Department of Pathology and Laboratory Medicine , Brown University , 70 Ship Street , Providence , Rhode Island 02912 , United States.
Chem Res Toxicol. 2018 Nov 19;31(11):1172-1184. doi: 10.1021/acs.chemrestox.8b00182. Epub 2018 Nov 6.
Epidemiological studies in chromate production have established hexavalent chromium as a potent lung carcinogen. Inhalation of chromium(VI) most often occurs in mixtures with other metals as among stainless steel welders, which is the largest occupational group with Cr(VI) exposure. Surprisingly, carcinogenicity of Cr(VI)-containing welding fumes is moderate and not consistently higher than that of Cr-free welding. Here, we investigated interactions between chromate and three other metal ions [Fe(III), Mn(II), Ni(II)] that are typically released from stainless steel welding particles. In human lung epithelial cells with physiological levels of ascorbate and glutathione, Cr(VI) was by far the most cytotoxic metal in single exposures. Coexposure with Fe(III) suppressed cytotoxicity and genotoxicity of Cr(VI), which resulted from a severe inhibition of Cr uptake by cells and required extracellular ascorbate/glutathione. Chemically, detoxification of Cr(VI) occurred via its rapid extracellular reduction by Fe(II) that primarily originated from ascorbate-reduced Fe(III). Glutathione was a significant contributor to reduction of Cr(VI) by Fe only in the presence of ascorbate. We further found that variability in Cr(VI) metabolism among common cell culture media was caused by their different Fe content. Ni(II) and Mn(II) had no detectable effects on metabolism, cellular uptake or cytotoxicity of Cr(VI). The main biological findings were confirmed in three human lung cell lines, including stem cell-like and primary cells. We discovered extracellular detoxification of carcinogenic chromate in coexposures with Fe(III) ions and identified the underlying chemical mechanism. Our findings established an important case when exposure to mixtures causes inactivation of a potent human carcinogen.
流行病学研究表明,六价铬是一种强有力的肺部致癌物质。铬(VI)的吸入通常发生在与其他金属的混合物中,如不锈钢焊工,这是接触 Cr(VI)的最大职业群体。令人惊讶的是,含 Cr(VI)的焊接烟尘的致癌性适中,并不总是高于无 Cr 焊接。在这里,我们研究了铬酸盐与其他三种金属离子[Fe(III)、Mn(II)、Ni(II)]之间的相互作用,这些金属离子通常是从不锈钢焊接颗粒中释放出来的。在含有生理浓度抗坏血酸和谷胱甘肽的人肺上皮细胞中,Cr(VI)是迄今为止在单一暴露中最具细胞毒性的金属。Fe(III)共暴露抑制了 Cr(VI)的细胞毒性和遗传毒性,这是由于细胞对 Cr 的摄取严重抑制,并且需要细胞外抗坏血酸/谷胱甘肽。从化学上讲,Cr(VI)的解毒是通过 Fe(II)的快速细胞外还原来实现的,Fe(II)主要来自抗坏血酸还原的 Fe(III)。只有在存在抗坏血酸的情况下,谷胱甘肽才是 Fe 还原 Cr(VI)的重要贡献者。我们还发现,常见细胞培养基中 Cr(VI)代谢的差异是由于它们不同的 Fe 含量造成的。Ni(II)和 Mn(II)对 Cr(VI)的代谢、细胞摄取或细胞毒性没有检测到影响。主要的生物学发现得到了三种人肺细胞系的证实,包括干细胞样和原代细胞。我们在与 Fe(III)离子的共暴露中发现了致癌铬的细胞外解毒,并确定了潜在的化学机制。我们的研究结果确立了一种重要的情况,即在暴露于混合物时,会使一种有效的人类致癌物失活。