MicroRNA-98 reduces amyloid [beta]-protein production and improves oxidative stress and mitochondrial dysfunction through the Notch signaling pathway via HEY2 in Alzheimer's disease mice

• Published in: International journal of molecular medicine 2019-01, Vol.43 (1), p.91
• Main Authors: Chen, Fang-Zhou, Zhao, Ying, Chen, Hui-Zhao
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Amyloid beta-protein; Cellular signal transduction; MicroRNA; Mitochondrial diseases; Oxidative stress
• ISSN: 1107-3756
• DOI: 10.3892/ijmm.2018.3957

Alzheimer's disease (AD) is a chronic neurodegenerative disease that often occurs at a slow pace yet deteriorates with time. MicroRNAs (miRs) have been demonstrated to offer novel therapeutic hope for disease treatment. The aim of the present study was to investigate the effect of miR-98 on amyloid [beta] (A[beta])-protein production, oxidative stress and mitochondrial dysfunction through the Notch signaling pathway by targeting hairy and enhancer of split (Hes)-related with YRPW motif protein 2 (HEY2) in mice with AD. A total of 70 Kunming mice were obtained and subjected to behavioral assessment. The levels of oxidative stress-related proteins glutathione peroxidase, reduced glutathione, superoxide dismutase, malondialdehyde, acetylcholinesterase and [Na.sup.+]-[K.sup.+]-ATP were measured. Morphological changes in brain tissue, HEY2-positivity levels, neuronal apoptotic index (AI) and neuron mitochondrial DNA (mtDNA) levels were also determined. Subsequently, the levels of miR-98 and the mRNA and protein levels of HEY2, Jagged1, Notchl, Hesl, Hes5, [beta]-amyloid precursor protein, B-cell lymphoma 2 (Bcl-2) and Bcl-2-associated X protein in tissues and hippocampal neurons were determined by reverse transcription-quantitative polymerase chain reaction and western blot analyses, respectively. Finally, hippocampal neuron viability and apoptosis were determined using an MTT assay and flow cytometry, respectively. The levels of miR-98-targeted HEY2 and miR-98 were low and the levels of HEY2 were high in the AD mice. The AD mice exhibited poorer learning and memory abilities, oxidative stress function, and morphological changes of pyramidal cells in the hippocampal CA1 region. Furthermore, the AD mice exhibited increased protein levels of HEY2 and AI in the CA1 region of brain tissues with reduced mtDNA levels and dysfunctional neuronal mitochondria. miR-98 suppressed hippocampal neuron apoptosis and promoted hippocampal neuron viability by inactivating the Notch signaling pathway via the inhibition of HEY2. In conclusion, the results demonstrated that miR-98 reduced the production of A[beta] and improved oxidative stress and mitochondrial dysfunction through activation of the Notch signaling pathway by binding to HEY2 in AD mice.