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

被引:44
作者
Azim, Kasum [1 ,2 ,3 ]
Angonin, Diane [4 ]
Marcy, Guillaume [4 ]
Pieropan, Francesca [5 ]
Rivera, Andrea [5 ]
Donega, Vanessa [4 ]
Cantu, Claudio [6 ]
Williams, Gareth [7 ]
Berninger, Benedikt [2 ,3 ]
Butt, Arthur M. [5 ]
Raineteau, Olivier [1 ,4 ]
机构
[1] Univ Zurich ETHZ, Brain Res Inst, Zurich, Switzerland
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Physiol Chem, Adult Neurogenesis & Cellular Reprogramming, Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Focus Program Translat Neurosci, Mainz, Germany
[4] Univ Claude Bernard Lyon 1, Univ Lyon, INSERM, Stem Cell & Brain Res Inst U1208, Bron, France
[5] Univ Portsmouth, Sch Pharm & Biomed Sci, Portsmouth, Hants, England
[6] Univ Zurich, IMLS, Zurich, Switzerland
[7] Kings Coll London, Wolfson Ctr Age Related Dis, Guys Campus, London, England
基金
英国生物技术与生命科学研究理事会; 瑞士国家科学基金会;
关键词
NEURAL STEM-CELLS; ADULT NEUROGENESIS; OLFACTORY-BULB; SONIC HEDGEHOG; IN-VIVO; EXPRESSION; OLIGODENDROCYTES; BRAIN; DIFFERENTIATION; NEURONS;
D O I
10.1371/journal.pbio.2000698
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
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页数:27
相关论文
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