人精子蛋白17增强型绿色荧光蛋白共表达卵巢癌细胞模型的建立  被引量:4

Establishment of an ovarian carcinoma cell model with co-expression of human sperm protein 17 and enhanced green fluorescent protein

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作  者:韩艳玲[1] 李芳秋[1] 刘群[1] 周万青[1] 张蕾[1] 王立魁[1] 

机构地区:[1]南京军区南京总医院解放军临床检验医学研究所,江苏南京210002

出  处:《医学研究生学报》2008年第9期904-906,910,I0001,共5页Journal of Medical Postgraduates

基  金:国家自然科学基金资助项目(批准号:30670599);南京军区医学科技"十一五"研究计划重点项目(批准号:06Z43);国家973计划项目基金资助(批准号:2006CB705707)

摘  要:目的:建立人精子蛋白17(hSp17)与增强型绿色荧光蛋白(EGFP)共表达的卵巢癌细胞模型。方法:用PCR方法获取hSp17基因片段,HindⅢ/KpnⅠ双酶切、T4 DNA连接酶连接的方法将hSp17基因片段克隆至含报告基因EGFP的真核表达载体pEGFP-N1中,脂质体介导转染卵巢癌细胞HO8910,荧光倒置显微镜观察及Westernblot检测转染细胞中hSp17/EGFP融合蛋白的表达,G418筛选稳定表达的细胞株。结果:酶切和测序结果均证实pEGFP-N1/hSp17重组质粒的构建完全正确。荧光观察与Western blot均证实了hSp17/EGFP蛋白的共表达,且成功筛选出稳定表达的细胞株。结论:成功构建hSp17/EGFP共表达的卵巢癌细胞模型,为研究hSp17异常表达对肿瘤细胞生物学行为的影响,以及hSp17为靶标的肿瘤诊断和生物治疗奠定基础。Objective: To establish a human ovarian carcinoma (OC) cell model that stably co-expresses the human sperm protein 17 and enhanced green fluorescent protein (hSpl7/EGFP). Methods: hSpl7 cDNA was obtained by PCR and cloned into the vector pEGFP-N1 that contained a report gene-enhanced green fluorescent protein. The recombinant plasmid was transfected into HO8910 cells with lipofectamine 2000. The expression of fusion hSp17/EGFP was observed under the fluorescent inverted microscope and detected by Western blotting. Cells with stable expression of hSpl7 were selected by G418. Results : Correct construction of pEGFP-N1/hSpl7 recombinant plasmid was confirmed by restriction enzyme digestion and sequencing. Conclusion: An ovarian carcinoma cell model that highly expressed hSp17/EGFP was successfully established, which may contribute to further studies on the effect of the abnormal hSp17 expression on the biological behavior of tumor cells and its role as a target in the diagnosis and biological treatment of tumors.

关 键 词:人精子蛋白17 卵巢癌 绿色荧光蛋白 

分 类 号:R737.31[医药卫生—肿瘤]

 

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