RNA干扰神经纤毛蛋白-2基因对结肠癌细胞HCT-8增殖和凋亡的影响

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目的:探讨应用RNAi技术降低神经纤毛蛋白-2(NRP-2)表达后对结肠癌细胞HCT-8增殖和凋亡的影响。方法:通过脂质体lip2000分别将NRP2-siRNA和NControl-siRNA转染入HCT-8中作为转染组和阴性对照组,加入磷酸盐缓冲液作为空白对照组,通过实时荧光定量PCR(RT-qPCR)和Western印迹法验证转染效果,采用细胞计数试剂盒(CCK)法、平板克隆实验和Ki-67蛋白染色实验检测3组细胞的增殖情况,吖啶橙/碘化丙啶(AO/PI)荧光染色实验检测3组细胞的凋亡情况。结果:RT-qPCR和Western印迹法结果表明转染组细胞NRP-2 mRNA相对表达量和NRP-2蛋白含量降低(0.46±0.05比0.99±0.05和1.00±0.06,1.04±0.06比1.73±0.09和1.65±0.11)(均n P<0.05),CCK法表明,转染组各时段的增殖能力较阴性对照组和空白对照组显著降低(24 h为0.53±0.04比0.82±0.07和0.87±0.07,48 h为0.54±0.05比1.00±0.09和1.17±0.05,72 h为0.75±0.05比1.31±0.13和1.50±0.03,96 h为1.05±0.04比1.46±0.09和1.86±0.06)(均n P<0.05);平板克隆实验显示转染组细胞较其他两组克隆形成能力显著下降(134.67±8.74比245.33±19.14和300.33±14.01,n P<0.05);Ki-67蛋白检测显示与对照组相比,转染组的细胞Ki-67含量显著下降(5.93±0.22比8.36±0.09和8.70±0.21,n P<0.05);AO/PI实验显示转染组较对照组相比凋亡细胞/活细胞比例显著上升(0.43±0.07比0.14±0.04和0.11±0.04,n P<0.05)。n 结论:降低NRP-2表达可使结肠癌细胞HCT-8的增殖能力下降,凋亡能力上升。“,”Objective:To investigate the effects of down-regulation of expression of neuropilin-2 (NRP-2) by RNA interference (RNAi) technique on proliferation and apoptosis of HCT-8 colon cancer cells.Methods:NRP2-siRNA and negative control (NControl)-siRNA were transferred into HCT-8 colon cancer cells by liposomes (lip2000) as transfection group and negative control group, and phosphate buffered solution (PBS) was added as blank control group. Quantitative reverse transcription PCR (RT-qPCR) and Western blot were used to detect the transfection effect. The proliferation of cells in the three groups was examined by cell counting kit (CCK) assay, colony-forming unit assay and Ki-67 protein staining assay, respectively. Moreover, the apoptosis of cells in the three groups was determined by acridine orange/propranidine iodide (AO/PI) staining method.Results:The results of RT-qPCR and Western blot showed that the relative expression of NRP-2 mRNA and the content of NRP-2 protein in the transfer group decreased (0.46±0.05 vs 0.99±0.05 and 1.00±0.06; 1.04±0.06 vs 1.73±0.09 and 1.65±0.11) (all n P<0.05). The results of CCK-8 demonstrated that the optical density of transfection group was significantly lower than that of the negative control group and the blank control group(24 h: 0.53±0.04 vs 0.82±0.07 and 0.87±0.07; 48 h: 0.54±0.05 vs 1.00±0.09 and 1.17±0.05; 72 h: 0.75±0.05 vs 1.31±0.13 and 1.50±0.03; 96 h:1.05±0.04 vs 1.46±0.09 and 1.86±0.06) (all n P<0.05). The results of colony-forming unit assay indicated that the proliferation ability of the cells in the transfer group was significantly lower than that in the other two groups (134.67±8.74 vs 245.33±19.14 and 300.33±14.01, n P<0.05). The results of Ki-67 protein staining assay showed that compared with the negative control group and blank control group, the expression of Ki-67 protein was significantly decreased in the transfection group (5.93±0.22 vs 8.36±0.09 and 8.70±0.21, n P<0.05). The results of AO/PI assay revealed that the ratio of apoptotic cells to living cells in the transfer group was significantly higher than that in the other two groups (0.43±0.07 vs 0.14±0.04 and 0.11±0.04, n P<0.05).n Conclusion:The proliferation ability of HCT-8 colon cancer cells decreases, and the apoptosis ability increases by decreasing the expression of NRP-2.
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