| Literature DB >> 28350803 |
Kasum Azim1,2,3, Diane Angonin4, Guillaume Marcy4, Francesca Pieropan5, Andrea Rivera5, Vanessa Donega4, Claudio Cantù6, Gareth Williams7, Benedikt Berninger2,3, Arthur M Butt5, Olivier Raineteau1,4.
Abstract
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.Entities:
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Year: 2017 PMID: 28350803 PMCID: PMC5370089 DOI: 10.1371/journal.pbio.2000698
Source DB: PubMed Journal: PLoS Biol ISSN: 1544-9173 Impact factor: 8.029