Article Summary
李海燕,贺红艳,黄凤霞,黄君华,张逍港,姚子淳.乙肝病毒X蛋白通过上调NOX4的表达活化肝星状细胞[J].现代生物医学进展英文版,2019,19(2):227-230.
乙肝病毒X蛋白通过上调NOX4的表达活化肝星状细胞
HBx Protein Activated Hepatic Stellate Cells Through Up-regulationof NOX4 Expression
Received:May 27, 2018  Revised:July 09, 2018
DOI:10.13241/j.cnki.pmb.2019.02.006
中文关键词: 乙肝病毒X蛋白  NOX4  肝星状细胞  活化
英文关键词: HBx  NOX4  Hepatic stellate cells  Activation
基金项目:国家自然科学基金青年基金项目(81700546);陕西省教育厅西安医学院专项科研计划项目(16JK1664);西安医学院2016年博士科研启动基金项目(2016DOC15);西安医学院2017年配套基金项目(2017PT13)
Author NameAffiliationE-mail
LI Hai-yan Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China lihaiyan319@126.com 
HE Hong-yan Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China  
HUANG Feng-xia Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China  
HUANG Jun-hua Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China  
ZHANG Xiao-gang Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China  
YAO Zi-chun Medical Technology Department, Xi'an Medical College, Xi'an, Shaanxi, 710000, China  
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中文摘要:
      摘要 目的:探讨乙肝病毒X蛋白(HBx)对肝星状细胞(HSC)活化的影响及其可能的分子机制。方法:构建稳定转染HBx基因的L02肝细胞(L02-HBx),Western Blot鉴定细胞株中HBx蛋白的稳定表达。以L02-HBx、转染空质粒(L02-pcDNA3.1)和未转染肝细胞(L02)的条件培养基,分别孵育肝星状细胞株LX-2,即LX-2/L02-HBx、LX-2/L02-pcDNA3.1、LX-2/L02,Western Blot检测上述各组细胞α-SMA(肝星状细胞活化标志)和NOX4的蛋白表达。以L02-HBx的条件培养基孵育LX-2细胞,分为转染si-NOX4(LX-2/L02-HBx+ si-NOX4)、无关干扰片段(LX-2/L02-HBx+snc-RNA)、未转染(LX-2/L02-HBx)3组,Western Blot检测各组LX-2细胞的α-SMA蛋白表达。结果:L02-HBx中稳定表达HBx蛋白;LX-2/L02-HBx细胞中α-SMA和NOX4的蛋白表达显著高于LX-2/L02-pcDNA3.1、LX-2/L02细胞(P<0.01);LX-2/L02-HBx细胞敲减NOX4后(LX-2/L02-HBx+si-NOX4),α-SMA的蛋白表达显著低于LX-2/L02-HBx+snc-RNA和LX-2/L02-HBx细胞(P<0.05)。结论:肝细胞中表达的HBx蛋白可以通过HSC中NOX4上调α-SMA的表达,促进HSC的活化。
英文摘要:
      ABSTRACT Objective: To explore the mechanism of HSC activation by HBxprotein. Methods: HBx-transfected human non-tu- mour hepatic L02 cell line, named L02-HBx was established and showed HBx expression by western blot analysis. Western blot tested the effects of HBx on NOX4 and α-SMA expression in human HSC HSC cell line(LX-2) after exposure to conditioned medium from L02-HBx , L02-pcDNA3.1, and L02 cells. After LX-2/L02-HBx cells treated with si-NOX4, the NOX4 and α-SMAexpression were tested by western blot analysis. Results: The L02-HBx cell models were successfully constructed. The expression of HBx was significantly ex- pressed. Compared with LX-2/L02-pcDNA3.1 and LX-2/L0 groups, NOX4 and α-SMAexpression were increased significantly in LX-2/L02-HBx group(P<0.01). α-SMA in LX-2/L02-HBx expressions were depressed, coupled with the fact that the NOX4 was si- lenced(P<0.05). Conclusion: HBx protein activate hepatic stellate cells, and NOX4 play a vital role in the activation.
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