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Transcriptomics analysis of early embryonic stem cell differentiation under osteoblast culture conditions: Applications for detection of developmental toxicity.

Citation
Chen, X., et al. “Transcriptomics Analysis Of Early Embryonic Stem Cell Differentiation Under Osteoblast Culture Conditions: Applications For Detection Of Developmental Toxicity.”. Reproductive Toxicology (Elmsford, N.y.), pp. 75-83.
Center Albert Einstein College of Medicine
Author Xinrong Chen, Tao Han, Edward Fisher, Wafa Harrouk, Melissa S Tassinari, Gwenn E Merry, Daniel Sloper, James C Fuscoe, Deborah K Hansen, Amy L Inselman
Keywords Embryonic stem cell test, Embryotoxicity, OSTEOBLAST, transcriptomics
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.

Year of Publication
2017
Journal
Reproductive toxicology (Elmsford, N.Y.)
Volume
69
Number of Pages
75-83
Date Published
12/2017
ISSN Number
1873-1708
DOI
10.1016/j.reprotox.2017.02.001
Alternate Journal
Reprod. Toxicol.
PMID
28189605
PMCID
PMC5427642
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