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自闭症基因小鼠模型中的“既视感”改变了社会习俗。

"Déjà vu" in an autism gene mouse model modifies social mores.

机构信息

Department of Neurobiology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL, USA; Civitan International Research Center at UAB Heersink School of Medicine, Birmingham, AL, USA.

Department of Neurobiology, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL, USA; Civitan International Research Center at UAB Heersink School of Medicine, Birmingham, AL, USA.

出版信息

Neuron. 2022 May 4;110(9):1433-1435. doi: 10.1016/j.neuron.2022.04.007.

DOI:10.1016/j.neuron.2022.04.007
PMID:35512633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9641719/
Abstract

Genetic and environmental factors during development are involved in autism, and in this issue of Neuron Krüttner et al. (2022) find environment may play a more acute role in modulating autism behavior in a Shank3 exon 21 deletion mutant mouse (Shank3). The authors explore the underlying circuit mechanisms in detail.

摘要

遗传和环境因素在自闭症的发展中起作用,在本期《神经元》杂志上,Krüttner 等人(2022)发现环境可能在 Shank3 外显子 21 缺失突变小鼠(Shank3)中更急性地调节自闭症行为方面发挥更重要的作用。作者详细探讨了潜在的电路机制。

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Neuron. 2022 May 4;110(9):1433-1435. doi: 10.1016/j.neuron.2022.04.007.
2
Early life sleep disruption potentiates lasting sex-specific changes in behavior in genetically vulnerable Shank3 heterozygous autism model mice.早期生活中的睡眠中断会使 Shank3 杂合子自闭症模型小鼠中存在遗传易感性的行为产生持久的性别特异性变化。
Mol Autism. 2022 Aug 29;13(1):35. doi: 10.1186/s13229-022-00514-5.
3
Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism.抑制 TRPV4 可挽救 Shank3 自闭症小鼠模型中急性炎症反应所揭示的回路和社交缺陷。
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Absence of familiarity triggers hallmarks of autism in mouse model through aberrant tail-of-striatum and prelimbic cortex signaling.缺乏熟悉感通过纹状体尾部和前额皮质信号的异常触发自闭症小鼠模型的标志性特征。
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Genes Brain Behav. 2018 Jan;17(1):4-22. doi: 10.1111/gbb.12405. Epub 2017 Sep 5.
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Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function.自闭症小鼠模型中 Shank3 突变导致 S-亚硝基化蛋白质组发生变化,并影响参与囊泡释放和突触功能的关键蛋白。
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A cross-talk between nitric oxide and the glutamatergic system in a Shank3 mouse model of autism.自闭症 Shank3 模型中一氧化氮与谷氨酰胺能系统的串扰。
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Juvenile Shank3b deficient mice present with behavioral phenotype relevant to autism spectrum disorder.幼年缺失Shank3b基因的小鼠表现出与自闭症谱系障碍相关的行为表型。
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本文引用的文献

1
Absence of familiarity triggers hallmarks of autism in mouse model through aberrant tail-of-striatum and prelimbic cortex signaling.缺乏熟悉感通过纹状体尾部和前额皮质信号的异常触发自闭症小鼠模型的标志性特征。
Neuron. 2022 May 4;110(9):1468-1482.e5. doi: 10.1016/j.neuron.2022.02.001. Epub 2022 Feb 25.
2
Reset of hippocampal-prefrontal circuitry facilitates learning.海马-前额叶回路的重置促进了学习。
Nature. 2021 Mar;591(7851):615-619. doi: 10.1038/s41586-021-03272-1. Epub 2021 Feb 24.
3
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
大规模外显子组测序研究表明自闭症的神经生物学既有发育性变化也有功能性变化。
Cell. 2020 Feb 6;180(3):568-584.e23. doi: 10.1016/j.cell.2019.12.036. Epub 2020 Jan 23.
4
CLK2 inhibition ameliorates autistic features associated with SHANK3 deficiency.CLK2 抑制改善了与 SHANK3 缺乏相关的自闭症特征。
Science. 2016 Mar 11;351(6278):1199-203. doi: 10.1126/science.aad5487. Epub 2016 Feb 4.
5
Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits.Shank3基因第21外显子的自闭症相关插入突变(InsG)导致突触传递受损和行为缺陷。
J Neurosci. 2015 Jul 1;35(26):9648-65. doi: 10.1523/JNEUROSCI.3125-14.2015.
6
Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators.靶向肌动蛋白调节因子可挽救Shank3基因缺陷小鼠的自闭症样缺陷。
Cell Rep. 2015 Jun 9;11(9):1400-1413. doi: 10.1016/j.celrep.2015.04.064. Epub 2015 May 28.
7
Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission.缺失主要的 Shank3 异构体导致海马依赖的行为和突触传递损伤。
J Neurosci. 2013 Nov 20;33(47):18448-68. doi: 10.1523/JNEUROSCI.3017-13.2013.
8
Modulation of striatal projection systems by dopamine.多巴胺对纹状体投射系统的调制。
Annu Rev Neurosci. 2011;34:441-66. doi: 10.1146/annurev-neuro-061010-113641.
9
Pten regulates neuronal arborization and social interaction in mice.Pten调节小鼠的神经元分支和社交互动。
Neuron. 2006 May 4;50(3):377-88. doi: 10.1016/j.neuron.2006.03.023.
10
Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice.五个近交系小鼠的社交性及对社交新奇性的偏好:一种评估小鼠自闭症样行为的方法。
Genes Brain Behav. 2004 Oct;3(5):287-302. doi: 10.1111/j.1601-1848.2004.00076.x.