Valproic acid-induced gene expression responses in rat whole embryo culture and comparison across in vitro developmental and non-developmental models

•Transcriptomics was used to identify VPA-induced gene expression changes in WEC.•VPA-induced responses were compared across in vitro-based developmental models.•We observed conservation of VPA-induced gene regulation across in vitro developmental models.•Developmental models provide added value whe...

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Veröffentlicht in:Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2013-11, Vol.41, p.57-66
Hauptverfasser: Tonk, Elisa C.M., Robinson, Joshua F., Verhoef, Aart, Theunissen, Peter T., Pennings, Jeroen L.A., Piersma, Aldert H.
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Sprache:eng
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Zusammenfassung:•Transcriptomics was used to identify VPA-induced gene expression changes in WEC.•VPA-induced responses were compared across in vitro-based developmental models.•We observed conservation of VPA-induced gene regulation across in vitro developmental models.•Developmental models provide added value when assessing developmental-specific effects. 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.
ISSN:0890-6238
1873-1708
DOI:10.1016/j.reprotox.2013.06.069