Applicability of a human cell co-culture model to evaluate antioxidant responses triggered by chemical mixtures in fish and oyster homogenates

Food Chem Toxicol. 2019 Jun:128:154-162. doi: 10.1016/j.fct.2019.04.005. Epub 2019 Apr 6.

Abstract

The accumulation of chemical compounds in fish tissue represents significant health concerns for seafood consumers, but little is known about the risks to human health associated with such substances. The identification of adverse biological responses upon exposure to contaminants has been facilitated by the development of in vitro systems resembling the human dietary pathway. The present study explores the applicability of an organotypic co-culture system, using intestinal (Caco-2) and hepatic (HepaRG) cell lines, to provide insight into the toxicity of chemical mixtures found in commercially available seafood. Chemical extractions were conducted utilizing fish and oyster standard reference material (SRM) from the U.S. National Institute of Standards and Technology (NIST). Cells were seeded in monoculture and co-culture systems and exposed to SRM extracts before measurements of cytotoxicity and antioxidant responses. Exposure to oyster extracts led to significant cell mortality in monocultures. HepaRG cells in monoculture expressed lower levels of glutathione peroxidase and superoxide dismutase than HepaRG cells in co-culture, upon exposure to both oyster and fish extracts. These observations illustrate the importance of organotypic co-culture models to explore biological responses that could be otherwise difficult to evaluate in monocultures, and the adverse effects associated with the consumption of contaminated seafood.

Keywords: Antioxidant enzymes; Caco-2; Chemical mixtures; Co-culture; Cytotoxicity; HepaRG.

MeSH terms

  • Animals
  • Antioxidants / metabolism*
  • Catalase / metabolism
  • Cell Line
  • Coculture Techniques
  • Dietary Exposure
  • Fishes / metabolism*
  • Food Contamination / analysis
  • Glutathione Peroxidase / metabolism
  • Humans
  • Intestines / cytology
  • Intestines / drug effects*
  • Intestines / enzymology
  • Liver / cytology
  • Liver / drug effects*
  • Liver / metabolism
  • Ostreidae / metabolism*
  • Seafood / analysis
  • Superoxide Dismutase / metabolism

Substances

  • Antioxidants
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase