TY - JOUR
T1 - Homogeneous differentiation of hepatocyte-like cells from embryonic stem cells
T2 - Applications for the treatment of liver failure
AU - Cho, Cheul H.
AU - Parashurama, Natesh
AU - Park, Eric Y.H.
AU - Suganuma, Kazuhiro
AU - Nahmias, Yaakov
AU - Park, Jaesung
AU - Tilles, Arno W.
AU - Berthiaume, François
AU - Yarmush, Martin L.
PY - 2008/3
Y1 - 2008/3
N2 - One of the major hurdles of cellular therapies for the treatment of liver failure is the low availability of functional human hepatocytes. While embryonic stem (ES) cells represent a potential cell source for therapy, current methods for differentiation result in mixed cell populations or low yields of the cells of interest. Here we describe a rapid, direct differentiation method that yields a homogeneous population of endoderm-like cells with 95% purity. Mouse ES cells cultured on top of collagen-sandwiched hepatocytes differentiated and proliferated into a uniform and homogeneous cell population of endoderm-like cells. The endoderm-like cell population was positive for Foxa2, Sox17, and AFP and could be further differentiated into hepatocyte-like cells, demonstrating hepatic morphology, functionality, and gene and protein expression. Incorporating the hepatocyte-like cells into a bioartificial liver device to treat fulminant hepatic failure improved animal survival, thereby underscoring the therapeutic potential of these cells.
AB - One of the major hurdles of cellular therapies for the treatment of liver failure is the low availability of functional human hepatocytes. While embryonic stem (ES) cells represent a potential cell source for therapy, current methods for differentiation result in mixed cell populations or low yields of the cells of interest. Here we describe a rapid, direct differentiation method that yields a homogeneous population of endoderm-like cells with 95% purity. Mouse ES cells cultured on top of collagen-sandwiched hepatocytes differentiated and proliferated into a uniform and homogeneous cell population of endoderm-like cells. The endoderm-like cell population was positive for Foxa2, Sox17, and AFP and could be further differentiated into hepatocyte-like cells, demonstrating hepatic morphology, functionality, and gene and protein expression. Incorporating the hepatocyte-like cells into a bioartificial liver device to treat fulminant hepatic failure improved animal survival, thereby underscoring the therapeutic potential of these cells.
KW - Animal model
KW - Bioartificial liver device
KW - Coculture
KW - Endoderm
UR - http://www.scopus.com/inward/record.url?scp=40449118677&partnerID=8YFLogxK
U2 - 10.1096/fj.06-7764com
DO - 10.1096/fj.06-7764com
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 17942827
AN - SCOPUS:40449118677
SN - 0892-6638
VL - 22
SP - 898
EP - 909
JO - FASEB Journal
JF - FASEB Journal
IS - 3
ER -