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来自相分离晶状体的抑制性突触后致密物。

Inhibitory postsynaptic density from the lens of phase separation.

作者信息

Bai Guanhua, Zhang Mingjie

机构信息

School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055, China.

Greater Bay Biomedical Innocenter, Shenzhen Bay Laboratory, Shenzhen 518036, China.

出版信息

Oxf Open Neurosci. 2022 May 4;1:kvac003. doi: 10.1093/oons/kvac003. eCollection 2022.

DOI:10.1093/oons/kvac003
PMID:38596704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10913824/
Abstract

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.

摘要

为了忠实地传递和解码从突触前终末释放的信号,神经元突触的突触后区室部署了数百种不同的蛋白质。除了不同的蛋白质组外,兴奋性和抑制性突触后装置还表现出非常不同的组织特征和调节特性。数十年来的广泛研究已经产生了关于兴奋性突触后区室的分子组成、组装结构和活性依赖性调节机制的丰富知识。相比之下,我们对抑制性突触后装置的了解则较为滞后。最近的研究表明,相分离是兴奋性和抑制性突触后分子组装形成和可塑性的新范式。在这篇综述中,我们通过相分离概念的视角并与兴奋性突触后致密物进行比较,讨论抑制性突触后致密物的分子组成、组织和调节特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/025f90146cd2/kvac003f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/55f170811ec9/kvac003f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/1475a55603cb/kvac003f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/1c60a4522797/kvac003f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/025f90146cd2/kvac003f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/55f170811ec9/kvac003f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/1475a55603cb/kvac003f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/1c60a4522797/kvac003f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c23/10913824/025f90146cd2/kvac003f4.jpg

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Unique properties of dually innervated dendritic spines in pyramidal neurons of the somatosensory cortex uncovered by 3D correlative light and electron microscopy.通过三维共聚焦光镜和电子显微镜发现躯体感觉皮层锥体神经元中双重支配树突棘的独特性质。
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Presynaptic bouton compartmentalization and postsynaptic density-mediated glutamate receptor clustering via phase separation.
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Neuropharmacology. 2021 Aug 1;193:108622. doi: 10.1016/j.neuropharm.2021.108622. Epub 2021 May 26.
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CaMKII activation persistently segregates postsynaptic proteins via liquid phase separation.CaMKII 的激活通过液-液相分离持久地分隔突触后蛋白。
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The α3 subunit of GABA receptors promotes formation of inhibitory synapses in the absence of collybistin.GABA 受体的 α3 亚基在没有 collybistin 的情况下促进抑制性突触的形成。
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Reciprocal stabilization of glycine receptors and gephyrin scaffold proteins at inhibitory synapses.抑制性突触处甘氨酸受体和网格蛋白支架蛋白的相互稳定。
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