| Literature DB >> 27315491 |
Xian Shuang Liu1, Bao Yan Fan1, Wan Long Pan1,2, Chao Li1, Albert M Levin3,4, Xinli Wang1, Rui Lan Zhang1, Thomas M Zervos1, Jiani Hu5, Xiao Ming Zhang6, Michael Chopp1,7, Zheng Gang Zhang1.
Abstract
Neurogenesis is associated with functional recovery after stroke. However, the underlying molecular mechanisms have not been fully investigated. Using an Ago2-based RNA immunoprecipitation to immunoprecipated Ago2-RNA complexes followed by RNA sequencing (Ago2 RIP-seq) approach, we profiled the miRNomes in neural progenitor cells (NPCs) harvested from the subventricular zone (SVZ) of the lateral ventricles of young adult rats. We identified more than 7 and 15 million reads in normal and ischemic NPC libraries, respectively. We found that stroke substantially changed Ago2-associated miRNA profiles in NPCs compared to those in non-ischemic NPCs. We also discovered a new complex repertoire of isomiRs and multiple miRNA-miRNA* pairs and numerous novel miRNAs in the non-ischemic and ischemic NPCs. Among them, pc-3p-17172 significantly regulated NPC proliferation and neuronal differentiation. Collectively, the present study reveals profiles of Ago2-associated miRNomes in non-ischemic and ischemic NPCs, which provide a molecular basis to further investigate the role of miRNAs in mediating adult neurogenesis under physiological and ischemic conditions.Entities:
Keywords: Ago2; RNA sequencing; microRNA; neural progenitor cells; neurogenesis; stroke
Mesh:
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Year: 2016 PMID: 27315491 PMCID: PMC5449080 DOI: 10.1080/15476286.2016.1196320
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652