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作 者:刘藻滨 蒋晓帆[1] 张磊[1] 饶维[1] 杨悦凡[1] 戴舒惠 陈涛[1] 李三中[1] 罗鹏[1] 李娟[1] 费舟[1]
机构地区:[1]第四军医大学西京医院神经外科,陕西西安710032
出 处:《现代生物医学进展》2014年第17期3232-3235,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(30930093;81071034)
摘 要:目的:研究ADAR1 shRNA对人胶质瘤细胞U87细胞增殖和凋亡的影响。方法:通过构建ADAR1-shRNA的干扰质粒,经脂质体法转染胶质瘤U87细胞系,通过荧光倒置显微镜观察转染效率,选择转染效率最高的细胞系。取转染48h细胞,采用RT-PCR和Western-blot分别检测ADAR1 mRNA及蛋白的表达,流式细胞仪检测其细胞凋亡率,MTT法检测细胞增殖情况。结果:①经ADAR1-shRNA转染48h后的转染效率最高,此时U87细胞系中ADAR1 mRNA及蛋白的表达均被显著抑制,较阴性对照组及空白组均明显降低(P<0.05)。②在转染ADAR1-shRNA后,细胞凋亡率为(28.14%±3.76%),明显高于阴性对照组(3.20%±1.57%)和空白组(2.80%±1.49%),细胞增殖率较阴性对照组及空白组明显下降(P<0.05)。结论:通过shRNA抑制ADAR1的表达能明显促进人胶质瘤细胞U87细胞的凋亡和抑制其增殖,ADAR1基因可能成为治疗治疗胶质瘤的新靶点。Objective: Thisstudywasdesigned to investigate the effects of transfection withsmall hairpinRNA(shRNA)-DAR1 onthe proliferation and apoptosis of human glioma U87 cell line. Methods: The shRNA expression vector which expresses the specific shRNA targeting ADAR1 mRNA (ADARI-hRNA) or independent sequence (Negative-hRNA) was transfected into U87 cells, and then the U87 cells with stable expression of shRNA were selected. The expressions of ADAR1 were detected by RT-CR and Western blotting. The cellular proliferation activity, and the apoptotic rate were determined by MTT assay and flow cytometry, respectively. Results: Compared with the Negative-hRNA group and the non-ransfection group, the mRNA and protein expression levels of ADAR1 in U87 cells with transfection of ADARI-hRNA (interference group) was significantly suppressed and the cell proliferation was slowed down after transfection for 48h (P〈0.05). The apoptotic rate in the interference group (28.14%±3.76%) was significantly higher than those in the Negative-hRNA group (3.20%± 1.57%) and the non-ransfection group (2.80%± 1.49%) (P〈0.05). The proliferation ratio of U87 cells significantly decreased after transfection of ADAR1 shRNA (P〈0.05). Conclusion: ADARI-hRNA transfection increases the apoptotic rate, inhibits the proliferation of U87 glioma cells, which provides a potential target in gene therapy for glioma.
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