| Literature DB >> 17942827 |
Cheul H Cho1, Natesh Parashurama, Eric Y H Park, Kazuhiro Suganuma, Yaakov Nahmias, Jaesung Park, Arno W Tilles, François Berthiaume, Martin L Yarmush.
Abstract
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.Entities:
Mesh:
Year: 2007 PMID: 17942827 DOI: 10.1096/fj.06-7764com
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191