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神经元路径寻找、突触重组和神经元再生中的时间机制。

Timing mechanisms in neuronal pathfinding, synaptic reorganization, and neuronal regeneration.

作者信息

Ivakhnitskaia Evguenia, Hamada Kana, Chang Chieh

机构信息

Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL, 60607, USA.

Medical Scientist Training Program, University of Illinois at Chicago, Chicago, IL, 60612, USA.

出版信息

Dev Growth Differ. 2016 Jan;58(1):88-93. doi: 10.1111/dgd.12259. Epub 2016 Jan 9.

Abstract

Precise temporal control of neuro differentiation and post-differentiation events are necessary for the creation of appropriate wiring diagram in the brain. To make advances in the treatment of neurodevelopmental and neurodegenerative disorders, and traumatic brain injury, it is important to understand these mechanisms. Caenorhabditis elegans has emerged as a revolutionary tool for the study of neural circuits due to its genetic homology to vertebrates and ease of genetic manipulation. microRNA (miRNA), a ubiquitous class of small non-coding RNA, that inhibits the expression of target genes, has emerged as an important timing control molecule through research conducted on C. elegans. This review will focus on the temporal control of neurodifferentiation and post-differentiation events exerted by two conserved miRNAs, lin-4 and let-7. We summarize recent findings on the role of lin-4 as a timing regulator controlling transition of sequential events in neuronal pathfinding and synaptic remodeling, and the role of let-7 as a timing regulator that limits the regeneration potential of post-differentiated AVM neurons as they age.

摘要

神经分化和分化后事件的精确时间控制对于在大脑中创建合适的布线图至关重要。为了在神经发育和神经退行性疾病以及创伤性脑损伤的治疗方面取得进展,了解这些机制很重要。秀丽隐杆线虫由于其与脊椎动物的基因同源性以及易于进行基因操作,已成为研究神经回路的革命性工具。微小RNA(miRNA)是一类普遍存在的小非编码RNA,可抑制靶基因的表达,通过对秀丽隐杆线虫的研究,它已成为一种重要的时间控制分子。本综述将聚焦于由两个保守的miRNA,lin-4和let-7所施加的神经分化和分化后事件的时间控制。我们总结了关于lin-4作为控制神经元路径寻找和突触重塑中连续事件转变的时间调节因子的作用,以及let-7作为随着分化后的AVM神经元衰老而限制其再生潜力的时间调节因子的作用的最新发现。

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本文引用的文献

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