Long noncoding RNA SRY-box transcription factor 2 overlapping transcript participates in Parkinson's disease by regulating the microRNA-942-5p/nuclear apoptosis-inducing factor 1 axis

被引:21
作者
Guo, Yabi [1 ]
Liu, Yanyang [1 ]
Wang, Hong [1 ]
Liu, Peijun [1 ]
机构
[1] Hubei Univ Arts & Sci, Affiliated Hosp, Rehabil Med Ctr, Xiangyang Cent Hosp, 136 Jingzhou St, Xiangyang 441000, Peoples R China
关键词
LncRNA SOX2-OT; miRNA-942-5p; NAIF1; parkinson's disease; MPP+; SH-SY5Y cells; GASTRIC-CANCER; EXPRESSION; MODEL; MICRORNAS; GENES; BRAIN;
D O I
10.1080/21655979.2021.1987126
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Parkinson's disease (PD) is a neurodegenerative disorder. Studies have shown that long noncoding RNA SRY-box transcription factor 2 overlapping transcript (lncRNA SOX2-OT) is highly expressed in PD patients, but its specific functions and mechanisms require further research. To address this gap, this study utilized an in vitro PD cell model induced by 1-methyl-4-phenylpyridinium (MPP+). Cell viability, apoptosis, lactate dehydrogenase (LDH) activity, inflammatory factor secretion, and oxidative stress indicators were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-dipheyltetrazolium bromide assay, LDH assay, flow cytometry, enzyme linked immunosorbent assay (ELISA), and corresponding kits, respectively. Gene and protein expression were measured using quantitative real-time-PCR and western blotting, respectively. The results indicated that microRNA-942-5p (miR-942-5p) was a direct target of lncRNA SOX2-OT and nuclear apoptosis-inducing factor 1 (NAIF1) was a direct target of miR-942-5p. The expression levels of lncRNA SOX2-OT and NAIF1 were increased, and miR-942-5p expression was decreased in SH-SY5Y cells following MPP+ treatment. In addition, MPP+ treatment reduced SH-SY5Y cell viability, increased apoptosis; increased cleaved caspase-3 protein expression and cleaved caspase-3/caspase-3 ratio; enhanced lactate dehydrogenase viability; increased tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, and reactive oxygen species, and decreased superoxide dismutase activity in SH-SY5Y cells were inhibited by SOX2-OT-siRNA, and these inhibitions were reversed by miR-942-5p inhibitor. Moreover, the protective role of miR-942-5p mimic in MPP+-induced SH-SY5Y cells was eliminated by the NAIF1 plasmid. Overall, lncRNA SOX2-OT-mediated regulation of oxidative stress, inflammation, and neuronal apoptosis were directly controlled by the miR-942-5p/NAIF1 signal axis in MPP+-induced SH-SY5Y cells.
引用
收藏
页码:8570 / 8582
页数:13
相关论文
共 41 条
[21]   Molecular pathophysiology of Parkinson's disease [J].
Moore, DJ ;
West, AB ;
Dawson, VL ;
Dawson, TM .
ANNUAL REVIEW OF NEUROSCIENCE, 2005, 28 :57-87
[22]   Long noncoding RNAs in development and disease of the central nervous system [J].
Ng, Shi-Yan ;
Lin, Lin ;
Soh, Boon Seng ;
Stanton, Lawrence W. .
TRENDS IN GENETICS, 2013, 29 (08) :461-468
[23]   Integrated Analysis of microRNA and mRNA Expression Profiles: An Attempt to Disentangle the Complex Interaction Network in Attention Deficit Hyperactivity Disorder [J].
Nuzziello, Nicoletta ;
Craig, Francesco ;
Simone, Marta ;
Consiglio, Arianna ;
Licciulli, Flavio ;
Margari, Lucia ;
Grillo, Giorgio ;
Liuni, Sabino ;
Liguori, Maria .
BRAIN SCIENCES, 2019, 9 (10)
[24]   Status of antioxidant defense system and expression of toxicant responsive genes in striatum of maneb- and paraquat-induced Parkinson's disease phenotype in mouse: Mechanism of neurodegeneration [J].
Patel, S ;
Singh, V ;
Kumar, A ;
Gupta, YK ;
Singh, MP .
BRAIN RESEARCH, 2006, 1081 :9-18
[25]   Quantification of apoptosis and necroptosis at the single cell level by a combination of Imaging Flow Cytometry with classical Annexin V/propidium iodide staining [J].
Pietkiewicz, Sabine ;
Schmidt, Joern H. ;
Lavrik, Inna N. .
JOURNAL OF IMMUNOLOGICAL METHODS, 2015, 423 :99-103
[26]   Long non-coding RNA SOX2OT: expression signature, splicing patterns, and emerging roles in pluripotency and tumorigenesis [J].
Shahryari, Alireza ;
Jazi, Marie Saghaeian ;
Samaei, Nader M. ;
Mowla, Seyed J. .
FRONTIERS IN GENETICS, 2015, 6
[27]  
Shahryari AR., 2013, CELL J, V15, P77
[28]   The brain as a target for inflammatory processes and neuroprotective strategies [J].
Skaper, Stephen D. .
NEUROPROTECTIVE AGENTS: EIGHTH INTERNATIONAL NEUROPROTECTION SOCIETY MEETING, 2007, 1122 :23-34
[29]   Long Non-Coding RNA and Alternative Splicing Modulations in Parkinson's Leukocytes Identified by RNA Sequencing [J].
Soreq, Lilach ;
Guffanti, Alessandro ;
Salomonis, Nathan ;
Simchovitz, Alon ;
Israel, Zvi ;
Bergman, Hagai ;
Soreq, Hermona .
PLOS COMPUTATIONAL BIOLOGY, 2014, 10 (03)
[30]   Small RNA sequencing-microarray analyses in Parkinson leukocytes reveal deep brain stimulation-induced splicing changes that classify brain region transcriptornes [J].
Soreq, Lilach ;
Salomonis, Nathan ;
Bronstein, Michal ;
Greenberg, David S. ;
Israel, Zvi ;
Bergman, Hagai ;
Soreq, Hermona .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2013, 6