陈中原,皇昊,申淑娜,等.以HIF2α为靶点的化合物筛选的细胞模型构建[J].中国海洋药物,2022,41(6):69-75.
以HIF2α为靶点的化合物筛选的细胞模型构建
Constructing a cell model for compounds screening targeted on HIF2α
投稿时间:2021-12-16  修订日期:2022-03-01
DOI:10.13400/j.cnki.cjmd.2022.06.002
中文关键词:  786-O细胞  缺氧诱导因子  缺氧反应原件  萤光素酶报告基因
English Keywords:786-o cells  hypoxia inducible factor  hypoxia responsive element  luciferase reporter gene
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作者单位E-mail
陈中原 中国海洋大学医药学院 742574734@qq.com 
皇昊 中国海洋大学医药学院 626117868@qq.com 
申淑娜 中国海洋大学医药学院 shenshuna0124@163.com 
张博奇 中国海洋大学医药学院 2867653686@qq.com 
樊范 中国海洋大学医药学院 2819955087@qq.com 
杜珂欣 中国海洋大学医药学院 2752533860@qq.com 
刘云章 中国海洋大学医药学院 liuyz@ouc.edu.cn 
李筠 中国海洋大学医药学院 yunlisun@ouc.edu.cn 
卢玲* 中国海洋大学医药学院 linglu@ouc.edu.cn 
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中文摘要:
      目的 建立稳定表达血管内皮生长因子A(VEGFA)启动子区5×缺氧反应元件(5×HRE)和萤光素酶(Luc)报告基因的人肾透明细胞癌(786-O)单克隆细胞系,构建以缺氧诱导因子2α(HIF2α)为靶点的化合物筛选的细胞模型,并对其应用加以初步验证。方法 采用基因重组技术,构建含有VEGFA启动子区5×HRE以及Luc报告基因的慢病毒载体,并感染786-O细胞,经过嘌呤霉素筛选获得能稳定表达Luc活性的786-O-5×HRE-Luc细胞系;采用等浓度梯度稀释获得单克隆细胞系,运用HIF2α抑制剂PT2385和PT2399处理,检测Luc活性变化,筛选对PT2385和PT2399反应更灵敏的单克隆细胞系。结果 通过基因测序鉴定,VEGFA启动子区5×HRE和Luc报告基因慢病毒表达载体构建成功,经过嘌呤霉素(Puro)筛选获得稳定表达Luc的786-O-5×HRE-Luc细胞;PT2385和PT2399可剂量依赖性的降低细胞Luc的活性;得到对PT2385和PT2399反应灵敏的单克隆细胞系。结论 建立了786-O-5×HRE-Luc稳定表达5×HRE和Luc报告基因细胞系,为高通量筛选靶向HIF2α的药物提供一类新的细胞模型。
English Summary:
      Objective To establish a human clear cell carcinoma monoclonal cell line stably expressing human vascular endothelial growth factor A(VEGFA) promoter 5×hypoxia response element (5×HRE) and luciferase (Luc) reporter gene and to preliminarily verify its application targeting hypoxia inducible factor 2α (HIF2α). Methods Using genetic recombination technology, the lentiviral vector carrying 5×HRE and Luc reporter sequence was designed and constructed to infect 786-O cells and obtain 786-O-5×HRE-Luc cell lines by the selection with puromycin. Monoclonal cell lines were obtained by equal concentration gradient dilution, and treated with HIF2α inhibitors PT2385 and PT2399 to detect the change of Luc activity, and screened monoclonal cell lines that were more sensitive to PT2385 and PT2399. Results Lentivirus-infected 786-O cells were screened by puromycin, the 786-O-5×HRE-Luc cells stably expressing firefly Luc was obtained. PT2385 and PT2399 decreased the Luc luminescence value of 786-O-5×HRE-Luc cells in a dose-dependent manner, which provides a new cell model for high-throughput screening of compounds targeting HIF2α. Conclusion The cell line of 786-O-5×HRE-Luc containing VEGFA promoter 5×HRE and Luc reporter gene has been successfully constructed, which provides a new cell model for high throughput screening of HIF2α-targeting drugs.
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