Möller L, Grzybowska E, Zeisig M, Cimander B, Hemminki K, Chorazy M
Karolinska Institute, Department for Biosciences, Huddinge, Sweden.
Carcinogenesis. 1996 Jan;17(1):61-6. doi: 10.1093/carcin/17.1.61.
32P-HPLC is a recently published method to generate DNA adduct profiles after exposure to a complex of genotoxic substances. The low detection limit enables characterization of individual DNA adducts in the general population. The 32P-HPLC method was applied to human lymphocytes and granulocytes from Silesia, a polluted industrial region in the south of Poland. Human samples were collected at the end of winter and summer to investigate the seasonal influence on DNA adduct formation. In lymphocytes a strong seasonal variation was seen in total DNA adducts, with winter values exceeding the summer values by 7.33 +/- 3.56 times. Granulocytes did not show any seasonal variation. In winter-collected lymphocytes the DNA adduct levels were 21.4 +/- 16.6/10(8) normal nucleotides (NN) while the summer values were 2.96 +/- 2.46/10(8) NN. Granulocytes had 8.06 +/- 7.76 and 9.59 +/- 6.19 DNA adducts/10(8) NN during winter and summer respectively. The lymphocyte DNA adduct profile consisted of at least 16 individual or clusters of DNA adducts. All 16 had a clear winter influence, with a winter:summer ratio of 1.6-15.3, indicating exposure to a complex mixture of genotoxic substances. The DNA adducts analyzed in human lymphocytes had retention times similar to DNA adducts generated by polycyclic aromatic hydrocarbons. The suggested candidates for DNA adducts displayed a similar seasonal variation in airborne particles to that found in DNA adducts in lymphocytes of humans living in the area. This is the first application of the 32P-HPLC method to analysis of DNA adducts in human tissues.
32P - 高效液相色谱法是一种最近发表的方法,用于在暴露于遗传毒性物质复合物后生成DNA加合物谱。低检测限能够对普通人群中的个体DNA加合物进行表征。32P - 高效液相色谱法应用于来自西里西亚(波兰南部一个污染严重的工业区)的人类淋巴细胞和粒细胞。在冬季末和夏季采集人类样本,以研究季节对DNA加合物形成的影响。在淋巴细胞中,总DNA加合物呈现出强烈的季节变化,冬季值比夏季值高出7.33±3.56倍。粒细胞未显示出任何季节变化。冬季采集的淋巴细胞中DNA加合物水平为21.4±16.6/10⁸正常核苷酸(NN),而夏季值为2.96±2.46/10⁸NN。粒细胞在冬季和夏季的DNA加合物分别为8.06±7.76和9.59±6.19/10⁸NN。淋巴细胞DNA加合物谱由至少16种个体或DNA加合物簇组成。所有16种加合物都受到明显的冬季影响,冬季与夏季的比值为1.6 - 15.3,表明暴露于遗传毒性物质的复杂混合物中。在人类淋巴细胞中分析的DNA加合物保留时间与多环芳烃产生的DNA加合物相似。推测的DNA加合物候选物在空气中颗粒物中的季节变化与该地区居民淋巴细胞中DNA加合物的季节变化相似。这是32P - 高效液相色谱法首次应用于人体组织中DNA加合物的分析。