Session 32
Advanced human liver model systems for translational integrated chemical safety testing strategies
Programme of the Session
- S32-01
A 2D & 3D fluorescent toxicity pathway reporter platform for high throughput imaging-based evaluation of hepatotoxicity liabilities
Bob van de Water
Leiden Academic Centre for Drug Research, Leiden University, Leiden, Netherlands - S32-02
Combined genome, metabolic and environmental engineering to create more functional hepatocytes from pluripotent stem cellsCatherine Verfaillie
Stem Cell Institute, KU Leuven, Leuven, Belgium -
S32-03
Application of 3D liver microtissues for assessment of drug-induced liver injury (DILI) and for studying liver steatosis
Radina Kostadinova, Fabrice Müller, Tobias Strassfeld, Simon Messner, Monika Kijanska, Wolfgang Moritz, Patrick Guye, David Fluri
InSphero AG, Zurich, Switzerland -
S32-04
Multi-organ on a chip: human physiology-based assessment of liver toxicity
Eva-Maria Dehne, Tobias Hasenberg, Reyk Horland, Uwe Marx
TissUse GmbH, Berlin, Germany
Session Abstract
The EU-ToxRisk project develops integrated strategies for human chemical safety assessment using animal free methods. A focus is on systemic repeated dose toxicity with the liver as one of the primary target organs. In EU-ToxRisk we systematically assess the applicability of different liver model systems for hepatotoxicity testing. The vision is to evaluate case study compound series in different cell systems and for each model define the feasibility to predict hepatotoxicity. Both high throughput microscopy, biochemical assessment as well as omics readouts are applied in the different systems. We anticipate to establish a proof-of-concept for tiered testing strategies for hepatotoxicity evaluation. In this symposium we will discuss the applicability domain of the different liver model systems, ranging from high throughput imaging based toxicity pathway reporter liver cell systems, primary human hepatocytes, human iPSC-derived hepatocytes, human liver microtissues and organ on a chip model systems. The application of case study compounds within the EU-ToxRisk project allows us to assess fit-for-purpose clarification for the individual models.