Skip to main content
Log in

MHC class II interaction with CD4 mediated by a region analogous to the MHC class I binding site for CD8

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

INTERACTIONS between major histocompatibility complex (MHC) molecules and the CD4 or CDS coreceptors have a major role in intrathymic T-cell selection1. On mature T cells, each of these two glycoproteins is associated with a class-specific bias in MHC molecule recognition by the T-cell receptor. CD4+ T cells respond to antigen in association with MHC class II molecules and CD8+ T cells respond to antigen in association with MHC class I molecules. Physical interaction between the CD4/MHC class II molecules and CD8/MHC class I molecules has been demonstrated by cell adhesion assay2–5, and a binding site for CDS on class I has been identified6,7. Here we demonstrate that a region of the MHC class IIβ-chain β2 domain, structurally analogous to the CDS-binding loop in the MHC class I α3 domain, is critical for function with both mouse and human CD4.

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. von Boehmer, H. A. Rev. Immun. 6, 309–326 (1988).

    Article  CAS  Google Scholar 

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

    Article  ADS  CAS  PubMed  Google Scholar 

  3. Norment, A. M., Salter, R. D., Parham, P., Engelhard, V. H. & Littman, D. R. Nature 336, 79–81 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

  4. Rosenstein, Y. Ratnofsky, S., Burakoff, S. J. & Herrmann, S. H. J. exp. Med. 169, 149–160 (1989).

    Article  CAS  PubMed  Google Scholar 

  5. Clayton, L. K., Sieh, M., Pious, D. A. & Reinherz, E. L. Nature 339, 548–551 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  6. Potter, T. A., Rajan, T. V., Dick, R. F. II & Bluestone, J. A. Nature 337, 73–75 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  7. Salter, R. D. et al. Nature 345, 41–46 (1990).

    Article  ADS  CAS  PubMed  Google Scholar 

  8. Lamarre, D. et al. Science 245, 743–746 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  9. von Hoegen, P., Miceli, M. C., Tourvieille, B., Schilham, M. & Parnes, J. E. J. exp. Med. 170, 1879–1886 (1989).

    Article  CAS  PubMed  Google Scholar 

  10. Kaufman, J. F., Auffray, C., Korman, A. J., Shackelford, D. A. & Strominger, J. Cell 36, 1–13 (1984).

    Article  CAS  PubMed  Google Scholar 

  11. Travers, P., Blundell, T. L., Sternberg, M. J. E. & Bodmer, W. F. Nature 310, 235–238 (1984).

    Article  ADS  CAS  PubMed  Google Scholar 

  12. Braunstein, N. S. & Germain, R. N. Proc. natn. Acad. Sci. U.S.A. 84, 2921–2925 (1987).

    Article  ADS  CAS  Google Scholar 

  13. Brown, J. H. et al. Nature 332, 845–850 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

  14. Gorga, J. C., et al. Proc. natn. Acad. Sci. U.S.A. 86, 2321–2325 (1989).

    Article  ADS  CAS  Google Scholar 

  15. Lemke, H., Hämmerling, G. J. & Hämmerling, U. Immunol. Rev. 47, 175–206 (1979).

    Article  CAS  PubMed  Google Scholar 

  16. Kappler, J., Skidmore, B., White, J. & Marrack, P. J. exp. Med. 153, 1198–1214 (1981).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Bhattacharya, A., Dorf, M. E. & Springer, T. A. J. Immun. 127, 2488–2495 (1981).

    CAS  PubMed  Google Scholar 

  18. Saper, M. A., Bjorkman, P. J. & Wiley, D. C. J. molec. Biol. 219, 277–319 (1991).

    Article  CAS  PubMed  Google Scholar 

  19. Wang, J. et al. Nature 348, 411–418 (1990).

    Article  ADS  CAS  PubMed  Google Scholar 

  20. Fleury, S. et al. Cell 66, 1037–1049 (1991).

    Article  CAS  PubMed  Google Scholar 

  21. Golding, H. et al. Nature 317, 425–427 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  22. Kabat, E. A., Wu, T. T., Reid-Miller, M., Perry, H. M. & Gottesman, K. S. in Sequences of Proteins of Immunological Interest (US Department of Health and Human Services, PHS, NIH 1987).

    Google Scholar 

  23. Miller, J. & Germain, R. N. J. exp. Med. 164, 1478–1489 (1986).

    Article  CAS  PubMed  Google Scholar 

  24. Dalbadie-McFarland, G. et al. Proc. natn. Acad. Sci. U.S.A. 79, 6409–6413 (1982).

    Article  ADS  CAS  Google Scholar 

  25. Ho, S. N., Hunt, H. D., Horton, R. M., Pullen, J. K. & Pease, L. R. Gene 77, 51–59 (1989).

    Article  CAS  PubMed  Google Scholar 

  26. Crowe, J. S. et al. Nucleic Acids Res. 19, 184 (1991).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  27. Layet, C. & Germain, R. N. Proc. natn. Acad. Sci. U.S.A. 88, 2346–2350 (1991).

    Article  ADS  CAS  Google Scholar 

  28. Margulies, D. H. et al. J. Immun. 130, 463–470 (1981).

    Google Scholar 

  29. Ronchese, F., Brown, M. A. & Germain, R. N. J. Immun. 139, 629–638 (1987).

    CAS  PubMed  Google Scholar 

  30. Marrack, P., et al. J. exp. Med. 158, 1077–1091 (1983).

    Article  CAS  PubMed  Google Scholar 

  31. Littman, D. R. & Gettner, S. N. Nature 325, 453–455 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  32. Zamoyska, R., Vollmer, A. C., Sizer, K. C., Liaw, C. W. & Parnes, J. R. Cell 43, 153–163 (1985).

    Article  CAS  PubMed  Google Scholar 

  33. Sleckman, B. P. et al. Nature 328, 351–353 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  34. Ronchese, F., Schwartz, R. H. & Germain, R. N. Nature 329, 254–256 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  35. Glaichenhaus, N., Shastri, N., Littman, D. R. & Turner, J. M. Cell 64, 511–520 (1991).

    Article  CAS  PubMed  Google Scholar 

  36. Cammarota, G. et al. Nature 356, 799–801 (1992).

    Article  ADS  CAS  PubMed  Google Scholar 

  37. Lombardi, G. et al. J. Immun. 147, 2034–2040 (1991).

    CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

König, R., Huang, LY. & Germain, R. MHC class II interaction with CD4 mediated by a region analogous to the MHC class I binding site for CD8. Nature 356, 796–798 (1992). https://doi.org/10.1038/356796a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/356796a0

  • Springer Nature Limited

This article is cited by

Navigation