Molecular and Cellular Aspects of Embryonal Carcinoma Cell Differentiation
Joel Schindler
Abstract
Joel Schindler
Abstract
Embryonal carcinoma cells represent a subpopulation of undifferentiated stem cells contained within a mixture of differentiated cell phenotypes of teratocarcinoma tumors (1). Such tumors can develop spontaneously in gonadal tissue of certain mouse strains (2,3) and can be induced experimentally (4,5). The undifferentiated EC cells are the primary malignant cells of the tumor and are similar to early embryonic ectoderm morphologically (6), biochemically (7) and antigenically (8). Like early ectoderm cells, EC cells are pluripotent since injection of EC cells into host blastocysts leads to formation of chimeric mice (9–11).
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Embryonal carcinoma cells represent a subpopulation of undifferentiated stem cells contained within a mixture of differentiated cell phenotypes of teratocarcinoma tumors (1). Such tumors can develop spontaneously in gonadal tissue of certain mouse strains (2,3) and can be induced experimentally (4,5). The undifferentiated EC cells are the primary malignant cells of the tumor and are similar to early embryonic ectoderm morphologically (6), biochemically (7) and antigenically (8). Like early ectoderm cells, EC cells are pluripotent since injection of EC cells into host blastocysts leads to formation of chimeric mice (9–11).
Key concepts: Teratocarcinoma, Ectoderm, Embryonal carcinoma, Embryonic stem cell, Biology, Cell biology, Cellular differentiation, Phenotype