Centre for Health Protection, National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Reprod Toxicol. 2013 Nov;41:57-66. doi: 10.1016/j.reprotox.2013.06.069. Epub 2013 Jun 28.
Transcriptomic evaluations may improve toxicity prediction of in vitro-based developmental models. In this study, transcriptomics was used to identify VPA-induced gene expression changes in rat whole embryo culture (WEC). Furthermore, VPA-induced responses were compared across in vitro-based developmental models, such as the cardiac and neural embryonic stem cells (ESTc and ESTn, respectively) and the zebrafish embryotoxicity model. VPA-induced gene regulation in WEC corresponded with observed morphological effects and previously suggested mechanisms of toxicity. Gene Ontology term-directed analysis showed conservation of VPA-induced gene expression changes across in vitro-based developmental models, with ESTc and ESTn exhibiting complementary responses. Furthermore, comparison of in vitro-based developmental and non-developmental models revealed that more generalized VPA-induced effects can be detected using non-developmental models whereas developmental models provide added value when assessing developmental-specific effects. These analyses can be used to optimize test batteries for the detection of developmental toxicants in vitro.
转录组评估可能会提高基于体外的发育模型的毒性预测。在这项研究中,使用转录组学来鉴定 VPA 诱导的大鼠全胚胎培养 (WEC) 中的基因表达变化。此外,还比较了基于体外的发育模型之间的 VPA 诱导反应,例如心脏和神经胚胎干细胞 (ESTc 和 ESTn) 和斑马鱼胚胎毒性模型。WEC 中的 VPA 诱导基因调控与观察到的形态效应和先前提出的毒性机制相对应。基因本体论 (GO) 术语定向分析表明,基于体外的发育模型之间存在 VPA 诱导基因表达变化的保守性,其中 ESTc 和 ESTn 表现出互补反应。此外,基于体外的发育和非发育模型的比较表明,使用非发育模型可以检测到更广泛的 VPA 诱导效应,而发育模型在评估发育特异性效应时提供了附加值。这些分析可用于优化体外检测发育毒物的测试组合。