International Journal of Molecular Sciences (Feb 2024)

Xeno-Free 3D Bioprinted Liver Model for Hepatotoxicity Assessment

  • Ahmed S. M. Ali,
  • Johanna Berg,
  • Viola Roehrs,
  • Dongwei Wu,
  • Johannes Hackethal,
  • Albert Braeuning,
  • Lisa Woelken,
  • Cornelia Rauh,
  • Jens Kurreck

DOI
https://doi.org/10.3390/ijms25031811
Journal volume & issue
Vol. 25, no. 3
p. 1811

Abstract

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Three-dimensional (3D) bioprinting is one of the most promising methodologies that are currently in development for the replacement of animal experiments. Bioprinting and most alternative technologies rely on animal-derived materials, which compromises the intent of animal welfare and results in the generation of chimeric systems of limited value. The current study therefore presents the first bioprinted liver model that is entirely void of animal-derived constituents. Initially, HuH-7 cells underwent adaptation to a chemically defined medium (CDM). The adapted cells exhibited high survival rates (85–92%) after cryopreservation in chemically defined freezing media, comparable to those preserved in standard medium (86–92%). Xeno-free bioink for 3D bioprinting yielded liver models with high relative cell viability (97–101%), akin to a Matrigel-based liver model (83–102%) after 15 days of culture. The established xeno-free model was used for toxicity testing of a marine biotoxin, okadaic acid (OA). In 2D culture, OA toxicity was virtually identical for cells cultured under standard conditions and in CDM. In the xeno-free bioprinted liver model, 3-fold higher concentrations of OA than in the respective monolayer culture were needed to induce cytotoxicity. In conclusion, this study describes for the first time the development of a xeno-free 3D bioprinted liver model and its applicability for research purposes.

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