Isolation and characterization of a bovine visceral endoderm cell line derived from a parthenogenetic blastocyst

In Vitro Cellular and Developmental Biology - Animal

Volumn 41, Issue 5-6, 2005, Pages 130-141

  Talbot, Neil C ^a   Caperna, Thomas J ^a   Powell, Anne M ^a   Ealy, Alan D ^b   Blomberg, Le Ann ^a   Garrett, Wesley M ^a  

^a AGRICULTURAL RESEARCH SERVICE   (United States)

^b UNIVERSITY OF FLORIDA   (United States)

Author keywords

Bovine; Cell; Endoderm; Line; Parthenogenic

Indexed keywords

ANIMAL CELL; ARTICLE; BLASTOCYST; CELL ISOLATION; CELL LINE; CELL NUCLEUS TRANSPLANTATION; DESMOSOME; EMBRYO; EMBRYO TRANSFER; ENDODERM; FERTILIZATION IN VITRO; IMMUNOHISTOCHEMISTRY; METAPHASE; NONHUMAN; PARTHENOGENESIS; ROUGH ENDOPLASMIC RETICULUM; TIGHT JUNCTION; TRANSMISSION ELECTRON MICROSCOPY;

ANIMALS; BLASTOCYST; CATTLE; CELL LINE; CHROMOSOMES, MAMMALIAN; CYTOGENETIC ANALYSIS; ENDODERM; IMMUNOHISTOCHEMISTRY; INTERFERON TYPE I; MICROSCOPY, ELECTRON, TRANSMISSION; PARTHENOGENESIS; PREGNANCY PROTEINS;

BOVINAE;

EID: 24944508545     PISSN: 10712690     EISSN: None     Source Type: Journal    
DOI: 10.1290/040901.1     Document Type: Article

References (43)

