Skip to main content
Log in

Demonstration of components of serum-free culture medium effecting maximum in vitro expression of mouse mammary tumor virus

  • Published:
In Vitro Aims and scope Submit manuscript

Summary

By using a chemically defined serum-free (SF) medium for propagation of Mm5mtc1 mouse adenocarcinoma cell cultures and clonal derivatives, medium components including hormones, glucose and individual amino acids were evaluated as to modulation of mouse mammary tumor virus (MMTV) production. Insulin, hydrocortisone and dexamethasen each increased MMTV production on a per cell basis over constitutive expression that ocures in SF medium devoid of hormones. Maximum production occurred when all three hormones were present. Hormone-stimulated virus expression also was influenced by glucose concentration. Cell growth and maximum MMTV expression increased when thyroxine, asparagine, proline and serine were omitted from the medium formulation. The resulting modified SF medium provides and ideal system for the propagation of high MMTV-producer clones and for the study of the biochemical regulation of MMTV expression.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Mühbock, O., and P. Bentvelzen. 1969. The transmission of the mammary tumor viruses. Perspect. Virol. 6: 75–81.

    Google Scholar 

  2. Bentvelzen, P., and J. H. Daams. 1969. Hereditary infections with mammary tumor viruses in mice. J. Nat. Cancer Inst. 43: 1025–1035.

    PubMed  CAS  Google Scholar 

  3. Bentvelzen, P., J. H. Daams, P. C. Hageman, and J. Calafat. 1970. Genetic transmission of viruses that incite mammary tumors in mice. Proc. Nat. Acad. Sci. U.S.A. 67: 377–384.

    Article  CAS  Google Scholar 

  4. Hageman, P., J. Calafat, and J. H. Daams. 1972. The mammary tumor viruses. In: P. Emmelot, and P. Bentvelzen (Eds.),RNA Viruses and Host Genome in Oncogenesis. North Holland Publ. Co., Amsterdam, pp. 283–300.

    Google Scholar 

  5. Cardiff, R. D., P. B. Blair, and K. B. Deome. 1968.In vitro cultivation of the mouse mammary tumor virus: Replication of MTV in tissue culture. Virology 36: 313–317.

    Article  PubMed  CAS  Google Scholar 

  6. McGrath, C. M. 1971. Replication of mammary tumor virus in tumor cell cultures: Dependence on hormone induced cellular organization. J. Nat. Cancer Inst. 47: 455–461.

    PubMed  CAS  Google Scholar 

  7. Sykes, J. A., J. Whitescarver, and L. Briggs. 1968. Observations on a cell line producing mammary tumor virus. J. Nat. Cancer Inst. 41: 1315–1327.

    PubMed  CAS  Google Scholar 

  8. Lasfargues, E. Y., B. Kramarsky, N. H. Sarkar, J. C. Lasfargues, and D. H. Moore. 1972. An established RIII mouse mammary tumor cell line; kinetics of mammary tumor virus (MTV) production. Proc. Soc. Exp. Biol. Med. 139: 242–247.

    PubMed  CAS  Google Scholar 

  9. Sheffield, J. B., T. M. Daly, and D. H. Moore. 1974. External and metabolic labeling of glycoproteins in the mouse mammary tumor virus (MMTV). In: F. Squartini (Ed.),IXth Meeting of Mammary Cancer in Experimental Animals and Man. Univ. Pisa, Pisa, Italy, p. 45.

    Google Scholar 

  10. Owens, R. B., and A. J. Hackett. 1972. Tissue culture studies of mouse mammary tumor cells and associated viruses. J. Nat. Cancer Inst. 49: 1321–1332.

    PubMed  CAS  Google Scholar 

  11. Young, L. J. T., R. D. Cardiff, and R. L. Ashley. 1975. Long-term primary culture of mouse mammary tumor cells: Production of virus. J. Nat. Cancer Inst. 54: 1215–1221.

    PubMed  CAS  Google Scholar 

  12. Fine, D. L., L. O. Arthur, J. K. Plowman, E. A. Hillman, and F. Klein. 1974.In vitro system for production of mouse mammary tumor virus. Appl. Microbiol. 28: 1040–1046.

    PubMed  CAS  Google Scholar 

  13. Parks, W. P., E. M. Scolnick, and E. H. Kozikowski. 1974. Dexamethasone stimulation of murine mammary tumor virus expression. A tissue culture source of virus. Science 12: 158–160.

