来自相分离透镜的抑制性突触后密度

Oxford open neuroscience Pub Date : 2022-05-04 eCollection Date: 2022-01-01 DOI:10.1093/oons/kvac003
Guanhua Bai, Mingjie Zhang
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引用次数: 0

摘要

为了忠实地传输和解码突触前末端释放的信号,神经元突触后区段需要部署数百种不同的蛋白质。除了不同的蛋白质集之外,兴奋性和抑制性突触后装置还显示出截然不同的组织特征和调控特性。经过几十年的广泛研究,我们对兴奋性突触后区室的分子组成、装配结构和活动依赖性调控机制有了丰富的了解。相比之下,我们对抑制性突触后装置的了解则相对滞后。最近的研究表明,相分离是兴奋性和抑制性突触后分子装配形成和可塑性的一种新模式。在这篇综述中,我们将通过相分离概念的视角,并与兴奋性突触后密度进行比较,讨论抑制性突触后密度的分子组成、组织和调控特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory postsynaptic density from the lens of phase separation.

To faithfully transmit and decode signals released from presynaptic termini, postsynaptic compartments of neuronal synapses deploy hundreds of various proteins. In addition to distinct sets of proteins, excitatory and inhibitory postsynaptic apparatuses display very different organization features and regulatory properties. Decades of extensive studies have generated a wealth of knowledge on the molecular composition, assembly architecture and activity-dependent regulatory mechanisms of excitatory postsynaptic compartments. In comparison, our understanding of the inhibitory postsynaptic apparatus trails behind. Recent studies have demonstrated that phase separation is a new paradigm underlying the formation and plasticity of both excitatory and inhibitory postsynaptic molecular assemblies. In this review, we discuss molecular composition, organizational and regulatory features of inhibitory postsynaptic densities through the lens of the phase separation concept and in comparison with the excitatory postsynaptic densities.

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