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在缺乏N - 乙基马来酰亚胺敏感因子基因的小鼠中,类似自闭症的行为以及血清素转运体和AMPA受体转运的损伤

Autistic-Like Behavior and Impairment of Serotonin Transporter and AMPA Receptor Trafficking in -Ethylmaleimide Sensitive Factor Gene-Deficient Mice.

作者信息

Xie Min-Jue, Iwata Keiko, Ishikawa Yasuyuki, Nomura Yuki, Tani Tomomi, Murata Koshi, Fukazawa Yugo, Matsuzaki Hideo

机构信息

Division of Development of Mental Functions, Research Center for Child Mental Development, University of Fukui, Fukui, Japan.

Life Science Innovation Center, University of Fukui, Fukui, Japan.

出版信息

Front Genet. 2021 Oct 20;12:748627. doi: 10.3389/fgene.2021.748627. eCollection 2021.

DOI:10.3389/fgene.2021.748627
PMID:34745222
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8563833/
Abstract

Autism spectrum disorder (ASD), characterized by profound impairment in social interactions and communication skills, is the most common neurodevelopmental disorder. Many studies on the mechanisms underlying the development of ASD have focused on the serotonergic system; however, these studies have failed to completely elucidate the mechanisms. We previously identified -ethylmaleimide-sensitive factor (NSF) as a new serotonin transporter (SERT)-binding protein and described its importance in SERT membrane trafficking and uptake . In the present study, we generated mice and investigated their behavioral, neurotransmitter, and neurophysiological phenotypes . mice exhibited abnormalities in sociability, communication, repetitiveness, and anxiety. Additionally, loss led to a decrease in membrane SERT expression in the raphe and accumulation of glutamate alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors at the synaptic membrane surface in the hippocampal CA1 region. We found that postsynaptic density and long-term depression were impaired in the hippocampal CA1 region of mice. Taken together, these findings demonstrate that NSF plays a role in synaptic plasticity and glutamatergic and serotonergic systems, suggesting a possible mechanism by which the gene is linked to the pathophysiology of autistic behaviors.

摘要

自闭症谱系障碍(ASD)是最常见的神经发育障碍,其特征是社交互动和沟通技能严重受损。许多关于ASD发病机制的研究都集中在血清素能系统;然而,这些研究未能完全阐明其机制。我们之前鉴定出N - 乙基马来酰亚胺敏感因子(NSF)是一种新的血清素转运体(SERT)结合蛋白,并描述了其在SERT膜转运和摄取中的重要性。在本研究中,我们构建了Nsf基因敲除小鼠,并研究了它们的行为、神经递质和神经生理学表型。Nsf基因敲除小鼠在社交性、沟通、重复性和焦虑方面表现出异常。此外,Nsf缺失导致中缝核中膜SERT表达减少,海马CA1区突触膜表面谷氨酸α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体积累。我们发现Nsf基因敲除小鼠海马CA1区的突触后致密物和长时程抑制受损。综上所述,这些发现表明NSF在突触可塑性以及谷氨酸能和血清素能系统中发挥作用,提示该基因与自闭症行为病理生理学相关的一种可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/bc7665812766/fgene-12-748627-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/0471c6113dda/fgene-12-748627-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/a916d8fd6825/fgene-12-748627-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/4810fb381401/fgene-12-748627-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/11b6ebd11af5/fgene-12-748627-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/cb2a9755bfdb/fgene-12-748627-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/e32c33e1863e/fgene-12-748627-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/f2920d8f531a/fgene-12-748627-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/1329822b4682/fgene-12-748627-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/bc7665812766/fgene-12-748627-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/0471c6113dda/fgene-12-748627-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/a916d8fd6825/fgene-12-748627-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/4810fb381401/fgene-12-748627-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/11b6ebd11af5/fgene-12-748627-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/cb2a9755bfdb/fgene-12-748627-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/e32c33e1863e/fgene-12-748627-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/f2920d8f531a/fgene-12-748627-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/1329822b4682/fgene-12-748627-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca55/8563833/bc7665812766/fgene-12-748627-g009.jpg

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