期刊文献+

拉米夫定与原儿茶酸药物组合对HBV X蛋白入核的影响 被引量:6

Effect of Lamivudine Combined with Protocatechuic Acid on the Distribution of HBV X Protein in Cellular Nucleus
原文传递
导出
摘要 目的研究拉米夫定与原儿茶酸药物组合对乙肝病毒(HBV)X蛋白入核的影响。方法 Huh7细胞转染外源性GFP-HBx融合质粒后,与药物作用一定时间,利用共聚焦荧光显微镜观察药物对外源性HBV X蛋白在细胞内分布的影响。HepG2.2.15细胞与药物作用一定时间后,用Western blot分析药物对内源性HBV X蛋白在细胞核内含量的影响。结果拉米夫定及其与原儿茶酸的药物组合对HBV X蛋白的入核有抑制作用,且联合用药效果最好。结论原儿茶酸能增强拉米夫定对HBV X蛋白入核的抑制,这是该药物组合抑制HBV复制的重要作用途径之一。 OBJECTIVE To investigate the effect of lamivudine(3TC) combined with protocatechuic acid(PA) on the distribution of HBV X protein in cellular nucleus.METHODS Huh7 cell was transfected with ectogenic GFP-HBx fused plasmid,and treated by 3TC,PA and 3TC PA combination respectively the effect of drug treatment on the distribution of HBV X protein(HBx) in Huh7 cell was analyzed by using confocal microscopy.Furthermore,HepG2.2.15 cell was treated by 3TC,PA and 3TC PA combination respectively.The effect of drug treatment on the content of endogenic HBx in cellular nucleus of HepG2.2.15 cell was analyzed by Western blot.RESULTS 3TC and 3TC PA combination inhibited HBx into cellular nucleus,and the inhibitory action of 3TC PA combination was more powerful than that of 3TC.CONCLUSION The inhibitory action of 3TC PA on HBx may be an important mechanism of action on HBV replication.
出处 《中国药学杂志》 CAS CSCD 北大核心 2010年第11期832-835,共4页 Chinese Pharmaceutical Journal
基金 国家科技重大专项课题资助项目(2008ZX10204) 武汉大学病毒学国家重点实验室开放研究基金(Ⅲ-2005010)
关键词 乙肝病毒 X蛋白 拉米夫定 原儿茶酸 Hepatitis B virus X protein lamivudine protocatechuic acid
  • 相关文献

参考文献12

  • 1CHEN H S, KANEKO S, GIRONES R. et al. The woodchuck hepatitis virus X gene is important for establishment of virus infection in woodchucks [J ]. J Virol, 1993, 67(3) :1218-1226.
  • 2MADDEN C R, FINEGOI,D M J, SI.AGI,E B L. Expression of hepatitis B virus X protein does not alter the accumulation of spontaneous mutalinns in transgenic miee [J]. J Virol, 2000,74 ( 11 ) :5266-5272.
  • 3YU D Y, MOON tt B, SON J K. et al. Incidence of hepalocellulay carcinoma in transgenic mice expressing the hepatitis B virus X-protein [ J]. J Hepatol, 1999, 31 ( 1 ) :123-132.
  • 4BOUCHARD M J, PURO R J, WANG L, et al. Activation and inhibition of cellular calcium and tyrosine kinase signaling pathways identify targets of the HBx protein involved in hepatitis B virus replication [J]. J Virol, 2003, 77(14) :7713-7719.
  • 5NOMURA T, LIN Y, DORJSUREN D. et al. Human hepatitis B virus X prutcin is detectable in nuclei of transfected cells, and is active for transactivation[ J ]. Biochim Biophys Acta, 1999, 1453 (3) :330-340.
  • 6HOARE J, HENKKER F, DOWLING J J, et al. Subcellular localisation of the X protein in HBV infected hepatocytes [J]. Virol, 2001, 64 (4):419-426.
  • 7WANGXZ LINN.The function of HBV X gene and X protein .世界华人消化杂志,2006,14(26):2579-2585.
  • 8NOMURA T, LIN Y, DORJSUREN D, et al. Human hepatitis B virus X protein is detectable in nuclei of transfected cells, and is active for transactivation[ J]. Biochim Biophys Acta, 1999, 1453 ( 3 ) : 330-340.
  • 9ZHUOGY LIUSL XUGL.The research proga’ess of the anti- HBV activities of the constituents of medicinal plants in vitro recent 20 years.世界华人消化杂志,2006,14(13):1241-1246.
  • 10HENKLER F, HOARE J, WASEEM N, et al. Intracellular location of the hepatitis B virus HBx protein [ J ] . J Gen Viorol. 2001,82(4) :871-877.

同被引文献54

引证文献6

二级引证文献26

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部