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内体分选蛋白SNX4限制突触小泡的对接和释放。

Endosomal sorting protein SNX4 limits synaptic vesicle docking and release.

作者信息

Poppinga Josse, Barrett Nolan J, Cornelisse L Niels, Verhage Matthijs, van Weering Jan R T

机构信息

Department of Functional Genomics, Center for Neurogenomics and Cognitive Research (CNCR), VU University, Amsterdam, Netherlands.

Department of Human Genetics, CNCR, Amsterdam UMC, Amsterdam, Netherlands.

出版信息

Elife. 2024 Dec 19;13:RP97910. doi: 10.7554/eLife.97910.

Abstract

Sorting nexin 4 (SNX4) is an evolutionary conserved organizer of membrane recycling. In neurons, SNX4 accumulates in synapses, but how SNX4 affects synapse function remains unknown. We generated a conditional SNX4 knock-out mouse model and report that SNX4 cKO synapses show enhanced neurotransmission during train stimulation, while the first evoked EPSC was normal. SNX4 depletion did not affect vesicle recycling, basic autophagic flux, or the levels and localization of SNARE-protein VAMP2/synaptobrevin-2. However, SNX4 depletion affected synapse ultrastructure: an increase in docked synaptic vesicles at the active zone, while the overall vesicle number was normal, and a decreased active zone length. These effects together lead to a substantially increased density of docked vesicles per release site. In conclusion, SNX4 is a negative regulator of synaptic vesicle docking and release. These findings suggest a role for SNX4 in synaptic vesicle recruitment at the active zone.

摘要

分选连接蛋白4(SNX4)是一种在进化上保守的膜回收组织者。在神经元中,SNX4在突触中积累,但SNX4如何影响突触功能仍不清楚。我们构建了一个条件性SNX4基因敲除小鼠模型,并报告称SNX4基因敲除的突触在串刺激期间显示出增强的神经传递,而首次诱发的兴奋性突触后电流(EPSC)是正常的。SNX4的缺失不影响囊泡循环、基本自噬通量或SNARE蛋白VAMP2/突触小泡蛋白-2的水平和定位。然而,SNX4的缺失影响了突触超微结构:活性区对接的突触囊泡增加,而囊泡总数正常,且活性区长度减小。这些效应共同导致每个释放位点对接囊泡的密度大幅增加。总之,SNX4是突触囊泡对接和释放的负调节因子。这些发现表明SNX4在活性区突触囊泡募集过程中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91ce/11658762/99abe1ec9435/elife-97910-fig1.jpg

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