首页> 外文期刊>International Journal of Radiation Biology: Covering the Physical, Chemical, Biological, and Medical Effects of Ionizing and Non-ionizing Radiations >Lentivirus-mediated RNA interference of Ku70 to enhance radiosensitivity of human mammary epithelial cells.
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Lentivirus-mediated RNA interference of Ku70 to enhance radiosensitivity of human mammary epithelial cells.

机译:慢病毒介导的Ku70 RNA干扰可增强人类乳腺上皮细胞的放射敏感性。

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摘要

PURPOSE: To investigate the radiosensitising effect of Ku autoantigen 70 (Ku70) and Ku autoantigen 80 (Ku80) knockdown by lentivirus-mediated RNA interference (RNAi) in the MCF10A immortalised human mammary epithelial cell line. MATERIALS AND METHODS: MCF10A cells were infected with lentiviral vectors for RNAi of Ku70. The Ku70-knockdown cell line (Ku70i) and a mock-infected control cell line (LVTHM) were used to perform radiation experiments. For the in vitro Micronucleus (MN) assay, both cell lines were irradiated with doses of 2 and 4 Gy (60)Co gamma-rays. For cell survival experiments, doses ranging between 0 and 8 Gy were used. RESULTS: Western blot analysis showed that the Ku70 lentiviral vector was effective in silencing the expression of both Ku70 and Ku80. A significantly higher radiation-induced MN yield was obtained in the Ku70i cell line compared to the control LVTHM cell line. RNAi of Ku70 also resulted in a lower survival yield after irradiation compared to the control cell line. Analysis of cell death mechanisms showed that MCF10A cells (Ku70i and LVTHM) do not undergo apoptosis, but undergo post-irradiation cellular senescence. CONCLUSION: RNAi of Ku70 resulted in increased chromosomal and cellular radiosensitivity in the MCF10A human mammary cell line after irradiation with (60)Co gamma-rays. These results further strengthen the role of the Ku protein in correct DNA double strand break (DSB) repair.
机译:目的:研究慢病毒介导的RNA干扰(RNAi)对Ku自身抗原70(Ku70)和Ku自身抗原80(Ku80)的抑制作用对永生化的人乳腺上皮细胞系MCF10A的放射增敏作用。材料与方法:MCF10A细胞用Ku70 RNAi慢病毒载体感染。使用Ku70组合式细胞系(Ku70i)和模拟感染的对照细胞系(LVTHM)进行放射实验。对于体外微核(MN)分析,两种细胞系均以2和4 Gy(60)Coγ射线辐照。对于细胞存活实验,使用0至8 Gy的剂量。结果:Western blot分析表明,Ku70慢病毒载体可有效沉默Ku70和Ku80的表达。与对照LVTHM细胞系相比,在Ku70i细胞系中获得了明显更高的辐射诱导MN产量。与对照细胞系相比,Ku70的RNAi在辐射后还导致较低的存活率。细胞死亡机制的分析表明,MCF10A细胞(Ku70i和LVTHM)不发生凋亡,而是在照射后发生细胞衰老。结论:(70)Coγ射线照射后,Ku70的RNAi导致MCF10A人乳腺细胞系的染色体和细胞放射敏感性增加。这些结果进一步加强了Ku蛋白在正确的DNA双链断裂(DSB)修复中的作用。

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