Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1978 Dec 1;79(3):672–679. doi: 10.1083/jcb.79.3.672

Primary avian tendon cells in culture. An improved system for understanding malignant transformation

PMCID: PMC2110262  PMID: 215595

Abstract

Primary avian tendon (PAT) cells which maintain their differentiated state in culture are rapidly transformed by Rous sarcoma virus. By criteria of morphology, increased rate of 2-deoxyglucose uptake, and loss of density dependent growth control, PAT cells transform as well as their less differentiated counterpart, chick embryo fibroblasts. In addition, the percentage of collagen produced by PAT cells drops on transformation by an order of magnitude, from 23 to 2.5%, but is unaffected by viral replication of a transformation-defective mutant. The responsiveness of normal and transformed PAT cells to various environmental factors changes dramatically upon transformation. Normal PAT cells respond to the presence of ascorbate and high cell density by raising the level of collagen synthesis from 5 to 23%. Transformed PAT cells are totally unresponsive. These and previously reported results lead us to postulate that the break-down in the normal regulatory mechanisms used by the cell to maintain the differentiated state is related to or is responsible for the onset of malignant transformation.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barnes M. J. Function of ascorbic acid in collagen metabolism. Ann N Y Acad Sci. 1975 Sep 30;258:264–277. doi: 10.1111/j.1749-6632.1975.tb29287.x. [DOI] [PubMed] [Google Scholar]
  2. Bissell M. J., Farson D., Tung A. S. Cell shape and hexose transport in normal and virus-transformed cells in culture. J Supramol Struct. 1977;6(1):1–12. doi: 10.1002/jss.400060102. [DOI] [PubMed] [Google Scholar]
  3. Bissell M. J., Hatie C., Tischler A. N., Calvin M. Preferential inhibition of the growth of virus-transformed cells in culture by rifazone-82, a new rifamycin derivative. Proc Natl Acad Sci U S A. 1974 Jun;71(6):2520–2524. doi: 10.1073/pnas.71.6.2520. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bissell M. J., Hatié C., Rubin H. Patterns of glucose metabolism in normal and virus-transformed chick cells in tissue culture. J Natl Cancer Inst. 1972 Aug;49(2):555–565. [PubMed] [Google Scholar]
  5. DAVIDSON E. H. DIFFERENTIATION IN MONOLAYER TISSUE CULTURE CELLS. Adv Genet. 1964;12:143–280. doi: 10.1016/s0065-2660(08)60416-2. [DOI] [PubMed] [Google Scholar]
  6. Dolberg D. S., Bassham J. A., Bissell M. J. Selective inhibition of the facilitated mode of sugar uptake by cytochalasin B in cultured chick fibroblasts. Exp Cell Res. 1975 Nov;96(1):129–137. doi: 10.1016/s0014-4827(75)80045-0. [DOI] [PubMed] [Google Scholar]
  7. Green H., Todaro G. J., Goldberg B. Collagen synthesis in fibroblasts transformed by oncogenic viruses. Nature. 1966 Feb 26;209(5026):916–917. doi: 10.1038/209916a0. [DOI] [PubMed] [Google Scholar]
  8. HAM R. G. CLONAL GROWTH OF MAMMALIAN CELLS IN A CHEMICALLY DEFINED, SYNTHETIC MEDIUM. Proc Natl Acad Sci U S A. 1965 Feb;53:288–293. doi: 10.1073/pnas.53.2.288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Schwarz R. I., Bissell M. J. Dependence of the differentiated state on the cellular environment: modulation of collagen synthesis in tendon cells. Proc Natl Acad Sci U S A. 1977 Oct;74(10):4453–4457. doi: 10.1073/pnas.74.10.4453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Szabo C., Bissell M. J., Calvin M. Inhibition of infectious Rous sarcoma virus production by rifamycin derivative. J Virol. 1976 May;18(2):445–453. doi: 10.1128/jvi.18.2.445-453.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES