Liver organoids: from basic research to therapeutic applications.
Published version
Peer-reviewed
Repository URI
Repository DOI
Change log
Authors
Prior, Nicole https://orcid.org/0000-0003-2856-7052
Inacio, Patricia
Huch, Meritxell https://orcid.org/0000-0002-1545-5265
Abstract
Organoid cultures have emerged as an alternative in vitro system to recapitulate tissues in a dish. While mouse models and cell lines have furthered our understanding of liver biology and associated diseases, they suffer in replicating key aspects of human liver tissue, in particular its complex architecture and metabolic functions. Liver organoids have now been established for multiple species from induced pluripotent stem cells, embryonic stem cells, hepatoblasts and adult tissue-derived cells. These represent a promising addition to our toolbox to gain a deeper understanding of this complex organ. In this perspective we will review the advances in the liver organoid field, its limitations and potential for biomedical applications.
Description
Keywords
disease modelling, liver, organoid, personalised medicine, Animals, Biomedical Research, Cell Culture Techniques, Cell Line, Humans, Liver, Models, Biological, Organoids, Regenerative Medicine
Journal Title
Gut
Conference Name
Journal ISSN
0017-5749
1468-3288
1468-3288
Volume Title
68
Publisher
BMJ
Publisher DOI
Sponsorship
Wellcome Trust (104151/Z/14/Z)
European Commission Horizon 2020 (H2020) Research Infrastructures (RI) (668350)
National Centre for the Replacement Refinement and Reduction of Animals in Research (NC/R001162/1)
Wellcome Trust (092096/Z/10/Z)
Cancer Research Uk (None)
European Commission Horizon 2020 (H2020) Research Infrastructures (RI) (668350)
National Centre for the Replacement Refinement and Reduction of Animals in Research (NC/R001162/1)
Wellcome Trust (092096/Z/10/Z)
Cancer Research Uk (None)
Acknowledgements
M.H. is a Wellcome Trust Sir Henry Dale Fellow and is jointly funded by the Wellcome Trust and the Royal Society (104151/Z/14/Z). This work was partially funded by a H2020 LSMF4LIFE awarded to M.H. PI is funded by the NC3Rs (NC/R001162/1). The authors acknowledge core funding to the Gurdon Institute from the Wellcome Trust (092096) and CRUK (C6946/A14492).