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慢性应激对 PFC 转录组的影响:基于公开 RNA-seq 数据集的生物信息学荟萃分析。

The impact of chronic stress on the PFC transcriptome: a bioinformatic meta-analysis of publicly available RNA-sequencing datasets.

机构信息

Brain & Mind Centre, The University of Sydney, Sydney, Australia.

出版信息

Stress. 2022 Jan;25(1):305-312. doi: 10.1080/10253890.2022.2111211.

Abstract

The prefrontal cortex (PFC) is one of several brain structures that are sensitive to chronic stress exposure. There have been several studies which have examined the effects on chronic stress, using various protocols such as chronic unpredictable stress and chronic social defeat stress, on the PFC transcriptome. In this report, a bioinformatic meta-analysis of publicly available RNA sequencing datasets (101 samples) from seven chronic stress studies was carried out to identify core PFC transcriptional signatures that underpin behavioral phenotypes including resilience and susceptibility. The results showed 160 differentially expressed genes in chronic stress mice compared to controls with significant enrichment in mechanisms associated with translation and localization of membrane-bound proteins with a putative effect on synaptic plasticity in glutamatergic neurons. Moreover, the meta-analysis revealed no differentially expressed genes in resilient mice but 144 in susceptible mice compared to controls, of which 44 were not identified in the individual studies. Enrichment analysis revealed that susceptibility genes were most affected in oligodendrocytes and linked to mechanisms which mediate biochemical, bidirectional communication between this cell-type and myelinated axons. These results provide new avenues for further research into the neurobiology and treatment of chronic stress-induced disorders.

摘要

前额皮质(PFC)是对慢性应激暴露敏感的几种大脑结构之一。已经有几项研究使用慢性不可预测应激和慢性社会挫败应激等各种方案来检查慢性应激对 PFC 转录组的影响。在本报告中,对来自七个慢性应激研究的公开可用 RNA 测序数据集(101 个样本)进行了生物信息学元分析,以鉴定核心 PFC 转录特征,这些特征是行为表型(包括弹性和易感性)的基础。结果显示,与对照组相比,慢性应激小鼠中有 160 个差异表达基因,这些基因在与翻译和膜结合蛋白定位相关的机制中显著富集,可能对谷氨酸能神经元的突触可塑性产生影响。此外,元分析显示,弹性小鼠中没有差异表达的基因,但与对照组相比,易感小鼠中有 144 个差异表达的基因,其中 44 个在个别研究中未被识别。富集分析表明,易感基因在少突胶质细胞中受到的影响最大,与介导该细胞类型与髓鞘轴突之间生化双向通讯的机制有关。这些结果为进一步研究慢性应激诱导的疾病的神经生物学和治疗提供了新途径。

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