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神经元特异性基因 1 的全球缺失导致雄性小鼠运动协调能力改变、焦虑增加和昼夜活动过度。

Global loss of Neuron-specific gene 1 causes alterations in motor coordination, increased anxiety, and diurnal hyperactivity in male mice.

机构信息

Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, New Mexico, USA.

Department of Clinical Medicine, Translational Neuropsychiatry Unit, Aarhus University, Aarhus C, Denmark.

出版信息

Genes Brain Behav. 2022 Jul;21(6):e12816. doi: 10.1111/gbb.12816. Epub 2022 May 16.

Abstract

The Neuron-specific gene family (NSG1-3) consists of small endolysosomal proteins that are critical for trafficking multiple receptors and signaling molecules in neurons. NSG1 has been shown to play a critical role in AMPAR recycling from endosomes to plasma membrane during synaptic plasticity. However, to date nothing is known about whether NSG1 is required for normal behavior at an organismal level. Here we performed a battery of behavioral tests to determine whether loss of NSG1 would affect motor, cognitive, and/or affective behaviors, as well as circadian-related activity. Consistent with unique cerebellar expression of NSG1 among family members, we found that NSG1 was obligatory for motor coordination but not for gross motor function or learning. NSG1 knockout (KO) also altered performance across other behavioral modalities including anxiety-related and diurnal activity paradigms. Surprisingly, NSG1 KO did not cause significant impairments across all tasks within a given modality, but had specific effects within each modality. For instance, we found increases in anxiety-related behaviors in tasks with multiple stressors (e.g., elevation and exposure), but not those with a single main stressor (e.g., exposure). Interestingly, NSG1 KO animals displayed a significant increase in locomotor activity during subjective daytime, suggesting a possible impact on diurnal activity rhythms or vigilance. Surprisingly, loss of NSG1 had no effect on hippocampal-dependent learning despite previous studies showing deficits in CA1 long-term potentiation. Together, these findings do not support a role of NSG1 in hippocampal-dependent learning, but support a role in mediating proper neuronal function across amygdalar and cerebellar circuits.

摘要

神经元特异性基因家族(NSG1-3)由小内体蛋白组成,对于神经元中多种受体和信号分子的运输至关重要。已有研究表明,NSG1 在突触可塑性过程中 AMPAR 从内体到质膜的再循环中起着关键作用。然而,迄今为止,尚不清楚 NSG1 是否需要在机体水平上发挥正常行为。在这里,我们进行了一系列行为测试,以确定 NSG1 的缺失是否会影响运动、认知和/或情感行为以及与昼夜节律相关的活动。与 NSG1 在家族成员中独特的小脑表达一致,我们发现 NSG1 是运动协调所必需的,但不是粗大运动功能或学习所必需的。NSG1 敲除(KO)也改变了包括焦虑相关和昼夜活动范式在内的其他行为模式的表现。令人惊讶的是,NSG1 KO 在给定模态中的所有任务中都不会导致明显的损伤,但在每个模态中都有特定的影响。例如,我们发现,在具有多个应激源(例如,升高和暴露)的焦虑相关任务中,焦虑相关行为增加,但在具有单个主要应激源(例如,暴露)的任务中则没有。有趣的是,NSG1 KO 动物在主观白天表现出明显增加的运动活性,这表明昼夜活动节律或警觉性可能受到影响。令人惊讶的是,尽管先前的研究表明 CA1 长时程增强作用存在缺陷,但 NSG1 的缺失对海马依赖性学习没有影响。总之,这些发现不支持 NSG1 在海马依赖性学习中的作用,但支持其在调节杏仁核和小脑回路中适当神经元功能中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1dc/9744474/1dd7fd5985ed/GBB-21-e12816-g004.jpg

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