Zhao Ran, Zhang Shu-zhi, Yao Geng-dong, Lu De-qiang, Jiang Huai, Xu Zheng-ping
Bioelectromagnetics Laboratory, Zhejiang University School of Medicine, Hangzhou 310031, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2006 Apr;24(4):222-5.
To investigate the changes of gene expression in rat neurons induced by 1.8 GHz radiofrequency electromagnetic fields (RF EMF) and to screen for the RF EMF-responsive genes.
Newly-born SD rats in 24 hours were sacrificed to obtain cortex and hippocampus neurons. The cells were divided randomly into two groups: the experiment group (the irradiation group) and the control group (the false irradiation group). In the irradiation group, after twelve days' culture, neurons were exposed to 1.8 GHz RF EMF modulated by 217 Hz at a specific absorption rate (SAR) of 2 W/kg for 24 hours (5 minutes on/10 minutes off) while in the false control group, the neurons were put in the same waveguide as in the irradiation group, but were not exposed to any irradiation. The total RNA was isolated and purified immediately after exposure. The affymetrix rat neurobiology U34 assay was used for detecting the changes in gene expression profile according to the manufacturer's instruction. RF EMF-responsive candidate gene was confirmed by using ribonuclease protection assay (RPA).
Among 1200 candidate genes, the expression levels of 34 genes were up or down regulated. Microtubule associated protein 2 (Map2) gene was selected as the candidate and subjected to further analysis. RPA data clearly revealed that Map2 was statistically significantly up-regulated after neurons were exposed to the RF EMF (P < 0.05).
The modulation of gene expression and function of Map2 as a neuron specific cytoskeleton protein is crucial to maintain the normal framework and function of neurons. The finding that 1.8 GHz RF EMF exposure increases the expression of Map2 might indicate some unknown effects of RF EMF on neurons.
研究1.8 GHz射频电磁场(RF EMF)诱导大鼠神经元基因表达的变化,并筛选RF EMF反应基因。
处死出生24小时内的新生SD大鼠,获取皮质和海马神经元。将细胞随机分为两组:实验组(照射组)和对照组(假照射组)。照射组在培养12天后,神经元暴露于以217 Hz调制、比吸收率(SAR)为2 W/kg的1.8 GHz RF EMF下24小时(开5分钟/关10分钟),而假对照组的神经元置于与照射组相同的波导中,但不进行任何照射。暴露后立即分离并纯化总RNA。根据制造商的说明,使用Affymetrix大鼠神经生物学U34检测法检测基因表达谱的变化。通过核糖核酸酶保护试验(RPA)确认RF EMF反应候选基因。
在1200个候选基因中,34个基因的表达水平上调或下调。选择微管相关蛋白2(Map2)基因作为候选基因并进行进一步分析。RPA数据清楚地显示,神经元暴露于RF EMF后,Map2在统计学上显著上调(P < 0.05)。
Map2作为神经元特异性细胞骨架蛋白,其基因表达和功能的调节对于维持神经元的正常结构和功能至关重要。1.8 GHz RF EMF暴露增加Map2表达这一发现可能表明RF EMF对神经元有一些未知的影响。