文章摘要
王辉区裕升沈晗黄树林△.TCR BV12-3 重组载体构建及其抗肿瘤作用的初步研究*[J].,2014,14(2):206-208
TCR BV12-3 重组载体构建及其抗肿瘤作用的初步研究*
Construction and Primary Study on the Anti-Tumor Effect of TCR BV12-3Recombinant Vector*
  
DOI:
中文关键词: T 细胞受体  BV12-3  克隆  肿瘤
英文关键词: TCR  BV12-3  Clone  Tumor
基金项目:国家“重大新药创制”科技重大专项(2009ZX09103-708);广东省医学科研课题(B2002070)
作者单位
王辉区裕升沈晗黄树林△ 广东药学院生命科学与生物制药学院广东省生物技术候选药物研究重点实验室 
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中文摘要:
      摘要目的:构建pEGFP-C3-TCR BV12-3 表达载体并初步研究其抗肿瘤作用。方法:TCR BV12-3 基因片段从pGEM-T-TCR BV12-3 载体上酶切并克隆至pEGFP-C3 载体中,通过脂质体将pEGFP-C3-TCR BV12-3 表达载体转染外周血单个核细胞 (PBMCs),48 小时后荧光显微镜观察转染效率。PBMCs细胞、pEGFP-C3 载体转染的PBMCs 细胞、pEGFP-C3-TCR BV12-3 表达 载体转染的PBMCs 细胞分别与肝癌细胞BEL-7402 和宫颈癌细胞HeLa 共培养24 h,显微镜观察肿瘤细胞的生长情况。结果:测 序证实TCR BV12-3 基因片段成功亚克隆至pEGFP-C3 载体中,荧光显微镜证实重组体转染PBMCs 细胞48 h后可有效表达绿 色荧光。显微镜观察发现pEGFP-C3-TCR BV12-3载体转染的PBMCs 对肝癌细胞有杀伤作用,但对宫颈癌杀伤作用不明显。结 论:成功构建pEGFP-C3-TCR BV12-3 表达载体,初步证实TCRBV12-3 对肝癌细胞有杀伤作用。
英文摘要:
      ABSTRACT Objective:To construct pEGFP-C3-TCR BV12-3 vector, and to investigate the effect of TCR BV12-3 on anti-tumor. Methods:TCR BV12-3 gene was digested from pGEM-T-TCR BV12-3, and was cloned into pEGFP-C3 vector. The pEGFP-C3-TCR BV12-3 recombinant vector was transfected into peripheral blood mononuclear cells (PBMCs) via liposome. After 48 h, the transfection efficiency was measured by fluorescence microscope. Then, the PBMCs, pEGFP-C3-TCR BV12-3 and pEGFP-C3 transfection were co-cultured with hepatocarcinoma cells BEL-7402 and cervical cancer cells HeLa, respectively. After 24 h incubation, the anti-tumor effect of TCR BV12-3 was investigated by microscope. Results:The DNA sequencing analysis showed that TCR BV12-3 gene was successfully subcloned into pEGFP-C3 vector, and the green fluorescence could be detected by fluorescence microscope in PBMCs transfected with pEGFP-C3-TCR BV12-3. PBMCs transfected with pEGFP-C3-TCR BV12-3 showed cytotoxicity in BEL-7402 cells. Conclusion:The pEGFP-C3-TCR BV 12-3 vector was successfully constructed, and the anti-tumor effect of TCR BV12-3 was proved initially.
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