结合单细胞RNA测序和孟德尔随机化探索帕金森病的新药物靶点。

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-06-01 Epub Date: 2025-01-31 DOI:10.1007/s12035-025-04700-3
Xiaolong Wu, Kailiang Wang, Qinghua Li, Yuqing Zhang, Penghu Wei, Yongzhi Shan, Guoguang Zhao
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引用次数: 0

摘要

神经炎症是帕金森病的一个关键病理因素,而T细胞在神经炎症的进展中起着核心作用。然而,T细胞相关基因与PD风险的因果关系尚不清楚。我们研究了PD患者和健康对照组外周血T细胞的单细胞RNA测序(scRNA-Seq)数据集,并筛选了细胞毒性CD4 + T细胞相对于其他T细胞亚群的差异表达基因(DEGs)。对细胞毒性CD4 + T细胞进行假时间序列分析、细胞间通讯分析和代谢途径分析。通过GO和KEGG途径富集分析,对deg进行了功能注释。MR方法用于确定DEGs(暴露)对PD风险(结局)的因果关系,并探索新的PD药物靶点。通过Steiger滤波、双向MR、贝叶斯共定位分析和表型扫描进一步验证MR分析的结果,并使用来自独立PD病例对照队列的GWAS数据对结果进行外部验证。最后,通过scRNA-Seq和大量转录组测序数据进一步验证PD患者与健康对照之间的基因表达差异。我们发现IL-32、GNLY、MT2A和ARPC2的表达增加与PD的高风险显著相关。相反,ARRB2的增加与PD风险的降低密切相关。IL32、GNLY、MT2A、ARRB2和ARPC2是PD的致病基因和潜在的药物靶点。细胞毒性CD4 + T细胞可能是pd相关神经炎症的关键效应因子。这些发现为PD的发病机制和治疗方案提供了新的见解,基于这五个潜在的药物靶点和神经炎症的进一步研究和临床试验是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combining Single-Cell RNA Sequencing and Mendelian Randomization to Explore Novel Drug Targets for Parkinson's Disease.

Neuroinflammation is a key pathological factor of PD, and T cells play a central role in neuroinflammatory progression. However, the causal effect of T cell-related genes on the risk of PD is still unclear. We explored single-cell RNA sequencing (scRNA-Seq) datasets of the peripheral blood T cells of PD patients and healthy controls, and screened the differentially expressed genes (DEGs) in the cytotoxic CD4 + T cells relative to the other T cell subsets. Pseudo-time series analysis, cell-cell communication analysis, and metabolic pathway analysis was performed for the cytotoxic CD4 + T cells. The DEGs were also functionally annotated through GO and KEGG pathway enrichment analyses. The MR approach was used to establish causal effects of the DEGs (exposure) on PD risk (outcome), and explore new drug targets for PD. The findings of MR analysis were further validated by Steiger filtering, bidirectional MR, Bayesian colocalization analysis, and phenotype scanning, and the GWAS data from an independent PD case-control cohort was used for external validation of the results. Finally, differences in gene expression between PD patients and healthy controls were further validated in scRNA-Seq and bulk transcriptome sequencing data. We found that increased expression of IL-32, GNLY, MT2A, and ARPC2 was significantly associated with a higher risk of PD. In contrast, the increase in ARRB2 was closely related to a lower risk of PD. IL32, GNLY, MT2A, ARRB2, and ARPC2 are the causal genes and potential drug targets of PD. Cytotoxic CD4 + T cells are likely the key effectors of PD-related neuroinflammation. These findings provide new insights into the pathogenesis and treatment options for PD, and further research and clinical trials based on the five potential drug targets and neuroinflammation are necessary.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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