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长链非编码 RNA LINC00473 在抑郁症中的性别特异性作用

Sex-Specific Role for the Long Non-coding RNA LINC00473 in Depression.

机构信息

Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

Nash Family Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; School for Mental Health and Neuroscience, Department of Psychiatry and Neuropsychology, Maastricht University, 6229 ER, Maastricht, the Netherlands.

出版信息

Neuron. 2020 Jun 17;106(6):912-926.e5. doi: 10.1016/j.neuron.2020.03.023. Epub 2020 Apr 17.

Abstract

Depression is a common disorder that affects women at twice the rate of men. Here, we report that long non-coding RNAs (lncRNAs), a recently discovered class of regulatory transcripts, represent about one-third of the differentially expressed genes in the brains of depressed humans and display complex region- and sex-specific patterns of regulation. We identified the primate-specific, neuronal-enriched gene LINC00473 as downregulated in prefrontal cortex (PFC) of depressed females but not males. Using viral-mediated gene transfer to express LINC00473 in adult mouse PFC neurons, we mirrored the human sex-specific phenotype by inducing stress resilience solely in female mice. This sex-specific phenotype was accompanied by changes in synaptic function and gene expression selectively in female mice and, along with studies of human neuron-like cells in culture, implicates LINC00473 as a CREB effector. Together, our studies identify LINC00473 as a female-specific driver of stress resilience that is aberrant in female depression.

摘要

抑郁症是一种常见的疾病,其在女性中的发病率是男性的两倍。在这里,我们报告说,长非编码 RNA(lncRNA)是一类新发现的调控转录本,它们约占抑郁患者大脑中差异表达基因的三分之一,并表现出复杂的区域和性别特异性调控模式。我们鉴定出灵长类特异性、神经元丰富的基因 LINC00473 在抑郁女性的前额叶皮层(PFC)中下调,但在男性中没有下调。我们使用病毒介导的基因转移在成年小鼠 PFC 神经元中表达 LINC00473,通过仅在雌性小鼠中诱导应激弹性,模拟了人类的性别特异性表型。这种性别特异性表型伴随着突触功能和基因表达的变化,这些变化在雌性小鼠中是选择性的,并且与体外培养的人类神经元样细胞的研究一起,表明 LINC00473 是 CREB 效应物。总之,我们的研究将 LINC00473 确定为应激弹性的女性特异性驱动因素,而在女性抑郁症中这种驱动因素是异常的。

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