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神经元特异性基因 2(NSG2)编码一种 AMPA 受体相互作用蛋白,可调节兴奋性神经传递。

Neuron-Specific Gene 2 (NSG2) Encodes an AMPA Receptor Interacting Protein That Modulates Excitatory Neurotransmission.

机构信息

Department of Neurosciences, University of New Mexico-Health Science Center, Albuquerque, NM 87131.

Department of Pharmacology, University of Colorado-Denver, Aurora, CO 80045.

出版信息

eNeuro. 2019 Jan 24;6(1). doi: 10.1523/ENEURO.0292-18.2018. eCollection 2019 Jan-Feb.

Abstract

Neurons have evolved a number of unique protein-coding genes that regulate trafficking of protein complexes within small organelles throughout dendrites and axons. Neuron-specific gene 2 (NSG2) encodes for one of the most abundant proteins in the nervous system during perinatal development. NSG2 belongs to a family of small neuronal endosomal proteins but its function has remained uncharacterized to date. Here, we show that NSG2 is found in discrete punctae restricted to the somatodendritic arbors of developing mouse and human neurons, and a significant proportion of NSG2 punctae colocalize with postsynaptic HOMER1 and surface-expressed AMPA-type glutamate receptors (AMPARs) at excitatory synapses. Immunoprecipitation revealed that NSG2 physically interacts with both the GluA1 and GluA2 AMPAR subunits in mouse brain. Knock-out of NSG2 in mouse hippocampal neurons selectively impaired the frequency of miniature EPSCs (mEPSCs) and caused alterations in PSD95 expression at postsynaptic densities (PSDs). In contrast, NSG2 overexpression caused a significant increase in the amplitude of mEPSCs as well as GluA2 surface expression. Thus, NSG2 functions as an AMPAR-binding protein that is required for normal synapse formation and/or maintenance, and has unique functions compared with other NSG family members.

摘要

神经元进化出了许多独特的蛋白编码基因,这些基因可以调节蛋白复合物在树突和轴突中小细胞器内的运输。神经元特异性基因 2(NSG2)在围产期发育过程中编码神经系统中最丰富的蛋白质之一。NSG2 属于小神经元内体蛋白家族,但迄今为止其功能仍未被阐明。在这里,我们表明 NSG2 存在于离散的点状结构中,这些点状结构仅限于发育中的小鼠和人类神经元的体树突树突中,并且 NSG2 点状结构的很大一部分与兴奋性突触后 HOMER1 和表面表达的 AMPA 型谷氨酸受体(AMPAR)共定位。免疫沉淀显示 NSG2 与小鼠脑中的 GluA1 和 GluA2 AMPAR 亚基均发生物理相互作用。在小鼠海马神经元中敲除 NSG2 选择性地损害了微小 EPSC(mEPSC)的频率,并导致突触后密度(PSD)中 PSD95 表达的改变。相比之下,NSG2 的过表达导致 mEPSC 的幅度以及 GluA2 表面表达显著增加。因此,NSG2 作为一种 AMPAR 结合蛋白发挥作用,对于正常的突触形成和/或维持是必需的,并且与其他 NSG 家族成员具有独特的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea41/6345199/f9b73b5a6e7c/enu0011928240001.jpg

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