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.
J Alzheimers Dis. 2024;98(4):1329-1348. doi: 10.3233/JAD-231281.
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.
This study aims to elucidate the role of miRNA PC-5P-12969 in the pathogenesis of AD.
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.
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.
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.
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。
本研究旨在阐明 miRNA PC-5P-12969 在 AD 发病机制中的作用。
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。
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。
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。