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T-cell receptor δ-chain can substitute for α to form a βδ heterodimer

Abstract

SPECIFIC monoclonal antibodies have made possible the identification of two T-cell antigen receptor (TCR) heterodimers, αβ TCR (refs 1-3) and γδ TCR (ref. 4). Formation of these receptors is largely separated by the preferential pairing of α-TCR with β and γ-TCR with δ (refs 5 & 6), the sequential rearrangement and expression of the TCR loci during thymic development7-10 and the deletion of the δ-loci either prior to or concomitant with α-rearrangement in αβ TCR cells11-13. Here we show that δ-TCR can substitute for α in pairing with β to form a βδ heterodimer. This receptor is expressed on the cell surface of the T-leukaemia cell line DND41 as analysed with β- and δ-specific monoclonal antibodies. We suggest that a variety of factors including, for example, the deletion of the δ-TCR loci, can now be understood as exclusion mechanisms operating to prevent not only the formation of γδ receptors, but also of βδ T-cell receptors, thereby promoting the numerically dominant αβ TCR lineage. Nevertheless, some developing T cells that do not rearrange the α-loci may express the βδ TCR as described here.

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References

  1. Allison, J. P., McIntyre, B. W. & Bloch, D. J. Immun. 129, 2293–2300 (1982).

    CAS  PubMed  Google Scholar 

  2. Haskins, K. et al. J. exp. Med. 157, 1149–1169 (1983).

    Article  CAS  PubMed  Google Scholar 

  3. Meuer, S. C. et al. J. exp. Med. 157, 705–719 (1983).

    Article  CAS  PubMed  Google Scholar 

  4. Brenner, M. B. et al. Nature 322, 145–149 (1986).

    Article  ADS  CAS  PubMed  Google Scholar 

  5. Saito, T. et al. J. exp. Med. 168, 1003–1020 (1988).

    Article  CAS  PubMed  Google Scholar 

  6. De Waal Malefyt, R. et al. J. Immun. 142, 3634–3642 (1989).

    CAS  PubMed  Google Scholar 

  7. Raulet, D. H., Garman, R. D., Saito, H. & Tonegawa, S. Nature 314, 103–107 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  8. Snodgrass, H. R., Dembic, Z., Steinmetz, M. & Von Boehmer, H. Nature 315, 232–233 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  9. Born, W., Rathburn, G., Tucker, P., Marrack, P. & Kappler, J. Science 214, 479–482 (1986).

    Article  ADS  Google Scholar 

  10. Chien, Y.-h. et al. Nature 330, 722–727 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  11. Chien, Y.-h., Iwashima, M., Kaplan, K. B., Elliott, J. F. & Davis, M. M. Nature 327, 677–682 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  12. de Villartay, J.-P., Hockett, R. D., Coran, D., Korsmeyer, S. J. & Cohen, D. I. Nature 335, 170–174 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

  13. Hata, S., Brenner, M. B. & Krangel, M. S. Science 238, 678–682 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  14. Minowada, J. in Cancer Rev. Vol. 10 (ed. Nilsson, K.) (Munksgaard, Copenhagen, in the press).

  15. Faure, F., Jitsukawa, S., Triebel, F. & Hercend, T. J. Immun. 141, 3357–3360 (1988).

    CAS  PubMed  Google Scholar 

  16. Band, H. et al. Science 238, 682–684 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  17. Lanier, L. L., Ruitenberg, J. J., Allison, J. P. & Weiss, A. in Leukocyte Typing III (ed. McMichael, A. J.) 175–178 (Oxford Univ. Press, 1987).

    Google Scholar 

  18. Spits, H. et al. J. Immun. 135, 1922–1928 (1985).

    CAS  PubMed  Google Scholar 

  19. Brenner, M. B. et al. J. Immun. 138, 1502–1509 (1987).

    CAS  PubMed  Google Scholar 

  20. Fabbi, M., Acuto, O., Bensussan, A., Poole, C. B. & Reinherz, E. L. Eur. J. Immun. 15, 821–827 (1985).

    Article  CAS  Google Scholar 

  21. Hata, S. et al. J. exp. Med. 169, 41–57 (1989).

    Article  CAS  PubMed  Google Scholar 

  22. Hochstenbach, F. et al. J. exp. Med. 168, 761–776 (1988).

    Article  CAS  PubMed  Google Scholar 

  23. Bear, R., Boehm, T., Yssel, H., Spits, H. & Rabbitts, T. H. EMBO J. 7, 1661–1668 (1988).

    Article  Google Scholar 

  24. Champagne, E. et al. Eur. J. Immun. 18, 1033–1038 (1988).

    Article  CAS  Google Scholar 

  25. Marrack, P. & Kappler, J. Adv. Immun. 38, 1–30 (1986).

    Article  CAS  PubMed  Google Scholar 

  26. Brenner, M. B., Strominger, J. L. & Krangel, M. S. Adv. Immun. 43, 133–192 (1988).

    Article  CAS  PubMed  Google Scholar 

  27. Koning, F., Maloy, W. L., Cohen, D. & Coligan, J. E. J. exp. Med. 166, 595–600 (1987).

    Article  CAS  PubMed  Google Scholar 

  28. Germain, R. N. & Quill, H. Nature 320, 72–75 (1986).

    Article  ADS  CAS  PubMed  Google Scholar 

  29. Takeshita, S., Toda, M. & Yamagishi, H. EMBO J., in the press.

  30. Winoto, A. & Baltimore, D. Nature 338, 430–432 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  31. Grynkiewicz, G., Poenie, M. & Tsien, R. Y. J. biol. Chem. 260, 3440–3450 (1985).

    CAS  PubMed  Google Scholar 

  32. Murre, C. et al. Nature 316, 549–552 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  33. Toyonaga, B. & Mak, T. W. A. Rev. Immun. 5, 585–620 (1987).

    Article  CAS  Google Scholar 

  34. Hata, S. et al. Science 240, 1541–1544 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

  35. Sim, G. K. et al. Nature 312, 771–775 (1984).

    Article  ADS  CAS  PubMed  Google Scholar 

  36. Leiden, J. M. et al. Molec. cell. Biol. 6, 3207–3214 (1986).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Krangel, M. S., Band, H., Hata, S., McLean, J. & Brenner, M. B. Science 237, 64–67 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  38. Duby, A. D., Klein, K. A., Murre, C. & Seidman, J. G. Science 228, 1204–1206 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  39. Saiki, R. K. et al. Science 239, 487–491 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

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Hochstenbach, F., Brenner, M. T-cell receptor δ-chain can substitute for α to form a βδ heterodimer. Nature 340, 562–565 (1989). https://doi.org/10.1038/340562a0

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