Hindman Andrea R, Mo Xiaokui Molly, Helber Hannah L, Kovalchin Claire E, Ravichandran Nanditha, Murphy Alina R, Fagan Abigail M, St John Pamela M, Burd Craig J
Department of Molecular Genetics, The Ohio State University, Columbus, Ohio 43210.
The Ohio State University Comprehensive Cancer Center, Columbus, Ohio 43210.
Endocrinology. 2017 Oct 1;158(10):3435-3447. doi: 10.1210/en.2017-00116.
In utero exposure to the endocrine disrupting compound bisphenol A (BPA) is known to disrupt mammary gland development and increase tumor susceptibility in rodents. It is unclear whether different periods of in utero development might be more susceptible to BPA exposure. We exposed pregnant CD-1 mice to BPA at different times during gestation that correspond to specific milestones of in utero mammary gland development. The mammary glands of early-life and adult female mice, exposed in utero to BPA, were morphologically and molecularly (estrogen receptor-α and Ki67) evaluated for developmental abnormalities. We found that BPA treatment occurring before mammary bud invasion into the mesenchyme [embryonic day (E)12.5] incompletely resulted in the measured phenotypes of mammary gland defects. Exposing mice up to the point at which the epithelium extends into the precursor fat pad (E16.5) resulted in a nearly complete BPA phenotype and exposure during epithelial extension (E15.5 to E18.5) resulted in a partial phenotype. Furthermore, the relative differences in phenotypes between exposure windows highlight the substantial correlations between early-life molecular changes (estrogen receptor-α and Ki67) in the stroma and the epithelial elongation defects in mammary development. These data further implicate BPA action in the stroma as a critical mediator of epithelial phenotypes.
已知子宫内暴露于内分泌干扰化合物双酚A(BPA)会扰乱啮齿动物的乳腺发育并增加肿瘤易感性。尚不清楚子宫内发育的不同时期是否对BPA暴露更敏感。我们在妊娠期间的不同时间将怀孕的CD-1小鼠暴露于BPA,这些时间点对应于子宫内乳腺发育的特定里程碑。对子宫内暴露于BPA的幼年和成年雌性小鼠的乳腺进行形态学和分子水平(雌激素受体-α和Ki67)评估,以检测发育异常情况。我们发现,在乳腺芽侵入间充质之前(胚胎第12.5天)进行BPA处理,并未完全导致所测量的乳腺缺陷表型。在乳腺上皮延伸至前体脂肪垫之前(胚胎第16.5天)对小鼠进行暴露,会导致近乎完全的BPA表型,而在乳腺上皮延伸期间(胚胎第15.5天至18.5天)进行暴露,则会导致部分表型。此外,不同暴露时间段之间表型的相对差异突出了早期基质中分子变化(雌激素受体-α和Ki67)与乳腺发育中上皮伸长缺陷之间的显著相关性。这些数据进一步表明,基质中的BPA作用是上皮表型的关键介导因素。