    Article  Google Scholar 

  14. Fine, D. L., J. K. Plowman, S. P. Kelley, L. O. Arthur, and E. A. Hillman. 1974. Enhanced production of mouse mammary tumor virus in dexamethasone-treated, 5-iododeoxyuridine-stimulated mammary tumor cell cultures. J. Nat. Cancer Inst. 52: 1881–1886.

    PubMed  CAS  Google Scholar 

  15. Ringold, G., E. Y. Lasfargues, J. M. Bishop, and H. E. Varmus. 1975. Production of mouse mammary tumor virus by cultured cells in the absence and presence of hormones. Assay by molecular hybridization. Virology 65: 135–147.

    Article  PubMed  CAS  Google Scholar 

  16. Parks, W. P., J. C. Ransom, H. A. Young, and E. M. Scolnick. 1975. Mammary tumor virus induction by glucocorticoids. J. Biol. Chem. 250: 3330–3336.

    PubMed  CAS  Google Scholar 

  17. Young, H. A., E. M. Scolnick, and W. P. Parks. 1975. Glucocorticoid receptor interaction and induction of murine mammary tumor virus. J. Biol. Chem. 250: 3337–3343.

    PubMed  CAS  Google Scholar 

  18. Ringold, G. M., K. R. Yamamoto, and G. M. Tomkins. 1975. Dexamethasone-mediated induction of mouse mammary tumor virus RNA. A system for studying glucocorticoid action. Cell 6: 299–305.

    Article  PubMed  CAS  Google Scholar 

  19. Scolnick, E. M., H. A. Young, and W. P. Parks. 1976. Biochemical and physiological mechanisms in glucocorticoid hormone induction of mouse mammary tumor virus. Virology 69: 148–156.

    Article  PubMed  CAS  Google Scholar 

  20. Schochetman, G., and J. Schlom. 1976. Independent polypeptide chain initiation sites for the synthesis of different classes of proteins for an RNA tumor virus: Mouse mammary tumor virus. Virology 73: 431–441.

    Article  PubMed  CAS  Google Scholar 

  21. Dickson, C., S. Haslam, and S. Nandi. 1974. Conditions for optimal MTV synthesisin vitro and the effect of steroid hormones on virus production. Virology 62: 242–252.

    Article  PubMed  CAS  Google Scholar 

  22. Fine, D. L., L. O. Arthur, and L. J. T. Young. 1976. Cell culture factors influencing in vitro expression of mouse mammary tumor virus. In Vitro 12: 693–701.

    PubMed  CAS  Google Scholar 

  23. Bauer, R. F., L. O. Arthur, and D. L. Fine. 1976. Propagation of mouse mammary tumor cell lines and production of mouse mammary tumor virus in a serum-free medium. In Vitro 12: 558–563.

    PubMed  CAS  Google Scholar 

  24. Higuchi, K., and R. C. Robinson. 1973. Studies on the cultivation of mammalian cell lines in a serum-free chemically defined medium. In Vitro 9: 114–121.

    Article  PubMed  CAS  Google Scholar 

  25. Sandberg, A. A., W. R. Slaunwhite, and H. N. Antoniades. 1957. The binding of steroids and steroid conjugates to human plasma proteins. Recent Prog. Horm. Res. 13: 209–260.

    PubMed  CAS  Google Scholar 

  26. Arthur, L. O., D. L. Fine, and J. K. Plowman. 1975. Variations in phenotypic expression of MMTV in mouse mammary tumor-derived cell clones. Proc. Amer. Assoc. Cancer Res. 16: 168.

    Google Scholar 

  27. Fine, D. L., and L. O. Arthur. 1974. Divalent cation requirements of RNA dependent DNA polymerase from type-B and type-C virus particles. Proc. Am. Soc. Microbiol. 74: 246.

    Google Scholar 

  28. Olpin, J., S. Oroszlan, and R. V. Gilden. 1974. Biophysical-immunological assay for ribonucleic acid type C viruses. Appl. Microbiol. 28: 100–105.

    PubMed  CAS  Google Scholar 

  29. Mancini, G., A. O., Carbonara, and J. F. Heremans. 1965. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry 2: 235–254.

    Article  PubMed  CAS  Google Scholar 

  30. Monroe, J. H., and P. M. Brandt. 1970. Rapid semi-quantitation method for screening large numbers of virus by negative staining electron microscopy. Appl. Microbiol. 20: 259–262.

    PubMed  CAS  Google Scholar 

  31. Chantler, J. K., and W. S. Stevely. 1976. The absence of one class of virus induced proteins in arginine-deprived cells infected with pig herpes-virus. Virology 70: 88–96.

