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本文引用的文献

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microRNA-132 regulates dendritic growth and arborization of newborn neurons in the adult hippocampus.microRNA-132 调控成年海马体新生神经元的树突生长和分支。
Proc Natl Acad Sci U S A. 2010 Nov 23;107(47):20382-7. doi: 10.1073/pnas.1015691107. Epub 2010 Nov 8.
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The widespread regulation of microRNA biogenesis, function and decay.广泛调节 microRNA 的生物发生、功能和降解。
Nat Rev Genet. 2010 Sep;11(9):597-610. doi: 10.1038/nrg2843. Epub 2010 Jul 27.
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MicroRNA miR-137 regulates neuronal maturation by targeting ubiquitin ligase mind bomb-1.MicroRNA miR-137 通过靶向泛素连接酶 mind bomb-1 调节神经元成熟。
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Glucocorticoids and lithium in adult hippocampal neurogenesis.糖皮质激素和锂在成年海马神经发生中的作用。
Vitam Horm. 2010;82:421-31. doi: 10.1016/S0083-6729(10)82021-7.
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miR-132 regulates antiviral innate immunity through suppression of the p300 transcriptional co-activator.miR-132 通过抑制 p300 转录共激活因子来调节抗病毒先天免疫。
Nat Cell Biol. 2010 May;12(5):513-9. doi: 10.1038/ncb2054. Epub 2010 Apr 25.
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MicroRNA-9 coordinates proliferation and migration of human embryonic stem cell-derived neural progenitors.MicroRNA-9 协调人胚胎干细胞源性神经祖细胞的增殖和迁移。
Cell Stem Cell. 2010 Apr 2;6(4):323-335. doi: 10.1016/j.stem.2010.02.015.
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Recombinant Adeno-Associated Virus-Mediated microRNA Delivery into the Postnatal Mouse Brain Reveals a Role for miR-134 in Dendritogenesis in Vivo.腺相关病毒介导的 microRNA 递送至新生小鼠脑内揭示了 miR-134 在体内树突发生中的作用。
Front Neural Circuits. 2010 Jan 12;3:16. doi: 10.3389/neuro.04.016.2009. eCollection 2010.
8
Input-specific GABAergic signaling to newborn neurons in adult dentate gyrus.成年齿状回中新生神经元的输入特异性γ-氨基丁酸能信号传导。
J Neurosci. 2009 Dec 2;29(48):15063-72. doi: 10.1523/JNEUROSCI.2727-09.2009.
9
A reduced number of hippocampal granule cells does not associate with an anhedonia-like phenotype in a rat chronic mild stress model of depression.在大鼠慢性轻度应激抑郁模型中,海马颗粒细胞数量减少与快感缺失样表型无关。
Stress. 2010 Mar;13(2):95-105. doi: 10.3109/10253890902951786.
10
An activity-induced microRNA controls dendritic spine formation by regulating Rac1-PAK signaling.一种活性诱导的 microRNA 通过调节 Rac1-PAK 信号来控制树突棘形成。
Mol Cell Neurosci. 2010 Jan;43(1):146-56. doi: 10.1016/j.mcn.2009.10.005. Epub 2009 Oct 20.

齿状回神经发生、整合与 microRNAs。

Dentate gyrus neurogenesis, integration and microRNAs.

机构信息

The Vollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.

出版信息

Behav Brain Res. 2012 Feb 14;227(2):348-55. doi: 10.1016/j.bbr.2011.03.048. Epub 2011 Apr 1.

DOI:10.1016/j.bbr.2011.03.048
PMID:21443907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3153561/
Abstract

Neurons are born and become a functional part of the synaptic circuitry in adult brains. The proliferative phase of neurogenesis has been extensively reviewed. We therefore focus this review on a few topics addressing the functional role of adult-generated newborn neurons in the dentate gyrus. We discuss the evidence for a link between neurogenesis and behavior. We then describe the steps in the integration of newborn neurons into a functioning mature synaptic circuit. Given the profound effects of neural activity on the differentiation and integration of newborn neurons, we discuss the role of activity-dependent gene expression in the birth and maturation of newborn neurons. The differentiation and maturation of newborn neurons likely involves the concerted action of many genes. Thus we focus on transcription factors that can direct large changes to the transcriptome, and microRNAs, a newly-discovered class of molecules that can effect the expression of hundreds of genes. How microRNAs affect the generation and integration of newborn neurons is just being explored, but there are compelling clues hinting at their involvement.

摘要

神经元在成年大脑中产生并成为突触回路的功能部分。神经发生的增殖阶段已经得到了广泛的研究。因此,我们将重点放在几个主题上,讨论成年产生的新神经元在齿状回中的功能作用。我们讨论了神经发生与行为之间的联系的证据。然后,我们描述了新神经元整合到成熟的突触回路中的步骤。鉴于神经活动对新神经元的分化和整合有深远的影响,我们讨论了活性依赖性基因表达在新神经元的产生和成熟中的作用。新神经元的分化和成熟可能涉及许多基因的协同作用。因此,我们专注于可以指导转录组发生重大变化的转录因子,以及 microRNAs,这是一类新发现的分子,可以影响数百个基因的表达。microRNAs 如何影响新神经元的产生和整合才刚刚开始探索,但有一些令人信服的线索暗示了它们的参与。