1. Adamson, E. D.; Strickland, S.; Tu, M., et al. A teratocarcinoma-derived endoderm stem cell line (1H5) that can differentiate into extra-embryonic endoderm cell types. Differentiation 29:68-76; 1985.
2. Beckman, D. A.; Lloyd, J. B.; Brent, R. L. Investigations into mechanisms of amino acid supply to the rat embryo using whole-embryo culture. Int. J. Dev. Biol. 41:315-318; 1997.
3. Boediono, A.; Suzuki, T. Pregnancies after transfer of aggregated parthenogenetic bovine activated oocytes. Theriogenology 41:166; 1994.
4. Carlson, B. M. Patten's foundations of embryology. New York, NY: McGraw-Hill; 1981:197-200.
5. Cezar, G. G.; Bartolomei, M. S.; Forsberg, E. J., et al. Genome-wide epigenetic alterations in cloned bovine fetuses. Biol. Reprod. 68:1009-1014; 2003.
6. Chang, M. C. Development of bovine blastocyst with a note on implantation. Anat. Rec. 113:43-161; 1952.
7. De La Fuente, R.; King W. A. Developmental consequences of karyokinesis without cytokinesis during the first mitotic cell cycle of bovine parthenotes. Biol. Reprod. 58:952-962; 1998.
8. De Sousa, P. A.; King, T.; Harkness, L., et al. Evaluation of gestional deficiencies in cloned sheep fetuses and placentae. Biol. Reprod. 65:23-30; 2001.
9. Freshney, R. I. Culture of animal cells. 3rd ed. New York, NY: Wiley-Liss; 1994:12, 254.
10. Fukui, Y.; Sawai, K.; Furudate, M., et al. Parthenogenetic development of bovine oocytes treated with ethanol and cytochalasin B after in vitro maturation. Mol. Reprod. Dev. 33:357-362; 1992.
11. Hagemann, L. J.; Peterson, A. J.; Weilert, L. L., et al. In vitro and early development of sheep gynogenones and putative androgenones. Mol. Reprod. Dev. 50:154-162; 1998.
12. Hashizume, K.; Ishiwata, H.; Kizaki, K., et al. Implantation and placental development in somatic cell clone recipient cows. Cloning Stem Cells 4:197-209; 2002.
13. Hill, J. R.; Burghardt, R. C.; Jones, K., et al. Evidence for placental abnormalities as the major cause of mortality in first-trimester somatic cell cloned bovine fetuses. Biol. Reprod. 63:1787-1794; 2000.
14. Humpherys, D.; Eggan, K.; Akutsu, H., et al. Abnormal gene expression in cloned mice derived from embryonic stem cell and cumulus cell nuclei. Proc. Natl. Acad. Sci. USA 99:12889-12894; 2002.
15. Inoue, K.; Kodha, T.; Lee, J., et al. Faithful expression of imprinted genes in cloned mice. Science 295:297; 2002.
16. Janzen, R. G.; Mably, E. R.; Tamaoki, T., et al. Synthesis of alpha-fetoprotein by the pre-implantation and post-implantation bovine embryo. J. Reprod. Fertil. 65:105-110; 1982.
17. Kadokawa, Y.; Kato, Y.; Eguchi, G. Cell lineage analysis of the primitive and visceral endoderm of mouse embryos cultured in vitro. Cell Differ. 21:69-76; 1987.
18. Kaufman, M. H.; Robertson, E. J.; Handyside, A. H., et al. Establishment of pluripotential cell lines from haploid mouse embryos. J. Embryol. Exp. Morphol. 73:249-261; 1983.
19. Kharroubi, A. B.; Piras, G.; Stewart, C. L. DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts. J. Biol. Chem. 276:8674-8680; 2001.
20. Laemmli, U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 277:680-685; 1970.
21. Loi, P.; Ledda, S.; Fulka, J., Jr., et al. Development of parthenogenetic and cloned ovine embryos: effect of activation protocols. Biol. Reprod. 58:1177-1187; 1998.
22. Marnaeva, S. E. Karyotypic evolution of cells in culture: a new concept. Int. Rev. Cytol. 178:1-40; 1998.
23. Mossman, H. W. Vertebrate fetal membranes. New Brunswick, NJ: Rutgers University Press; 1987:279-291.
24. Mummery, C. L.; van Achterberg, T. A. E.; van den Eijnden-van Raaji, A. J. M., et al. Visceral-endoderm-like cell lines induce differentiation of murine P19 embryonal carcinoma cells. Differentiation 46:51-60; 1991.
25. Niimi, G.; Usuda, N.; Shinzato, M., et al. A light and electron microscopic study of the mouse visceral yolk sac endodermal cells in the middle and late embryonic periods, showing the possibility of definitive erythropoiesis. Ann. Anat. 184:425-429; 2002.
26. Pera, M. F.; Blasco-Lafita, M. J.; Mills, J. Cultured stem-cells from human testicular teratomas: the nature of human embryonal carcinoma, and its comparison with two types of yolk-sac carcinoma. Int. J. Cancer 40:334-343; 1987.
27. Roberts, R. M.; Imakawa, K.; Niwano, Y., et al. Interferon production by the preimplanation sheep embryo. J. Interferon Res. 9:175-187; 1989.
28. Rüsse, I.; Sinowatz, F.; Richter, L., et al. Development of the yolk sac of ruminants (sheep and cattle). Anat. Histol. Embryol. 21:324-347; 1992.
29. Santos, F.; Zakhartchenko, V.; Stojkovic, M., et al. Epigenetic marking correlates with developmental potential in cloned bovine preimplantation embryos. Curr. Biol. 13:1116-1121; 2003.
30. Shi, W. K.; Hopkins, B.; Thompson, S., et al. Synthesis of apolipoproteins, alphafoetoprotein, albumin, and transferrin by the human foetal yolk sac and other foetal organs. J. Embryol. Exp. Morphol. 85:191-206; 1985.
31. Starling, D.; Duncan, R.; Lloyd, J. B. The role of microtubules in pinocytosis. Inhibition of fluid-phase pinocytosis in rat visceral yolk sac by mitoclasic and related agents. Cell Biol. Int. Rep. 7:593-602; 1983.
32. Surani, M. A. H.; Barton, S. C. Development of gynogenetic eggs in the mouse: implications for parthenogenetic embryos. Science 222:1034-1036; 1983.
33. Surani, M. A. H., Kothary, R., Allen, N. D., et al. Genome imprinting and development in the mouse. Development (Suppl.):89-98; 1990.
34. Susko-Parrish, J. L.; Leibfried-Rutledge, M. L.; Northey, D. L., et al. Inhibition of protein kinases after an induced calcium transient causes transition of bovine oocytes to embryonic cycles without meiotic completion. Dev. Biol. 166:729-739; 1994.
35. Tada, T.; Takagi, N. Early development and X-chromosome inactivation in mouse parthenogenetic embryos. Mol. Reprod. Dev. 31:20-27; 1992.
36. Talbot, N. C.; Caperna, T. J.; Edwards, J. L., et al. Bovine blastocyst-derived trophectoderm and endoderm cell cultures: interferon-tau and transferrin expression as respective in vitro markers. Biol. Reprod. 62:235-247; 2000a.
37. Talbot, N. C.; Garrett, W. M.; Caperna, T. J. 2003. Analysis of the expression of aquaporin-1 and -9 in pig liver tissue: comparison with rat liver tissue. Cells Tissues Organs 174:17-28; 2003.
38. Talbot, N. C.; Powell, A.; Garrett, W., et al. Ultrastructural and karyotypic examination of in vitro produced bovine embryos developed in the sheep uterus. Tissue Cell 32:9-27; 2000b.
39. Talbot, N. C.; Powell, A. M.; Rexroad, C. E., Jr. In vitro pluripotency of epiblasts derived from bovine blastocysts. Mol. Reprod. Dev. 42:35-52; 1995.
40. Talbot, N. C.; Rexroad, C. E., Jr.; Pursel, V. G., et al. Culturing the epiblast cells of the pig blastocyst. In Vitro Cell. Dev. Biol. 29A:543-554; 1993.
41. Walter, G.; Intek, A.; Wobus, A. M., et al. Serological characterization of a pluripotent mouse embryonal stem cell line, two transformed derivatives, and an endoderm-like cell line. Cell Differ. 15:147-151; 1984.
42. Winger, Q. A., De La Fuente, R., King, W. A., et al. Bovine parthenogenesis is characterized by abnormal chromosomal complements: implications for maternal and paternal co-dependence during early bovine development. Dev. Genet. 21:160-166; 1997.
43. Young, M. F.; Klein, N. W. Synthesis of serum proteins by cultures of chick embryo yolk sac endodermal cells. Dev. Biol. 100:50-58; 1983.