Utilizing a human embryonic stem cell model to assess for developmental neurotoxicity

Human embyronic stem cells (hESC) have an unlimited potential for self-renewal and the capacity to differentiate into all somatic cell types of the central nervous system. Due to their unique characteristics of being able to capture early in vivo human developmental events in vitro, hESCs can be utilized to study the effects of environmental chemicals on cellular transitions occruing during early CNS development. In our laboratory, we established a hESC model of neurogenesis to identify chemical hazards that cause developmental neurotoxicity as well as the underlying mechanisms that lead to disease.

Using a Multi-Stage hESC Model to Characterize BDE-47 Toxicity during Neurogenesis. Toxicol Sci. 2019 Jun 07. Chen H, Seifikar H, Larocque N, Kim Y, Khatib I, Fernandez CJ, Abello N, Robinson JF. PMID: 31173147.

A genomics-based framework for identifying biomarkers of human neurodevelopmental toxicity. Reprod Toxicol. 2016 04; 60:1-10. Robinson JF, Gormley MJ, Fisher SJ. PMID: 26827931.

Compound-specific effects of diverse neurodevelopmental toxicants on global gene expression in the neural embryonic stem cell test (ESTn). Toxicol Appl Pharmacol. 2012 Aug 01; 262(3):330-40. Theunissen PT, Robinson JF, Pennings JL, van Herwijnen MH, Kleinjans JC, Piersma AH. PMID: 22634333.