This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bédard, P A
Right arrow Articles by Erikson, R L
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bédard, P A
Right arrow Articles by Erikson, R L

 Previous Article  |  Next Article 

Mol Cell Biol. 1987 April; 7(4): 1450-1458

Repression of quiescence-specific polypeptides in chicken heart mesenchymal cells transformed by Rous sarcoma virus.

P A Bédard, S D Balk, H S Gunther, A Morisi and R L Erikson

ABSTRACT

Chicken heart mesenchymal cells do not proliferate in medium of physiological composition containing plasma (S. Balk, Proc. Natl. Acad. Sci. USA 77:6606-6610, 1980). To understand the molecular events involved in cell quiescence and in the initiation of cell division under physiological conditions, we examined the differences in the patterns of protein synthesis of quiescent, hormone-stimulated, and Rous sarcoma virus-transformed chicken heart mesenchymal cells. We describe the expression of a 20,000-kilodalton (kDa) polypeptide actively synthesized by quiescent cells but not by their transformed counterparts. Normal chicken heart mesenchymal cells stimulated with epidermal growth factor and insulin also repressed the synthesis of the 20,000-kDa polypeptide while actively growing but synthesized increasing amounts of the protein at high cell density (confluence). The synthesis of the 20,000-kDa protein is not restricted to chicken heart mesenchymal cells, since confluent, density-arrested chicken embryo fibroblasts also expressed high levels of the protein. Transformed chicken heart mesenchymal cells and embryo fibroblasts did not synthesize the protein even at high cell density. The 20,000-kDa polypeptide accumulated in the culture medium.


Mol Cell Biol. 1987 April; 7(4): 1450-1458




This article has been cited by other articles:

  • Lillehoj, H. S., Kim, C. H., Keeler, C. L. Jr., Zhang, S. (2007). Immunogenomic Approaches to Study Host Immunity to Enteric Pathogens. Poult. Sci. 86: 1491-1500 [Abstract] [Full Text]  
  • Gagliardi, M., Maynard, S., Miyake, T., Rodrigues, N., Tjew, S. L., Cabannes, E., Bedard, P.-A. (2003). Opposing Roles of C/EBP{beta} and AP-1 in the Control of Fibroblast Proliferation and Growth Arrest-specific Gene Expression. J. Biol. Chem. 278: 43846-43854 [Abstract] [Full Text]  
  • Kim, S., Mao, P.-L., Gagliardi, M., Bedard, P.-A. (1999). C/EBPbeta (NF-M) Is Essential for Activation of the p20K Lipocalin Gene in Growth-Arrested Chicken Embryo Fibroblasts. Mol. Cell. Biol. 19: 5718-5731 [Abstract] [Full Text]  
  • Jahn, L, Sadoshima, J, Greene, A, Parker, C, Morgan, K., Izumo, S (1996). Conditional differentiation of heart- and smooth muscle-derived cells transformed by a temperature-sensitive mutant of SV40 T antigen. J. Cell Sci. 109: 397-407 [Abstract]  
  • Erikson, R.L., Alcorta, D., Bedard, P.-A., Blenis, J., Biemann, H.-P., Erikson, E., Jones, S.W., Maller, J.L., Martins, T.J., Simmons, D.L. (1988). Molecular Analyses of Gene Products Associated with the Response of Cells to Mitogenic Stimulation. Cold Spring Harb Symp Quant Biol 53: 143-151 [Abstract]