INRS, Institut Armand-Frappier, Laval, Québec, Canada.
Centre de Recherche Biomed, Université du Québec à Montréal, Montréal, Québec, Canada.
Toxicol Sci. 2017 Sep 1;159(1):114-123. doi: 10.1093/toxsci/kfx123.
Proper mammary gland development and function require precise hormonal regulation and bidirectional cross talk between cells provided by means of paracrine factors as well as intercellular junctions; exposure to environmental endocrine disruptors can disturb these processes. Exposure to one such family of chemicals, the brominated flame retardants (BFRs), is ubiquitous. Here, we tested the hypothesis that BFR exposures disrupt signaling pathways and intercellular junctions that control mammary gland development. Before mating, during pregnancy and throughout lactation, female Sprague-Dawley rats were fed diets containing that BFR mixture based on house dust, delivering nominal exposures of BFR of 0 (control), 0.06, 20, or 60 mg/kg/d. Dams were euthanized and mammary glands collected on postnatal day 21. BFR exposure had no significant effects on mammary gland/body weight ratios or the levels of proteins involved in milk synthesis, epithelial-mesenchymal transition, cell-cell interactions, or hormone signalling. However, BFR exposure (0.06 mg/kg/d) down-regulated phospho-ser675 β-catenin (p-β-catSer675) levels in the absence of any effect on total β-catenin levels. Levels of p-CREB were also down-regulated, suggesting that PKA inhibition plays a role. p-β-catSer675 co-localized with β-catenin at the mammary epithelial cell membrane, and its expression was decreased in animals from the 0.06 and 20 mg/kg/d BFR treatment groups. Although β-Catenin signaling was not affected by BFR exposure, the interaction between p-β-catSer675 and E-cadherin was significantly reduced. Together, our results demonstrate that exposure to an environmentally relevant mixture of BFR during pregnancy and lactation decreases p-β-catser675 at cell adhesion sites, likely in a PKA-dependant manner, altering mammary gland signaling.
乳腺的正常发育和功能需要精确的激素调节以及细胞间通过旁分泌因子和细胞连接进行的双向交流;而环境内分泌干扰物的暴露会干扰这些过程。一种此类化学物质家族——溴化阻燃剂(BFRs)的暴露无处不在。在这里,我们检验了这样一个假设,即 BFR 暴露会破坏控制乳腺发育的信号通路和细胞间连接。在交配前、怀孕期间和整个哺乳期,雌性 Sprague-Dawley 大鼠通过饮食摄入基于家庭灰尘的 BFR 混合物,接受名义上的 BFR 暴露剂量分别为 0(对照)、0.06、20 或 60mg/kg/d。在产后第 21 天处死母鼠并收集乳腺。BFR 暴露对乳腺/体重比或参与乳汁合成、上皮-间充质转化、细胞-细胞相互作用或激素信号的蛋白质水平没有显著影响。然而,BFR 暴露(0.06mg/kg/d)在不影响总β-catenin 水平的情况下下调了磷酸化 Ser675 β-catenin(p-β-catSer675)水平。p-CREB 水平也下调,表明 PKA 抑制起作用。p-β-catSer675 与β-catenin 在乳腺上皮细胞膜上共定位,并且其表达在来自 0.06 和 20mg/kg/d BFR 处理组的动物中减少。尽管 BFR 暴露没有影响β-catenin 信号,但 p-β-catSer675 与 E-cadherin 的相互作用显著减少。总之,我们的结果表明,在怀孕期间和哺乳期暴露于环境相关的 BFR 混合物会降低细胞黏附部位的 p-β-catSer675,可能以 PKA 依赖的方式改变乳腺信号。