| Literature DB >> 28189605 |
Xinrong Chen1, Tao Han2, J Edward Fisher3, Wafa Harrouk4, Melissa S Tassinari5, Gwenn E Merry6, Daniel Sloper7, James C Fuscoe8, Deborah K Hansen9, Amy L Inselman10.
Abstract
The mouse embryonic stem cell test (mEST) is a promising in vitro assay for predicting developmental toxicity. In the current study, early differentiation of D3 mouse embryonic stem cells (mESCs) under osteoblast culture conditions and embryotoxicity of cadmium sulfate were examined. D3 mESCs were exposed to cadmium sulfate for 24, 48 or 72h, and whole genome transcriptional profiles were determined. The results indicate a track of differentiation was identified as mESCs differentiate. Biological processes that were associated with differentiation related genes included embryonic development and, specifically, skeletal system development. Cadmium sulfate inhibited mESC differentiation at all three time points. Functional pathway analysis indicated biological pathways affected included those related to skeletal development, renal and reproductive function. In summary, our results suggest that transcriptional profiles are a sensitive indicator of early mESC differentiation. Transcriptomics may improve the predictivity of the mEST by suggesting possible modes of action for tested chemicals. Published by Elsevier Inc.Entities:
Keywords: Embryonic stem cell test; Embryotoxicity; Osteoblast; Transcriptomics
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Year: 2017 PMID: 28189605 PMCID: PMC5427642 DOI: 10.1016/j.reprotox.2017.02.001
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143