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揭示新型 miRNA PC-5P-12969 在缓解阿尔茨海默病中的作用。

Unveiling the Role of Novel miRNA PC-5P-12969 in Alleviating Alzheimer's Disease.

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.

Department of Pharmacology and Neuroscience Department, Texas Tech University Health Sciences Center, Lubbock, TX, USA.

出版信息

J Alzheimers Dis. 2024;98(4):1329-1348. doi: 10.3233/JAD-231281.

Abstract

BACKGROUND

The intricate and complex molecular mechanisms that underlie the progression of Alzheimer's disease (AD) have prompted a concerted and vigorous research endeavor aimed at uncovering potential avenues for therapeutic intervention.

OBJECTIVE

This study aims to elucidate the role of miRNA PC-5P-12969 in the pathogenesis of AD.

METHODS

We assessed the differential expression of miRNA PC-5P-12969 in postmortem AD brains, AD animal and cell models using real-time reverse-transcriptase RT-PCR, we also checked the gene and protein expression of GSK3α and APP.

RESULTS

Our investigation revealed a notable upregulation of miRNA PC-5P-12969 in postmortem brains of AD patients, in transgenic mouse models of AD, and in mutant APP overexpressing-HT22 cells. Additionally, our findings indicate that overexpression of miRNA PC-5P-12969 exerts a protective effect on cell survival, while concurrently mitigating apoptotic cell death. Further-more, we established a robust and specific interaction between miRNA PC-5P-12969 and GSK3α. Our luciferase reporter assays provided confirmation of the binding between miRNA PC-5P-12969 and the 3'-UTR of the GSK3α gene. Manipulation of miRNA PC-5P-12969 levels in cellular models of AD yielded noteworthy alterations in the gene and protein expression levels of both GSK3α and APP. Remarkably, the manipulation of miRNA PC-5P-12969 levels yielded significant enhancements in mitochondrial respiration and ATP production, concurrently with a reduction in mitochondrial fragmentation, thus unveiling a potential regulatory role of miRNA PC-5P-12969 in these vital cellular processes.

CONCLUSIONS

In summary, this study sheds light on the crucial role of miRNA PC-5P-12969 and its direct interaction with GSK3α in the context of AD.

摘要

背景

阿尔茨海默病(AD)进展的复杂分子机制促使人们进行了协调一致的大力研究,旨在寻找潜在的治疗干预途径。

目的

本研究旨在阐明 miRNA PC-5P-12969 在 AD 发病机制中的作用。

方法

我们使用实时逆转录 RT-PCR 评估了 miRNA PC-5P-12969 在 AD 患者死后大脑、AD 动物和细胞模型中的差异表达,还检查了 GSK3α 和 APP 的基因和蛋白表达。

结果

我们的研究表明,miRNA PC-5P-12969 在 AD 患者死后大脑、AD 转基因小鼠模型和过表达突变 APP 的 HT22 细胞中显著上调。此外,我们的研究结果表明,miRNA PC-5P-12969 的过表达对细胞存活具有保护作用,同时减轻细胞凋亡。进一步,我们建立了 miRNA PC-5P-12969 与 GSK3α 之间强大而特异的相互作用。我们的荧光素酶报告基因检测证实了 miRNA PC-5P-12969 与 GSK3α 基因 3'UTR 之间的结合。在 AD 细胞模型中操纵 miRNA PC-5P-12969 水平导致 GSK3α 和 APP 的基因和蛋白表达水平发生显著改变。值得注意的是,操纵 miRNA PC-5P-12969 水平可显著增强线粒体呼吸和 ATP 生成,同时减少线粒体碎片化,从而揭示了 miRNA PC-5P-12969 在这些重要细胞过程中的潜在调节作用。

结论

总之,本研究揭示了 miRNA PC-5P-12969 及其与 GSK3α 的直接相互作用在 AD 中的关键作用。

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