Division of Genetic and Reproductive Toxicology, National Center for Toxicological Research, Jefferson, AR 72079, USA.
Toxicol In Vitro. 2010 Mar;24(2):439-44. doi: 10.1016/j.tiv.2009.10.004. Epub 2009 Oct 14.
Vitamin A (all-trans-retinol; retinol) is an essential human nutrient and plays an important role in several biological functions. However, under certain circumstances, retinol treatment can cause free radical generation and induce oxidative stress. In this study, we investigated photocytotoxicity and photomutagenicity of retinol using L5178Y/Tk(+/-) mouse lymphoma cells concomitantly exposed to retinol and ultraviolet A (UVA) light. While the cells treated with retinol alone at the doses of 5 or 10microg/ml in the absence of light did not increase the mutant frequency (MF) in the Tk gene, the treatment of the cells with 1-4microg/ml retinol under UVA light (1.38mW/cm(2) for 30min) increased the MF in the Tk gene in a dose-responsive manner. To elucidate the underlying mechanism of action, we also examined the mutational types of the Tk mutants by determining their loss of heterozygosity (LOH) at four microsatellite loci spanning the entire chromosome 11 on which the Tk gene is located. The mutational spectrum for the retinol+UVA treatment was significantly different from those of the control and UVA alone. More than 93% of the mutants from retinol+UVA treatment lost heterozygosity at the Tk1 locus and the major type (58%) of mutations was LOHs extending to D11Mit42, an alternation involving approximately 6cM of the chromosome, whereas the main type of mutations in the control was non-LOH mutations. These results suggest that retinol is mutagenic when exposed to UVA in mouse lymphoma cells through a clastogenic mode-of-action.
维生素 A(全反式视黄醇;视黄醇)是人体必需的营养物质,在多种生物学功能中发挥重要作用。然而,在某些情况下,视黄醇治疗会引起自由基生成,并诱导氧化应激。在这项研究中,我们使用 L5178Y/Tk(+/-) 小鼠淋巴瘤细胞,同时暴露于视黄醇和紫外线 A(UVA)光下,研究了视黄醇的光细胞毒性和光致突变性。虽然单独用视黄醇处理,剂量为 5 或 10μg/ml,在没有光照的情况下,不会增加 Tk 基因的突变频率(MF),但在 UVA 光(1.38mW/cm(2) 照射 30min)下,用 1-4μg/ml 的视黄醇处理细胞,会以剂量依赖的方式增加 Tk 基因的 MF。为了阐明作用机制,我们还通过确定横跨 Tk 基因所在的整个第 11 号染色体的四个微卫星位点的杂合性丢失(LOH),来检测 Tk 突变体的突变类型。视黄醇+UVA 处理的突变谱与对照和单独 UVA 处理的突变谱明显不同。超过 93%的来自视黄醇+UVA 处理的突变体在 Tk1 基因座失去杂合性,主要类型(58%)的突变是延伸到 D11Mit42 的 LOHs,涉及染色体约 6cM 的改变,而对照的主要突变类型是非 LOH 突变。这些结果表明,视黄醇在小鼠淋巴瘤细胞中通过断裂剂作用模式暴露于 UVA 时具有致突变性。