Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1974 Nov 30;140(6):1511–1521. doi: 10.1084/jem.140.6.1511

GENERATION OF CYTOTOXIC T LYMPHOCYTES IN VITRO

III. Velocity Sedimentation Studies of the Differentiation and Fate of Effector Cells in Long-Term Mixed Leukocyte Cultures

H Robson MacDonald 1, Jean-Charles Cerottini 1, K Theodor Brunner 1
PMCID: PMC2139763  PMID: 4279270

Abstract

Separation of cells by velocity sedimentation at unit gravity was utilized to investigate the physical properties of cytotoxic thymus-derived lymphocytes (CTL) generated in long-term mixed leukocyte cultures (MLC). In kinetic studies, CTL were found almost exclusively in the large cell fractions at the peak of the response on day 4, whereas the majority of CTL in day 14 MLC had the sedimentation properties of small lymphocytes. Reculture until day 14 of cells fractionated on the basis of size on day 4 indicated that the small CTL were derived exclusively from cells which had been large on day 4. Re-exposure of day 14 MLC cells to the original stimulating alloantigens resulted in significant cell proliferation and rapid regeneration of CTL activity. Cell fractionation experiments demonstrated that the cells in the day 14 MLC population which responded to the secondary allogeneic stimulus were small T lymphocytes, and that these cells rapidly developed into large, highly cytotoxic CTL following stimulation. Moreover, by restimulating on day 14 fractions which were selected on the basis of size on day 4, it was found that the responding small lymphocytes were themselves the progeny of cells which were large at the peak of the response. Since CTL and CTL progenitors showed concomitant changes in physical properties with time, the possibility exists that they belong to the same cell lineage, and hence that CTL can differentiate into cells which are no longer cytotoxic, but capable of mounting an anamnestic response.

Full Text

The Full Text of this article is available as a PDF (822.6 KB).

Selected References

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

  1. Andersson L. C., Häyry P. Specific priming of mouse thymus-dependent lymphocytes to allogeneic cells in vitro. Eur J Immunol. 1973 Sep;3(9):595–599. doi: 10.1002/eji.1830030913. [DOI] [PubMed] [Google Scholar]
  2. Brunner K. T., Mauel J., Cerottini J. C., Chapuis B. Quantitative assay of the lytic action of immune lymphoid cells on 51-Cr-labelled allogeneic target cells in vitro; inhibition by isoantibody and by drugs. Immunology. 1968 Feb;14(2):181–196. [PMC free article] [PubMed] [Google Scholar]
  3. Canty T. G., Wunderlich J. R., Fletcher F. Qualitative and quantitative studies of cytotoxic immune cells. J Immunol. 1971 Jan;106(1):200–208. [PubMed] [Google Scholar]
  4. Cerottini J. C., Brunner K. T. Cell-mediated cytotoxicity, allograft rejection, and tumor immunity. Adv Immunol. 1974;18:67–132. doi: 10.1016/s0065-2776(08)60308-9. [DOI] [PubMed] [Google Scholar]
  5. Cerottini J. C., Engers H. D., Macdonald H. R., Brunner T. Generation of cytotoxic T lymphocytes in vitro. I. Response of normal and immune mouse spleen cells in mixed leukocyte cultures. J Exp Med. 1974 Sep 1;140(3):703–717. doi: 10.1084/jem.140.3.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Clark W., Nedrud J. Effect of BUdR on proliferation and development of cytotoxicity in mixed leukocyte culture. Cell Immunol. 1974 Jan;10(1):159–164. doi: 10.1016/0008-8749(74)90160-9. [DOI] [PubMed] [Google Scholar]
  7. Greenberg A. H. Fractionation of cytotoxic T lymphoblasts on Ficoll gradients by velocity sedimentation. Eur J Immunol. 1973 Dec;3(12):793–797. doi: 10.1002/eji.1830031211. [DOI] [PubMed] [Google Scholar]
  8. Häyry P., Defendi V. Mixed lymphocyte cultures produce effector cells: model in vitro for allograft rejection. Science. 1970 Apr 3;168(3927):133–135. doi: 10.1126/science.168.3927.133. [DOI] [PubMed] [Google Scholar]
  9. MacDonald H. R., Phillips R. A., Miller R. G. Allograft immunity in the mouse. 1. Quantitation and specificity of cytotoxic effector cells after in vitro sensitization. J Immunol. 1973 Aug;111(2):565–574. [PubMed] [Google Scholar]
  10. MacDonald H. R., Phillips R. A., Miller R. G. Allograft immunity in the mouse. II. Physical studies of the development of cytotoxic effector cells from their immediate progenitors. J Immunol. 1973 Aug;111(2):575–589. [PubMed] [Google Scholar]
  11. Macdonald H. R., Engers H. D., Cerottini J. C., Brunner K. T. Generation of cytotoxic T lymphocytes in vitro. II. Effect of repeated exposure to alloantigens on the cytotoxic activity of long-term mixed leukocyte cultures. J Exp Med. 1974 Sep 1;140(3):718–730. doi: 10.1084/jem.140.3.718. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Macdonald H. R., Miller R. G. Synchronization of mouse L-cells by a velocity sedimentation technique. Biophys J. 1970 Sep;10(9):834–842. doi: 10.1016/S0006-3495(70)86338-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Miller R. G., Phillips R. A. Separation of cells by velocity sedimentation. J Cell Physiol. 1969 Jun;73(3):191–201. doi: 10.1002/jcp.1040730305. [DOI] [PubMed] [Google Scholar]
  14. Pelet J., Brunner K. T., Nordin A. A., Cerottini J. C. The relative distribution of cytotoxic lymphocytes and of alloantibody-forming cells in albumin density gradients. Eur J Immunol. 1971 Aug;1(4):238–242. doi: 10.1002/eji.1830010405. [DOI] [PubMed] [Google Scholar]
  15. Shortman K., Brunner K. T., Cerottini J. C. Separation of stages in the development of the "T" cells involved in cell-mediated immunity. J Exp Med. 1972 Jun 1;135(6):1375–1391. doi: 10.1084/jem.135.6.1375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Wagner H., Feldmann M. Cell-mediated immune response in vitro. I. A new in vitro system for the generation of cell-mediated cytotoxic activity. Cell Immunol. 1972 Mar;3(3):405–420. doi: 10.1016/0008-8749(72)90246-8. [DOI] [PubMed] [Google Scholar]

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

RESOURCES