Department of Biophysics, Faculty of Medicine and Gazi Non-ionizing Radiation Protection (GNRP) Center, Gazi University, Beşevler, 06510, Ankara, Turkey,
Cell Biochem Biophys. 2013;67(3):1371-8. doi: 10.1007/s12013-013-9669-6.
In the present study we aimed to investigate the effects of 2.1 GHz Wideband Code Division Multiple Access (W-CDMA) modulated Microwave (MW) Radiation on cell survival and apoptotic activity of human breast fibroblast cells. The cell cultures were exposed to W-CDMA modulated MW at 2.1 GHz at a SAR level of 0.607 W/kg for 4 and 24 h. The cell viability was assessed by MTT [3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] method. The percentage of apoptotic cells was analyzed by Annexin V-FITC and PI staining. 5,5',6,6'-Tetrachloro-1,1',3,3'- tetraethylbenzimidazolcarbocyanine iodide (JC-1) was used to measure Mitochondrial Membrane Potential (ΔΨm). sFasL and Fas/APO-1 protein levels were determined by ELISA method. 2.1 GHz MW radiation was shown to be able to inhibit cell proliferation and induce apoptosis in human breast fibroblast cells. The cell viability of MW-exposed cells was decreased significantly. The percentages of Annexin V-FITC positive cells were higher in MW groups. ΔΨm was decreased significantly due to MW radiation exposure. However, neither sFas nor FasL level was significantly changed in MW-exposed fibroblast cells. The results of this study showed that 2.1 GHz W-CDMA modulated MW radiation-induced apoptotic cell death via the mitochondrial pathway.
在本研究中,我们旨在研究 2.1GHz 宽带码分多址(W-CDMA)调制微波(MW)辐射对人乳腺成纤维细胞存活和凋亡活性的影响。将细胞培养物暴露于 2.1GHz 的 W-CDMA 调制 MW 下,SAR 水平为 0.607W/kg,暴露 4 小时和 24 小时。通过 MTT[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐]法评估细胞活力。通过 Annexin V-FITC 和 PI 染色分析凋亡细胞的百分比。使用 5,5',6,6'-四氯-1,1',3,3'-四乙基苯并咪唑羰花青碘化物(JC-1)测量线粒体膜电位(ΔΨm)。通过 ELISA 法测定 sFasL 和 Fas/APO-1 蛋白水平。结果显示,2.1GHz MW 辐射能够抑制人乳腺成纤维细胞的增殖并诱导其凋亡。MW 照射细胞的细胞活力明显下降。MW 组 Annexin V-FITC 阳性细胞的百分比更高。由于 MW 辐射暴露,ΔΨm 明显降低。然而,MW 暴露的成纤维细胞中 sFas 或 FasL 水平均无明显变化。本研究结果表明,2.1GHz W-CDMA 调制 MW 辐射通过线粒体途径诱导凋亡性细胞死亡。