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. 1974 Jul;17(3):455–462.

In vitro preferential effect of irradiation on cultured T lymphoid cell line

T Han, J L Pauly, J Minowada
PMCID: PMC1554081  PMID: 4549689

Abstract

The present report describes a comparative study of cytocidal effect of irradiation on human cultured T and B lymphoid cells. Cytocidal effect of irradiation was expressed as percentage inhibition or percentage reduction, which was calculated by comparing the [3H]thymidine incorporations or viable cell counts in irradiated and unirradiated cultures, respectively. A higher percentage inhibition was observed in each and every T-cell culture, irradiated with 100–4000 rads at days 1–4 of incubation. The most significant difference of percentage inhibition between T and B cells (P<0·05–P<0·01) was observed at each irradiation dose level at day 3. A significant percentage reduction of viable T cells (98–100%) was noted at 100 rad dose level, whereas only 0–3% of B lymphoid cells were killed by this dose of irradiation at days 2–4 of incubation. Our data clearly indicate that human cultured T lymphoid cells are extremely radiosensitive and B lymphoid cells, on the other hand, are fairly radioresistant.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bianco C., Patrick R., Nussenzweig V. A population of lymphocytes bearing a membrane receptor for antigen-antibody-complement complexes. I. Separation and characterization. J Exp Med. 1970 Oct 1;132(4):702–720. doi: 10.1084/jem.132.4.702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. DIXON F. J., TALMAGE D. W., MAURER P. H. Radiosensitive and radioresistant phases in the antibody response. J Immunol. 1952 Jun;68(6):693–700. [PubMed] [Google Scholar]
  3. Drewinko B., Humphrey R. M., Trujillo J. M. The radiation response of a long-term culture of human lymphoid cells. I. Asynchronous populations. Int J Radiat Biol Relat Stud Phys Chem Med. 1972 Apr;21(4):361–373. doi: 10.1080/09553007214550431. [DOI] [PubMed] [Google Scholar]
  4. HEMPELMANN L. H., LISCO H., HOFFMAN J. G. The acute radiation syndrome: a study of nine cases and a review of the problem. Ann Intern Med. 1952 Feb;36(21):279–510. doi: 10.7326/0003-4819-36-2-279. [DOI] [PubMed] [Google Scholar]
  5. Han T. Blastogenic response of normal lymphocytes to cultured lymphoid cells and non-lymphoid neoplastic cells. Immunology. 1972 Sep;23(3):355–359. [PMC free article] [PubMed] [Google Scholar]
  6. Han T., Minowada J. A unique 'leukaemic' T lymphoid cell line: absence of stimulating effect in mixed lymphocyte reaction. Lack of MLR-S in leukaemic T lymphoid cells. Clin Exp Immunol. 1973 Dec;15(4):535–541. [PMC free article] [PubMed] [Google Scholar]
  7. Jondal M., Holm G., Wigzell H. Surface markers on human T and B lymphocytes. I. A large population of lymphocytes forming nonimmune rosettes with sheep red blood cells. J Exp Med. 1972 Aug 1;136(2):207–215. doi: 10.1084/jem.136.2.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. LIEBOW A. A., WARREN S., DeCOURSEY E. Pathology of atomic bomb casualties. Am J Pathol. 1949 Sep;25(5):853–1027. [PMC free article] [PubMed] [Google Scholar]
  9. Minowada J., Onuma T., Moore G. E. Rosette-forming human lymphoid cell lines. I. Establishment and evidence for origin of thymus-derived lymphocytes. J Natl Cancer Inst. 1972 Sep;49(3):891–895. [PubMed] [Google Scholar]
  10. Nettesheim P., Williams M. L., Hammons A. S. Regenerative potential of immunocompetent cells. 3. Recovery of primary antibody-forming potential from X-irradiation. The role of the thymus. J Immunol. 1969 Sep;103(3):505–518. [PubMed] [Google Scholar]
  11. Osoba D. Some physical and radiobiological properties of immunologically reactive mouse spleen cells. J Exp Med. 1970 Aug 1;132(2):368–383. doi: 10.1084/jem.132.2.368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Pribnow J. F., Silverman M. S. Studies on the radiosensitive phase of the antibody response in rabbits. II. Recovery and the secondary response. J Immunol. 1969 Aug;103(2):276–281. [PubMed] [Google Scholar]
  13. ROSS M. H., FURTH J., BIGELOW R. R. Changes in cellular composition of the lymph caused by ionizing radiations. Blood. 1952 Apr;7(4):417–428. [PubMed] [Google Scholar]
  14. SALVIN S. B., SMITH R. F. Delayed hypersensitivity in the development of circulating antibody; the effect of x-irradiation. J Exp Med. 1959 Apr 1;109(4):325–338. doi: 10.1084/jem.109.4.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. SCHREK R. Cytologic changes in thymic glands exposed in vivo to X-rays. Am J Pathol. 1948 Sep;24(5):1055–1065. [PMC free article] [PubMed] [Google Scholar]
  16. SCHREK R. In vitro longevity and radiosensitivity of lymphocytes of man and other species. Am J Clin Pathol. 1959 Feb;31(2):112–116. doi: 10.1093/ajcp/31.2.112. [DOI] [PubMed] [Google Scholar]
  17. SCHREK R., OTT J. N., Jr Study of the death of irradiated and non-irradiated cells by time-lapse cinemicrography. AMA Arch Pathol. 1952 Apr;53(4):363–378. [PubMed] [Google Scholar]
  18. Sato C. Change in the type of radiation cell-killing on human lymphocytes after blast formation by phytohaemagglutinin. Int J Radiat Biol Relat Stud Phys Chem Med. 1970;18(5):483–485. doi: 10.1080/09553007014551381. [DOI] [PubMed] [Google Scholar]
  19. Shevach E. M., Herberman R., Frank M. M., Green I. Receptors for complement and immunoglobulin on human leukemic cells and human lymphoblastoid cell lines. J Clin Invest. 1972 Aug;51(8):1933–1938. doi: 10.1172/JCI106999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Stjernswärd J., Jondal M., Vánky F., Wigzell H., Sealy R. Lymphopenia and change in distribution of human B and T lymphocytes in peripheral blood induced by irradiation for mammary carcinoma. Lancet. 1972 Jun 24;1(7765):1352–1356. doi: 10.1016/s0140-6736(72)91091-4. [DOI] [PubMed] [Google Scholar]
  21. Swasdikul D., Block M. Effect of radiation upon the "embryonic" thymus. Radiat Res. 1972 Apr;50(1):73–84. [PubMed] [Google Scholar]
  22. VOGEL F. S., BALLIN J. C. Morphological changes in thymus of rats following wholebody exposure to massive doses of radiation. Proc Soc Exp Biol Med. 1955 Nov;90(2):419–423. doi: 10.3181/00379727-90-22053. [DOI] [PubMed] [Google Scholar]

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