Development and Use of Avian In Vitro and In Vivo Models for Toxicological Screening and Prioritization of Five Bisphenol A Replacement Compounds: Bisphenol F, TGSH, DD-70, Bisphenol AF, and BPSIP

Toxicity testing is moving from animal-based studies to faster, more ethical in vitro approaches that focus on mechanistic toxicology. The use of bisphenol A (BPA) replacement compounds is increasing and there is limited toxicity data available for these compounds in avian species. The overall goals of this thesis were to: a) determine if avian cell lines are suitable alternatives to primary hepatocytes for chemical screening; b) generate toxicity data for five BPA replacement compounds: bis(4-hydroxyphenyl)methane (BPF), bis(3-allyl-4-hydroxyphenyl)sulfone (TGSH), 7-bis(4-hydroxyphenylthio)-3,5-dioxaheptane (DD-70), 2,2-bis(4-hydroxyphenyl)hexafluoropropane (BPAF) and 4-hydroxyphenyl 4-isoprooxyphenylsulfone (BPSIP) in three in vitro models: primary chicken embryonic hepatocytes (CEH), double-crested cormorant (DCCO) embryonic hepatocytes (DCEH) and chicken LMH cell line; and 3) prioritize two replacements for early-life stage testing (ELS). LMH cells cultured as 3D spheroids, as opposed to 2D monolayer, had enhanced mRNA expression and CYP1A activity and were therefore used for screening. Additionally, an immortalized DCCO hepatic cell line, DCH22, was established, which may be useful for future avian toxicity testing. DD-70 and BPAF were the most cytotoxic across the three in vitro models. TGSH and DD-70 altered expression of genes associated with multiple toxicity pathways, but not estrogen response, and are potential non-estrogenic replacements. BPAF, BPF and BPSIP are potential estrogenic replacements. In general, the replacements were more cytotoxic and/or transcriptionally active than BPA. There was species-specific variability in toxicity; the replacements were more transcriptionally active in CEH compared to DCEH. LMH spheroids were more sensitive to estrogenic endpoints than CEH. DD-70 and BPAF were prioritized for ELS studies based on in vitro results. All of the replacements modulated the expression of genes related to bile acid regulation in vitro and an increase in gallbladder mass was observed in chicken embryos after exposure to DD-70 or BPAF. Overall, this thesis evaluated the utility of LMH cells cultured as spheroids as an animal free alternative for chemical screening, established a DCCO cell line, and generated novel cytotoxicity and gene expression data for five BPA replacement compounds in three in vitro avian models and determined ELS toxicity of two replacement compounds.