Immonen E, Serpi R, Vähäkangas K, Myllynen P
Institute of Biomedicine, Department of Pharmacology and Toxicology, University of Oulu, Oulu, Finland.
Chem Biol Interact. 2009 Nov 10;182(1):73-83. doi: 10.1016/j.cbi.2009.07.020. Epub 2009 Aug 6.
To compare the effects of the food toxin 2-amino-1-methyl-6-phenyl-imidazo[4,5-b]pyridine (PhIP) and estradiol in hormone-responsive MCF-7 cells, the cells were exposed to different concentrations of either PhIP or estradiol. The effect of various culture conditions (e.g. phenol red, FBS, vehicle (DMSO/EtOH) and seeding density) on responses was studied. Cells were continuously grown with steroid-containing or -deprived medium, or switched from steroid-containing to -deprived medium for the experiments to minimize the effect of background estrogenicity. Effects of PhIP and estradiol on cell viability and proliferation were determined by ATP analysis and Ki-67 immunocytochemistry. Expression of estrogen receptor alpha, cell stress markers (p53 and ERK) and estrogen responsive proteins (c-myc and ERK) were immunoblotted. All concentrations of estradiol induced cell proliferation, viability and changes in protein expression, typical for estrogenic responses. PhIP, however, increased viability only at low concentrations and depending on culture conditions. No changes in protein expressions by PhIP were noted, not even when switching cells from steroid-containing to -deprived medium which down-regulated the expression of proteins at basal level. Vehicle affected significantly viability, especially after exposure to PhIP, but not protein expression while medium changes affected both. In conclusion, the effects of PhIP and estradiol in MCF-7 cells are dependent on culture conditions. The detected PhIP-induced changes are weaker compared to those induced by estradiol.
为了比较食物毒素2-氨基-1-甲基-6-苯基咪唑并[4,5-b]吡啶(PhIP)和雌二醇对激素反应性MCF-7细胞的影响,将细胞暴露于不同浓度的PhIP或雌二醇中。研究了各种培养条件(如酚红、胎牛血清、溶剂(二甲基亚砜/乙醇)和接种密度)对反应的影响。为了尽量减少背景雌激素的影响,细胞在含类固醇或不含类固醇的培养基中连续培养,或在实验中从含类固醇培养基转换为不含类固醇的培养基。通过ATP分析和Ki-67免疫细胞化学测定PhIP和雌二醇对细胞活力和增殖的影响。对雌激素受体α、细胞应激标志物(p53和ERK)和雌激素反应蛋白(c-myc和ERK)的表达进行免疫印迹分析。所有浓度的雌二醇均诱导细胞增殖、活力以及蛋白质表达变化,这是雌激素反应的典型表现。然而,PhIP仅在低浓度时增加细胞活力,且取决于培养条件。未观察到PhIP引起的蛋白质表达变化,即使将细胞从含类固醇培养基转换为不含类固醇的培养基(这会下调基础水平的蛋白质表达)时也未观察到。溶剂显著影响细胞活力,尤其是在暴露于PhIP后,但不影响蛋白质表达,而培养基变化则对两者均有影响。总之,PhIP和雌二醇在MCF-7细胞中的作用取决于培养条件。与雌二醇诱导的变化相比,检测到的PhIP诱导的变化较弱。