Skip to main content
Log in

Glucocorticoid-induced apoptosis in lymphoid organs is associated with a delayed increase in circulating deoxyribonucleic acid

  • Published:
Apoptosis Aims and scope Submit manuscript

Abstract

Pathological processes like cancer, chronic inflammation and autoimmune phenomena, all of which involve massive cell death, are associated with significant increases in circulating DNA. In order to clarify whether massive apoptosis occurring under physiological circumstances also causes DNA release into the circulation, we correlated the time-course of dexamethasone-induced intra thymic cell apoptosis with plasma DNA dynamics in rats. Animals were given 10 mg/l dexamethasone in their drinking water for up to 7 days. Sequential plasma samples were obtained during the treatment and DNA was quantitated by a micro fluorometric assay. Thymus and spleen weight as well as apoptotic cell levels were assessed at different times. Seven days of glucocorticoid treatment reduced thymic and spleen mass by 82 and 31%, respectively. Intra thymic apoptosis was maximal 24 h after the beginning of glucocorticoid treatment, declining markedly by 48 h. Very little apoptosis was observed in the spleen. Plasma DNA increased steadily during the first 4 days of glucocorticoid treatment (11.8 ± 1.2 μg/ml on day 0; 24.2 ± 1.6 μg/ml on day 4) beginning to decline afterward. Thymectomy but not splenectomy, drastically reduced the glucocorticoid-induced increase in plasma DNA. It is concluded that hormone-induced massive intra thymic cell death is followed by a delayed release of nucleosomal DNA into the circulation.

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. Beaulaton J, Lockshin RA. The relation of programmed cell death to development and reproduction: Comparative studies and an attempt at classification. Int Rev Cytol 1982; 79: 215–235.

    Google Scholar 

  2. Wyllie AH. Cell death: The significance of apoptosis. Int Rev Cytol 1980; 68: 251–306.

    Google Scholar 

  3. Cotter TG, Lennon SV, Glynn JG, Martin SJ. Cell death via apoptosis and its relationship to growth, development and differentiation of both tumour and normal cells. Anticancer Res 1990; 10: 1153–1160.

    Google Scholar 

  4. Kerr JFR, Wyllie AH, Currie AR. Apoptosis:Abasic biological phenomenon with wide ranging implications in tissue kinetics. Br J Cancer 1972; 26: 239–257.

    Google Scholar 

  5. Kerr JF, Winterford CM, Harmon BV. Apoptosis. Its significance in cancer and cancer therapy. Cancer 1994; 73: 2013–2026.

    Google Scholar 

  6. Arends MJ, Morris RJ, Wyllie AH. Apoptosis: The role of endonuclease. Am J Pathol 1990; 136: 593–608.

    Google Scholar 

  7. Kornberg R. Structure of the chromatin. Annu Rev Biochem 1977; 46: 931–954.

    Google Scholar 

  8. Luger K, Mader AW, Richmond RK, Sargent DF, Richmond TJ. Crystal structure of the nucleosome core particle at 2,8 A resolution. Nature (London) 1997; 389: 251–260.

    Google Scholar 

  9. Wyllie AH. Death from inside out: An overview. Philos Trans Royal Soc Lond 1994; 345: 237–241.

    Google Scholar 

  10. Steinman CR. Free DNA in serum and plasma from normal adults. J Clin Invest 1975; 56: 512–515.

    Google Scholar 

  11. Shapiro B, Chakrabarty M, Cohn EM, Leon SA. Determination of circulating DNAlevels in patients with benign or malignant gastrointestinal disease. Cancer 1983; 51: 2116–2120.

    Google Scholar 

  12. Raptis L, Menard HA. Quantitation and characterization of plasma DNA in normals and patients with systemic lupus erythematosus. J Clin Invest 1980; 66: 1391–1399.

    Google Scholar 

  13. Leon SA, Shapiro B, Sklaroff DM, Yaros MJ. Free DNA in the serum of cancer patients and the effect of therapy. Cancer Res 1977; 37: 646–650.

    Google Scholar 

  14. Fournié GJ, Courtin JP, Laval F, et al. Plasma DNA as a marker of cancerous cell death. Investigations in patients suffering from lung cancer and in nude mice bearing human tumours. Cancer Lett 1995; 91: 221–227.

    Google Scholar 

  15. Maebo A. Plasma DNA level as a tumor marker in primary lung cancer. Nihon Kyobu Shikkan Gakkai Zasshi 1990; 28: 1085–1091.

    Google Scholar 

  16. Anker P. Quantitative aspects of plasma/serum DNA in cancer patients. Ann NY Acad Sci USA 2000; 906: 5–7.

    Google Scholar 

  17. Koffler D, Agnello V, Winchester R, Kunkel HG. The occurrence of single-stranded DNA in the serum of patients with SLE and other diseases. J Clin Invest 1973; 52: 198–204.

