In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration (original) (raw)
- Letter
- Published: 27 January 2013
- Craig Dorrell2 na1,
- Sylvia F. Boj1,
- Johan H. van Es1,
- Vivian S. W. Li1,
- Marc van de Wetering1,
- Toshiro Sato1 nAff5,
- Karien Hamer1,
- Nobuo Sasaki1,
- Milton J. Finegold3,
- Annelise Haft2,
- Robert G. Vries1,
- Markus Grompe2 &
- …
- Hans Clevers1
Nature volume 494, pages 247–250 (2013)Cite this article
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Abstract
The Wnt target gene Lgr5 (leucine-rich-repeat-containing G-protein-coupled receptor 5) marks actively dividing stem cells in Wnt-driven, self-renewing tissues such as small intestine and colon1, stomach2 and hair follicles3. A three-dimensional culture system allows long-term clonal expansion of single Lgr5+ stem cells into transplantable organoids (budding cysts) that retain many characteristics of the original epithelial architecture2,4,5. A crucial component of the culture medium is the Wnt agonist RSPO16, the recently discovered ligand of LGR57,8. Here we show that Lgr5-lacZ is not expressed in healthy adult liver, however, small Lgr5-LacZ+ cells appear near bile ducts upon damage, coinciding with robust activation of Wnt signalling. As shown by mouse lineage tracing using a new Lgr5-IRES-creERT2 knock-in allele, damage-induced Lgr5+ cells generate hepatocytes and bile ducts in vivo. Single Lgr5+ cells from damaged mouse liver can be clonally expanded as organoids in Rspo1-based culture medium over several months. Such clonal organoids can be induced to differentiate in vitro and to generate functional hepatocytes upon transplantation into _Fah_−/− mice. These findings indicate that previous observations concerning Lgr5+ stem cells in actively self-renewing tissues can also be extended to damage-induced stem cells in a tissue with a low rate of spontaneous proliferation.
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The data for the microarray analysis have been deposited to the Gene Expression Omnibus under the accession number GSE32210.
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Acknowledgements
We thank H. Begthel, A. Buijs, W. Karthaus, C. Kroon-Veenboer, M. van den Born, S. van der Brink, and L. Zeinstra for technical assistance. This work was supported by grants to M.H. (EU/236954), S.F.B. (EU/232814), and V.S.W.L. and J.H.v.E. (Ti Pharma/T3-106).
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Author notes
- Toshiro Sato
Present address: Present address: Department of Gastroenterology, School of Medicine, Keio University, 35 Shinanomachi, Shinnjukuku, Tokyo, 160-8582, Japan., - Meritxell Huch and Craig Dorrell: These authors contributed equally to this work.
Authors and Affiliations
- Hubrecht Institute for Developmental Biology and Stem Cell Research, Uppsalalaan 8, 3584CT Utrecht & University Medical Centre Utrecht, Netherlands
Meritxell Huch, Sylvia F. Boj, Johan H. van Es, Vivian S. W. Li, Marc van de Wetering, Toshiro Sato, Karien Hamer, Nobuo Sasaki, Robert G. Vries & Hans Clevers - Oregon Stem Cell Center, Papé Family Pediatric Research Institute, Oregon Health and Science University, Portland, 97239, Oregon, USA
Craig Dorrell, Annelise Haft & Markus Grompe - Department of Pathology, Texas Children’s Hospital, Houston, 77030, Texas, USA
Milton J. Finegold
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- Meritxell Huch
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Contributions
Experiments were conceived and designed by M.H and H.C. Transplantation experiments were conceived and designed by M.H., C.D., M.G. and H.C. Experiments were performed by M.H., C.D., S.F.B. and V.S.W.L. A.H. helped with the transplantation experiments. M.v.d.W. and N.S. performed the sortings and K.H. the karyotyping experiments. J.H.v.E. designed and generated the _Lgr5_-IRES-creERT2 allele. V.S.W.L. performed the bioinformatic analysis of the microarrays and M.J.F. the Y-chromosome staining. M.H. and T.S. developed the isolation protocol. T.S. helped in the beginning phase of the project. R.G.V. helped with sorting experiments. M.H. analysed the data. M.H. and H.C. wrote the manuscript. The other authors commented on the manuscript.
Corresponding author
Correspondence toHans Clevers.
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Competing interests
M.H. and H.C. are inventors on a patent application related to this work.
Supplementary information
Supplementary Information
This file contains Supplementary Figures 1-9 and Supplementary Tables 4 -5. (PDF 4291 kb)
Supplementary Table 1
This file contains overlapping genes between CCl4 treated Liver and small intestine Wnt target genes published in Lau et al. (ref.8). (XLSX 63 kb)
Supplementary Table 2
This file contains overlapping genes between Lgr5-cells and small intestine Wnt target genes published in de Lau et al. (ref.8). (XLSX 33 kb)
Supplementary Table 3
This file contains overlapping genes between Liver Lgr5-cells and small intestine stem cell signature genes published in Munoz et al. (ref. 18). (XLSX 17 kb)
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Huch, M., Dorrell, C., Boj, S. et al. In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration.Nature 494, 247–250 (2013). https://doi.org/10.1038/nature11826
- Received: 10 September 2011
- Accepted: 07 December 2012
- Published: 27 January 2013
- Issue Date: 14 February 2013
- DOI: https://doi.org/10.1038/nature11826
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Editorial Summary
Wake-up call for liver stem cells
Hans Clevers and colleagues have identified a quiescent population of adult liver stem cells that can be 'woken up' by damage. In mice subject to liver damage, small cells expressing the Wnt target gene Lgr5 accumulate near the bile ducts. One of these cells was used to grow large numbers of bipotent stem cells in vitro. The stem cells were converted to functional hepatocytes in vitro, and when liver organoids were transplanted into a mouse model of tyrosinemia type I liver disease, islands of apparently normal hepatocytes appeared in the liver. Whether these hepatocytes are fully functional is not yet known, but the results are promising for regenerative approaches in the liver.