Department of Hematology, the First Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, Shaanxi 710061, P.R. China.
Mol Med Rep. 2012 Dec;6(6):1288-92. doi: 10.3892/mmr.2012.1105. Epub 2012 Sep 27.
To investigate the possibility of prohibitin (PHB) inhibition by lentiviral vector-mediated RNA interference (RNAi) and its influence on cell apoptosis in the retinoic acid-resistant acute promyelocytic leukemia cell line NB4-R1, a lentiviral vector encoding a short hairpin RNA (shRNA) targeted against PHB (pGCSIL-GFP-PHB) was constructed and transfected into the packaging cells 293T, and the viral supernatant was collected to transfect NB4-R1 cells. Quantitative real-time fluorescent PCR and western blotting were used to detect the expression levels of PHB. Flow cytometry and detection of enzymatic activity of caspase-3 by western blotting were employed to examine cell apoptosis. Our results provide evidence that the lentiviral vector pGCSIL-GFP-PHB was constructed successfully, and the PHB mRNA and the protein expression inhibitory rates were 90.3 and 95.8%, respectively. When compared to the control group, the activity of caspase-3 decreased significantly, which showed a 57.3% downregulation, and the apoptosis rate was reduced by 44.6% (P<0.05). In conclusion, downregulation of the PHB gene may inhibit apoptosis of NB4-R1 cells, and it is speculated that this was at least partly due to the downregulation of caspase-3, and PHB may be a novel target for gene therapy for retinoic acid-resistant acute promyelocytic leukemia.
为了研究通过慢病毒载体介导的 RNA 干扰(RNAi)抑制 prohibitin(PHB)的可能性及其对维甲酸耐药急性早幼粒细胞白血病细胞系 NB4-R1 细胞凋亡的影响,构建了一种靶向 PHB 的短发夹 RNA(shRNA)的慢病毒载体(pGCSIL-GFP-PHB),并转染至包装细胞 293T,收集病毒上清液转染 NB4-R1 细胞。采用实时荧光定量 PCR 和 Western blot 检测 PHB 的表达水平。采用流式细胞术和 Western blot 检测 caspase-3 的酶活性来检测细胞凋亡。我们的结果表明成功构建了慢病毒载体 pGCSIL-GFP-PHB,PHB mRNA 和蛋白表达抑制率分别为 90.3%和 95.8%。与对照组相比,caspase-3 的活性显著降低,下调了 57.3%,凋亡率降低了 44.6%(P<0.05)。结论:下调 PHB 基因可能抑制 NB4-R1 细胞凋亡,推测这至少部分是由于 caspase-3 的下调,PHB 可能是维甲酸耐药急性早幼粒细胞白血病基因治疗的新靶点。