Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Engagement of the CD4 molecule influences cell surface expression of the T-cell receptor on thymocytes

Abstract

The intrathymic differentiation process by which precursor cells derived from the bone marrow develop into immune-competent T lymphocytes is poorly understood. Most thymocytes express both CD4 and CDS accessory molecules1, yet little is known about either the function of these molecules or the responsiveness of the CD4+8+ double positive thymocytes that bear them2–7. Here, we address the possibility that CD4 engagement influences T-cell receptor (TCR) expression on developing thymocytes. We engaged CD4 molecules on murine thymocytes by in vivo injection of an anti-CD4 monoclonal antibody, which reduced the surface expression of CD4 on CD4+ thymocytes. More importantly, CD4 engagement also affected TCR expression on CD4+ thymocytes, but the effect on CD4+8+ double positive and CD4+8- single positive thymocytes was very different. CD4+8+ thymocytes responded to CD4 engagement by dramatically increasing surface expression of TCR, whereas CD4+8- thymocytes decreased surface expression of TCR. These results demonstrate that the effect of CD4 engagement on TCR expression is dependent upon the developmental state of the responding thymocyte, and, most interestingly, results in increased TCR expression by double positive thymocytes.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Fowlkes, B. J., Edison, E., Mathieson, B. J. & Chused, T. M. J. exp. Med. 162, 802–888 (1985).

    Article  CAS  PubMed  Google Scholar 

  2. Reinherz, E. L. & Schlossman, S. F. Cell 19, 821–827 (1980).

    Article  CAS  PubMed  Google Scholar 

  3. Shortman, K. & Jackson, H. Cell. Immun. 12, 230–246 (1974).

    Article  CAS  Google Scholar 

  4. McPhee, D., Pye, J. & Shortman, K. Thymus 1, 151–162 (1979).

    CAS  PubMed  Google Scholar 

  5. Havran, W. L. et al. Nature 330, 170–173 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  6. Finkel, T. H., McDuffie, M., Kappler, J. W., Marrack, P. & Cambier, J. C. Nature 330, 179–181 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  7. McDuffie, M., Born, W., Marrack, P. & Kappler, J. Proc. natn. Acad. Sci. U.S.A. 83, 8728–8732 (1986).

    Article  ADS  CAS  Google Scholar 

  8. Biddison, W. E., Rao, P. A., Talle, M. A., Goldstein, G. & Shaw, S. J. exp. Med. 156, 1065–1076 (1982).

    Article  CAS  PubMed  Google Scholar 

  9. Swain, S. Immunol. Rev. 74, 129–142 (1983).

    Article  CAS  PubMed  Google Scholar 

  10. MacDonald, H. R., Glasebrook, A. L., Bron, C., Kelso, A. & Cerottini, J.-C. Immunol. Rev. 68, 89–115 (1982).

    Article  CAS  PubMed  Google Scholar 

  11. Greenstein, J. L., Kappler, J., Marrack, P. & Burakoff, S. J. J. exp. Med. 159, 1213–1224 (1984).

    Article  CAS  PubMed  Google Scholar 

  12. Golding, H. et al. Nature 317, 425–428 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  13. Doyle, C. & Strominger, J. L. Nature 330, 256–259 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  14. Bluestone, J. A., Pardoll, D., Sharrow, S. O. & Fowlkes, B. J. Nature 326, 82–84 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  15. Crispe, I. N., Shimonkevitz, R. P., Husmann, L. A., Kimura, J. & Allison, J. P. J. Immun. 139, 3585–3589 (1987).

    CAS  PubMed  Google Scholar 

  16. Kruisbeek, A. M., Fultz, M. J., Sharrow, S. O., Singer, A. & Mond, J. J. J. exp. Med. 157, 1932–1946 (1983).

    Article  CAS  PubMed  Google Scholar 

  17. Kruisbeek, A. M. et al. J. exp. Med. 161, 1029–1047 (1985).

    Article  CAS  PubMed  Google Scholar 

  18. Mizuochi, T., Tentori, L., Sharrow, S. O., Kruisbeek, A. M. & Singer, A. J. exp. Med. 168, 437–442 (1988).

    Article  CAS  PubMed  Google Scholar 

  19. Dialynas, D. P. et al. J. Immun. 131, 2445–2451 (1983).

    CAS  PubMed  Google Scholar 

  20. Leo, O., Foo, M., Sachs, D. H., Samelson, L. E. & Bluestone, J. A. Proc. natn. Acad. Sci. U.S.A. 84, 1374–1378 (1987).

    Article  ADS  CAS  Google Scholar 

  21. Staerz, U. D., Rammensee, H.-G., Benedetto, J. D. & Bevan, M. J. J. Immun. 134, 3994–4000 (1985).

    CAS  PubMed  Google Scholar 

  22. Lanier, L. L., Gutman, G. A., Lewis, D. E., Griswold, S. T. & Warner, N. L. Hybridoma 1, 125–131 (1982).

    Article  CAS  PubMed  Google Scholar 

  23. Sarmiento, M., Glasebrook, A. L. & Fitch, F. W. J. Immun. 125, 2665–2672 (1980).

    CAS  PubMed  Google Scholar 

  24. Janeway, C. A. Jr et al. J. immun. 132, 662–667 (1984).

    PubMed  Google Scholar 

  25. Pierres, A. et al. J. Immun. 132, 2275–2785 (1984).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

McCarthy, S., Kruisbeek, A., Uppenkamp, I. et al. Engagement of the CD4 molecule influences cell surface expression of the T-cell receptor on thymocytes. Nature 336, 76–79 (1988). https://doi.org/10.1038/336076a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/336076a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing