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偏头痛患者外周血单个核细胞中与疾病和头痛相关的 microRNA 特征及其预测的 mRNA 靶标:炎症信号和氧化应激的作用。

Disease- and headache-specific microRNA signatures and their predicted mRNA targets in peripheral blood mononuclear cells in migraineurs: role of inflammatory signalling and oxidative stress.

机构信息

Department of Pharmacology and Pharmacotherapy, Medical School & Szentágothai Research Centre, Molecular Pharmacology Research Group, Centre for Neuroscience, University of Pécs, Pécs, Hungary.

Cardiometabolic and MTA-SE System Pharmacology Research Group, Department of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.

出版信息

J Headache Pain. 2022 Sep 2;23(1):113. doi: 10.1186/s10194-022-01478-w.

Abstract

BACKGROUND

Migraine is a primary headache with genetic susceptibility, but the pathophysiological mechanisms are poorly understood, and it remains an unmet medical need. Earlier we demonstrated significant differences in the transcriptome of migraineurs' PBMCs (peripheral blood mononuclear cells), suggesting the role of neuroinflammation and mitochondrial dysfunctions. Post-transcriptional gene expression is regulated by miRNA (microRNA), a group of short non-coding RNAs that are emerging biomarkers, drug targets, or drugs. MiRNAs are emerging biomarkers and therapeutics; however, little is known about the miRNA transcriptome in migraine, and a systematic comparative analysis has not been performed so far in migraine patients.

METHODS

We determined miRNA expression of migraineurs' PBMC during (ictal) and between (interictal) headaches compared to age- and sex-matched healthy volunteers. Small RNA sequencing was performed from the PBMC, and mRNA targets of miRNAs were predicted using a network theoretical approach by miRNAtarget.com™. Predicted miRNA targets were investigated by Gene Ontology enrichment analysis and validated by comparing network metrics to differentially expressed mRNA data.

RESULTS

In the interictal PBMC samples 31 miRNAs were differentially expressed (DE) in comparison to healthy controls, including hsa-miR-5189-3p, hsa-miR-96-5p, hsa-miR-3613-5p, hsa-miR-99a-3p, hsa-miR-542-3p. During headache attacks, the top DE miRNAs as compared to the self-control samples in the interictal phase were hsa-miR-3202, hsa-miR-7855-5p, hsa-miR-6770-3p, hsa-miR-1538, and hsa-miR-409-5p. MiRNA-mRNA target prediction and pathway analysis indicated several mRNAs related to immune and inflammatory responses (toll-like receptor and cytokine receptor signalling), neuroinflammation and oxidative stress, also confirmed by mRNA transcriptomics.

CONCLUSIONS

We provide here the first evidence for disease- and headache-specific miRNA signatures in the PBMC of migraineurs, which might help to identify novel targets for both prophylaxis and attack therapy.

摘要

背景

偏头痛是一种具有遗传易感性的原发性头痛,但病理生理机制尚不清楚,这仍然是未满足的医学需求。我们之前的研究表明,偏头痛患者的 PBMC(外周血单核细胞)转录组存在显著差异,提示神经炎症和线粒体功能障碍的作用。基因的转录后表达受 miRNA(microRNA)调控,miRNA 是一组短的非编码 RNA,它们是新兴的生物标志物、药物靶点或药物。miRNA 是新兴的生物标志物和治疗药物;然而,目前对于偏头痛患者的 miRNA 转录组知之甚少,迄今为止尚未进行系统的比较分析。

方法

我们比较了偏头痛患者在头痛发作期间(发作期)和头痛发作之间(发作间期)的 PBMC 中的 miRNA 表达,与年龄和性别匹配的健康志愿者进行比较。从 PBMC 中进行了小 RNA 测序,并使用 miRNAtarget.com™通过网络理论方法预测了 miRNA 的 mRNA 靶标。通过基因本体论富集分析研究了预测的 miRNA 靶标,并通过将网络指标与差异表达的 mRNA 数据进行比较来验证。

结果

在发作间期 PBMC 样本中,与健康对照组相比,有 31 个 miRNA 表达差异(DE),包括 hsa-miR-5189-3p、hsa-miR-96-5p、hsa-miR-3613-5p、hsa-miR-99a-3p、hsa-miR-542-3p。与发作间期的自我对照样本相比,在头痛发作期间,DE 最多的 miRNA 是 hsa-miR-3202、hsa-miR-7855-5p、hsa-miR-6770-3p、hsa-miR-1538 和 hsa-miR-409-5p。miRNA-mRNA 靶标预测和通路分析表明,几个与免疫和炎症反应( Toll 样受体和细胞因子受体信号)、神经炎症和氧化应激相关的 mRNAs 存在靶标,这也得到了 mRNA 转录组学的证实。

结论

我们在这里首次提供了偏头痛患者 PBMC 中疾病和头痛特异性 miRNA 特征的证据,这可能有助于为预防和攻击治疗确定新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f593/9438144/6bae040bf877/10194_2022_1478_Fig1_HTML.jpg

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