Journal of Hebei University(Natural Science Edition) ›› 2023, Vol. 43 ›› Issue (2): 179-187.DOI: 10.3969/j.issn.1000-1565.2023.02.010

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miR-194-5p inhibits activation of human hepatic stellate cells through Wnt5a

LI Yaqi1, ZHANG Ronghua1, LIU Yutan1, CAO Yumeng1, XIONG Yanan1, ZHANG Guangling2   

  1. 1.Hebei Key Laboratory for Chronic Diseases, School of Basic Medicine, North China University of Science and Technology, Tangshan 063200, China; 2. Hebei Provincial Key Laboratory of Medical-Industrial Integration Precision Medicine, School of Clinical Medicine, North China University of Science and Technology, Tangshan 063200, China
  • Received:2022-06-07 Online:2023-03-25 Published:2023-04-06

Abstract: To investigate the effects and mechanism of miR-194-5p on the activation of hepatic stellate cells(HSCs), CCK-8, β-galactosidase staining, Transwell, wound healing, colony formation assays, RT-qPCR and Western blot were used to detect the effects of miR-194-5p on the cell biological properties, the expression of HSC activation markers and target gene, respectively. The candidate target genes of miR-194-5p were confirmed by the bioinformatics website and dual luciferase reporter assay. The results showed that the proliferation, cell colony formation, migration ability and HSC activation markers expression of LX-2 cells were inhibited by miR-194-5p; the senescence was promoted by miR-194-5p; and- DOI:10.3969/j.issn.1000-1565.2023.02.010miR-194-5p通过Wnt5a抑制肝星状细胞活化李亚琦1,张荣花1,刘雨潭1,曹雨萌1,熊亚南1,章广玲2(1.华北理工大学 基础医学院, 河北省慢性疾病重点实验室, 河北 唐山 063200;2.华北理工大学 临床医学院,河北省医工融合精准医疗重点实验室, 河北 唐山 063200)摘 要:为研究miR-194-5p对肝星状细胞(HSCs)活化的影响及作用机制,采用CCK-8、β-半乳糖苷酶染色、Transwell、划痕、集落形成实验和RT-qPCR、Western blot分别检测miR-194-5p 对LX-2细胞生物学特性、细胞活化标志物和靶基因表达的影响,并用生物信息学和双荧光素酶报告实验确定miR-194-5p靶基因. 结果显示:miR-194-5p抑制LX-2细胞增殖、细胞集落形成、迁移能力以及LX-2细胞中活化标志物的表达,促进LX-2细胞衰老;Wnt5a为miR-194-5p的直接靶基因.研究表明miR-194-5p通过靶定Wnt5a抑制LX-2细胞活化,miR-194-5p和Wnt5a可能是治疗肝纤维化新的靶点.关键词:miR-194-5p;肝纤维化;肝星状细胞活化;增殖;迁移中图分类号:R575.2 文献标志码:A 文章编号:1000-1565(2023)02-0179-09miR-194-5p inhibits activation of human hepatic stellate cells through Wnt5aLI Yaqi1, ZHANG Ronghua1, LIU Yutan1, CAO Yumeng1, XIONG Yanan1, ZHANG Guangling2(1.Hebei Key Laboratory for Chronic Diseases, School of Basic Medicine, North China University of Science and Technology, Tangshan 063200, China; 2. Hebei Provincial Key Laboratory of Medical-Industrial Integration Precision Medicine, School of Clinical Medicine, North China University of Science and Technology, Tangshan 063200, China)Abstract: To investigate the effects and mechanism of miR-194-5p on the activation of hepatic stellate cells(HSCs), CCK-8, β-galactosidase staining, Transwell, wound healing, colony formation assays, RT-qPCR and Western blot were used to detect the effects of miR-194-5p on the cell biological properties, the expression of HSC activation markers and target gene, respectively. The candidate target genes of miR-194-5p were confirmed by the bioinformatics website and dual luciferase reporter assay. The results showed that the proliferation, cell colony formation, migration ability and HSC activation markers expression of LX-2 cells were inhibited by miR-194-5p; the senescence was promoted by miR-194-5p; and- 收稿日期:2022-06-07 基金项目:河北省自然科学基金资助项目(H2021209026);河北省人力资源和社会保障厅项目(C20210340);2020年政府资助临床医学优秀人才培养项目(冀财预付[2020]397号) 第一作者:李亚琦(1997—),女,河北邯郸人,华北理工大学在读硕士研究生,主要从事肝纤维化分子机制方向研究. E-mail:871528007@qq.com 通信作者:熊亚南(1978—),女,河北唐山人,华北理工大学副教授,主要从事肝纤维化分子机制方向研究.E-mail:xiongyanan@ncst.edu.cn章广玲(1972—),女,河北唐山人,华北理工大学教授,博士,主要从事肝纤维化分子机制方向研究.E-mail:zhanggl@ncst.edu.cn第2期李亚琦等:miR-194-5p通过Wnt5a抑制肝星状细胞活化河北大学学报(自然科学版) 第43卷Wnt5a was a target gene of miR-194-5p. Our findings provide evidence that miR-194-5p inhibits LX-2 cell activation by targeting Wnt5a. Therefore, miR-194-5p and Wnt5a may be possible novel therapeutic targets for hepatic fibrosis.

Key words: miR-194-5p, hepatic fibrosis, hepatic stellate cell activation, proliferation, migration

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