基础医学与临床 ›› 2011, Vol. 31 ›› Issue (2): 144-148.

• 研究论文 • 上一篇    下一篇

乙型肝炎病毒X蛋白通过激活ERKs和NF-κB上调大鼠系膜细胞表达TNF-α

卢宏柱1,樊启红1,刘丹1,邓开琴1,周建华2   

  1. 1. 长江大学
    2. 华中科技大学
  • 收稿日期:2010-02-24 修回日期:2010-06-30 出版日期:2011-02-05 发布日期:2011-03-14
  • 通讯作者: 卢宏柱 E-mail:lucas215@163.com
  • 基金资助:
    省卫生厅科研基金

Hepatitis B virus X protein upregulates tumor necrosis factor-α expression of rat mesangial cell line via ERKs and NF-κB pathway

LU Hong-Zhu1,FAN Qi-hong 2,LIU Dan 2,DENG Kai-qin 2,ZHOU Jian-hua 2   

  1. 1. Yangtze University
    2.
  • Received:2010-02-24 Revised:2010-06-30 Online:2011-02-05 Published:2011-03-14
  • Contact: LU Hong-Zhu E-mail:lucas215@163.com

摘要: 目的 探讨乙型肝炎病毒(HBV)X基因转染大鼠系膜细胞肿瘤坏死因子-α(TNF-α)高表达的细胞外蛋白调节激酶(ERKs)、核因子κB(NF-κB)、p38MAPK信号转导机制。方法 将含有HBV X基因的质粒pCI-neo-X导入体外培养的大鼠系膜细胞,分别采用特异性抑制剂U0126阻断ERK1/2通路,Lactacystin阻断NF-κB通路和SB203580阻断p38MAPK通路,观察培养细胞TNF-α 及其mRNA表达,以不加抑制剂作为对照。RT-PCR检测TNF-α mRNA表达,ELISA检测培养上清液中TNF-α表达。Western blot 检测HBx表达。结果 转染pCI-neo-X后,系膜细胞TNF-α mRNA及上清液TNF-α表达均增高,通过阻断ERK1/2或NF-κB通路,细胞TNF-α mRNA及上清液TNF-α表达均下降。而阻断p38MAPK通路对系膜细胞TNF-α mRNA及上清液TNF-α表达无明显影响。结论HBx蛋白通过激活ERKs和NF-κB信号通路使系膜细胞高表达TNF-α,而与p38MAPK通路无关。

关键词: 乙型肝炎病毒, X蛋白, 系膜细胞, 细胞外蛋白调节激酶, 肿瘤坏死因子α, 核因子-κB

Abstract: Objectives To investigate the signal transduction pathway of hepatitis B virus X protein (HBx) in glomerular mesangial cell(GMC) TNF-α expression. Methods PCI-neo-X was transfected into cultured glomerular mesangial cells. TNF-α and its mRNA expression of GMC were compared between treated or untreated with ERKs inhibitor U0126, NF-κB inhibitor lactacystin and p38 inhibitor SB203580, respectively. HBx expression in glomerular mesangial cells was assessed by Western-blot. TNF-α mRNA expression was assessed by semi-quantitative RT-PCR. TNF-α levels in supernatants were measured by ELISA. Results HBx expression was found in transfected glomerular mesangial cells, and became prominent at 36 and 48 hours after transfection whatever with or without inhibitors in culture media. TNF-α mRNA expression was significantly decreased in U0126 or lactacytin group compared with U0126-free or lactacytin-free group. TNF-α levels in supernatants in pCI-neo-X transfection was also partially inhibited when treated with ERKs inhibitor U0126 or NF-κB inhibitor lactacystin, but no effect was observed in p38 inhibitor SB203580 treated group at 36 and 48h after transfection. Conclussion HBx upregulated TNF-α expression of GMC line partly through ERK1/2 and NF-κB signal transduction pathway, but not p38MAPK pathway.

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