Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver

M Huch, H Gehart, R van Boxtel, K Hamer, F Blokzijl, Monique Verstegen, E Ellis, M van Wenum, SA Fuchs, J de Ligt, M van de Wetering, N Sasaki, SJ Boers, H Kemperman, Jeroen de Jonge, J.N.M. IJzermans, EES Nieuwenhuis, R Hoekstra, S Strom, RRG VriesLuc van der Laan, E Cuppen, H Clevers

Research output: Contribution to journalArticleAcademicpeer-review

831 Citations (Scopus)
2 Downloads (Pure)


Despite the enormous replication potential of the human liver, there are currently no culture systems available that sustain hepatocyte replication and/or function in vitro. We have shown previously that single mouse Lgr5+ liver stem cells can be expanded as epithelial organoids in vitro and can be differentiated into functional hepatocytes in vitro and in vivo. We now describe conditions allowing long-term expansion of adult bile duct-derived bipotent progenitor cells from human liver. The expanded cells are highly stable at the chromosome and structural level, while single base changes occur at very low rates. The cells can readily be converted into functional hepatocytes in vitro and upon transplantation in vivo. Organoids from alpha 1-antitrypsin deficiency and Alagille syndrome patients mirror the in vivo pathology. Clonal long-term expansion of primary adult liver stem cells opens up experimental avenues for disease modeling, toxicology studies, regenerative medicine, and gene therapy.
Original languageUndefined/Unknown
Pages (from-to)299-312
Number of pages14
Issue number1-2
Publication statusPublished - 2015

Cite this