实用肝脏病杂志 ›› 2018, Vol. 21 ›› Issue (3): 388-392.doi: 10.3969/j.issn.1672-5069.2018.03.018

• 实验性肝炎 • 上一篇    下一篇

脯氨酰寡肽酶抑制剂体外对肝星状细胞凋亡、增殖和肝纤维化相关基因表达的影响*

周达, 王晶, 李冰航, 孙超, 陈源文, 范建高   

  1. 200092 上海市 上海交通大学医学院附属新华医院消化内科
  • 收稿日期:2017-11-17 出版日期:2018-05-10 发布日期:2018-05-25
  • 通讯作者: 孙超,E-mail:sunchao@xinhuamed.com.cn
  • 作者简介:周达,男,28岁,医学博士。E-mail:mubing2007@foxmail.com
  • 基金资助:
    *国家自然科学基金资助项目(编号:81170410/81000173)

Inhibition of proliferation and regulation of heaptic fibrosis-related genes in HSC-T6 cells by prolyloligopeptidase inhibitor in vitro

Zhou Da, Wang Jing, Li Binghang, et al   

  1. Department of Gastroenterology,Xinhua Hospital,Jiaotong University School of Medicine,Shanghai 200092,China
  • Received:2017-11-17 Online:2018-05-10 Published:2018-05-25

摘要: 目的 体外探讨肝星状细胞(HSC)脯氨酰寡肽酶(POP)的生物学功能,以进一步阐述其在肝脏炎症和纤维化发生发展中的作用。方法 取HSC-T6细胞,经不同浓度的POP抑制剂(S17092)处理,采用ELISA法检测HSC-T6细胞N-乙酰基-丝氨酸-天冬氨酸-赖氨酸-脯氨酸(Ac-SDKP)水平,使用流式细胞术和CCK8检测HSC-T6凋亡和增殖水平,采用实时定量-PCR法检测相关炎症和肝纤维化基因转化生长因子-β1(TGF-β1)、α-平滑肌肌动蛋白(α-SMA)、单核细胞趋化蛋白-1(MCP-1)、Ⅰ型胶原(Col I)水平,采用Western blot法检测相关蛋白(POP、TGF-β1、α-SMA、Smad7、p-Smad2/3、PPAR-γ)表达。结果 与对照组比,POP抑制剂干预组细胞内Ac-SDKP水平显著下降(P<0.05);POP被抑制后对HSC-T6凋亡没有显著的影响(P>0.05),但可抑制其增殖(P<0.05);与对照组比,抑制剂组HSC内α-SMA蛋白表达显著升高(P<0.05),而Smad7和PPAR-γ蛋白表达显著下降(P均<0.05);抑制剂组HSC内MCP-1和α-SMA mRNA水平显著上调(P均<0.05)。结论 POP在肝星状细胞内可能发挥重要的抗炎抗纤维化作用,其机制可能与其调节Ac-SDKP及Smad7和PPAR-γ的表达有关。

关键词: HSC-T6细胞, 脯氨酰寡肽酶, 转化生长因子-β-Smad蛋白信号通路, 过氧化物酶体增殖剂激活受体-&#x003b3, 体外

Abstract: Objective To investigate the inhibition of proliferation and regulation of heaptic fibrosis-related genes in HSC-T6 cells by prolyloligopeptidase(POP) inhibitor in vitro. Methods The HSC-T6 cells were cultured,and the POP activity was inhibited by increasing concentrations of POP inhibitor(S17092). The intracellular level of N-acetyl- seryl-aspartyl-lysyl-proline(Ac-SDKP) was determined by ELISA. The cell apoptosis and cell proliferation were detected by flow cytometry and CCK-8 assay,respectively. The mRNA levels of TGF-β1,α-SMA,monocyte chemoattractant protein 1(MCP-1) and collagen I(Col I) were detected by realtime-PCR,and the POP,TGF-β1,α-SMA, Smad7,p-Smad2/3 and PPAR-γ expression were detected by Western blot. Results The intracellular Ac-SDKP level decreased significantly after co-culture with S17092,the POP inhibitor(P<0.05) as compared to that in the control; the proliferation of HSC-T6 cells was significantly inhibited(P<0.05) and the cell apoptosis was not influenced obviously after S17092 intervention(P>0.05);the Smad7(P<0.05) and PPAR-γ(P<0.05) protein levels were significantly down-regulated,and the α-SMA protein level was significantly up-regulated(P<0.05) after S17092 intervention;the MCP-1(P<0.05) and α-SMA(P<0.05) mRNA level were significantly up-regulated. Conclusion POP plays a pivotal role in anti-inflammation and anti-fibrosis in HSC cells, which might be related to the regulation of Smad7 and PPAR-γ expression.

Key words: HSC-T6 cells, Prolyloligopeptidase, Transforming growth factor-&#x003b2, -Smad signaling, Peroxisome proliferator activated receptor-&#x003b3, In vitro