| Literature DB >> 28673813 |
Hee Young Kang1, Young-Kwon Choi2, Na Rae Jo3, Jae-Hwan Lee2, Changhwan Ahn2, Il Young Ahn4, Tae Sung Kim4, Ki-Suk Kim5, Kyung-Chul Choi6, Jong Kwon Lee4, Sung Duck Lee3, Eui-Bae Jeung7.
Abstract
Embryonic stem cell test (EST) evaluates the embryotoxic potential of substances and measures the half inhibition in viability of mouse embryonic stem cells (ESCs), fibroblasts (3T3 cells) and in cardiac differentiation of ESC. In this study, we suggest the developmental toxicity test method (termed EBT) applying area of embryoid bodies (EBs) instead of cardiac differentiation of EST. In the assessment of 21 substances, EB area was logarithmically decreased in dose-dependent manner. Decline in EB area resulted in decrease of beating ratio during differentiation of ESCs. In classification by the EBT-based prediction model reflecting decline in cell viability and EB area, toxicity for 21 chemicals showed 90.5% accuracy. In the results of next generation sequencing, reduction in EB area resulted from cell cycle arrest mediated by HDAC2 and CDKN2A. Conclusively, EBT is advanced and is a useful tool to assess and classify various embryotoxicants in a short time with less effort.Entities:
Keywords: Cardiac differentiation; Developmental toxicity; Embryoid bodies; Embryonic stem cell test
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Year: 2017 PMID: 28673813 DOI: 10.1016/j.reprotox.2017.06.185
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143