Department of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China; Institute of Neurosciences, Department of Neurobiology, Collaborative Innovation Center for Brain Science, School of Basic Medicine, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Department of Medical Genetics and Developmental Biology, Fourth Military Medical University, Chang-Le Xi Street #17, Xi'an 710032, China.
Stem Cell Reports. 2017 Apr 11;8(4):1032-1045. doi: 10.1016/j.stemcr.2017.02.017. Epub 2017 Mar 23.
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.
Notch 信号通路在神经发育中起着至关重要的作用,但下游效应器仍不完全清楚。在这项研究中,我们从 Nestin-Cre 介导的条件性 Rbp-j 敲除(Rbp-j cKO)和对照胚胎中培养神经球,并使用微阵列比较它们的 miRNA 表达谱。在差异表达的 miRNA 中,miR-342-5p 的表达上调,表明 Notch 信号通路被遗传或药物阻断。一致地,miR-342-5p 宿主基因 Ena-vasodilator stimulated phosphoprotein-like(Evl)的启动子受到 Notch 信号通路的负调控,可能通过 HES5。miR-342-5p 的转染促进了体外神经干细胞(NSCs)向中间神经祖细胞(INPs)的分化,并减少了体内 NSCs 的干性。此外,miR-342-5p 通过直接靶向 GFAP 抑制了神经干细胞/中间祖细胞向星形胶质细胞的分化。我们的结果表明,miR-342-5p 可以作为 Notch 信号通路的下游效应子,调节 NSCs 向 INPs 和星形胶质细胞分化的过程。