Nakamura Masato, Kanda Tatsuo, Sasaki Reina, Haga Yuki, Jiang Xia, Wu Shuang, Nakamoto Shingo, Yokosuka Osamu
Department of Gastroenterology and Nephrology, Chiba University, Graduate School of Medicine, Chiba, 260-8677, Japan.
Department of Molecular Virology, Chiba University, Graduate School of Medicine, Chiba, 260-8677, Japan.
PLoS One. 2015 Dec 4;10(12):e0144295. doi: 10.1371/journal.pone.0144295. eCollection 2015.
MicroRNA-122 (miR-122) is one of the most abundant miRs in the liver. Previous studies have demonstrated that miR-122 plays a role in inflammation in the liver and functions in hepatic stellate cells (HSCs), which reside in the space of Disse. Here, we showed that the transient inhibition of PKR-activating protein (PACT) expression, by miR-122 or siRNA targeting of PACT, suppressed the production of proinflammatory cytokines, such as interleukin (IL)-6, monocyte chemoattractant protein-1 (MCP-1) and IL-1β, in human HSC LX-2. Sequence and functional analyses confirmed that miR-122 directly targeted the 3'-untranslated region of PACT. Immunofluorescence analysis revealed that miR-122 blocked NF-κB-nuclear translocation in LX-2 cells. We also showed that conditioned medium from miR-122-transfected LX-2 cells suppressed human monocyte-derived THP-1 cell migration. Taken together, our study indicates that miR-122 may downregulate cytokine production in HSCs and macrophage chemotaxis and that the targeting of miR-122 may have therapeutic potential for preventing the progression of liver diseases.
微小RNA-122(miR-122)是肝脏中含量最丰富的微小RNA之一。先前的研究表明,miR-122在肝脏炎症中发挥作用,并在位于狄氏间隙的肝星状细胞(HSC)中起作用。在此,我们发现,通过miR-122或靶向PACT的小干扰RNA(siRNA)瞬时抑制PKR激活蛋白(PACT)的表达,可抑制人HSC LX-2中促炎细胞因子的产生,如白细胞介素(IL)-6、单核细胞趋化蛋白-1(MCP-1)和IL-1β。序列和功能分析证实,miR-122直接靶向PACT的3'-非翻译区。免疫荧光分析显示,miR-122可阻断LX-2细胞中NF-κB的核转位。我们还发现,来自miR-122转染的LX-2细胞的条件培养基可抑制人单核细胞来源的THP-1细胞迁移。综上所述,我们的研究表明,miR-122可能下调HSC中的细胞因子产生和巨噬细胞趋化性,并且靶向miR-122可能具有预防肝脏疾病进展的治疗潜力。