| 注册
首页|期刊导航|中国药科大学学报|人胰岛素样生长因子-1的体外抗肝纤维化活性

人胰岛素样生长因子-1的体外抗肝纤维化活性

万爱妮 徐栋生 蔡燕飞 陈蕴 金坚 李华钟

中国药科大学学报2017,Vol.48Issue(4):476-482,7.
中国药科大学学报2017,Vol.48Issue(4):476-482,7.DOI:10.11665/j.issn.1000-5048.20170413

人胰岛素样生长因子-1的体外抗肝纤维化活性

Anti-liver fibrosis activities of human insulin-like growth factor-1 in vitro

万爱妮 1徐栋生 2蔡燕飞 2陈蕴 2金坚 2李华钟1

作者信息

  • 1. 江南大学生物工程学院,无锡214122
  • 2. 江南大学药学院,无锡214122
  • 折叠

摘要

Abstract

This study was focus on investigating the anti-liver fibrosis effects of insulin-like growth factor-1 (IGF-1) in vitro.The effects of IGF-1 on human liver L-02 cell viability and cell cycle were observed.CC14-induced L-02 cell injury was set up to detect the anti-apoptotic activity of insulin-like growth factor-1 (IGF-1).Transforming growth factor β1 (TGF-β1) induced hepatic stellate cell line (HSC-T6) were used as a liver fibrosis model in vitro to analyze the effects of IGF-1 on the expression of liver fibrosis proteins and intracellular TGF-β1/Smad signaling pathway in HSC-T6 cells.The results showed that IGF-1 could relieve the growth inhibition effects of TGF-β1 on L-02 cells,increase the viability of L-02 cells injured by CCl4,decrease the expression of liver fibrosis proteins,and inhibit the TGF-β1/Smad signaling pathway by inhibiting the phosphorylation of Smad3.Our study suggested that IGF-1 exerted anti-liver fibrosis effects by stimulating L-02 cells proliferation,reducing cell damage and inhibiting ECM accumulation via interfering TGF-β1/Smad signaling pathway.

关键词

胰岛素样生长因子-1/转化生长因子-β1/肝细胞/肝星状细胞/肝纤维化

Key words

insulin-like growth factor-1/transforming growth factor β1/liver cells/hepatic stellate cells/liver fibrosis

分类

生物科学

引用本文复制引用

万爱妮,徐栋生,蔡燕飞,陈蕴,金坚,李华钟..人胰岛素样生长因子-1的体外抗肝纤维化活性[J].中国药科大学学报,2017,48(4):476-482,7.

基金项目

国家高技术研究发展计划(863计划)资助项目(No.2014AA021003) (863计划)

江苏省优势学科建设工程资助项目(PADA)This study was supported by the National High Technology Research and Development Program of China (863 Program) (No.2014AA021003) and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PADA) (PADA)

中国药科大学学报

OA北大核心CSCDCSTPCD

1000-5048

访问量0
|
下载量0
段落导航相关论文