In Vitro Expansion of Single Lgr5+ Liver Stem Cells Induced by Wnt-driven Regeneration

Overview

Journal Nature

Specialty Science

Date 2013 Jan 29

PMID 23354049

Citations 748

Authors

Meritxell Huch

Craig Dorrell

Sylvia F Boj

Johan H van Es

Vivian S W Li

Marc van de Wetering

Toshiro Sato

Karien Hamer

Nobuo Sasaki

Milton J Finegold

Annelise Haft

Robert G Vries

Markus Grompe

Hans Clevers

Affiliations

Soon will be listed here.

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 colon, stomach and hair follicles. 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 architecture. A crucial component of the culture medium is the Wnt agonist RSPO1, the recently discovered ligand of LGR5. 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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