Long-Term Adult Feline Liver Organoid Cultures for Disease Modeling of Hepatic Steatosis
Kruitwagen, Hedwig S.; Oosterhoff, Loes A.; Vernooij, Ingrid G.W.H.; Schrall, Ingrid M.; van Wolferen, Monique E.; Bannink, Farah; Roesch, Camille; van Uden, Lisa; Molenaar, Martijn R.; Helms, J. Bernd; Grinwis, Guy C.M.; Verstegen, Monique M.A.; van der Laan, Luc J.W.; Huch, Meritxell; Geijsen, Niels; Vries, Robert G.; Clevers, Hans; Rothuizen, Jan; Schotanus, Baukje A.; Penning, Louis C.; Spee, Bart
(2017) Stem Cell Reports [E], volume 8, issue 4, pp. 822 - 830
(Article)
Abstract
Hepatic steatosis is a highly prevalent liver disease, yet research is hampered by the lack of tractable cellular and animal models. Steatosis also occurs in cats, where it can cause severe hepatic failure. Previous studies demonstrate the potential of liver organoids for modeling genetic diseases. To examine the possibility of
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using organoids to model steatosis, we established a long-term feline liver organoid culture with adult liver stem cell characteristics and differentiation potential toward hepatocyte-like cells. Next, organoids from mouse, human, dog, and cat liver were provided with fatty acids. Lipid accumulation was observed in all organoids and interestingly, feline liver organoids accumulated more lipid droplets than human organoids. Finally, we demonstrate effects of interference with β-oxidation on lipid accumulation in feline liver organoids. In conclusion, feline liver organoids can be successfully cultured and display a predisposition for lipid accumulation, making them an interesting model in hepatic steatosis research.
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Keywords: adult liver stem cells, disease modeling, feline hepatic lipidosis, feline liver organoids, hepatic steatosis, species differences, Biochemistry, Genetics, Developmental Biology, Cell Biology, Journal Article
ISSN: 2213-6711
Publisher: Cell Press
Note: Funding Information: The authors would like to thank the Utrecht University Center for Cell Imaging for technical assistance with imaging, Stefan van der Elst from the Hubrecht Institute for technical assistance with flow cytometry experiments, Dr. Sathidpak Nantasanti for technical advice, Dr. Hilda Toussaint for providing surplus mouse liver samples, and Sarah Opitz for editing the manuscript. This study was sponsored by the Winn Feline Foundation (grant no. W15-037). Parts of this work were funded by the Dutch Research Council NWO ZON/MW (116004121). Publisher Copyright: © 2017 The Author(s)
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