An Yan, Kato Koichi, Nakano Masayuki, Otsu Hiroshi, Okada Shoji, Yamanaka Kenzo
Department of Biochemical Toxicology, College of Pharmacy, Nihon University, 7-7-1 Narashinodai, Funabashi, Chiba 274-8555, Japan.
Cancer Lett. 2005 Dec 8;230(1):57-64. doi: 10.1016/j.canlet.2004.12.029.
The induction of oxidative stress in pulmonary cells during the process of lung tumor promotion by dimethylarsinic acid (DMA), a main metabolite of inorganic arsenics in mammals, was examined by immunohistochemical analysis using a specific antibody against 4-hydroxy-2-nonenal (4HNE) adducts, which are major aldehydic metabolites of lipid peroxidation. We demonstrated that 4HNE-modified proteins existed specifically in the secretory granules in terminal bronchiolar Clara cells. Furthermore, the degree of positive staining increased with the duration of DMA administration. Transmission electron microscopy revealed morphological changes in the Clara cells of DMA-treated mice. These results suggest that Clara cells are the major target cell for DMA-induced oxidative stress and that the cells may play an important role in the lung tumor promotion process in mice.
通过使用针对4-羟基-2-壬烯醛(4HNE)加合物的特异性抗体进行免疫组织化学分析,检测了二甲基胂酸(DMA)(哺乳动物体内无机砷的主要代谢产物)在肺肿瘤促进过程中对肺细胞氧化应激的诱导作用,4HNE加合物是脂质过氧化的主要醛类代谢产物。我们证明,4HNE修饰的蛋白特异性存在于终末细支气管克拉拉细胞的分泌颗粒中。此外,阳性染色程度随DMA给药时间的延长而增加。透射电子显微镜揭示了DMA处理小鼠克拉拉细胞的形态变化。这些结果表明,克拉拉细胞是DMA诱导氧化应激的主要靶细胞,并且这些细胞可能在小鼠肺肿瘤促进过程中发挥重要作用。