Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1973 Oct 1;138(4):812–824. doi: 10.1084/jem.138.4.812

POKEWEED MITOGEN-, CONCANAVALIN A-, AND PHYTOHEMAGGLUTININ-INDUCED DEVELOPMENT OF CYTOTOXIC EFFECTOR LYMPHOCYTES

AN EVALUATION OF THE MECHANISMS OF T CELL-MEDIATED CYTOTOXICITY

Holger Kirchner 1, R Michael Blaese 1
PMCID: PMC2180558  PMID: 4542736

Abstract

Cultures of chicken lymphoid tissues were tested for their capacity to lyse 51Cr-labeled chicken, burro (BRC), and human red blood cells (HRC) in the presence of phytomitogens. PHA-stimulated cultures lysed all three types of targets, while PWM and Con A showed a "target cell specificity" for HRC and BRC, respectively. In mixtures of target cells only the appropriate targets were lysed by lymphocytes activated by either Con A or PWM indicating that soluble lymphotoxins do not play a major role in these reactions. Preincubation experiments suggested that there may be a population of pre-existing aggressor cells which only require linking to the targets by the mitogens for activation of their cytotoxic potential. Strong cytotoxic reactions were found with spleen cells, peripheral blood leucocytes, and bone marrow cells. Thymocytes were less active but could be stimulated for significant cytotoxicity, while bursal cells were generally unreactive. Spleen cells from agammaglobulinemic chickens totally lacking serum immunoglobulins and B cells with surface-bound immunoglobulins were as active as cells from normal chickens. The activity of spleen cells, from which phagocytic cells were removed was also unimpaired. These results indicate that the development of cytotoxic effector lymphocytes in mitogen-treated leucocyte cultures is a property of T lymphocytes. Although bone marrow cells fail to proliferate in response to these phytomitogens, they do have strong cytotoxic reactivity suggesting that different subsets of thymic-derived lymphocytes are responsible for mitogen-induced transformation and mitogen-induced cytotoxicity.

Full Text

The Full Text of this article is available as a PDF (735.3 KB).

Selected References

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

  1. Cerottini J. C., Nordin A. A., Brunner K. T. Specific in vitro cytotoxicity of thymus-derived lymphocytes sensitized to alloantigens. Nature. 1970 Dec 26;228(5278):1308–1309. doi: 10.1038/2281308a0. [DOI] [PubMed] [Google Scholar]
  2. Ginsburg H. Lysis of target cell monolayers by lymphocytes stimulated with pokeweed mitogen. Transplantation. 1971 Apr;11(4):408–412. doi: 10.1097/00007890-197104000-00009. [DOI] [PubMed] [Google Scholar]
  3. Holm G., Perlmann P. Inhibition of cytotoxic lymphocytes by anti-lymphocytic serum. Transplant Proc. 1969 Mar;1(1):420–423. [PubMed] [Google Scholar]
  4. Holm G., Perlmann P., Johansson B. Impaired phytohaemagglutinin-induced cytotoxicity in vitro of lymphocytes from patients with Hodgkin's disease or chronic lymphatic leukaemia. Clin Exp Immunol. 1967 May;2(3):351–360. [PMC free article] [PubMed] [Google Scholar]
  5. Holm G. The in vitro cytotoxicity of human lymphocytes: the effect of metabolic inhibitors. Exp Cell Res. 1967 Nov;48(2):334–349. doi: 10.1016/0014-4827(67)90359-x. [DOI] [PubMed] [Google Scholar]
  6. Kincade P. W., Lawton A. R., Cooper M. D. Restriction of surface immunoglobulin determinants to lymphocytes of the plasma cell line. J Immunol. 1971 May;106(5):1421–1423. [PubMed] [Google Scholar]
  7. Kirchner H., Oppenheim J. J., Blaese M. R., Hofstrand H. J. Defective in vitro spleen cell proliferative response to antigens in agammaglobulinemic chickens. J Immunol. 1972 Aug;109(2):348–352. [PubMed] [Google Scholar]
  8. Lydyard P., Ivanyi J. Suppression of graft-versus-host-reactive lymphocytes by heterologous antithymus serum in vitro. Transplantation. 1971 Dec;12(6):493–499. doi: 10.1097/00007890-197112000-00014. [DOI] [PubMed] [Google Scholar]
  9. Mogensen C. E. The glomerular permeability determined by dextran clearance using Sephadex gel filtration. Scand J Clin Lab Invest. 1968;21(1):77–82. doi: 10.3109/00365516809076979. [DOI] [PubMed] [Google Scholar]
  10. Möller G., Sjöberg O., Andersson J. Mitogen-induced lymphocyte-mediated cytotoxicity in vitro: effect of mitogens selectively activating T or B cells. Eur J Immunol. 1972 Dec;2(6):586–592. doi: 10.1002/eji.1830020621. [DOI] [PubMed] [Google Scholar]
  11. Perlmann P., Nilsson H., Leon M. A. Inhibition of cytotoxicity of lymphocytes by concanavalin A in vitro. Science. 1970 May 29;168(3935):1112–1115. doi: 10.1126/science.168.3935.1112. [DOI] [PubMed] [Google Scholar]
  12. Rosenstreich D. L., Blake J. T., Rosenthal A. S. The peritoneal exudate lymphocyte. I. Differences in antigen responsiveness between peritoneal exudate and lymph node lymphocytes from immunized guinea pigs. J Exp Med. 1971 Nov 1;134(5):1170–1186. doi: 10.1084/jem.134.5.1170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Van Boxel J. A., Stobo J. D., Paul W. E., Green I. Antibody-dependent lymphoid cell-mediated cytotoxicity: no requirement for thymus-derived lymphocytes. Science. 1972 Jan 14;175(4018):194–196. doi: 10.1126/science.175.4018.194. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES