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MicroRNAs 对于发育中的脊髓从神经发生到神经胶质发生的发育转换是必不可少的。

MicroRNAs are essential for the developmental switch from neurogenesis to gliogenesis in the developing spinal cord.

机构信息

College of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, Zhejiang 310036, China.

出版信息

J Neurosci. 2010 Jun 16;30(24):8245-50. doi: 10.1523/JNEUROSCI.1169-10.2010.

DOI:10.1523/JNEUROSCI.1169-10.2010
PMID:20554876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2918643/
Abstract

In the developing CNS, neurons and glia are sequentially produced from the ventricular neural progenitor cells. One fundamental question in developmental neurobiology is what signals or factors control the developmental switch from neurogenesis to gliogenesis. Here we report that microRNAs (miRNAs) play an essential role in this important developmental process. Inhibition of miRNA formation in Olig1(Cre)-mediated Dicer conditional knock-out mice disrupted both oligodendrogenesis and astrogliogenesis in the ventral neuroepithelial cells. By contrast, the early patterning and development of motor neurons were not affected in the mutant spinal cord tissue.

摘要

在中枢神经系统的发育过程中,神经元和神经胶质细胞是从脑室神经祖细胞中依次产生的。发育神经生物学的一个基本问题是,是什么信号或因素控制着从神经发生到神经胶质发生的发育转变。在这里,我们报告说 microRNAs(miRNAs)在这个重要的发育过程中起着至关重要的作用。在 Olig1(Cre)-介导的 Dicer 条件性敲除小鼠中抑制 miRNA 的形成,破坏了腹侧神经上皮细胞中的少突胶质细胞发生和星形胶质细胞发生。相比之下,突变脊髓组织中的运动神经元的早期模式形成和发育没有受到影响。

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MicroRNAs are essential for the developmental switch from neurogenesis to gliogenesis in the developing spinal cord.MicroRNAs 对于发育中的脊髓从神经发生到神经胶质发生的发育转换是必不可少的。
J Neurosci. 2010 Jun 16;30(24):8245-50. doi: 10.1523/JNEUROSCI.1169-10.2010.
2
Mir-17-3p controls spinal neural progenitor patterning by regulating Olig2/Irx3 cross-repressive loop.miR-17-3p 通过调控 Olig2/Irx3 交叉抑制环路控制脊髓神经祖细胞的模式形成。
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Development. 2007 Apr;134(8):1617-29. doi: 10.1242/dev.001255. Epub 2007 Mar 7.

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WNT signaling suppresses oligodendrogenesis via Ngn2-dependent direct inhibition of Olig2 expression.WNT 信号通过 Ngn2 依赖性直接抑制 Olig2 表达来抑制少突胶质细胞生成。
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The Therapeutic Potential of Mesenchymal Stem Cell-Derived Exosomes in Treatment of Neurodegenerative Diseases.间充质干细胞衍生的外泌体在治疗神经退行性疾病中的治疗潜力。
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本文引用的文献

1
MicroRNA-mediated control of oligodendrocyte differentiation.微小 RNA 介导的少突胶质细胞分化调控。
Neuron. 2010 Mar 11;65(5):612-26. doi: 10.1016/j.neuron.2010.02.018.
2
Dicer1 and miR-219 Are required for normal oligodendrocyte differentiation and myelination.Dicer1 和 miR-219 对于正常少突胶质细胞分化和髓鞘形成是必需的。
Neuron. 2010 Mar 11;65(5):597-611. doi: 10.1016/j.neuron.2010.01.027.
3
Origins and Mechanisms of miRNAs and siRNAs.微小RNA(miRNA)和小干扰RNA(siRNA)的起源与机制。
Cell. 2009 Feb 20;136(4):642-55. doi: 10.1016/j.cell.2009.01.035.
4
miRNAs are essential for survival and differentiation of newborn neurons but not for expansion of neural progenitors during early neurogenesis in the mouse embryonic neocortex.在小鼠胚胎新皮质的早期神经发生过程中,微小RNA(miRNA)对于新生神经元的存活和分化至关重要,但对于神经祖细胞的增殖并非必需。
Development. 2008 Dec;135(23):3911-21. doi: 10.1242/dev.025080.
5
Identification of dynamically regulated microRNA and mRNA networks in developing oligodendrocytes.发育中的少突胶质细胞中动态调控的微小RNA和信使核糖核酸网络的鉴定
J Neurosci. 2008 Nov 5;28(45):11720-30. doi: 10.1523/JNEUROSCI.1932-08.2008.
6
Identification of positionally distinct astrocyte subtypes whose identities are specified by a homeodomain code.鉴定由同源结构域编码指定其身份的位置不同的星形胶质细胞亚型。
Cell. 2008 May 2;133(3):510-22. doi: 10.1016/j.cell.2008.02.046.
7
MicroRNAs in gene regulation: when the smallest governs it all.基因调控中的微小RNA:当最小者掌控一切时。
J Biomed Biotechnol. 2006;2006(4):69616. doi: 10.1155/JBB/2006/69616.
8
Competing waves of oligodendrocytes in the forebrain and postnatal elimination of an embryonic lineage.前脑少突胶质细胞的竞争浪潮与胚胎谱系的出生后消除。
Nat Neurosci. 2006 Feb;9(2):173-9. doi: 10.1038/nn1620. Epub 2005 Dec 25.
9
Oligodendrocyte wars.少突胶质细胞之战。
Nat Rev Neurosci. 2006 Jan;7(1):11-8. doi: 10.1038/nrn1826.
10
In situ detection of miRNAs in animal embryos using LNA-modified oligonucleotide probes.使用锁核酸(LNA)修饰的寡核苷酸探针原位检测动物胚胎中的微小RNA(miRNA)
Nat Methods. 2006 Jan;3(1):27-9. doi: 10.1038/nmeth843.