Tait Sabrina, Tassinari Roberta, Maranghi Francesca, Mantovani Alberto
Food and Veterinary Toxicology Unit, Dept. Veterinary Public Health and Food Safety, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy.
Genom Data. 2015 Apr 11;4:109-11. doi: 10.1016/j.gdata.2015.04.004. eCollection 2015 Jun.
Bisphenol A (BPA), a widespread Endocrine Disrupter mainly used in food contact plastics, may induce adverse effects especially on susceptible lifestages, first of all pregnancy. The present study considered placental development as a potential target of BPA and investigated potential differences in the modes of action of two doses of BPA by a toxicogenomic approach. Pregnant CD-1 mice were administered with vehicle, 0.5 (BPA05) or 50 mg/kg (BPA50) body weight (bw)/die of BPA, from gestational day (GD) 1 to GD11. At GD12 dams were sacrificed and transcriptomic analysis was performed on placenta samples. Histological, histomorphometrical and immunohistochemical analyses were also performed to phenotypically anchor transcriptional changes associated with BPA exposure. The interpretation and description of the overall data are included in a manuscript under revision [1]. Here we describe the experimental design and the analysis performed on the gene expression data which are publicly available through the Gene Expression Omnibus (GEO) database with accession number GSE63852.
双酚A(BPA)是一种广泛存在的内分泌干扰物,主要用于食品接触塑料,可能会产生不良影响,尤其是对易感生命阶段,首先是孕期。本研究将胎盘发育视为BPA的一个潜在靶点,并通过毒理基因组学方法研究了两种剂量BPA作用模式的潜在差异。从妊娠第1天(GD)至GD11,给怀孕的CD-1小鼠分别灌胃给予溶媒、0.5(BPA05)或50毫克/千克体重(bw)/天的BPA。在GD12处死母鼠,并对胎盘样本进行转录组分析。还进行了组织学、组织形态计量学和免疫组化分析,以从表型上确定与BPA暴露相关的转录变化。对总体数据的解读和描述包含在一篇正在修订的论文中[1]。在此,我们描述了实验设计以及对通过基因表达综合数据库(GEO)数据库公开获取的基因表达数据所进行的分析,该数据库的登录号为GSE63852。