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微小RNA-122通过靶向人肝星状细胞中的PKR激活剂PACT抑制炎性细胞因子的产生。

MicroRNA-122 Inhibits the Production of Inflammatory Cytokines by Targeting the PKR Activator PACT in Human Hepatic Stellate Cells.

作者信息

Nakamura Masato, Kanda Tatsuo, Sasaki Reina, Haga Yuki, Jiang Xia, Wu Shuang, Nakamoto Shingo, Yokosuka Osamu

机构信息

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.

出版信息

PLoS One. 2015 Dec 4;10(12):e0144295. doi: 10.1371/journal.pone.0144295. eCollection 2015.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6704/4670168/34ed09e1bae4/pone.0144295.g001.jpg

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