CD19
绿色荧光蛋白
荧光素酶
流式细胞术
细胞培养
嵌合抗原受体
分子生物学
转染
化学
癌症研究
T细胞
医学
生物
免疫学
免疫系统
生物化学
遗传学
基因
作者
Yujie Guo,Haixiao Duan,Yining Chen,Binfeng Yang,Han Hu,Binlei Liu,Yang Wang
出处
期刊:PubMed
日期:2024-02-25
卷期号:40 (2): 458-472
标识
DOI:10.13345/j.cjb.230468
摘要
Solid tumors lack well-defined targets for chimeric antigen receptor T-cell (CAR-T) therapy. Therefore, introducing a known target molecule, CD19, into solid tumor cell lines via lentiviral transduction to investigate the cytotoxicity of CD19 CAR-T cells can potentially support CAR-T cell therapy against solid tumors. In this study, a stable colon cancer CT26 cell line, CT26-CD19-FLUC-GFP, expressing CD19, firefly luciferase (FLUC), and green fluorescent protein (GFP), was constructed using a triple-plasmid lentiviral system. The growth characteristics of this cell line were consistent with those of the CT26 cell line. Subsequent flow cytometry analysis confirmed stable expression of CD19 and GFP in CT26-CD19-FLUC-GFP cells after serial passaging up to the 5th, 10th, and 22nd generations. Further validation revealed significantly higher levels of
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