Exploring the zebrafish embryo as an alternative model for the evaluation of liver toxicity by histopathology and expression profiling
- Authors
- Driessen, M., Kienhuis, A.S., Pennings, J.L., Pronk, T.E., van de Brandhof, E.J., Roodbergen, M., Spaink, H.P., van de Water, B., and van der Ven, L.T.
- ID
- ZDB-PUB-130416-19
- Date
- 2013
- Source
- Archives of toxicology 87(5): 807-23 (Journal)
- Registered Authors
- Spaink, Herman P., van der Ven, Leo
- Keywords
- whole zebrafish embryo model, hepatotoxicity, next-generation sequencing, adult zebrafish liver, gene expression profiles, pathway analysis, toxicogenomics, transcription factor analysis
- MeSH Terms
-
- Animal Testing Alternatives
- Animals
- Cell Line, Tumor
- Cyclosporine/toxicity
- Disease Models, Animal*
- Drug Evaluation, Preclinical/methods*
- Embryo, Nonmammalian/drug effects*
- Female
- Gene Expression/drug effects*
- Gene Expression Profiling
- Hepatocytes/drug effects
- High-Throughput Nucleotide Sequencing
- In Situ Hybridization
- Life Cycle Stages/drug effects
- Liver/drug effects*
- Liver/embryology
- Liver/metabolism
- Male
- Mice
- Sequence Analysis, RNA
- Species Specificity
- Xenobiotics/toxicity*
- Zebrafish/physiology*
- PubMed
- 23559145 Full text @ Arch. Toxicol.
The whole zebrafish embryo model (ZFE) has proven its applicability in developmental toxicity testing. Since functional hepatocytes are already present from 36 h post fertilization onwards, whole ZFE have been proposed as an attractive alternative to mammalian in vivo models in hepatotoxicity testing. The goal of the present study is to further underpin the applicability of whole ZFE for hepatotoxicity testing by combining histopathology and next-generation sequencing-based gene expression profiling. To this aim, whole ZFE and adult zebrafish were exposed to a set of hepatotoxic reference compounds. Histopathology revealed compound and life-stage-specific effects indicative of toxic injury in livers of whole ZFE and adult zebrafish. Next-generation sequencing (NGS) was used to compare transcript profiles in pooled individual RNA samples of whole ZFE and livers of adult zebrafish. This revealed that hepatotoxicity-associated expression can be detected beyond the overall transcription noise in the whole embryo. In situ hybridization verified liver specificity of selected highly expressed markers in whole ZFE. Finally, cyclosporine A (CsA) was used as an illustrative case to support applicability of ZFE in hepatotoxicity testing by comparing CsA-induced gene expression between ZFE, in vivo mouse liver and HepaRG cells on the levels of single genes, pathways and transcription factors. While there was no clear overlap on single gene level between the whole ZFE and in vivo mouse liver, strong similarities were observed between whole ZFE and in vivo mouse liver in regulated pathways related to hepatotoxicity, as well as in relevant overrepresented transcription factors. In conclusion, both the use of NGS of pooled RNA extracts analysis combined with histopathology and traditional microarray in single case showed the potential to detect liver-related genes and processes within the transcriptome of a whole zebrafish embryo. This supports the applicability of the whole ZFE model for compound-induced hepatotoxicity screening.