Chen Zhen, Xing Yi-qiao, Xu Chong
Renmin Hospital of Wuhan University, Wuhan, China.
Zhonghua Yan Ke Za Zhi. 2012 Feb;48(2):159-63.
To explore the effects of siRNA-mediated downregulation of integrin-linked kinase (ILK) gene expression on the proliferation and apoptosis in retinoblastoma cells.
Experiment study. Human retinoblastoma cells, HXO-Rb(44) cells, were divided into four groups: ILK siRNA intervention group, control siRNA intervention group, empty liposome group and blank control group. ILK siRNA was transfected into HXO-Rb(44) cells by lipofection. The expression of ILK mRNA and protein was detected at 48 hours after transfection by RT-PCR and Western blot, respectively. Cell proliferation inhibition was measured by Cell Counting Kit-8 assay. The apoptosis was detected by Annexin/PI double immunofluorescence and flow cytometry. Statistical method adopted one-way ANOVA between each group overall comparison.
The HXO-Rb(44) cells were transfected by ILK siRNA successfully with lipofection. RT-PCR analysis showed that the expression of ILK mRNA in the ILK siRNA intervention group was significantly decreased as compared to the control siRNA intervention group, empty liposome group and blank control group (0.12 ± 0.02 vs. 0.45 ± 0.04, 0.42 ± 0.05 and 0.40 ± 0.04, F = 12.781, P = 0.000). Similar results were obtained for protein expression as revealed by Western blot analysis (0.10 ± 0.03 vs. 0.38 ± 0.07, 0.40 ± 0.05 and 0.43 ± 0.03, F = 18.647, P = 0.000). The proliferation inhibition rate in the ILK siRNA intervention group (35.0%) was higher than that in the blank control group (0%), control siRNA intervention group (2.1%) and empty liposome group (1.8%) (F = 23.573, P = 0.000). The results of immunofluorescence and flow cytometry showed that ratio of Annexin positive cells was highest in the ILK siRNA intervention group (26.5%), which was 5.0%, 4.6%, 5.3% in the empty liposome group, blank control group, control siRNA intervention group, respectively (F = 65.217, P = 0.000).
ILK siRNA can downregulate the expression of ILK gene in HXO-Rb(44) cells inhibited the cell proliferation and induced their apoptosis.
探讨小干扰RNA(siRNA)介导的整合素连接激酶(ILK)基因表达下调对视网膜母细胞瘤细胞增殖和凋亡的影响。
实验研究。人视网膜母细胞瘤HXO-Rb(44)细胞分为四组:ILK siRNA干预组、对照siRNA干预组、空脂质体组和空白对照组。采用脂质体转染法将ILK siRNA转染至HXO-Rb(44)细胞。分别于转染后48小时通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(Western blot)检测ILK mRNA和蛋白表达。采用细胞计数试剂盒-8法检测细胞增殖抑制情况。通过膜联蛋白/碘化丙啶(Annexin/PI)双免疫荧光和流式细胞术检测细胞凋亡情况。统计方法采用单因素方差分析进行组间总体比较。
通过脂质体转染成功将ILK siRNA转染至HXO-Rb(44)细胞。RT-PCR分析显示,与对照siRNA干预组、空脂质体组和空白对照组相比,ILK siRNA干预组ILK mRNA表达显著降低(0.12±0.02 vs. 0.45±0.04、0.42±0.05和0.40±0.04,F = 12.781,P = 0.000)。蛋白质免疫印迹分析显示蛋白表达也得到类似结果(0.10±0.03 vs. 0.38±0.07、0.40±0.05和0.43±0.03,F = 18.647,P = 0.000)。ILK siRNA干预组的增殖抑制率(35.0%)高于空白对照组(0%)、对照siRNA干预组(2.1%)和空脂质体组(1.8%)(F = 23.573,P = 0.000)。免疫荧光和流式细胞术结果显示,ILK siRNA干预组膜联蛋白阳性细胞比例最高(26.5%),空脂质体组、空白对照组、对照siRNA干预组分别为5.0%、4.6%、5.3%(F = 65.217,P = 0.000)。
ILK siRNA可下调HXO-Rb(44)细胞中ILK基因的表达,抑制细胞增殖并诱导其凋亡。