Koizumi Shinji, Yamada Hirotomo
Department of Hazard Assessment, National Institute of Industrial Health, Kawasaki, Japan.
J Occup Health. 2003 Nov;45(6):331-4. doi: 10.1539/joh.45.331.
Cadmium (Cd) is a heavy metal known to be toxic and carcinogenic, but its mechanism of action remains to be elucidated. Development of the DNA microarray technology has recently made the comprehensive analysis of gene expression possible, and it could be a powerful tool also in toxicological studies. With microarray slides containing 7,000-9,000 genes, we have been studying the gene expression profiles of a human cell line exposed to Cd. By exposure to a non-lethal concentration of Cd, 46 upregulated and 10 downregulated genes whose expression levels changed twofold or greater were observed. The expression of genes related to cellular protection and damage control mechanisms such as those encoding metallothioneins, anti-oxidant proteins and heat shock proteins was simultaneously induced. In addition, altered expression of many genes involved in signaling, metabolism and so on was newly observed. As a whole, a number of genes appear to be coordinately regulated toward survival from Cd toxicity. When cells were exposed to a higher concentration of Cd, more remarkable effects were observed both in the number of affected genes and in the extent of altered expression. These findings will contribute to the understanding of the complicated biological effects of Cd.
镉(Cd)是一种已知具有毒性和致癌性的重金属,但其作用机制仍有待阐明。DNA微阵列技术的发展近来使得对基因表达进行全面分析成为可能,并且它在毒理学研究中也可能是一种强大的工具。利用包含7000 - 9000个基因的微阵列载玻片,我们一直在研究暴露于镉的人细胞系的基因表达谱。通过暴露于非致死浓度的镉,观察到46个上调和10个下调的基因,其表达水平变化两倍或更大。与细胞保护和损伤控制机制相关的基因,如编码金属硫蛋白、抗氧化蛋白和热休克蛋白的基因的表达同时被诱导。此外,新观察到许多参与信号传导、代谢等的基因表达发生改变。总体而言,许多基因似乎朝着从镉毒性中存活的方向被协同调节。当细胞暴露于更高浓度的镉时,在受影响基因的数量和表达改变的程度方面都观察到更显著的影响。这些发现将有助于理解镉的复杂生物学效应。