CircSATB2 modulates fear extinction memory via Robo3-driven synaptic plasticity

IF 3.5 3区 医学 Q2 NEUROSCIENCES Brain Research Bulletin Pub Date : 2025-01-01 DOI:10.1016/j.brainresbull.2024.111167
Ziyue Xu , Jichun Shi , Runming Liu , Zhehao Li , Shuangxiang Xu , Hao Gong , Mingyue Fu , Hongyu Xu , Shuangqi Yu , Junhui Liu , Huiqing Wu , Xiang Li , Sha Liu , Wei Wei
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Abstract

Circular RNAs (circRNAs) are novel class of stable regulatory RNAs abundantly expressed in the brain. However, their role in fear extinction (EXT) memory remains largely unexplored. To investigate the mechanisms of Circular Special AT-rich Sequence Binding Protein 2 (circSatb2) in EXT memory, we constructed a lentivirus overexpressing circSatb2 and injected it into the infralimbic prefrontal cortex (ILPFC) of the mouse brain. Following extinction training and subsequent testing, we observed an essential role of circSatb2 in this dynamic process. RNA sequencing (RNA-seq) and bioinformatics analyses revealed that circSatb2 enhances the transcription of Roundabout Guidance Receptor 3 (Robo3), a key gene implicated in axon guidance and synaptic plasticity, which was validated by RT-qPCR. Neuronal morphology was assessed using confocal microscopy to determine changes in dendritic spine density. Our results demonstrated that circSatb2 significantly enhances Robo3 transcription, leading to increased dendritic spine formation and improved synaptic plasticity. In conclusion, circSatb2 promotes the formation of EXT memory by upregulating Robo3 transcription and enhancing synaptic plasticity. These findings position circSatb2 as a potential therapeutic target for disorders associated with memory impairment.
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CircSATB2 通过 Robo3 驱动的突触可塑性调节恐惧消退记忆
环状rna (circRNAs)是一类在大脑中大量表达的新型稳定调控rna。然而,它们在恐惧消退(EXT)记忆中的作用在很大程度上仍未被探索。为了研究环状特殊at富集序列结合蛋白2 (Circular Special AT-rich Sequence Binding Protein 2, circSatb2)在EXT记忆中的作用机制,我们构建了过表达circSatb2的慢病毒,并将其注入小鼠大脑边缘下前额叶皮层(ILPFC)。经过消光训练和随后的测试,我们观察到circSatb2在这一动态过程中发挥了重要作用。RNA测序(RNA-seq)和生物信息学分析显示,circSatb2可增强Roundabout Guidance Receptor 3 (Robo3)的转录,Robo3是参与轴突引导和突触可塑性的关键基因,RT-qPCR证实了这一点。使用共聚焦显微镜评估神经元形态学以确定树突棘密度的变化。我们的研究结果表明,circSatb2显著增强Robo3转录,导致树突棘形成增加和突触可塑性改善。综上所述,circSatb2通过上调Robo3转录和增强突触可塑性来促进EXT记忆的形成。这些发现将circSatb2定位为与记忆障碍相关的疾病的潜在治疗靶点。
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来源期刊
Brain Research Bulletin
Brain Research Bulletin 医学-神经科学
CiteScore
6.90
自引率
2.60%
发文量
253
审稿时长
67 days
期刊介绍: The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.
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