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转录组测序揭示有氧运动后帕金森病样小鼠的环状RNA表达谱。

Transcriptome sequencing reveals circRNA expression profile in Parkinson's disease-like mice after aerobic exercise.

作者信息

Fan Tianlun, Li Xiating, Fu Chuan, Sun Lichun

机构信息

The First Affiliated Hospital of Hainan Medical College, Hainan, China.

出版信息

Turk J Biol. 2022 Mar 21;46(3):227-238. doi: 10.55730/1300-0152.2611. eCollection 2022.

DOI:10.55730/1300-0152.2611
PMID:37529258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10388083/
Abstract

Parkinson's disease (PD) is a common complex neurodegenerative disease, and aerobic exercise (EX) has potential to improve motor dysfunction. This study aimed to explore whether EX acts on PD in mice mode. Mice were administered 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and subjected to a 4-week physical exercise regimen (EX-PD group) and underwent RNA-Seq. Here, MPTP caused PD, which was characterized by neuron shrinkage and behavioral deficits, whereas EX improved PD by rescuing neuronal survival and motor function in mice. Moreover, circRNA expression profiles identified a total of 142 differentially expressed circRNAs (DEcircRNAs) between PD and EX-PD group. These DEcircRNAs were mainly involved in PD, dopaminergic synapses, and calcium signaling pathways. The expression of circZfp827 and circTshz2 were significantly elevated in PD group while reduced owing to EX intervention. In contrast, EX intervention significantly restored decline in circHivep2 expression due to PD. The circRNA-miRNA-mRNA network suggested that circZfp827, circHivep2, and circTshz2 were involved in ceRNA mechanism of EX to improve PD, and their target genes were significantly decreased after interference. The directly binding regulation relationship of circTshz2-mmu-miR-326-3p-Th was verified by double luciferase reporter assay. Our research revealed that EX improved motor behavioral deficits and pathological features of PD mice, and circRNA-based signatures are potential candidates for further assessment as PD biomarkers for improvement by EX.

摘要

帕金森病(PD)是一种常见的复杂性神经退行性疾病,有氧运动(EX)有改善运动功能障碍的潜力。本研究旨在探讨运动是否以小鼠模型作用于帕金森病。给小鼠注射1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)并进行为期4周的体育锻炼方案(运动-帕金森病组),然后进行RNA测序。在此,MPTP导致了帕金森病,其特征为神经元萎缩和行为缺陷,而运动通过挽救小鼠的神经元存活和运动功能改善了帕金森病。此外,环状RNA表达谱鉴定出帕金森病组和运动-帕金森病组之间共有142个差异表达的环状RNA(DEcircRNAs)。这些DEcircRNAs主要参与帕金森病、多巴胺能突触和钙信号通路。环状Zfp827和环状Tshz2的表达在帕金森病组显著升高,而由于运动干预而降低。相反,运动干预显著恢复了因帕金森病导致的环状Hivep2表达下降。环状RNA-微小RNA-信使RNA网络表明,环状Zfp827、环状Hivep2和环状Tshz2参与了运动改善帕金森病的竞争性内源RNA机制,并且它们的靶基因在干扰后显著降低。通过双荧光素酶报告基因测定验证了环状Tshz2-小鼠微小RNA-326-3p-Th的直接结合调控关系。我们的研究表明,运动改善了帕金森病小鼠的运动行为缺陷和病理特征,基于环状RNA的特征是作为运动改善帕金森病生物标志物进行进一步评估的潜在候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3dd/10388083/975924912df7/turkjbiol-46-3-227f6.jpg
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