Article Summary
王森 赵毅 康海仙 丁伟斌 姚运红 胡新荣 王云 罗兵 朱伟.EBV融合基因Z2A 腺病毒的制备及其在诱导EBV阳性 细胞凋亡的应用[J].现代生物医学进展英文版,2014,14(13):2426-2429.
EBV融合基因Z2A 腺病毒的制备及其在诱导EBV阳性 细胞凋亡的应用
Construction of Recombinant Adenovirus Expressing EBV fusion gene Z2Aand its Application on Apoptosis of EBV+ Cells
  
DOI:
中文关键词: LMP2A  BZLF1  融合基因  腺病毒载体  EBV
英文关键词: LMP2A  BZLF1  Fusion gene  Adenoviral vector  EBV
基金项目:国家自然科学基金项目(81302244);广东省自然科学基金博士启动项目(S2012040006311,S2012040006383); 广东医学院科研基金项目(B2011004,B2011012)
Author NameAffiliation
WANG Sen, ZHAO Yi, KANG Hai-xian, DING Wei-bin, YAO Yun-hong, HU Xin-rong, WANG Yun, LUO Bing,ZHU Wei 广东医学院肿瘤研究所广东医学院微免教研室广东医学院病理教研室青岛大学医学院微生物教研室 
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中文摘要:
      目的:构建EB 病毒基因LMP2A及BZLF1 的融合基因(Z2A)重组腺病毒表达载体,探讨Z2A 融合蛋白对EBV+细胞凋亡 的作用。方法:利用AdEasy系统构建重组腺病毒载体pAd-Z2A,而后将之转染293 细胞(人胚肾细胞)产生重组腺病毒rAd-Z2A。 后者用于感染EBV 阳性及阴性细胞,RT-PCR、Western-blotting检测Z2A的mRNA 和蛋白表达,以及流式细胞术检测其对EBV 阳性细胞凋亡的调控。结果: 序列测定和酶切实验均证实,Z2A 融合基因正确插入穿梭质粒,并成功获得重组腺病毒表达载体 pAd-Z2A及重组腺病毒rAd-Z2A。感染rAd-Z2A的NEC靶细胞检测到Z2A 的表达。流式细胞术检测发现,与EBV-细胞组及 EBV+空白质粒转染组相比,接种rAd-Z2A 的EBV+ 细胞组48h(P<0.05)凋亡细胞显著增多,72h 时细胞近乎全部凋亡(P<0.01)。 结论:重组腺病毒rAd-Z2A可有效感染EBV+及EBV- 细胞,从而显著促进EBV+细胞凋亡而不影响EBV- 细胞,为进一步特异 性靶向EBV+肿瘤的基因治疗奠定基础。
英文摘要:
      Objective:To construct recombinant adenovirus carrying EBV fusion gene Z2A (LMP2A/BZLF1) and to investigate its function on the apoptosis of EBV+ cells.Methods:The recombinant adenovirus vector carrying Z2A was constructed with AdEasy system. The resulting construct was linearized and then transfected to 293 cells to generate recombinant adenovirus rAd-Z2A. EBV+ and EBV- cells were infected with recombinant adenoviruses. The expression and its effect on EBV+ cells of target gene were tested by RT-PCR, Western-blotting, and FACS.Results:It was confirmed by sequencing identification and restrictive analysis that the recombinant adenovirus vector was constructed successfully. The recombinant adenovirus rAd-Z2A produced with 293 cells showed stable infectivity. Z2A expression was detected in EBV+ NEC cells infected by recombinant adenovirus rAd-Z2A. And the expression of Z2A promoted markedly the apoptosis of EBV+ cells, at 48h (P<0.05) and 72h (P<0.01) compared with that of EBV- cells and EBV+ cells infected with empty vector.Conclusion:The recombinant adenoviruses expressing Z2A can effectively infect EBV+ cells and promote the apoptosis of EBV+ cells without obvious effects on EBV- cells, which can be applied further to gene therapy of EBV infection-related tumors.
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