Johnson N F, Carpenter T R, Jaramillo R J, Liberati T A
Inhalation Toxicology Research Institute, Albuquerque, New Mexico 87185, USA.
Environ Health Perspect. 1997 Jun;105 Suppl 4(Suppl 4):913-8. doi: 10.1289/ehp.97105s4913.
A biodosimetric approach to determine alpha-particle dose to the respiratory tract epithelium from known exposures to radon has been developed in the rat. Cytotoxicity assays have been used to obtain dose-conversion factors for cumulative exposures typical of those encountered by underground uranium miners. However, this approach is not sensitive enough to derive dose-conversion factors for indoor radon exposures. The expression of DNA damage-inducible genes is being investigated as a biomarker of exposure to radon progeny. Exposure of cultures of A549 cells to alpha particles resulted in an increase in the protein levels of the DNA damage-inducible genes, p53, Cip1, and Gadd45. These protein changes were associated with a transient arrest of cells passing through the cell cycle. This arrest was typified by an increase in the number of cells in the G1 and G2 phases and a decrease in the number of cells in the S phase. The effect of inhaled alpha particles (radon progeny) in rats was examined in the epithelial cells of the lateral well of the anterior nasal cavity. Exposures to radon progeny resulted in a significant increase in the number of cells in the G1 phase and a decrease in the number of cells in the S phase. These cell-cycle changes were concomitant with an increase in the number of cells containing DNA strand breaks. These results suggest a commonality between cell-cycle events in vitro and in vivo following exposure to ionizing radiation. In addition to ionizing radiation, A549 cells were exposed to 4-nitroquinoline-1-oxide, methyl methanesulphonate, crocidolite asbestos, and glass microfiber. These studies showed that physical and chemical agents induce different expression patterns of p53, Cip1, and Gadd153 proteins and they could be used to discriminate between toxic and nontoxic materials such as asbestos and glass microfiber. The measurement of gene expression in A549 cells may provide a means to identify a broad spectrum of physical and chemical toxicants encountered in the environment.
已在大鼠中开发出一种生物剂量测定方法,用于根据已知的氡暴露情况确定呼吸道上皮细胞所接受的α粒子剂量。细胞毒性测定已用于获取地下铀矿工人所经历的典型累积暴露的剂量转换因子。然而,这种方法对于得出室内氡暴露的剂量转换因子不够敏感。DNA损伤诱导基因的表达正作为氡子体暴露的生物标志物进行研究。将A549细胞培养物暴露于α粒子会导致DNA损伤诱导基因p53、Cip1和Gadd45的蛋白质水平升高。这些蛋白质变化与细胞通过细胞周期的短暂停滞有关。这种停滞的典型表现是G1期和G2期细胞数量增加,S期细胞数量减少。在前鼻腔外侧孔的上皮细胞中检测了吸入的α粒子(氡子体)对大鼠的影响。暴露于氡子体导致G1期细胞数量显著增加,S期细胞数量减少。这些细胞周期变化与含有DNA链断裂的细胞数量增加同时出现。这些结果表明,暴露于电离辐射后,体外和体内的细胞周期事件存在共性。除了电离辐射外,还将A549细胞暴露于4-硝基喹啉-1-氧化物、甲基磺酸甲酯、青石棉和玻璃微纤维。这些研究表明,物理和化学试剂会诱导p53、Cip1和Gadd153蛋白质产生不同的表达模式,它们可用于区分有毒和无毒物质,如石棉和玻璃微纤维。测量A549细胞中的基因表达可能提供一种手段,用于识别环境中遇到的广泛的物理和化学毒物。