基础医学与临床 ›› 2012, Vol. 32 ›› Issue (4): 423-427.

• 研究论文 • 上一篇    下一篇

JAK/STAT通路调节IL-4诱导的肝星状细胞I型胶原基因的表达

王晓红   

  1. 安徽医科大学
  • 收稿日期:2011-05-26 修回日期:2011-10-13 出版日期:2012-04-05 发布日期:2012-03-21
  • 通讯作者: 王晓红 E-mail:wangxiaohongvvvv@163.com
  • 基金资助:
    安徽省高校优秀青年人才基金项目

JAK/STAT pathway mediates IL-4-induced collagen type I expression in human hepatic stellate cells

  • Received:2011-05-26 Revised:2011-10-13 Online:2012-04-05 Published:2012-03-21

摘要: 目的:探讨JAK/STAT通路在IL-4对肝星状细胞(HSC)中I型胶原基因表达的影响及其作用机制。方法 用RT-PCR法和ELISA法分别检测不同浓度IL-4对人肝星状细胞系LX-2 中I型胶原mRNA表达和蛋白合成的影响;用Western blot法和RT-PCR法分别观察JAK1抑制剂AG490对IL-4诱导的JAK1磷酸化以及I型胶原mRNA表达的影响;用Western blot法和RT-PCR法分别观察LX-2转染STAT6-ASON对IL-4诱导的STAT6磷酸化以及I型胶原mRNA表达的影响。结果 IL-4诱导LX-2中I型胶原mRNA表达及其蛋白的合成,呈现剂量依赖性效应;AG490完全阻断IL-4诱导的JAK1磷酸化和I型胶原mRNA的表达;LX-2转染STAT6-ASON完全阻断IL-4诱导的STAT6磷酸化和I型胶原mRNA的表达。结论 JAK/STAT信号传导通路参与调节IL-4诱导HSC 中I型胶原基因表达,并在肝纤维化发生过程中发挥重要的作用。

关键词: IL-4, 肝星状细胞, JAK/STAT信号传导通路, α1(I)型胶原

Abstract: Aim To investigate the effects of IL-4 on collagen type I mRNA expression and protein production, and the roles of Janus kinase/signal transducers and activators transcription(JAK/STAT) signaling transduction pathway in increased collagen type I mRNA expression stimulated by IL-4 in activated hepatic stellate cells(HSCs). Methods First, collagen type I mRNA expression and protein production induced by IL-4 at different doses in a human HSC cell line, LX-2 was determined by RT-PCR and ELISA. Second, the effects of JAK inhibitor AG490 on JAK1 phosphorylation and collagen type I mRNA expression stimulated by IL-4 were detected by Western blot and RT-PCR. Third, the roles of transfection with STAT6 antisense oligonucleotide (STAT6-ASON) in STAT6 phosphorylation after IL-4 were detected by Western blot. Finally, the effect of transfection with STAT6-ASON on collagen type I mRNA expression after IL-4 was measured by RT-PCR. Results IL-4 increased collagen type I mRNA expression and protein production in a dose-dependent manner in LX-2, reaching a maximal level at 50 ng/ml IL-4. In addition, JAK inhibitor AG490 completely blocked JAK1 and STAT6 phosphorylation and increase in collagen type I gene expression after IL-4 in LX-2. Transfection with STAT6-ASON blocked STAT6 phosphorylation and increased collagen type I mRNA by IL-4 in LX-2. Conclusion JAK/STAT signaling pathway had mediated IL-4-induced collagen type I mRNA expression and protein production in activated HSC.

Key words: IL-4, Hepatic stellate cell(HSC), JAK/STAT signaling pathway, Collagen type I