实用肝脏病杂志 ›› 2012, Vol. 15 ›› Issue (4): 327-331.doi: 10.3969/j.issn.1672-5069.2012.04.019

• 基础研究 • 上一篇    下一篇

TGF-β1对大鼠HSC-T6细胞增殖、细胞周期和胶原分泌的影响*

郑素军,邢欣悦,韩源平,武聚山,王世美,张莹,刘陈煜,刘霜,段钟平   

  1. 100056北京市首都医科大学附属北京佑安医院人工肝中心(郑素军, 韩源平, 武聚山, 王世美, 张莹, 刘梅, 陈煜, 刘霜, 段钟平);附属北京安贞医院EICU(邢欣悦)
  • 收稿日期:2011-10-18 出版日期:2012-08-10 发布日期:2017-03-15
  • 通讯作者: 段钟平,E-mail: duan2517@163.com
  • 作者简介:第一作者:郑素军 男,38岁,医学博士,副主任医师,主要从事肝病的基础与临床研究。
  • 基金资助:
    国家自然科学基金资助项目(30800979 ); 北京市自然科学基金资助项目(7102085); 北京市科技新星资助项目(2007B055); 北京市卫生系统高层次卫生技术人才基金资助(2011-3-083); 北京市教育委员会科技发展计划项目(KM201010025024)

The effect of TGF-β1 on cell proliferation,cell cycle regulation and collagen expression in HSC-T6 cells

Zheng Sujun, Xing Xinyue, Han Yuanping, et al.   

  1. Artificial Liver Centre,Beijing YouAn Hospital,Capital Medical Uuniversity,Beijing 100069,China
  • Received:2011-10-18 Online:2012-08-10 Published:2017-03-15

摘要: 目的 观察TGF-β 1对大鼠肝星状细胞系HSC-T6增殖、细胞周期以及分泌肝纤维化相关胶原的影响。方法 采用MTT法检测细胞增殖;使用流式细胞仪检测细胞周期;采用荧光定量RT-PCR法检测SMAD3、c-myc、cdk-2、cyclinE、EGF、HGF、Bcl-2、NF-κB、MMP1、MMP9、MMP14、TIMP-1、PAI-1、α-SMA、COLⅠ及COLⅢ等基因mRNA水平;采用ELISA法检测细胞培养液COLⅠ、COLⅢ和α-SMA含量。结果 与对照组比,TGF-β 1处理24h及36h时,细胞形态及生长状况均无明显变化;在24h和36h时,TGF-β 1处理组细胞G0/G1期细胞比率均减少(24h:57.3± 8.5% vs 60.6± 9.7%; 36h:53.0± 2.2% vs 56.6± 5.0%),S期细胞比例略高(24h:30.6± 7.2% vs 26.4± 10.1%; 36h:35.2± 3.7% vs 30.8± 2.5%),但差异无统计学意义(P> 0.05);TGF-β 1处理组SMAD3、c-myc、cdk2、cyclin E、EGF、Bcl-2、NF-κB、TIMP1、PAI-1、α-SMA及COLⅠmRNA在24h和36h表达均上调,HGF、MMP1、MMP9、MMP14及COL ⅢmRNA在24h时表达下调,36h时表达上调;TGF-β 1处理组HSC-T6细胞分泌COLⅠ[24h:(63.0± 7.4ng/ml vs 33.2± 10.8 ng/ml,P< 0.05; 36h:58.5± 6.0ng/ml vs 42.2± 6.3ng/ml,P< 0.05];α-SMA[24h:20.6± 2.6ng/ml vs 4.2± 0.7ng/ml,P< 36h:59.7± 14.6ng/ml vs 36.8± 5.6ng/ml,P< 0.05)均显著增加。结论 TGF-β 1对大鼠肝星状细胞系HSC-T6显示了促增殖作用,并能促进肝纤维化相关胶原的分泌。

关键词: HSC-T6, TGF-β, 1, SMAD3, 增殖, 细胞周期

Abstract: Objective To explore the effect of TGF-β1 on cell proliferation,cell cycle regulation and collagen expression by HSC-T6 cell line. Methods The HSC-T6 cell proliferation was detected by MTT at 24 and 36 hours, respectively;The HSC- T6 cells were treated with TGF-β1(10 ng/ml) or not as control group. Flow cytometry was performed to measure the cell cycle;Fluorescent quantitative real time RT-PCR was used to quantify the mRNA levels of SMAD3,c-myc,cdk-2,cyclinE,EGF,HGF,Bcl-2,NF-κB,MMP1,MMP9,MMP14,TIMP-1,PAI-1,α-SMA,Collagen-I and Collagen-Ⅲ genes;Collagen-I,Collagen-Ⅲ,and α-SMA secreted by HSC-T6 cells were detected by ELISA. Results In comparison to HSC-T6 cells in control group,TGF-β1 decreased the cell counts in G0-G1 phase(24h: 57.3±8.5% vs 60.6±9.7%;36h: 53.0±2.2% vs 56.6±5.0%,both P>0.05),while it increased the cells in S phase(24h:30.6±7.2% vs 26.4±10.1%;36h:35.2±3.7% vs 30.8±2.5%,both P>0.05);We found that TGF-β1 treatment increased the mRNA levels of SMAD3,c-myc,cdk2,cyclin E, EGF,Bcl-2,NF-κB,TIMP1,PAI-1,α-SMA,and Collagn-I after treatment for 24 and 36 hours. Conversely,the mRNA level of HGF,MMP1,MMP9,MMP14,and collagen-III decreased at 24 hr,but increased at 36 hr. TGF-β1 promoted the secretion of collagen-I [24h:63.0±7.4ng/ml vs. 33.2±10.8ng/ml,P<0.05;36h:58.5±6.0ng/ml vs. 42.2±6.3ng/ml,P<0.05],and α-SMA[24h: 20.6±2.6ng/ml vs 4.2±0.7ng/ml,P<0.05;36h:59.7±14.6ng/ml vs 36.8±5.6ng/ml,P<0.05] by HSC-T6 cells after the treatment. Conclusion TGF-β1 can promote cell proliferation and the secretion of collagen of rat HSC-T6 cell lines.

Key words: HSC-T6 cells, TGF-β1, SMAD3, Proliferation, Cell cycle