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