Elimination of tumorigenic stem cells from differentiated progeny and selection of definitive endoderm reveals a Pdx1 + foregut endoderm stem cell lineage

• Published in: Stem cell research 2011-03, Vol.6 (2), p.143-157
• Main Authors: Kahan, Brenda, Magliocca, Joseph, Merriam, Fabiola, Treff, Nathan, Budde, Melisa, Nelson, Jeffrey, Browning, Victoria, Ziehr, Benjamin, Odorico, Jon
• Format: Article
• Language: English
• Subjects: Animals; Antigens, Tumor-Associated, Carbohydrate - metabolism; Cell Differentiation; Cell Lineage; Cell Separation - methods; Cells, Cultured; Embryonic Stem Cells - cytology; Embryonic Stem Cells - physiology; Endoderm - cytology; Gastrointestinal Tract - cytology; Gastrointestinal Tract - embryology; Homeodomain Proteins - metabolism; Humans; Lewis X Antigen - metabolism; Male; Mice; Mice, Inbred NOD; Mice, SCID; Neoplasm Transplantation; Stage-Specific Embryonic Antigens - metabolism; Teratoma - metabolism; Teratoma - pathology; Trans-Activators - metabolism
• ISSN: 1873-5061; 1876-7753
• DOI: 10.1016/j.scr.2010.10.003

Embryonic stem cell (ESC) derivatives offer promise for generating clinically useful tissues for transplantation, yet the specter of producing tumors in patients remains a significant concern. We have developed a simple method that eliminates the tumorigenic potential from differentiated ESC cultures of murine and human origin while purifying lineage-restricted, definitive endoderm-committed cells. A three-stage scheme utilizing magnetic bead sorting and specific antibodies to remove undifferentiated ESCs and extraembryonic endoderm cells, followed by positive selection of definitive endoderm cells on the basis of epithelial cell adhesion molecule (EpCAM) expression, was used to isolate a population of EpCAM +SSEA1 –SSEA3 – cells. Sorted cells do not form teratomas after transplantation into immunodeficient mice, but display gene and protein expression profiles indicative of definitive endoderm cells. Sorted cells could be subsequently expanded in vitro and further differentiated to express key pancreas specification proteins. In vivo transplantation of sorted cells resulted in small, benign tissues that uniformly express PDX1. These studies describe a straightforward method without genetic manipulation that eliminates the risk of teratoma formation from ESC differentiated derivatives. Significantly, enriched populations isolated by this method appear to be lineage-restricted definitive endoderm cells with limited proliferation capacity.