实用肝脏病杂志 ›› 2012, Vol. 15 ›› Issue (3): 216-219.doi: 10.3969/j.issn.1672-5069.2012.03.014

• 基础研究 • 上一篇    下一篇

腺病毒载体在小鼠肝脏的分布及其表达规律研究*

王鸣, 郭健文, 习, 东, 刘君慧, 叶华丽, 罗小平, 宁, 琴   

  1. 430030武汉市 华中科技大学同济医学院附属同济医院感染性疾病研究所(王鸣,郭建文,习东,刘君慧,叶华丽,宁琴); 儿科(罗小平)
  • 收稿日期:2012-02-03 出版日期:2016-06-10 发布日期:2016-05-11
  • 通讯作者: 宁琴,E-mail:qning@tjh.tjmu.edu.cn
  • 作者简介:王鸣 女,30岁,博士研究生。主要从事肝衰竭发病机制研究。
  • 基金资助:
    国家973项目(2007CB512900); 国家自然科学基金项目(30700702); “十一五”国家科技支撑计划项目(2006BAI05A07)

Distribution and expression of adenovirus vector in mice with MHV-3-induced fulminant hepatitis

Wang Ming, Guo Jianwen, Xi Dong, et al.   

  1. Institute of Infectious Disease,Tongji Hospital,Tongji Medical College, Huazhong University of Science and Technology,Wuhan 430030,China
  • Received:2012-02-03 Online:2016-06-10 Published:2016-05-11

摘要: 目的研究腺病毒载体介导的β-半乳糖苷酶(LacZ)报告基因在小鼠肝脏的分布及表达情况,评价腺病毒载体作为基因治疗转导系统的有效性及安全性,为进一步的目的基因导入及表达奠定基础。方法将Balb/cJ 小鼠随机分为正常组及暴发性肝炎组,给小鼠经尾静脉注射2×108PFU腺病毒,收集24h、48h、72h、96h、120h和第7天小鼠血清,检测谷丙转氨酶和总胆红素,同时取肝脏、肺脏、心脏、肾脏标本进行X-gal 染色,以观察腺病毒载体在各脏器的表达情况。取MHV-3诱导的暴发性肝炎组小鼠24h、48h、72h、96h肝脏,检测腺病毒载体在肝脏的表达情况。结果腺病毒载体主要在小鼠肝脏表达,并于72小时表达最高,在正常小鼠及暴发性肝炎小鼠肝脏中表达效率分别约55.7%和25.7%,之后逐渐消减;正常组小鼠注射腺病毒载体后,肝功能无明显变化。结论腺病毒载体介导的报告基因可在肝脏高效表达且未见明显的肝损害,可作为基因治疗中安全有效的基因传递系统用于治疗肝脏疾病。

关键词: 暴发性肝炎, 腺病毒载体, 柯萨奇/腺病毒受体, 基因治疗

Abstract: Objective To study the distribution and expression of β-galactosidase(LacZ) reporter gene mediated by adenovirus vector in the liver of normal mice or mice with fulminant hepatitis, so as to evaluate the efficacy and safety of adenovirus as a gene therapy vector transduction system. Methods The normal Balb/cJ mice were randomly assigned to normal and fulminant hepatitis group. Each mouse was injected with adenovirus at 2×108PFU by tail vein injection,then the normal mice serum was collected to detect ALT and TBil at 24h,48h,72h,96h,120h, and the seventh day,meanwhile,the mice organs including liver,lung,heart,and kidney were collected and stained by X-gal in order to observe the expression of adenovirus vector in mice organ;the expression of adenovirus vector in liver of fulminant hepatitis mice induced by MHV-3 was detected. Results Adenovirus mainly expressed in the livers of mice;In normal group and fulminant hepatitis group,the highest expression efficiency was at 72 hours,reached 55.7% and 25.7%,respectively,then it followed by a gradual reduction of adenovirus expression; The adenovirus infection didn’t show obvious injury in liver function. Conclusions The adenovirus vector is highly expressed in the liver with no significantly liver damage; Adenovirus vector might be as an effective and safe gene delivery system for liver disease gene therapy.

Key words: fulminant hepatitis, Adenovirus vector, Coxsackie/adenovirus receptor, Gene therapy