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神经元轴突中的局部蛋白质合成:我们研究的原因及方式。

Local protein synthesis in neuronal axons: why and how we study.

作者信息

Kim Eunjin, Jung Hosung

机构信息

Department of Anatomy, Brain Research Institute, and Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea.

出版信息

BMB Rep. 2015 Mar;48(3):139-46. doi: 10.5483/bmbrep.2015.48.3.010.

Abstract

Adaptive brain function and synaptic plasticity rely on dynamic regulation of local proteome. One way for the neuron to introduce new proteins to the axon terminal is to transport those from the cell body, which had long been thought as the only source of axonal proteins. Another way, which is the topic of this review, is synthesizing proteins on site by local mRNA translation. Recent evidence indicates that the axon stores a reservoir of translationally silent mRNAs and regulates their expression solely by translational control. Different stimuli to axons, such as guidance cues, growth factors, and nerve injury, promote translation of selective mRNAs, a process required for the axon's ability to respond to these cues. One of the critical questions in the field of axonal protein synthesis is how mRNA-specific local translation is regulated by extracellular cues. Here, we review current experimental techniques that can be used to answer this question. Furthermore, we discuss how new technologies can help us understand what biological processes are regulated by axonal protein synthesis in vivo.

摘要

适应性脑功能和突触可塑性依赖于局部蛋白质组的动态调节。神经元将新蛋白质引入轴突末端的一种方式是从细胞体运输这些蛋白质,长期以来人们一直认为细胞体是轴突蛋白质的唯一来源。另一种方式,即本综述的主题,是通过局部mRNA翻译在原位合成蛋白质。最近的证据表明,轴突储存了一批翻译沉默的mRNA,并仅通过翻译控制来调节它们的表达。对轴突的不同刺激,如导向线索、生长因子和神经损伤,会促进选择性mRNA的翻译,这是轴突对这些线索作出反应的能力所必需的过程。轴突蛋白质合成领域的关键问题之一是细胞外线索如何调节mRNA特异性局部翻译。在这里,我们综述了可用于回答这个问题的当前实验技术。此外,我们讨论了新技术如何帮助我们理解体内轴突蛋白质合成调节哪些生物学过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e690/4453028/29692a7b0049/BMB-48-139-g001.jpg

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