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:

Cytotoxic T lymphocytes and glucocorticoids activate an endogenous suicide process in target cells

Abstract

Cytotoxic T lymphocytes (CTL) induce a cytolytic process in target cells which, like the glucocorticoid-mediated cytolysis of immature thymocytes, effects a rapid and characteristic degradation of chromosomal DNA. I have explored the possibility that these two lethal processes share a common pathway by studying the suscepti-bility of glucocorticoid-resistant mutants to CTL-mediated killing. Here, I report that an unusual thymoma mutant, which has normal hormone receptor activity, is resistant to both glucocorticoids and CTL. The failure to be killed by CTL is not due to an inability of this 'deathless' mutant to be recognized. Further, a single-step reversion can restore sensitivity to both glucocorticoids and CTL. The genetic locus thus identified may reveal one element of an endogenous suicide pathway that can be triggered by different effectors. Unlike complement-mediated lysis, the processes of glucocorticoid- and CTL-mediated cytolysis seem to require that target cells be active in their own death.

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. 1. Podack, E. R. & Tschopp, J. /. biol. Chem. 257, 15204–15212 (1982). 2. Tschopp, J., Miiller–Eberhard, H. J. & Podack, E. R. Nature 298, 534–538 (1982). 3. Dourmashkin, R. R., Deteix, P., Simone, C. B. & Henkart, P. Clin. exp. Immun. 42, 554–560 (1980). 4. Dennert, G. & Podack, E. R. / exp. Med. 157, 1483–1495 (1983). 5. Henney, C. S. /. Immun. 110, 73–84 (1973). 6. Martz, E., Burakoff, S. J. & Benacerraf, B. Proc. natn. Acad. Sci. U.S.A. 71, 177–181 (1974). 7. Henkart, M. P. & Henkart, P. A. Adv. exp. Med. Biol. 146, 227–242 (1982). 8. Podack, E. R. & Dennert, G. Nature 302, 442–445 (1983). 9. Henkart, P. A., Millard, P. J., Reynolds, C. W. & Henkart, M. P. /. exp. Med. 160, 75–93 (1984). 10. Podack, E. R. & Konigsberg, P. J. /. exp. Med. 160, 695–710 (1984). 11. Masson, D. & Tschopp, J. J. biol. Chem. 260, 9096–9072 (1985). 12. Young, J. D.–E., Hengartner, H., Podack, E. R. & Conn, Z. A. Cell 44, 849–859 (1986). 13. Young, J. D.–E., Nathan, C. F., Podack, E. R., Palladino, M. A. & Cohn, Z. A. Proc. natn. Acad. Sci. U.S.A. 83, 150–154 (1986). 14. Russell, J. H., Masakowski, V. R. & Dobos, C. B. / Immun. 124, 1100–1105 (1980). 15. Russell, J. H. & Dobos, C. B. J. Immun. 125, 1256–1261 (1980). 16. Russell, J. H., Masakowski, V., Rucinsky, T. & Phillips, G. /. Immun. 128,2087–2094 (1982). 17. Duke, R. C., Chervenak, R. & Cohen, J. J. Proc. natn. Acad. Sci. U.S.A. 80,6361–6365 (1983). 18. Nicholson, M. L. & Young, D. A. Cancer Res. 38, 3673–3680 (1978). 19. Wyllie, A. H. Nature 284, 555–556 (1980). 20. Cohen, J. J. & Duke, R. C. /. Immun. 132, 38–42 (1984). 21. Vedeckis, W. V. & Bradshaw, H. D. Jr Molec. Cell. Endocr. 30, 215–227 (1983). 22. Sibley, C. H. & Tomkins, G. M. Cell 2, 221–227 (1974). 23. Yamamoto, K. R., Gehring, U., Stampfer, M. R. & Sibley, C. H. Recent Progr. Horm. Res. 32, 3–32 (1976). 24. Podak, E. R. Immun. Today 6, 21–27 (1985). 25. Russell, J. H. Immun. Rev. 72, 97–118 (1983). 26. Rabindran, S. K., Danielsen, M., Firestone, G. L. & Stallcup, M. R. Somat. Cell molec. Genet., 13, 131–143 (1987). 27. Ozato, K., Mayer, N. M. & Sachs, D. H. Transplantation 34, 113–120 (1982).

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ucker, D. Cytotoxic T lymphocytes and glucocorticoids activate an endogenous suicide process in target cells. Nature 327, 62–64 (1987). https://doi.org/10.1038/327062a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/327062a0

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