Yang Jun-Hui, Zhang Run-Jiao, Lin Jia-Jie, Cao Ming-Chao, Wang Qie, Cui Hui-Xian, Sun Shao-Guang, Wang Lei
Department of Neurology, Hospital of Jingxing County, Hebei, China.
Department of Human Anatomy, Hebei Medical University, Hebei, China.
Cell Physiol Biochem. 2018;50(3):936-951. doi: 10.1159/000494478. Epub 2018 Oct 24.
BACKGROUND/AIMS: The nuclear factor erythroid 2-related factor 2 (Nrf2)-antioxidant response element (ARE) pathway plays a protective role in both acute neuronal damage and chronic neurodegeneration-related oxidative stress. Circular RNAs (circRNAs) are involved with various diseases in the central nervous system (CNS). This study aimed to identify the key circRNAs involved in Nrf2-neuroprotection against oxidative stress.
The differentially expressed circRNAs (DEcircRNAs) in the substantia nigra and corpus striatum between Nrf2 (-/-) and Nrf2 (+/+) mice were identified by microarray analysis. Quantitative real-time polymerase chain reaction (qRT-PCR) was then used to validate the expression of selected DEcircRNAs in the substantia nigra and corpus striatum between Nrf2 (-/-) and Nrf2 (+/+) mice. Based on our previous microarray analysis of the differentially expressed mRNAs (DEmRNAs) in the substantia nigra and corpus striatum between Nrf2 (-/-) and Nrf2 (+/+) mice, the DEcircRNA-miRNA-DEmRNA interaction network was constructed. Functional annotation of DEmRNAs that shared the same binding miRNAs with DEcircRNAs was performed using gene ontology (GO) and pathway analyses.
A total of 65 and 150 significant DEcircRNAs were obtained in the substantia nigra and corpus striatum of Nrf2 (-/-) mice, respectively, and seventeen shared DEcircRNAs were found in both these two tissues. The qRT-PCR results were generally consistent with the microarray results. The DEcircRNA-miRNA-DEmRNA interaction network and pathway analysis indicated that mmu_circRNA_34132, mmu_circRNA_017077 and mmu-circRNA-015216 might be involved with Nrf2-mediated neuroprotection against oxidative stress. Mmu_circRNA_015216 and mmu_circRNA_017077 might play roles in the Nrf2-related transcriptional misregulation and Nrf2-mediated processes of rheumatoid arthritis, respectively. In addition to these two processes, mmu_circRNA_34132 may be a potential regulator of Nrf2-mediated protection for diabetes mellitus and Nrf2-mediated defence against ROS in hearts.
In conclusion, our study identified the key DEcircRNAs in the substantia nigra and corpus striatum of Nrf2 (-/-) mice, which might provide new clues for further exploring the mechanism of Nrf2-mediated neuroprotection against oxidative stress and other Nrf2-mediated processes.
背景/目的:核因子红细胞2相关因子2(Nrf2)-抗氧化反应元件(ARE)通路在急性神经元损伤和慢性神经退行性变相关的氧化应激中均发挥保护作用。环状RNA(circRNA)与中枢神经系统(CNS)的多种疾病有关。本研究旨在鉴定参与Nrf2对氧化应激神经保护作用的关键circRNA。
通过微阵列分析鉴定Nrf2(-/-)和Nrf2(+/+)小鼠黑质和纹状体中差异表达的circRNA(DEcircRNA)。然后使用定量实时聚合酶链反应(qRT-PCR)验证Nrf2(-/-)和Nrf2(+/+)小鼠黑质和纹状体中所选DEcircRNA的表达。基于我们之前对Nrf2(-/-)和Nrf2(+/+)小鼠黑质和纹状体中差异表达的mRNA(DEmRNA)的微阵列分析,构建了DEcircRNA-miRNA-DEmRNA相互作用网络。使用基因本体论(GO)和通路分析对与DEcircRNA共享相同结合miRNA的DEmRNA进行功能注释。
在Nrf2(-/-)小鼠的黑质和纹状体中分别获得了65个和150个显著差异表达的circRNA,并且在这两个组织中发现了17个共享的差异表达circRNA。qRT-PCR结果与微阵列结果总体一致。DEcircRNA-miRNA-DEmRNA相互作用网络和通路分析表明,mmu_circRNA_34132、mmu_circRNA_017077和mmu-circRNA-015216可能参与Nrf2介导的对氧化应激的神经保护作用。Mmu_circRNA_015216和mmu_circRNA_017077可能分别在Nrf2相关的转录失调和类风湿性关节炎的Nrf2介导过程中发挥作用。除了这两个过程外,mmu_circRNA_34132可能是Nrf2介导的糖尿病保护作用和Nrf2介导的心脏抗氧化防御的潜在调节因子。
总之,我们的研究鉴定了Nrf2(-/-)小鼠黑质和纹状体中的关键差异表达circRNA,这可能为进一步探索Nrf2介导的对氧化应激的神经保护作用机制以及其他Nrf2介导的过程提供新线索。