Human embryonic stem cell and embryonic germ cell lines

Trends in Biotechnology

Volumn 18, Issue 2, 2000, Pages 53-57

  Thomson, James A ^a   Odorico, Jon S ^a  

^a UNIVERSITY OF WISCONSIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELL DIFFERENTIATION; CELL PROLIFERATION; EMBRYO CELL; EMBRYO DEVELOPMENT; GERM CELL; HUMAN; HUMAN CELL; PRIORITY JOURNAL; REVIEW; STEM CELL;

EID: 0033961920     PISSN: 01677799     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-7799(99)01410-9     Document Type: Short Survey

References (41)

1. Winkel G.K., Pedersen R.A. Fate of the inner cell mass in mouse embryos as studied by microinjection of lineage tracers. Dev. Biol. 127:1988;143-156.
2. Gardner R.L. Investigation of cell lineage and differentiation in the extraembryonic endoderm of the mouse embryo. J. Embryol. Exp. Morphol. 68:1982;175-198.
3. Lawson K.A., Hage W.J. Clonal analysis of the origin of primordial germ cells in the mouse. Ciba Found. Symp. 182:1994;68-84.
4. Damjanov I., Solter D. Animal model of human disease: teratoma and teratocarcinoma. Am. J. Pathol. 83:1976;241-244.
5. Roach S.et al. Cultured cell lines from human teratomas: windows into tumour growth and differentiation and early human development. Eur. Urol. 23:1993;82-88.
6. Evans M., Kaufman M. Establishment in culture of pluripotential cells from mouse embryos. Nature. 292:1981;154-156.
7. Martin G. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc. Natl. Acad. Sci. U. S. A. 78:1981;7634-7638.
8. Matsui Y.et al. Derivation of pluripotential embryonic stem cells from murine primordial germ cells in culture. Cell. 70:1992;841-847.
9. Resnick J.L.et al. Long-term proliferation of mouse primordial germ cells in culture. Nature. 359:1992;550-551.
10. Bradley A.et al. Formation of germ-line chimaeras from embryo-derived teratocarcinoma cell lines. Nature. 309:1984;255-256.
11. Stewart C.L.et al. Stem cells from primordial germ cells can reenter the germ line. Dev. Biol. 161:1994;626-628.
12. Thomson J.A.et al. Embryonic stem cell lines derived from human blastocysts. Science. 282:1998;1145-1147.
13. Shamblott M.J.et al. Derivation of pluripotent stem cells from cultured human primordial germ cells. Proc. Natl. Acad. Sci. U. S. A. 95:1998;13726-13731.
14. Thomson J.A.et al. Isolation of a primate embryonic stem cell line. Proc. Natl. Acad. Sci. U. S. A. 92:1995;7844-7848.
15. Thomson J.A., Marshall V.S. Primate embryonic stem cells. Curr. Top. Dev. Biol. 38:1998;133-165.
16. Andrews P.W.et al. Three monoclonal antibodies defining distinct differentiation antigens associated with different high molecular weight polypeptides on the surface of human embryonal carcinoma cells. Hybridoma. 3:1984;347-361.
17. Kannagi R.et al. Stage-specific embryonic antigens (SSEA-3 and -4) are epitopes of a unique globo-series ganglioside isolated from human teratocarcinoma cells. EMBO J. 2:1983;2355-2361.
18. Fox N.W.et al. Stage-specific embryonic antigen 3 as a marker of visceral extraembryonic endoderm. Dev. Biol. 103:1984;263-266.
19. Ozawa M.et al. SSEA-1, a stage-specific embryonic antigen of the mouse, is carried by the glycoprotein-bound large carbohydrate in embryonal carcinoma cells. Cell Differ. 16:1985;169-173.
20. Conover J.C.et al. Ciliary neurotrophic factor maintains the pluripotentiality of embryonic stem cells. Development. 119:1993;559-565.
21. Rose T.M.et al. Oncostatin M (OSM) inhibits the differentiation of pluripotent embryonic stem cells in vitro. Cytokine. 6:1994;48-54.
22. Williams R.et al. Myeloid leukaemia inhibitory factor maintains the developmental potential of embryonic stem cells. Nature. 336:1988;684-687.
23. Andrews P.W.et al. Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Lab. Invest. 50:1984;147-162.
24. Nagy A.et al. Derivation of completely cell culture-derived mice from early-passage embryonic stem cells. Proc. Natl. Acad. Sci. U. S. A. 90:1993;8424-8428.
25. Dean W.et al. Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes. Development. 125:1998;2273-2282.
26. Labosky P.A.et al. Mouse embryonic germ (EG) cell lines: transmission through the germline and differences in the methylation imprint of insulin-like growth factor 2 receptor (Igf2r) gene compared with embryonic stem (ES) cell lines. Development. 120:1994;3197-3204.
27. Tada T.et al. Epigenotype switching of imprintable loci in embryonic germ cells. Dev. Genes Evol. 207:1998;551-561.
28. Christofori G.et al. Deregulation of both imprinted and expressed alleles of the insulin-like growth factor 2 gene during beta-cell tumorigenesis. Nat. Genet. 10:1995;196-201.
29. McBride G. Mom and pop genetics: genomic imprinting changes may illuminate cancer. J. Natl. Cancer Inst. 89:1997;1256-1258.
30. Mori M.et al. Relaxation of insulin-like growth factor 2 gene imprinting in esophageal cancer. Int. J. Cancer. 68:1996;441-446.
31. Nonomura N.et al. Loss of imprinting of the insulin-like growth factor II gene in renal cell carcinoma. Cancer Res. 57:1997;2575-2577.
32. Braude P.et al. Human gene expression first occurs between the four- and eight-cell stages of preimplantation development. Nature. 332:1988;459-461.
33. Benirschke K., Kaufmann P. Pathology of the Human Placenta. 1990;Springer-Verlag.
34. Luckett W.P. Origin and differentiation of the yolk sac and extraembryonic mesoderm in presomite human and rhesus monkey embryos. Am. J. Anat. 152:1978;59-98.
35. O'Rahilly R., Muller F. Developmental Stages in Human Embryos. 1987;Carnegie Institution of Washington.
36. Bain G.et al. Embryonic stem cells express neuronal properties in vitro. Dev. Biol. 168:1995;342-357.
37. Keller G.M. In vitro differentiation of embryonic stem cells. Curr. Opin. Cell Biol. 7:1995;862-869.
38. Klug M.G.et al. Genetically selected cardiomyocytes from differentiating embronic stem cells form stable intracardiac grafts. J. Clin. Invest. 98:1996;216-224.
39. Brustle O.et al. In vitro generated neural precursors participate in mammalian brain development. Proc. Natl. Acad. Sci. U. S. A. 94:1997;14809-14814.
40. Burns R.S.et al. A primate model of parkinsonism: selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. Proc. Natl. Acad. Sci. U. S. A. 80:1983;4546-4550.
41. Jones C.W.et al. Streptozotocin diabetes in the monkey: plasma levels of glucose, insulin, glucagon, and somatostatin, with corresponding morphometric analysis of islet endocrine cells. Diabetes. 29:1980;536-546.