    Article  PubMed  CAS  Google Scholar 

  32. Hampar, B., G. Lenoir, M. Nonoyama, J. G. Derge, and S. Y. Chang. 1976. Cell cycle dependence for activation of Epstein-Barr virus by inhibitors of protein synthesis or medium deficient in arginine. Virology 69: 660–668.

    Article  PubMed  CAS  Google Scholar 

  33. Hearn, H. J., H. R. Tribble, S. C. Nagle, and O. C. Bowersox. 1971. Replication of Venezuelan Equine Encephalomyelitis virusin vitro. Appl. Microbiol. 21: 342–345.

    CAS  Google Scholar 

  34. Brunner, M.. 1973. Regulation of DNA synthesis by amino acid limitation. Cancer Res. 33: 29–32.

    PubMed  CAS  Google Scholar 

  35. Parks, W. P., and E. M. Scolnick. 1973. Murine mammary tumor cell clones with varying degrees of virus expression. Virology 55: 163–173.

    Article  PubMed  CAS  Google Scholar 

  36. Akedo, H., and H. N. Christensen. 1962. Nature of insulin action on amino acid uptake by the isolated diaphragm. J. Biol. Chem. 237: 118–122.

    PubMed  CAS  Google Scholar 

  37. Hadden, J. W., E. M. Hadden, E. E. Wilson, R. A. Good, and R. G. Coffey. 1971. Direct action of insulin on plasma membrane ATPase activity in human lymphocytes. Nature (London) New Biol. 235: 174–176.

    Google Scholar 

  38. Gillette, R. W.. 1976. Cyclic nucleotides, steroids and the expression of mammary tumor virus in tissue cultured mammary tumor cells. In Vitro 12: 316.

    Google Scholar 

  39. Cuatrecasas, P. 1973. Insulin receptor of liver and fat cell membranes. Fed. Proc. 32: 1838.

    PubMed  CAS  Google Scholar 

  40. Pitot, H. C., and M. B. Yatvin. 1973. Interrelationships of mammalian hormones and enzyme levelsin vitro. Physiol. Rev. 53: 228–235.

    PubMed  CAS  Google Scholar 

  41. Boyett, J. D., and J. F. Hofert, 1972. Stimulatory effect of insulin on glucose metabolism of thymus lymphocytes. Horm. Metab. Res. 4: 163–167.

    Article  PubMed  CAS  Google Scholar 

  42. Clifton, K. H., and B. N. Sridharan. 1975. Endocrine factors and tumor growth. In: F. F. Becker (Ed.),Cancer 3. Biology of Tumors: Cellular Biology and Growth. Plenum Press, New York, pp. 249–285.

    Google Scholar 

  43. Aksamit, R. R., and C. W. Long. 1977. Induction of endogenous murine type C virus by an arginine analog: L-canavanine. Virology 78: 284–287.

    Article  Google Scholar 

  44. Noon, M. C., R. G. Wolford, and W. P. Parks. 1975. Expression of mouse mammary tumor viral polypeptide in milks and tissues. J. Immunol. 115: 653–658.

    PubMed  CAS  Google Scholar 

  45. Nagle, S. C., D. L. Fine, and J. Kmetz. 1977. Nutritional factors that influence expression of mouse mammary tumor virus: Iron, Zinc and Lipids. In Vitro 13: 173.

    Google Scholar 

  46. Bando, Y., S. Morii, and Y. Kawakita. 1975. Influence of dietary fat on growth of mammary cancer in rats: especially delayed turnover of fatty acids in tumor tissues. In: Y. Tsubura (Ed.),10th Meeting of Mammary Cancer in Experimental Animals and Man, Kobe, Japan, p. 19.

  47. DeWaard, F. 1974. Diet and nutrition as environmental factors in the pathogenesis of breast cancer. In: B. Levine (Ed.)Report to the Profession: Breast Cancer. Breast Cancer Program Coordinating Branch, DCBD, Bethesda, Md., pp. 21–30.

    Google Scholar 

  48. Hirayama, T. 1975. Prospective studies on cancer epidemiology based on census population in Japan. Excerpta Med. 3: 26–35.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This work was supported in part by the Virus Cancer Program, Contract No. N01-CO-25423, National Cancer Institute, NIH, Bethesda, Maryland.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Nagle, S.C., Fine, D.L. Demonstration of components of serum-free culture medium effecting maximum in vitro expression of mouse mammary tumor virus. In Vitro 14, 218–226 (1978). https://doi.org/10.1007/BF02618226

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02618226

Key words

Navigation