adulthood, as well as in regenerative contexts. This study unravels new strategies for using small bioactive molecules to direct germinal activity in the SVZ, which has therapeutic potential in neurodegenerative diseases. Public Library of Science 2017-03-28 /pmc/articles/PMC5370089/ /pubmed/28350803 http://dx.doi.org/10.1371/journal.pbio.2000698 Text en © 2017 Azim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Azim, Kasum
Angonin, Diane
Marcy, Guillaume
Pieropan, Francesca
Rivera, Andrea
Donega, Vanessa
Cantù, Claudio
Williams, Gareth
Berninger, Benedikt
Butt, Arthur M.
Raineteau, Olivier
Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title_full Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title_fullStr Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title_full_unstemmed Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title_short Pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
title_sort pharmacogenomic identification of small molecules for lineage specific manipulation of subventricular zone germinal activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370089/
https://www.ncbi.nlm.nih.gov/pubmed/28350803
http://dx.doi.org/10.1371/journal.pbio.2000698
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