下调和上调
肝星状细胞
环状RNA
肝纤维化
小RNA
细胞生物学
细胞凋亡
肝细胞
癌症研究
化学
长非编码RNA
纤维化
核糖核酸
竞争性内源性RNA
生物
病理
生物化学
基因
内分泌学
医学
体外
作者
Hongwu Meng,Lingfeng Jiang,Peng-cheng Jia,Ruowen Niu,Fang‐tian Bu,Yan Zhu,Xue‐Yin Pan,Juanjuan Li,Jinyu Liu,Yilong Zhang,Cheng Huang,Xiongwen Lv,Jun Li
标识
DOI:10.1016/j.bcp.2023.115451
摘要
Circular RNAs (circRNAs) are a newly identified form of non-coding RNA that play a crucial role in various pathological processes. However, the expression profile and function of circRNAs in hepatic fibrosis (HF) remain largely unknown. In this study, we showed that a novel circRNA ASPH (circASPH) mediates HF by targeting the miR-139-5p/Notch1 axis. We investigated the expression profile of circRNAs in hepatocyte exosomes of mice with HF using circRNA-sequencing and found significant upregulation of circASPH. Loss- and gain-of-function analysis of circASPH was performed to assess its role in HF. Furthermore, we performed luciferase reporter assay, RNA pull-down, and fluorescence in situ hybridization analyses and confirmed that circASPH directly binds to miR-139-5p. We also found that circASPH was upregulated in liver fibrogenesis. Downregulation of circASPH expression inhibited hepatic stellate cell (HSC) activation and proliferation, induced apoptosis, and attenuated mouse liver fibrogenic injury. Mechanistically, circASPH directly targeted miR-139-5p to regulate the expression of Notch1 in HF. Thus, downregulation of circASPH may suppress the activation of HSCs and HF through the circASPH/miR-139-5p/Notch1 axis. Our findings indicated that circASPH may be a potential biomarker for HF diagnosis and therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI