中国组织工程研究

中国组织工程研究 ›› 0, Vol. ›› Issue (0): 11-16.doi: 10.3969/j.issn.1673-8225.2012.01.002

• 骨髓干细胞 • 上一篇    下一篇

携带双报告基因真核表达载体pHSV1-TK-IRES2-EGFP在小鼠骨髓间充质干细胞内的表达

吴立川1，杨  昆1，刘永哲1，陈  鹏1，徐文贵2
  

  1. 1天津医科大学公共卫生学院卫生毒理学教研室，天津市  300070；  2天津医科大学附属肿瘤医院，天津市  300060
  • 收稿日期:2011-07-19 修回日期:2011-09-16
  • 通讯作者: 杨昆，副教授，硕士生导师，天津医科大学公共卫生学院，天津市 300070 yangkun@tijmu.edu.cn 徐文贵，主任医师，硕士生导师，天津医科大学附属肿瘤医院，天津市300060 E-mail:lulizhongno.1@163.com
  • 作者简介:吴立川★，女，1986 年生，天津市人，汉族，天津医科大学在读硕士，主要从事骨髓间充质干细胞和肿瘤基因治疗方面的研究。 xihuzi0217@163.com

Construction and expression of pHSV1-TK- IRES2-EGFP eukaryotic vector in mouse bonemarrow mesenchymal stem cells

Wu Li-chuan1, Yang Kun1, Liu Yong-zhe1, Chen Peng1, Xu Wen-gui2
  

  1. 1Department of Toxicology, School of Public Health, Tianjin Medical University, Tianjin  300070, China; 2Tianjin Medical University Cancer Institute and Hospital, Tianjin  300060，China
  • Received:2011-07-19 Revised:2011-09-16
  • Contact: Yang Kun, Associateprofessor, Master’ssupervisor,Department ofToxicology, School ofPublic Health, TianjinMedical University,Tianjin 300070,Chinayangkun@tijmu.edu.cn Xu Wen-gui, Chiefphysician, Master’ssupervior, TianjinMedical UniversityCancer Institute andHospital, Tianjin300060, China Wenguixy@tom.com E-mail:lulizhongno.1@163.com
  • About author: Wu Li-chuan★,Studying for master’sdegree, Departmentof Toxicology, Schoolof Public Health,Tianjin MedicalUniversity, Tianjin300070, China xihuzi0217@163.com

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被引次数

1

摘要：

背景：单纯疱疹病毒胸腺嘧啶核苷激酶(herpes simplex virus 1-thymidine kinase，HSV1-TK)与绿色荧光蛋白(EGFP)双报告基因共表达载体构建及其在骨髓间充质干细胞内的表达研究报道较少。
目的：构建pHSV1-TK-IRES2-EGFP真核表达载体，并检测其在体外培养的小鼠骨髓间充质干细胞内的表达。
方法：应用聚合酶链式反应从质粒pHSV106中扩增出HSV1-TK基因后与pMD18-T载体连接，构成重组质粒pHSV1-TK/18T。重组质粒以限制性内切酶Bgl Ⅱ和Sal Ⅰ进行双酶切，将其插入同样双酶切处理的pIRES2-EGFP载体内；并将新构成的重组质粒pHSV1-TK-IRES2-EGFP以脂质体法转染小鼠骨髓间充质干细胞。
结果与结论：酶切鉴定结果表明，扩增的HSV1-TK基因序列正确，大小为1 130 bp；重组质粒载体内的HSV1-TK序列与Gene Bank报告的序列完全一致；骨髓间充质干细胞转染后在荧光显微镜下可以观察到有特异性绿色荧光出现，HSV1-TK的mRNA有表达。实验成功构建了pHSV1-TK-IRES2-EGFP真核表达载体，在体外培养的小鼠骨髓间充质干细胞内能有效的表达。

关键词: 单纯疱疹病毒胸腺嘧啶核苷激酶, 骨髓间充质干细胞, 构建；阳离子脂质体, 增强型绿色荧光蛋白, 基因表达

Abstract:

BACKGROUND: Up to date, thestudies regarding the construction of herpes simplex virus 1-thymidine kinase (HSV1-TK) and enhanced green fluorescent protein (EGFP) reporter gene co-expression vector and its expression in mouse bone marrow mesenchymal stem cells are few. OBJECTIVE: To construct a pHSV1-TK- IRES2-EGFP eukaryotic vector, and to observe the expression of HSV1-TK in mouse bone marrow mesenchymal stem cells. 
METHODS: The HSV1-TK cDNA fragments were obtained by polymerase chain reaction (PCR) from pHSV106 and Bgl Ⅱ, Sal Ⅰ two restriction sites were added, after T vector cloning, the recombinant plasmid pHSV1-TK/18T was digested by two restrictive endonucleases, and then HSV1-TK cDNA was collected and recombined with eukaryotic vector pIRES2-EGFP by using gene recombination technique. The recombinant plasmid pHSV1-TK- IRES2-EGFP was transfected into mouse bone marrow mesenchymal stem cells in vitro with lipofectamine transfection reagent.
RESULTS AND CONCLUSION: A length of 1 130 bp with Bgl Ⅱ and Sal Ⅰ target gene sequences was obtained by PCR. And the pHSV1-TK- IRES2-EGFP expression plasmid was constructed successfully. The TK/GFP green fluorescent protein was detected after transfection. At the same time, the expression of HSV1-TK mRNA was determined. The eukaryotic vector pHSV1-TK- IRES2-EGFP was successfully constructed, and effectively expressed HSV1-TK mRNA in mouse bone marrow mesenchymal stem cells in vitro.

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