    Google Scholar 

  18. Majno G, Joris I. Apoptosis, oncosis, and necrosis. An overview of cell death. Amer J Pathol 1995; 146: 3–15.

    Google Scholar 

  19. Brunk CF, Jones KC, James TW. Assay for nanogram quantities of DNA in cellular homogenates. Anal Biochem 1978; 92: 497–500.

    Google Scholar 

  20. Quaglino D, Ronchetti P. Cell death in the rat thymus: A minireview. Apoptosis 2001; 6: 389–401.

    Google Scholar 

  21. Ahmed SA, Sriranganathan N. Differential effects of dexamethasone on the thymus and spleen: Alterations in programmed cell death, lymphocyte subsets and activation of T cells. Immunopharmacol 1994; 28: 55–66.

    Google Scholar 

  22. Holdenrieder S, Stieber P, Bodenmüller H, et al. Nucleosomes in serum of patients with benign and malignant diseases. Int J Cancer (Pred Oncol) 2001; 95: 114–120.

    Google Scholar 

  23. Rumore P, Muralidhar B, Lin M, Lai C, Steinman CR. Haemodialysis as a model for studying endogenous plasma DNA: Oligonucleosome-like structure and clearance. Clin exp Immunol 1992; 90: 56–62.

    Google Scholar 

  24. Gauthier VJ, Tyler LN, Mannik M. Blood clearance kinetics and liver uptake of mononucleosomes in mice. J Immunol 1996; 156: 1151–1156.

    Google Scholar 

  25. Odaka C, Mizuochi T. Macrophages are involved in DNA degradation of apoptotic cells in murine thymus after administration of hydrocortisone. Cell Death Differ 2002; 9: 104–112.

    Google Scholar 

  26. Jacob L, Viard JP, Allenet B, et al. A monoclonal anti-doublestranded DNA autoantibody binds to a 94-kDa cell-surface protein on various cell types via nucleosomes or a DNAhistone complex. Proc Natl Acad Sci USA 1989; 86: 4669–4673.

    Google Scholar 

  27. Hefeneider SH, Cornell KA, Brown LE, Bakke AC, McCoy SL, Bennet RM. Nucleosomes and DNA bind to specific cellsurface molecules on murine cells and induce cytokine production. Clin Immunol Immunopathol 1992; 63: 245–251.

    Google Scholar 

  28. Bell DA, Morrison B, Vanden Bygaart P. Immunogenic DNA-related factors. J Clin Invest 1990; 85: 1487–1496.

    Google Scholar 

  29. Atkinson MJ, Bell DA, Singhal SK. Anaturally occurring polyclonal B cell activator of normal and autoantibody responses. J Immunol 1985; 135(4): 2524–2533.

    Google Scholar 

  30. Le Lann AD, Fournié GJ, Boissier L, Toutain PL, Benoist H. In vitro inhibition of natural killer-mediated lysis by chromatin fragments. Cancer Immunol Immunother 1994; 39: 185–192.

    Google Scholar 

  31. McCroskey MC, Palazuk BJ, Pierce-Ramsey PA, Colca JR, Pearson JD. Insulin-like effects of histones H3 and H4 on isolated rat adipocytes. Biochim Biophys Acta 1989; 1011: 212–219.

    Google Scholar 

  32. Reichhart R, Zeppezauer M, Jörnvall H. Preparations of homeostatic thymus hormone consist predominantly of histones 2A and 2B and suggest additional histone functions. Proc Natl Acad Sci USA 1985; 82: 4871–4875.

    Google Scholar 

  33. Goya RG, Quigley KL, Takahashi S, Reichhart R, Meites J. Differential effect of homeostatic thymus hormone on plasma thyrotropin and growth hormone in young and old rats. Mech Age Devel 1989; 49: 119–128.

    Google Scholar 

  34. Goya RG, Sosa YE, Quigley KL, Reichhart R, Meites J. Homeostatic thymus hormone stimulates corticosterone secretion in a dose-and age-dependent manner in rats. Neuroendocrinology 1990; 51: 59–63.

    Google Scholar 

  35. Brown OA, Sosa YE, Goya RG. Thyrotropin-releasing activity of histones H2A, H2B and peptide MB35. Peptides 1997; 18(8): 1315–1319.

    Google Scholar 

  36. Brown, OA, Sosa YE, Goya RG. Histones as extracellular messengers: Effects on growth hormone secretion. Cell Biol Int 1997; 21(12): 787–792.

    Google Scholar 

  37. Brown OA, Sosa YE, Goya RG. Gonadotrophin-releasing activity of histones H2A and H2B. Cell Molec Life Sci 1998; 54: 288–294.

    Google Scholar 

  38. Brown OA, Sosa YE, Castro MG, Goya RG. Studies on the prolactin-releasing mechanism of histones H2A and H2B. Life Sci 2000; 66: 2081–2089.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Goya, R.G., Cónsole, G.M., Spinelli, O.M. et al. Glucocorticoid-induced apoptosis in lymphoid organs is associated with a delayed increase in circulating deoxyribonucleic acid. Apoptosis 8, 171–177 (2003). https://doi.org/10.1023/A:1022922726418

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1022922726418

Navigation