Parker J E, Kiel J L, Winters W D
Department of Microbiology, University of Texas Health Science Center, San Antonio.
Physiol Chem Phys Med NMR. 1988;20(2):129-34.
Four rodent cell lines were exposed to 2450 MHz microwave radiation at a Specific Absorption Rate (SAR) of 103.5 +/- 4.2 W/kg for varying lengths of time at 37 degrees, 40 degrees, 42 degrees and 45 degrees C. mRNA was extracted from microwave-exposed and sham-exposed cells and dot blotted or Northern blotted to nitrocellulose. Radioisotope labelled DNA probes of oncogenes, heat shock protein or long terminal repeat sequences were hybridized to the mRNA, and the resulting autoradiographs analyzed for differences in levels of mRNA expression between exposed and nonexposed samples. With the cell lines and probes used in this study no significant differences in mRNA expression were observed after microwave exposure.
将四种啮齿动物细胞系在37摄氏度、40摄氏度、42摄氏度和45摄氏度下,以103.5±4.2瓦/千克的比吸收率(SAR)暴露于2450兆赫微波辐射下不同时长。从经微波照射和假照射的细胞中提取mRNA,并将其点杂交或Northern杂交到硝酸纤维素膜上。将癌基因、热休克蛋白或长末端重复序列的放射性同位素标记DNA探针与mRNA杂交,并分析所得放射自显影片,以检测照射和未照射样品之间mRNA表达水平的差异。使用本研究中所用的细胞系和探针,微波照射后未观察到mRNA表达有显著差异。