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作 者:金艳花[1] 訾晓渊[1] 姚玉成[1] 熊俊[1] 李建秀[1] 苏小平[1] 王新民[1] 倪文君[1] 丛文铭[2] 杨康鹃[3] 胡以平[1]
机构地区:[1]第二军医大学基础医学部细胞生物学教研室,上海200433 [2]第二军医大学东方肝胆外科医院病理科 [3]延边大学医学院生物学教研室,延吉133000
出 处:《第二军医大学学报》2003年第2期175-178,共4页Academic Journal of Second Military Medical University
基 金:国家"九五"攻关项目 (TJ99-LA0 1) ;国家自然科学基金 (3 9670 811) ;上海市科学技术发展基金项目 (9949190 3 3 )
摘 要:目的 :分析乙型肝炎病毒 pre S2蛋白在 3′末端缺失的 pre S/ S基因转基因小鼠肝脏中的分布及其病理学作用。方法 :采用原核显微注射法将质粒 pc DNA3.1- pre S/ St注射入小鼠受精卵雄原核 ,制备转基因小鼠。PCR法在基因组水平筛选 3′末端缺失的 pre S/ S基因转基因小鼠首建者 (founder)及后代 ;免疫组织化学法在蛋白水平检测 pre S2蛋白在这些小鼠中的表达 ;H- E染色分析转基因小鼠肝组织的病理学变化。结果 :经原核显微注射法将目的片段注射入受精卵雄原核后 ,共出生 15只新生小鼠 ,其中存活 7只 ,经 PCR检测后获得 2只 founder转基因小鼠 ,命名为 C5 7- Tg N (pre S/ St) SMMU。免疫组织化学检测发现转基因小鼠肝细胞质中有 pre S 2蛋白表达 ,H- E染色发现转基因小鼠肝组织中央静脉周围有淋巴细胞聚集。将这 2只转基因小鼠与正常同系异性小鼠交配 ,进行传代培育 ,PCR法筛选阳性转基因小鼠 ,目前已传至 F2 代。 结论 :本研究成功建立了稳定遗传 3′末端缺失的 pre S/ S基因并表达 pre S2蛋白的转基因小鼠 C5 7- Tg N((pre S/ St) SMMU,它将是体内研究 3′末端缺失的 pre S/Objective: To analyze the distribution of preS 2 protein and the pathological changes in liver tissue of hepatitis B virus 3′ truncated preS/S gene transgenic mice. Methods: After restriction enzyme digestion, the pcDNA3.1 preS/S t plasmids, including 3′ truncated preS/S gene and CMV promoter were microinjected into male pronuclei of mice zygotes. The pups and offsprings were evaluated by polymerase chain reaction (PCR) at genomic DNA level. Expression of preS/S t gene in transgenic mice were confirmed by immunohistochemistry. H E staining was used to analyze the pathological changes. Results: Following microinjection of coding sequence of pcDNA3.1 preS/S t, the embyros were transferred to oviducts of pseudopregnant females. Fifteen pups were born and 7 of them survived, two of them were verified to integrate the preS/S t gene in their genomic DNA by PCR assay, named C57 TgN( preS/S t)SMMU. With immunohistochemistry, preS 2 protein was detected in hepatocytes cytoplasm of C57 TgN( preS/S t)SMMU transgenic mice. Lymphocyte effusion was found near the central vein of liver tissue and NP of hepatocytes increased in transgenic mice by H E staining. Then the transgenic mice were mated with normal mice to establish transgenic mice strains. Now one of them had F 2 offsprings. Conclusion:We have established preS/S t gene transgenic mice C57 TgN( preS/S t)SMMU, which is a valuable animal system to study the roles of preS/S t gene in development of hepatocellular carcinoma in vivo .
关 键 词:乙型肝炎病毒 PRES2蛋白 转基因小鼠 preS/S基因 肝
分 类 号:R373.21[医药卫生—病原生物学]
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