雄性小鼠的反复社交失败诱导了杏仁核到海马体的投射神经元中独特的RNA谱。

IF 3.7 Q2 IMMUNOLOGY
Brain, behavior, & immunity - health Pub Date : 2024-11-29 eCollection Date: 2025-02-01 DOI:10.1016/j.bbih.2024.100908
Rebecca G Biltz, Wenyuan Yin, Ethan J Goodman, Lynde M Wangler, Amara C Davis, Braedan T Oliver, Jonathan P Godbout, John F Sheridan
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引用次数: 0

摘要

慢性压力会增加精神疾病的发病率,包括焦虑、抑郁和创伤后应激障碍。小鼠的重复性社会失败(RSD)概括了人类在慢性应激后明显的几个关键的生理、免疫和行为变化。例如,前额皮质、杏仁核和海马体中的神经元参与RSD后对恐惧和威胁性刺激的解释和反应。因此,本研究的目的是确定应激如何影响海马神经元和从威胁评估中心投射到海马体的神经元的RNA谱。在这里,RSD增加了雄性小鼠在高难度迷宫中的焦虑样行为,减少了海马依赖的新物体定位记忆。接下来,生成泛神经元(Baf53 b-Cre) RiboTag小鼠,以捕获海马中RSD激活的核糖体结合mRNA(即主动翻译)。RNAseq结果显示,RSD后海马神经元中存在1694个差异表达基因(DEGs)。这些deg与氧化应激、突触长期增强和神经炎症信号的增加有关。为了进一步研究与恐惧和焦虑相关的区域特异性神经回路,将表达cree -重组酶的逆行腺相关病毒(AAV2rg)注射到雄性RiboTag小鼠的海马中。这诱导了投射到海马体的神经元中血凝素表位的表达。对这些AAV2rg-RiboTag小鼠进行RSD,并从杏仁核中收集核糖体结合的mRNA进行rna测序。RSD诱导杏仁核投射677度。投射到海马体的杏仁核神经元的RNA谱与突触发生、白细胞介素-1信号传导、一氧化氮和活性氧产生的增加有关。使用类似的方法,在前额皮质投射的神经元中有1132个deg。这些前额皮质神经元的RNA谱与RSD后突触发生、整合素信号和多巴胺反馈信号的增加有关。总的来说,受压力影响的投射神经元有独特的RNA谱,这些谱与海马依赖的行为和认知缺陷有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Repeated social defeat in male mice induced unique RNA profiles in projection neurons from the amygdala to the hippocampus.

Chronic stress increases the incidence of psychiatric disorders including anxiety, depression, and posttraumatic stress disorder. Repeated Social Defeat (RSD) in mice recapitulates several key physiological, immune, and behavioral changes evident after chronic stress in humans. For instance, neurons in the prefrontal cortex, amygdala, and hippocampus are involved in the interpretation of and response to fear and threatful stimuli after RSD. Therefore, the purpose of this study was to determine how stress influenced the RNA profile of hippocampal neurons and neurons that project into the hippocampus from threat appraisal centers. Here, RSD increased anxiety-like behavior in the elevated plus maze and reduced hippocampal-dependent novel object location memory in male mice. Next, pan-neuronal (Baf53 b-Cre) RiboTag mice were generated to capture ribosomal bound mRNA (i.e., active translation) activated by RSD in the hippocampus. RNAseq revealed that there were 1694 differentially expressed genes (DEGs) in hippocampal neurons after RSD. These DEGs were associated with an increase in oxidative stress, synaptic long-term potentiation, and neuroinflammatory signaling. To further examine region-specific neural circuitry associated with fear and anxiety, a retrograde-adeno-associated-virus (AAV2rg) expressing Cre-recombinase was injected into the hippocampus of male RiboTag mice. This induced expression of a hemagglutinin epitope in neurons that project into the hippocampus. These AAV2rg-RiboTag mice were subjected to RSD and ribosomal-bound mRNA was collected from the amygdala for RNA-sequencing. RSD induced 677 DEGs from amygdala projections. Amygdala neurons that project into the hippocampus had RNA profiles associated with increased synaptogenesis, interleukin-1 signaling, nitric oxide, and reactive oxygen species production. Using a similar approach, there were 1132 DEGs in neurons that project from the prefrontal cortex. These prefrontal cortex neurons had RNA profiles associated with increased synaptogenesis, integrin signaling, and dopamine feedback signaling after RSD. Collectively, there were unique RNA profiles of stress-influenced projection neurons and these profiles were associated with hippocampal-dependent behavioral and cognitive deficits.

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来源期刊
Brain, behavior, & immunity - health
Brain, behavior, & immunity - health Biological Psychiatry, Behavioral Neuroscience
CiteScore
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