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RNA干扰下调bcl11b基因表达对Molt-4细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2010, 37(03): 247-250. DOI: 10.3971/j.issn.1000-8578.2010.03.001
引用本文: RNA干扰下调bcl11b基因表达对Molt-4细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2010, 37(03): 247-250. DOI: 10.3971/j.issn.1000-8578.2010.03.001
Effects of Down-regulating bcl11b Gene Expression on Proliferation and Apoptosis of Molt-4 Cells by RNA Interference[J]. Cancer Research on Prevention and Treatment, 2010, 37(03): 247-250. DOI: 10.3971/j.issn.1000-8578.2010.03.001
Citation: Effects of Down-regulating bcl11b Gene Expression on Proliferation and Apoptosis of Molt-4 Cells by RNA Interference[J]. Cancer Research on Prevention and Treatment, 2010, 37(03): 247-250. DOI: 10.3971/j.issn.1000-8578.2010.03.001

RNA干扰下调bcl11b基因表达对Molt-4细胞增殖和凋亡的影响

Effects of Down-regulating bcl11b Gene Expression on Proliferation and Apoptosis of Molt-4 Cells by RNA Interference

  • 摘要: 目的 分析下调bcl11b基因表达对人T淋巴细胞白血病细胞株Molt-4细胞增殖和凋亡的影响。 方法 通过核转技术将bcl11b-siRNA转染Molt-4细胞;在不同时间点分别采用荧光实时定量PCR观察其对bcl11b基因表达的影响;MTT法观察对Molt-4细胞体外增殖的抑制作用;流式细胞术及刘氏染色检测siRNA的诱导凋亡作用。 结果 转染后24小时开始细胞生存率均显著降低(P<0.01),细胞发生凋亡,bcl11b基因表达下调。 结论 bcl11b-siRNA可抑制Molt-4细胞中bcl11b基因表达,使肿瘤细胞增殖抑制和发生凋亡。

     

    Abstract: Objective To investigate the effects of down-regulating B-cell chronic lymphocytic leukemia /lymphoma 11B gene expression on the proliferation and apoptosis of Molt-4 cells. Methods The small interfering RNAs targeted on bcl11b gene were transfected into Molt-4 cells by nucleofector techique. The levels of bcl11b mRNA expression were analyzed at different time points after nucleofection by Real-time quantitative PCR. The cells proliferation rate was evaluated by MTT assay.Cell aapoptosis was detected by flow cytometry and modified Wright staining. Results The survival rates of siRNA-transfected cells had significantly decreased since the 24 hours after transfection (P<0.01). Apoptosis of treated molt-4 cells could be identified. The level of bcl11b mRNA expression was decreased. Conclusion bcl11b gene expression was inhibited by RNA interference selectively.Itmight inhibit the proliferation and induced the apoptosis of leukemia T cells.

     

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