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This Article Full Text Full Text (PDF) Supplemental Data All Versions of this Article: 2007-0718v1 26/4/894    most recent Alert me when this article is cited Alert me if a correction is posted Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints/Permissions Google Scholar Articles by Hay, D. C. Articles by Cui, W. PubMed PubMed Citation Articles by Hay, D. C. Articles by Cui, W.

EMBRYONIC STEM CELLS

Efficient Differentiation of Hepatocytes from Human Embryonic Stem Cells Exhibiting Markers Recapitulating Liver Development In Vivo

^aDepartment of Gene Function and Development, Roslin Institute, Roslin, Midlothian, United Kingdom;
^bCXR Biosciences Ltd. James Lindsay Place, Dundee, United Kingdom;
^cInstitute of Reproductive and Developmental Biology, Imperial College London, Du Cane Rd, London, United Kingdom;
^dTissue Injury and Repair Group, Chancellor's Building, University of Edinburgh, Edinburgh, United Kingdom

Key Words. Hepatocyte differentiation • Human embryonic stem cell • Cytochrome P450 • Liver development

Correspondence: Wei Cui, Ph.D., Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Rd, London W12 ONN UK, Telephone: +44-(0)20 7594 2124; Fax: +44-(0)20 7594 2154; e-mail: wei.cui{at}imperial.ac.uk

Received August 29, 2007; accepted for publication January 23, 2008.
First published online in STEM CELLS EXPRESS   January 31, 2008.



The potential to differentiate human embryonic stem cells (hESCs) in vitro to provide an unlimited source of human hepatocytes for use in biomedical research, drug discovery, and the treatment of liver diseases holds great promise. Here we describe a three-stage process for the efficient and reproducible differentiation of hESCs to hepatocytes by priming hESCs towards definitive endoderm with activin A and sodium butyrate prior to further differentiation to hepatocytes with dimethyl sulfoxide, followed by maturation with hepatocyte growth factor and oncostatin M. We have demonstrated that differentiation of hESCs in this process recapitulates liver development in vivo: following initial differentiation, hESCs transiently express characteristic markers of the primitive streak mesendoderm before turning to the markers of the definitive endoderm; with further differentiation, expression of hepatocyte progenitor cell markers and mature hepatocyte markers emerged sequentially. Furthermore, we have provided evidence that the hESC-derived hepatocytes are able to carry out a range of hepatocyte functions: storage of glycogen, and generation and secretion of plasma proteins. More importantly, the hESC-derived hepatocytes express several members of cytochrome P450 isozymes, and these P450 isozymes are capable of converting the substrates to metabolites and respond to the chemical stimulation. Our results have provided evidence that hESCs can be differentiated efficiently in vitro to functional hepatocytes, which may be useful as an in vitro system for toxicity screening in drug discovery.

Disclosure of potential conflicts of interest is found at the end of this article.