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聂思瑶, 刘波, 洪斌. 沉默TIPE2基因对T细胞共培养肺腺癌细胞LA795的免疫杀伤作用[J]. 肿瘤防治研究, 2016, 43(8): 673-677. DOI: 10.3971/j.issn.1000-8578.2016.08.005
引用本文: 聂思瑶, 刘波, 洪斌. 沉默TIPE2基因对T细胞共培养肺腺癌细胞LA795的免疫杀伤作用[J]. 肿瘤防治研究, 2016, 43(8): 673-677. DOI: 10.3971/j.issn.1000-8578.2016.08.005
NIE Siyao, LIU Bo, HONG Bin. Immune Killing Effect of Silencing TIPE2 Expression on T Lymphocytes Against Lung Adenocarcinoma Cells LA795[J]. Cancer Research on Prevention and Treatment, 2016, 43(8): 673-677. DOI: 10.3971/j.issn.1000-8578.2016.08.005
Citation: NIE Siyao, LIU Bo, HONG Bin. Immune Killing Effect of Silencing TIPE2 Expression on T Lymphocytes Against Lung Adenocarcinoma Cells LA795[J]. Cancer Research on Prevention and Treatment, 2016, 43(8): 673-677. DOI: 10.3971/j.issn.1000-8578.2016.08.005

沉默TIPE2基因对T细胞共培养肺腺癌细胞LA795的免疫杀伤作用

Immune Killing Effect of Silencing TIPE2 Expression on T Lymphocytes Against Lung Adenocarcinoma Cells LA795

  • 摘要:
    目的 利用特异性小干扰RNA(small interfering RNA, siRNA)技术沉默T细胞TIPE2基因表达, 体外观察转染T细胞对肺腺癌细胞LA795的免疫杀伤作用。
    方法 磁珠分选小鼠脾脏T细胞, 筛选并验证能有效沉默T淋巴细胞TIPE2基因的siRNA序列, 转染48 h后, 利用酶联免疫吸附法(ELISA)比较各分组细胞上清液中IFN-γ分泌水平;转染72 h后, 观察对比单纯T细胞(空白组)、阴性对照T细胞(阴性对照组)及转染T细胞(实验组)与小鼠肺腺癌细胞LA795共培养时肿瘤杀伤率。
    结果 我们筛选出一条能有效抑制TIPE2基因表达的siRNA序列, 细胞转染率79.63%, 蛋白表达抑制率达到79%, 转染48 h后, 检测实验组、阴性对照组、空白组细胞因子IFN-γ分泌水平分别为(678.96±26.91)pg/ml、(401.69±13.67)pg/ml、(387.03±15.14)pg/ml(P<0.001);转染72 h后, 与空白组及阴性对照组T细胞相比, 在不同的效靶比水平(20:1、40:1、80:1), 转染T细胞杀瘤活性均更高。当效靶比为80:1时, 实验组肿瘤细胞杀伤率达到(47.91±3.25)%。
    结论 利用特异性siRNA技术能有效沉默TIPE2基因, 并促进抗肿瘤活性细胞因子IFN-γ分泌, 增强T细胞对小鼠肺腺癌细胞LA795的体外免疫杀伤作用。

     

    Abstract:
    Objective To silence the expression of tumor necrosis factor-α-induced protein-8-like 2 (TIPE2) gene of T-lymphocytes by specific small interfering RNA (siRNA) and investigate the cytotoxicity activity of transfected T lymphocytes against lung adenocarcinoma cells LA795 in vitro.
    Methods Spleen T lymphocytes of mice were separated by magnetic bead, and we screened and validated an effective siRNA to silence TIPE2 gene of T lymphocytes. After 48h transfection, the secretion of IFN-γ was measured by enzyme-linked immuno-sorbent assay (ELISA). At the end, 72h after transfection, we compared the cytotoxicity activity changes against LA795 cells among transfected T lymphocytes(experimental group), negative control and simplex T lymphocytes(blank group) in vitro.
    Results We screened a siRNA sequences to effectively inhibit the expression of TIPE2 gene, the transfection rate was 79.63%, and the inhibition rate for TIPE2 protein expression reached 79%. After 48h transfection, the secretion level of IFN-γ in experimental group, negative control and blank group respectively were (678.96±26.91), (401.69±13.67) and (387.03±15.14)pg/ml (P<0.001). After 72h transfection, compared with negative control and blank group, the transfected T lymphocyte showed more efficient killing ability against LA795 cells in different level of effect/target(20:1, 40:1, 80:1). The killing rate of experimental group reached (47.91±3.25)% in effect/target of 80:1.
    Conclusion Silencing TIPE2 could significantly promote the secretion level of IFN-γ of mice T lymphocyte, enhance the cytotoxicity activity of T lymphocyte against LA795 lung adenocarcinoma cells in vitro.

     

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