Tsan Yao-Chang, Morell Maria H, O'Shea K Sue
Department of Cell and Developmental Biology, School of Medicine, University of Michigan, Ann Arbor, MI 48109, United States.
Department of Cell and Developmental Biology, School of Medicine, University of Michigan, Ann Arbor, MI 48109, United States.
Stem Cell Res. 2016 Sep;17(2):238-247. doi: 10.1016/j.scr.2016.07.003. Epub 2016 Jul 17.
Over-expression of the early neural inducer, Noggin, in nestin positive subventricular zone (SVZ), neural stem cells (NSC) promotes proliferation and neuronal differentiation of neural progenitors and inhibits the expression of a CNS-enriched microRNA-410 (miR-410) (Morell et al., 2015). When expressed in neurospheres derived from the adult SVZ, miR-410 inhibits neuronal and oligodendrocyte differentiation, and promotes astrocyte differentiation. miR-410 also reverses the increase in neuronal differentiation and decreased astroglial differentiation caused by Noggin over-expression. Conversely, inhibition of miR-410 activity promotes neuronal and decreases astroglial differentiation of NSC. Using computer prediction algorithms and luciferase reporter assays we identified multiple neurogenic genes including Elavl4 as downstream targets of miR-410 via the canonical miRNA-3'UTR interaction. Over-expression of Elavl4 transcripts without the endogenous 3'UTR rescued the decrease in neuronal differentiation caused by miR-410 overexpression. Interestingly, we also observed that miR-410 affected neurite morphology; over-expression of miR-410 resulted in the formation of short, unbranched neurites. We conclude that miR-410 expression provides a new link between BMP signaling and the crucial lineage choice of adult neural stem cells via its ability to bind and control the expression of neurogenic gene transcripts.
早期神经诱导因子Noggin在巢蛋白阳性的脑室下区(SVZ)神经干细胞(NSC)中的过表达,可促进神经祖细胞的增殖和神经元分化,并抑制中枢神经系统富集的微小RNA-410(miR-410)的表达(莫雷尔等人,2015年)。当在源自成年SVZ的神经球中表达时,miR-410会抑制神经元和少突胶质细胞的分化,并促进星形胶质细胞的分化。miR-410还可逆转由Noggin过表达引起的神经元分化增加和星形胶质细胞分化减少的现象。相反,抑制miR-410的活性可促进NSC的神经元分化并减少星形胶质细胞的分化。通过计算机预测算法和荧光素酶报告基因检测,我们确定了多个神经源性基因,包括Elavl4,它们是miR-410通过典型的miRNA-3'UTR相互作用的下游靶点。不含内源性3'UTR的Elavl4转录本的过表达挽救了由miR-410过表达引起的神经元分化减少。有趣的是,我们还观察到miR-410影响神经突形态;miR-410的过表达导致形成短的、无分支的神经突。我们得出结论,miR-410的表达通过其结合和控制神经源性基因转录本表达的能力,在骨形态发生蛋白(BMP)信号传导与成年神经干细胞关键的谱系选择之间提供了新的联系。