实用肝脏病杂志 ›› 2022, Vol. 25 ›› Issue (2): 165-169.doi: 10.3969/j.issn.1672-5069.2022.02.004

• 实验性肝炎 • 上一篇    下一篇

罗格列酮干预对HSC-T6细胞增殖及细胞PPARγ和HO-1 mRNA水平的影响*

时扣荣, 顾伟鹰, 刘娟, 罗兰, 翟巧利, 范伟   

  1. 200137 上海市 上海中医药大学附属第七人民医院药学部
  • 收稿日期:2021-05-11 出版日期:2022-03-10 发布日期:2022-03-15
  • 通讯作者: 范伟,E-mail:24882582@qq.com
  • 作者简介:时扣荣,女,38岁,医学硕士,副主任药师。E-mail:shikourong@163.com
  • 基金资助:
    *上海市科委科研基金资助项目(编号:16411951539)

Effects of rosiglitazone on cell proliferation and PPARγ and HO-1 mRNA levels in HSC-T6 cells in vitro

Shi Kourong, Gu Weiying, Liu Juan, et al   

  1. Department of Pharmacy, Seventh People' s Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 200137,China
  • Received:2021-05-11 Online:2022-03-10 Published:2022-03-15

摘要: 目的 探讨罗格列酮(RGZ)干预对HSC-T6细胞增殖及对细胞过氧化物酶体增殖物激活受体γ(PPARγ)和血红素加氧酶1(HO-1)mRNA水平的影响。 方法 将HSC-T6细胞分为对照组、RGZ干预组和RGZ联合HO-1抑制剂ZnPP-IX处理组,采用四甲基偶氮唑盐(MTT)法检测细胞活力,使用流式细胞仪检测细胞凋亡,采用Real-time PCR法检测细胞PPARγ和HO-1 mRNA水平,采用Western Blot法检测细胞纤维化相关因子蛋白表达。 结果 RGZ处理组细胞增殖A值为(0.6±0.1),显著低于对照组(1.0±0.1),细胞增殖活性降低了38.4%(P<0.05),而RGZ联合ZnPP-IX处理组为(0.8±0.1),比对照组细胞增殖活性降低了17.2%(P<0.05),但显著高于RGZ处理组(P<0.05);RGZ干预组细胞凋亡率显著高于对照组(P<0.05),而RGZ联合ZnPP-IX干预组细胞凋亡率显著低于RGZ组(P<0.05);RGZ干预组细胞PPARγ和HO-1 mRNA水平分别为(2.0±0.2)和(3.7±0.4),显著高于对照组[分别为(1.0±0.1)和(1.0±0.1),P<0.05],而RGZ联合ZnPP-IX处理组 HO-1 mRNA水平为(2.9±0.4),显著低于RGZ处理组(P<0.05);RGZ处理组细胞α-SMA、COLⅠ、COLⅢ和TGF-β1蛋白表达显著低于对照组,而RGZ联合ZnPP-IX处理组显著高于RGZ处理组(P<0.05)。 结论 RGZ干预可显著抑制HSC-T6细胞增殖,促进其凋亡,发挥抗肝纤维化作用,其机制可能与抑制了细胞PPARγ和HO-1 mRNA水平有关。

关键词: HSC-T6细胞, 罗格列酮, 细胞增殖, 凋亡, 过氧化物酶体增殖物激活受体γ, 血红素加氧酶1, 体外

Abstract: Objective The aim of this study was to investigate the effects of rosiglitazone (RGZ) on cell proliferation and peroxisome proliferator-activated receptor γ (PPARγ) and heme oxygenase 1 (HO-1) levels in HSC-T6 cells in vitro. Methods The HSC-T6 cells were divided into control, RGZ- and RGZ and ZnPP-IX ( a HO-1 antagonist) combination-intervened groups (n=8), and the cell viability was detected by methyl thiazolyl tetrazolium (MTT) and the cell apoptosis was detected by flow cytometry. The cell PPARγ and HO-1 mRNA levels were detected by Real-time PCR, and the cell fibrosis-related protein expressions were detected by Western blot. Results The proliferation activity (A value) of HSC-T6 cells in RGZ-intervened group was (0.6±0.1), 38.4% decreased compared with (1.0±0.1) in the control (P<0.05), while it was (0.8±0.1) in RGZ and ZnPP-IX combination-intervened group, 17.2% decreased compared with in control group (P<0.05), but significantly increased compared with RGZ-intervened group (P<0.05); the apoptosis rate in RGZ-intervened group significantly higher than that in the control group (P<0.05), and the apoptosis rate in RGZ and ZnPP-IX combination-intervened group was significantly lower than that in RGZ-treated group (P<0.05). Conclusion RGZ intervention could significantly inhibit the proliferation and promote apoptosis of HSC-T6 cells in vitro, which might be related to the down-regulation of PPARγ and HO-1 mRNA levels.

Key words: HSC-T6 cells, Rosiglitazone, Cell proliferation, Apoptosis, Peroxisome proliferator-activated receptor γ, Heme oxygenase 1, In vitro