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对重度抑郁症的大规模转录组分析揭示了兴奋性神经元中突触通路的趋同失调。

Large-scale transcriptomic analyses of major depressive disorder reveal convergent dysregulation of synaptic pathways in excitatory neurons.

作者信息

Goes Fernando S, Collado-Torres Leonardo, Zandi Peter P, Huuki-Myers Louise, Tao Ran, Jaffe Andrew E, Pertea Geo, Shin Joo Heon, Weinberger Daniel R, Kleinman Joel E, Hyde Thomas M

机构信息

Department of Psychiatry and Behavioral Sciences, Stanley and Elizabeth Star Precision Medicine Center of Excellence in Mood Disorders, Johns Hopkins School of Medicine, Baltimore, MD, USA.

Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

出版信息

Nat Commun. 2025 Apr 28;16(1):3981. doi: 10.1038/s41467-025-59115-4.

Abstract

Major Depressive Disorder (MDD) is a common, complex disorder that is a leading cause of disability worldwide and a significant risk factor for suicide. In this study, we have performed the largest molecular analysis of MDD in postmortem human brains (846 samples across 458 individuals) in the subgenual Anterior Cingulate Cortex (sACC) and the Amygdala, two regions central to mood regulation and the pathophysiology of MDD. We found extensive expression differences, particularly at the level of specific transcripts, with prominent enrichment for genes associated with the vesicular functioning, the postsynaptic density, GTPase signaling, and gene splicing. We find associated transcriptional features in 107 of 243 genome-wide significant loci for MDD and, through integrative analyses, highlight convergence of genetic risk, gene expression, and network-based analyses on dysregulated glutamatergic signaling and synaptic vesicular functioning. Together, these results provide an initial mechanistic understanding of MDD and highlight potential targets for novel drug discovery.

摘要

重度抑郁症(MDD)是一种常见的复杂疾病,是全球致残的主要原因,也是自杀的重要风险因素。在本研究中,我们对死后人类大脑中(458名个体的846个样本)膝下前扣带回皮质(sACC)和杏仁核这两个对情绪调节和MDD病理生理学至关重要的区域进行了最大规模的MDD分子分析。我们发现了广泛的表达差异,特别是在特定转录本水平,与囊泡功能、突触后密度、GTP酶信号传导和基因剪接相关的基因显著富集。我们在243个全基因组显著的MDD位点中的107个中发现了相关的转录特征,并通过综合分析,突出了遗传风险、基因表达和基于网络的分析在谷氨酸能信号传导失调和突触囊泡功能方面的趋同。总之,这些结果为MDD提供了初步的机制理解,并突出了新型药物发现的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/241f/12037741/fbb8d2bc5595/41467_2025_59115_Fig1_HTML.jpg

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