SNHG14 Elevates NFAT5 Expression Through Sequestering miR-375-3p to Promote MPP + -Induced Neuronal Apoptosis, Inflammation, and Oxidative Stress in Parkinson’s Disease

• Published in: Neurochemical research 2024-05, Vol.49 (5), p.1212-1225
• Main Authors: Xu, Furong, Bian, Na, Li, Xuewen
• Format: Article
• Language: English
• Subjects: 1-Methyl-4-phenylpyridinium; Animals; Apoptosis; Apoptosis - drug effects; Apoptosis - genetics; Assaying; Biochemistry; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cell Line, Tumor; Cholecystokinin; Damage; Dopamine receptors; Dopaminergic Neurons - metabolism; Enzyme-linked immunosorbent assay; Flow cytometry; Gene expression; Immunoprecipitation; In vivo methods and tests; Inflammation; Inflammation - chemically induced; Inflammation - genetics; Inflammation - metabolism; Mice; MicroRNAs - genetics; MicroRNAs - metabolism; Movement disorders; MPTP; Neurochemistry; Neurodegenerative diseases; Neurology; Neurons; Neurosciences; Nucleoli; Original Paper; Oxidative Stress; Parkinson Disease - genetics; Parkinson Disease - metabolism; Parkinson's disease; Pathogenesis; Ribonucleic acid; RNA; RNA, Long Noncoding - genetics; RNA, Long Noncoding - metabolism; Sequestering; snoRNA; Superoxide dismutase; Transcription Factors - genetics; Transcription Factors - metabolism
• ISSN: 0364-3190; 1573-6903; 1573-6903
• DOI: 10.1007/s11064-024-04106-y

Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the loss of dopaminergic neurons. LncRNA small nucleolar RNA host gene 14 (SNHG14) was found to promote neuron injury in PD. Here, we investigated the mechanisms of SNHG14 in PD process. In vivo or in vitro PD model was established by using 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced mice or 1-methyl-4-phenylpyridinium (MPP +)-stimulated SK-N-SH cells. The expression of genes and proteins was measured by qRT-PCR and Western blot. In vitro assays were conducted using ELISA, CCK-8, colony formation, EdU, flow cytometry, and Western blot assays, respectively. The oxidative stress was evaluated by determining the production of superoxide dismutase (SOD) and malondialdehyde (MDA). The direct interactions between miR-375-3p and NFAT5 (Nuclear factor of activated T-cells 5) or SNHG14 was verified using dual-luciferase reporter and RNA immunoprecipitation (RIP) assays. SNHG14 and NFAT5 were elevated, while miR-375-3p was decreased in MPTP-mediated PD mouse model and MPP + -induced SK-N-SH cells. Knockdown of SNHG14 or NFAT5, or overexpression of miR-375-3p reversed MPP + -induced neuronal apoptosis, inflammation, and oxidative stress. Mechanistically, SNHG14 directly bound to miR-375, which targeted NFAT5. Inhibition of miR-375-3p abolished the inhibitory activity of SNHG14 knockdown on MPP + -evoked neuronal damage. Besides that, NFAT5 up-regulation counteracted the effects of miR-375-3p on MPP + -mediated neuronal damage. SNHG14 contributed to MPP + -induced neuronal injury by miR-375/NFAT5 axis, suggesting a new insight into the pathogenesis of PD. Graphical Abstract MPP + elevated SNHG14, which then increased NFAT5 by sequestering miR-375, thereby contributing to MPP + -induced inflammation, apoptosis, oxidative stress, and arrest of proliferation in neurons.