College of Pharmacy, Guangxi Medical University Nanning 530021, P.R. China.
Biochemistry Center, University of South China Hengyang 421001, P.R. China.
Am J Transl Res. 2015 Feb 15;7(2):285-97. eCollection 2015.
This study aims to investigate the role of activator protein 1 (AP-1) in the effects of 27nt-miRNA on expression of endothelial nitric oxide synthase (eNOS) gene and proliferation of endothelial cells. Cell proliferation was analyzed by cell number counting, colony formation assay and MTT assay. Cell migration and invasion was detected by transwell assay and invasion assay. Expression of eNOS and AP-1 was measured by real-time RT-PCR (mRNA level) and Western blotting (protein level). Luciferase reporter assay was performed to detect the binding of 27nt-miRNA to AP-1. Overexpression of 27nt-miRNA significantly inhibited endothelial cells proliferation, invasion and migration in vitro. And, eNOS and AP-1 expression at mRNA and protein levels were down-regulated by overexpression of 27nt-miRNA. Interestingly, overexpression of AP-1 protein partially restored eNOS expression and endothelial cell proliferation. Furthermore, the luciferase reporter assay demonstrated that AP-1 was a direct target of 27nt-miRNA. These data demonstrate that overexpression of 27nt-miRNA inhibits endothelial cell proliferation, invasion, migration, eNOS expression and AP-1 expression. Moreover, AP-1, a direct target of 27nt-miRNA, reverses the inhibitory effects of 27nt-miRNA. Thus, the effects of 27nt-miRNA might be acted through targeting AP-1.
本研究旨在探讨激活蛋白 1(AP-1)在 27nt-miRNA 对内皮型一氧化氮合酶(eNOS)基因表达和内皮细胞增殖的影响中的作用。通过细胞计数、集落形成实验和 MTT 实验分析细胞增殖。通过 Transwell 实验和侵袭实验检测细胞迁移和侵袭。通过实时 RT-PCR(mRNA 水平)和 Western blot(蛋白水平)检测 eNOS 和 AP-1 的表达。通过荧光素酶报告实验检测 27nt-miRNA 与 AP-1 的结合。过表达 27nt-miRNA 显著抑制内皮细胞的体外增殖、侵袭和迁移。并且,过表达 27nt-miRNA 下调 eNOS 和 AP-1 的 mRNA 和蛋白水平表达。有趣的是,AP-1 蛋白的过表达部分恢复了 eNOS 的表达和内皮细胞的增殖。此外,荧光素酶报告实验表明 AP-1 是 27nt-miRNA 的直接靶标。这些数据表明,过表达 27nt-miRNA 抑制内皮细胞增殖、侵袭、迁移、eNOS 表达和 AP-1 表达。此外,AP-1 是 27nt-miRNA 的直接靶标,可逆转 27nt-miRNA 的抑制作用。因此,27nt-miRNA 的作用可能是通过靶向 AP-1 发挥的。