Iwamoto R, Fushimi K, Hiraki Y, Namba M
Department of Radiology, Okayama University Medical School, Japan.
Acta Med Okayama. 1997 Feb;51(1):19-23. doi: 10.18926/AMO/30807.
This study was conducted to evaluate the frequency of DNA transfection into human cells following X-ray irradiation. We transfected plasmid DNA (pSV2neo) into human cells, HeLa and PA-1, by either calcium phosphate precipitation or the lipofection method immediately after irradiating the cells with various doses of X-rays. The transfection frequency was evaluated by counting the number of G418-resistant colonies. When circular plasmid DNA was used, irradiation up to a dose of 2 Gy dose-dependently increased the transfection frequency, which reached a maximum of 5 to 10-fold that of the control unirradiated cells. When linear plasmid DNA was used, the transfection frequency was 2 times higher than that of circular DNA. All five of the clones that were randomly chosen expressed the transfected neo gene. In addition, the pSV2neo gene was randomly integrated into the genomic DNA of each clone. These findings indicate that X-ray treatment can facilitate foreign DNA transfer into human cells and that radiation-induced DNA breaks may promote the insertion of foreign DNA into host DNA. The enhancement of DNA transfection with X-rays may be instrumental in practicing gene therapy.
本研究旨在评估X射线照射后人细胞中DNA转染的频率。我们在以不同剂量的X射线照射细胞后,立即通过磷酸钙沉淀法或脂质体转染法将质粒DNA(pSV2neo)转染到人细胞HeLa和PA-1中。通过计数G418抗性菌落的数量来评估转染频率。当使用环状质粒DNA时,高达2 Gy的照射剂量依赖性地增加了转染频率,最高达到未照射对照细胞的5至10倍。当使用线性质粒DNA时,转染频率比环状DNA高2倍。随机选择的5个克隆均表达了转染的neo基因。此外,pSV2neo基因随机整合到每个克隆的基因组DNA中。这些发现表明,X射线处理可促进外源DNA转入人细胞,且辐射诱导的DNA断裂可能促进外源DNA插入宿主DNA。X射线增强DNA转染可能有助于基因治疗的实践。