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miR-342-5p Regulates Neural Stem Cell Proliferation and Differentiation Downstream to Notch Signaling in Mice

Notch signaling is critically involved in neural development, but the downstream effectors remain incompletely understood. In this study, we cultured neurospheres from Nestin-Cre-mediated conditional Rbp-j knockout (Rbp-j cKO) and control embryos and compared their miRNA expression profiles using mi...

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Detalles Bibliográficos
Autores principales: Gao, Fang, Zhang, Yu-Fei, Zhang, Zheng-Ping, Fu, Luo-An, Cao, Xiu-Li, Zhang, Yi-Zhe, Guo, Chen-Jun, Yan, Xian-Chun, Yang, Qin-Chuan, Hu, Yi-Yang, Zhao, Xiang-Hui, Wang, Ya-Zhou, Wu, Sheng-Xi, Ju, Gong, Zheng, Min-Hua, Han, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390133/
https://www.ncbi.nlm.nih.gov/pubmed/28344005
http://dx.doi.org/10.1016/j.stemcr.2017.02.017
Descripción
Sumario:Notch signaling is critically involved in neural development, but the downstream effectors remain incompletely understood. In this study, we cultured neurospheres from Nestin-Cre-mediated conditional Rbp-j knockout (Rbp-j cKO) and control embryos and compared their miRNA expression profiles using microarray. Among differentially expressed miRNAs, miR-342-5p showed upregulated expression as Notch signaling was genetically or pharmaceutically interrupted. Consistently, the promoter of the miR-342-5p host gene, the Ena-vasodilator stimulated phosphoprotein-like (Evl), was negatively regulated by Notch signaling, probably through HES5. Transfection of miR-342-5p promoted the differentiation of neural stem cells (NSCs) into intermediate neural progenitors (INPs) in vitro and reduced the stemness of NSCs in vivo. Furthermore, miR-342-5p inhibited the differentiation of neural stem/intermediate progenitor cells into astrocytes, likely mediated by targeting GFAP directly. Our results indicated that miR-342-5p could function as a downstream effector of Notch signaling to regulate the differentiation of NSCs into INPs and astrocytes commitment.