Skip to main content

Inhibition of c-jun Expression in F-Mel Cells Causes Cell Cycle Arrest and prevention of Apoptosis

  • Chapter
New Developments and New Applications in Animal Cell Technology

Abstract

We are able to provide an evidence that will support the suppression of cell proliferation to withdrawal from the cell cycle and suppression of onset apoptosis with conditional expression of c-jun antisense transcript in F-MEL cells. F-MEL cells were transfected with c-jun antisense gene located downstream of aglucocorticoid-inducible MMTV promoter, and named as c-jun AS cells. By treating the c-jun AS cells with dexamethasone (DEX)in DMEM supplemented with 10% serum, the growth could be suppressed for duration of 16 days with high cell viability of 92%. When DEX-treated c-jun AS cells were serum deprived, the cell viability remained at high of 86% for upto 10 days, the onset of apoptosis was suppressed, and the internucleosomal cleavage of DNA was not detected upto 8 days. In contrast, when wild type F-MEL cells were serum deprived, the cell viability is low (50%.) and the onset of apoptosis is induced within 2 days, and internucleosomal cleavage of DNA was detectable.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Anderson, A. J., Pike, C. J. and Cotman, C. W. 1995. Differential induction of immediate early gene proteins in cultured neurons by b-amyloid (Ab): association of c-Jun with Ab — induced apoptosis. J. Neurochem. 65: 1487–1498.

    CAS  PubMed  Google Scholar 

  • Colotta, F., Polentarutti, N., Sironi, M. and Mantovani, A. 1992. Expression and involvement of c-fos and c-jun protooncogenes in programmed cell death induced by growth factor deprivation in lymphoid celllines. J. Biol. Chem. 267: I8278–18283.

    Google Scholar 

  • Duval, D., Demangel, C., Geahel, I., Blondeau, K. and Marcadcd, A. 1990. Comparison of various methods for monitoring hybridoma cell proliferation. J. Immunol. Meth. 134: 177–185.

    Article  CAS  Google Scholar 

  • Estus, S., Zaks, W. J., Freeman, R. S., Gruda, M., Bravo, R., and Johnson, E. M. Jr. 1994. Altered gene expression in neurons during programmed cell death: identification of c-jun as necessary for neuronal apoptosis. J. Cell Biol. 127:1717–1727.

    Article  CAS  PubMed  Google Scholar 

  • Franek, F, and Chladkova-Sramkova, K. (1995) Apoptosis and nutrition: Involvement of amino acid transport system in repression of hybridoma cell death. Cytotechnology 18: 113–117.

    CAS  Google Scholar 

  • Glacken, M. W., Adema, E, and Sinskey, A. J. 1988. Mathematical descriptions of hybridoma culture kinetics: I. initial metabolic rates. Biotechnol. Bioeng. 32:491–506.

    Article  CAS  Google Scholar 

  • Mercille, S. and Massie, B. 1994. Induction of apoptosis in nutrient-deprived cultures of hybridoma and myeloma ells. Biotechnol. Bioeng. 44: 1140–1154.

    Article  CAS  Google Scholar 

  • Rampalli, A. M. and Zelenka, P. S. 1995. Insulin regulates expression of c-fos and c-jun and suppresses apoptosis of lens epithelial cells. Cell Growth Differ. 6:945–953.

    CAS  PubMed  Google Scholar 

  • Ryseck. R. P., Hirai, S. I., Yaniv, M. and Bravo, R. 1988. Transcriptional activation of c-jun during the G0/G1 transition in mouse fibroblasts. Nature 334: 535–537.

    Article  CAS  PubMed  Google Scholar 

  • Sawai, H., Okazaki, T. Yamamoto, H., Okano, H., Takeda, Y., Tashima, M., Sawada, H., Okuma, M., Ishikura, H., Umehara, H., and Domae, N. 1995. Requirement of AP-l for ceramide-induced apoptosis in human leukemia HL-60 cells. J. Biol. Chem. 270: 27326–27331.

    CAS  PubMed  Google Scholar 

  • Singh, R. P., Al-Rubeai, M., Gregory, C. D., and Emery, A. N. 1994. Cell death inbioreactors: a role for apoptosis. Biotechnol. Bioeng. 44: 720–726.

    Article  CAS  Google Scholar 

  • Smith, M. J. and Prochownik, E. V. 1992. Inhibition of c-jun causes reversible proliferative arrest and withdrawal from the cell cycle. Blood 79: 2107–2115.

    CAS  PubMed  Google Scholar 

  • Soprano, K. J., Cosenza, S. C., Yumet, G., and Soprano, D. R. 1992. Use of antisense oligomers to study the role of c-jun in G1 progression. Ann. N. Y. Acad. Sci. 660: 231–239.

    CAS  PubMed  Google Scholar 

  • Suzuki, E. and Ollis, D. F. 1990. Enhanced antibody production at slowed growth rates: experimental demonstration and a simple structured model. Biotechnol. Prog. 6: 231–236.

    Article  CAS  PubMed  Google Scholar 

  • Tohyama, N., Karasuyama, H. and Tada, T. 1990. Growth autonomy and tumorigenicity of interleukin-6-dependent B cells transfected with interleukin-6 cDNA. J. Exp. Med. 171: 389–400.

    Article  CAS  PubMed  Google Scholar 

  • Turner. R. and Tjlan, R. 1989. Lcucine repeats and an adjacent DNA binding domain mediate the formation offunctional cFos-cJun heterodimers. Science 243: 1689–1694

    CAS  PubMed  Google Scholar 

  • Vomastek, T. and Franek, F. 1993. Kinetics of development of spontaneous apoptosis in B cell hybridoma cultures. Immunol. Lett. 35: 19–24.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Otto-Wilhelm Merten Pierre Perrin Bryan Griffiths

Rights and permissions

Reprints and permissions

Copyright information

© 1998 Kluwer Academic Publishers

About this chapter

Cite this chapter

Kim, Y.H., Iida, T., Prochownik, E.V., Suzuki, E. (1998). Inhibition of c-jun Expression in F-Mel Cells Causes Cell Cycle Arrest and prevention of Apoptosis. In: Merten, OW., Perrin, P., Griffiths, B. (eds) New Developments and New Applications in Animal Cell Technology. Springer, Dordrecht. https://doi.org/10.1007/0-306-46860-3_45

Download citation

  • DOI: https://doi.org/10.1007/0-306-46860-3_45

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-0-7923-5016-3

  • Online ISBN: 978-0-306-46860-5

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics