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特发性帕金森病中的免疫系统与神经炎症:基因变异与微小RNA相互作用的关联分析

Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions.

作者信息

Strafella Claudia, Caputo Valerio, Termine Andrea, Assogna Francesca, Pellicano Clelia, Pontieri Francesco E, Macchiusi Lucia, Minozzi Giulietta, Gambardella Stefano, Centonze Diego, Bossù Paola, Spalletta Gianfranco, Caltagirone Carlo, Giardina Emiliano, Cascella Raffaella

机构信息

Genomic Medicine Laboratory, IRCCS Santa Lucia Foundation, Rome, Italy.

Medical Genetics Laboratory, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.

出版信息

Front Genet. 2021 Jun 3;12:651971. doi: 10.3389/fgene.2021.651971. eCollection 2021.

Abstract

The present study investigated the association of SNPs involved in the regulation of immune response, cellular degenerative and neuroinflammatory pathways with the susceptibility and progression of idiopathic Parkinson's Disease (PD). In particular, 342 PD patients were subjected to a genotyping analysis of a panel of 120 SNPs by Open Array Technology. As control group, 503 samples representative of the European general population were utilized. The genetic analysis identified 26 SNPs associated with PD susceptibility. Of them, 12 SNPs were described as significant expression Quantitative Loci (eQTL) variants in different brain regions associated with motor and non-motor PD phenomenology. Moreover, the study highlighted 11 novel susceptibility genes for PD, which may alter multiple signaling pathways critically involved in peripheral immune response, neuroinflammation, neurodegeneration and dopaminergic neurons wiring. The study of miRNA-target genes highlighted a possible role of miR-499a, miR-196a2, and miR-29a in the modulation of multiple neuroinflammatory and neurodegenerative mechanisms underlying PD physiopathology. The study described a network of interconnected genes (, , , , , , , , , and ), which may act as upstream regulators in the modulation of biological pathways relevant to PD. Intriguingly, stands out as a master gene regulator since it may indirectly regulate the network of interconnected genes. The study highlighted different genes and miRNAs interactions potentially involved in PD physiopathology, which are worth to be further explored to improve the knowledge of disease and the research of novel treatments strategies.

摘要

本研究调查了参与免疫反应、细胞退行性变和神经炎症途径调控的单核苷酸多态性(SNP)与特发性帕金森病(PD)易感性及病情进展之间的关联。具体而言,采用开放式阵列技术对342例PD患者进行了一组120个SNP的基因分型分析。作为对照组,使用了503份代表欧洲普通人群的样本。基因分析确定了26个与PD易感性相关的SNP。其中,12个SNP在与运动和非运动性PD症状相关的不同脑区被描述为显著的表达数量性状位点(eQTL)变异。此外,该研究还发现了11个新的PD易感基因,这些基因可能会改变多个关键参与外周免疫反应、神经炎症、神经退行性变和多巴胺能神经元连接的信号通路。对miRNA靶基因的研究突出了miR-499a、miR-196a2和miR-29a在调节PD病理生理学中多种神经炎症和神经退行性变机制方面可能发挥的作用。该研究描述了一个相互连接的基因网络(,,,,,,,,,和),这些基因可能作为上游调节因子参与调节与PD相关的生物学途径。有趣的是,作为一个主基因调节因子脱颖而出,因为它可能间接调节相互连接的基因网络。该研究突出了不同基因和miRNA之间潜在参与PD病理生理学的相互作用,值得进一步探索以增进对该疾病的了解并开展新治疗策略的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b61/8209518/fa3d5b418638/fgene-12-651971-g001.jpg

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