Open AccessDown regulation of miR ‐218, miR ‐124, and miR ‐144 relates to Parkinson's disease via activating NF‐κB signaling
Author(s) -
Xing RuiXian,
Li LongGuang,
Liu XueWen,
Tian BuXian,
Cheng Yan
Publication year - 2020
Publication title -
the kaohsiung journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.439
H-Index - 36
eISSN - 2410-8650
pISSN - 1607-551X
DOI - 10.1002/kjm2.12241
Subject(s) - microrna , downregulation and upregulation , pathogenesis , medicine , signal transduction , transfection , proinflammatory cytokine , chromosomal translocation , inflammation , microbiology and biotechnology , cancer research , immunology , biology , cell culture , gene , genetics
Abstract Parkinson's disease (PD) is a neurological degenerative disorder that is partially induced by inflammation in the neural system. To explore the roles of disordered microRNAs in the development of PD, we screened 10 miRNAs in the brain samples of 15 postmortem PD patients and 10 postmortem healthy controls by qRT‐PCR. The direct targets of miRNAs were predicted by informatics tools and further confirmed by dual luciferase assay and immunoblotting. The function of miRNAs in regulating NF‐κB/p65 translocation was examined by immunoblotting, and the overactivation of NF‐κB signaling was examined by ELISA. The relationship between dysregulated miRNAs and cytokines was analyzed by correlation analysis. Three miRNAs were found to be reduced in the brains of patients with PD. KPNB1, KPNA3, and KPNA4 were identified as direct targets of miR‐218, miR‐124, and miR‐144. Additionally, KPNA3 was identified as a direct target of miR‐124, and KPNA4 was a direct target of both miR‐124 and miR‐218. The p65 translocation from the cytoplasm to the nucleus was repressed by miR‐124, miR‐218, and miR‐144 in the SH‐SY5Y cells. The NF‐κB signaling pathway was overactivated after miRNA inhibitor transfection. The upregulation of KPNB1, KPNA3, and KPNA4 in the brain samples of PD patients was confirmed by immunoblotting, and negative correlations were found between dysregulated miRNAs and cytokines. In conclusion, we identified that the downregulation of miR‐218, miR‐124, and miR‐144 in the brain was related to PD via activation of NF‐κB signaling, helping to unveil the role played by dysregulated miRNAs in the pathogenesis of PD and provide new potential targets for PD treatment.