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shRNA干扰沉默Net1基因对电离辐射损伤反应的影响
引用本文:徐畅,王彦,杜利清,曹嘉,刘强.shRNA干扰沉默Net1基因对电离辐射损伤反应的影响[J].国际放射医学核医学杂志,2013,37(3):135-138.
作者姓名:徐畅  王彦  杜利清  曹嘉  刘强
作者单位:300192 天津,中国医学科学院放射医学研究所,天津市分子核医学重点实验室
基金项目:国家自然科学基金(项目编号:31200634),天津市回国人员绿色通道项目(项目编号:12JCYBJC32900)中国医学科学院放射医学研究所引进人才启动基金(项目编号:所人1232)协和青年基金和中央高校基本科研业务费专项资金(项目编号:2012J05,2012G01)
摘    要: 目的 研究神经上皮细胞转化基因1(NET1)在电离辐射损伤反应中的生物学功能。 方法 运用RNA干扰技术,在细胞中特异性沉默Net1基因,然后通过集落存活实验和免疫印迹法研究抑制Net1表达对细胞的电离辐射损伤反应的影响。 结果 Net1敲低表达的细胞对电离辐射的敏感性增强,表现为更多细胞发生了凋亡,并且在γ射线照射后,毛细血管扩张性共济失调症突变蛋白(ATM)和细胞周期检查点激酶2(Chk2)的磷酸化水平也比对照细胞增强。 结论 Net1对于受到电离辐射的细胞有一定的保护作用,很可能在电离辐射损伤修复中具有重要作用。

关 键 词:电离辐射    RNA干扰    细胞凋亡    神经上皮细胞转化基因1
收稿时间:2013-04-15

The effects of short hairpin RNA-mediated silencing Net1 on ionizing radiation-induced damage responses
Chang XU,Yan WANG,Li-qing DU,Jia CAO,Qiang LIU.The effects of short hairpin RNA-mediated silencing Net1 on ionizing radiation-induced damage responses[J].International Journal of Radiation Medicine and Nuclear Medicine,2013,37(3):135-138.
Authors:Chang XU  Yan WANG  Li-qing DU  Jia CAO  Qiang LIU
Institution:Institute of Radiation Medicine, Chinese Academy of Medical Sciences, Tianjin Key Laboratory of Molecular Nuclear Medicine, Tianjin 300192, China
Abstract: Objective To study the biological roles of the neuroepithelioma transforming gene 1 (Net1)in the cellular responses to ionizing radiation(IR)-induced damage. Methods Specific shRNA was used to deplete Net1 in cells. The effects of Net1 depletion on the cellular responses to ionizing radiation were investigated through the colonogenic survival assay and immunoblotting analysis of DNA damage response proteins′ phosphorylation. Results Net1-depleted cells were more sensitive to IR, with a significantly increased induction of apoptosis. In response to IR, the phosphorylation levels of ataxia-telangiectasia mutated and checkpoint kinase 2 were much higher in the Net1-depleted cells than that in the control cells. Conclusion Net1 protects IR-treated cells from apoptosis and possibly plays an important role in IR-induced damage response and repair.
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