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从突触到细胞核,再回到突触——神经元内的远距离通讯。

From synapse to nucleus and back again--communication over distance within neurons.

机构信息

Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

J Neurosci. 2011 Nov 9;31(45):16045-8. doi: 10.1523/JNEUROSCI.4006-11.2011.

Abstract

How do neurons integrate intracellular communication from synapse to nucleus and back? Here we briefly summarize aspects of this topic covered by a symposium at Neuroscience 2011. A rich repertoire of signaling mechanisms link both dendritic terminals and axon tips with neuronal soma and nucleus, using motor-dependent transport machineries to traverse the long intracellular distances along neuronal processes. Activation mechanisms at terminals include localized translation of dendritic or axonal RNA, proteolytic cleavage of receptors or second messengers, and differential phosphorylation of signaling moieties. Signaling complexes may be transported in endosomes, or as non-endosomal complexes associated with importins and dynein. Anterograde transport of RNA granules from the soma to neuronal processes, coupled with retrograde transport of proteins translated locally at terminals or within processes, may fuel ongoing bidirectional communication between soma and synapse to modulate synaptic plasticity as well as neuronal growth and survival decisions.

摘要

神经元如何整合来自突触到细胞核再返回的细胞内通讯?本文简要总结了 2011 年神经科学会议上一个专题研讨会涵盖的这一主题的各个方面。丰富的信号机制将树突末梢和轴突末梢与神经元胞体和细胞核联系起来,利用依赖运动的运输机制沿着神经元突起的长距离进行跨越。末梢的激活机制包括树突或轴突 RNA 的局部翻译、受体或第二信使的蛋白水解切割,以及信号分子的差异磷酸化。信号复合物可以在内体中运输,也可以作为与导入蛋白和动力蛋白相关的非内体复合物运输。从胞体到神经元突起的 RNA 颗粒的顺行运输,与在末梢或突起内局部翻译的蛋白质的逆行运输相耦合,可能为胞体和突触之间的持续双向通讯提供动力,从而调节突触可塑性以及神经元生长和存活决策。

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