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. 1977 Sep 1;146(3):747–758. doi: 10.1084/jem.146.3.747

Separation of helper and suppressor T lymphocytes. II. Ly phenotypes and lack of DNA synthesis requirement for the generation of concanavalin A helper and suppressor cells

PMCID: PMC2180807  PMID: 302306

Abstract

Using a Ficoll velocity sedimentation gradient, we have been able to fractionate concanavalin A (Con A)-induced helper and suppressor cells into separate pools. Cells activated by Con A to mediate helper activity are Ly1+, do not require DNA synthesis for induction, and remain as small cells after activation. Suppressor cells are Ly23+, are found in the blast cell fraction and their induction is not inhibitable by prior treatment with mitomycin C or irradiation, both of which inhibit DNA synthesis. The implications of such findings are discussed.

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Selected References

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  1. Cantor H., Boyse E. A. Functional subclasses of T-lymphocytes bearing different Ly antigens. I. The generation of functionally distinct T-cell subclasses is a differentiative process independent of antigen. J Exp Med. 1975 Jun 1;141(6):1376–1389. doi: 10.1084/jem.141.6.1376. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chan E. L., Henry C. Coexistence of helper and suppressor activities in carrier-primed spleen cells. J Immunol. 1976 Oct;117(4):1132–1138. [PubMed] [Google Scholar]
  3. Dutton R. W. Inhibitory and stimulatory effects of concanavalin A on the response of mouse spleen cell suspensions to antigen. I. Characterization of the inhibitory cell activity. J Exp Med. 1972 Dec 1;136(6):1445–1460. doi: 10.1084/jem.136.6.1445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dutton R. W. Inhibitory and stimulatory effects of concanavalin A on the response of mouse spleen cell suspensions to antigen. II. Evidence for separate stimulatory and inhibitory cells. J Exp Med. 1973 Dec 1;138(6):1496–1505. doi: 10.1084/jem.138.6.1496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dutton R. W., Mishell R. I. Cell populations and cell proliferation in the in vitro response of normal mouse spleen to heterologous erythrocytes. Analysis by the hot pulse technique. J Exp Med. 1967 Sep 1;126(3):443–454. doi: 10.1084/jem.126.3.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eardley D. D., Sercarz E. E. Modulation of help and suppression in a hapten-carrier system. J Immunol. 1976 Mar;116(3):600–605. [PubMed] [Google Scholar]
  7. Frelinger J. A., Niederhuber J. E., Shreffler D. C. Effects of anti-Ia sera on mitogenic responses. III. Mapping the genes controlling the expression of Ia determinants on concanavalin A-reactive cells to the I-J subregion of the H-2 gene complex. J Exp Med. 1976 Oct 1;144(4):1141–1146. doi: 10.1084/jem.144.4.1141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jandinski J., Cantor H., Tadakuma T., Peavy D. L., Pierce C. W. Separation of helper T cells from suppressor T cells expressing different Ly components. I. Polyclonal activation: suppressor and helper activities are inherent properties of distinct T-cell subclasses. J Exp Med. 1976 Jun 1;143(6):1382–1390. doi: 10.1084/jem.143.6.1382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Kappler J. W., Marrack P. C. Functional heterogeneity among the T-derived lymphocytes of the mouse. III. Helper and suppressor T-cells activated by concanavalin A. Cell Immunol. 1975 Jul;18(1):9–20. doi: 10.1016/0008-8749(75)90031-3. [DOI] [PubMed] [Google Scholar]
  10. MacDonald H. R., Sordat B., Cerottini J. C., Brunner K. T. Generation of cytotoxic T lymphocytes in vitro. IV. Functional activation of memory cells in the absence of DNA synthesis. J Exp Med. 1975 Sep 1;142(3):622–636. doi: 10.1084/jem.142.3.622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Mishell R. I., Dutton R. W. Immunization of dissociated spleen cell cultures from normal mice. J Exp Med. 1967 Sep 1;126(3):423–442. doi: 10.1084/jem.126.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Niederhuber J. E., Frelinger J. A., Dine M. S., Shoffner P., Dugan E., Shreffler D. C. Effects of anti-Ia sera on mitogenic responses. II. Differential expression of the Ia marker on phytohemagglutinin and concanavalin A-reactive T cells. J Exp Med. 1976 Feb 1;143(2):372–381. doi: 10.1084/jem.143.2.372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Okumura K., Herzenberg L. A., Murphy D. B., McDevitt H. O., Herzenberg L. A. Selective expression of H-2 (i-region) loci controlling determinants on helper and suppressor T lymphocytes. J Exp Med. 1976 Sep 1;144(3):685–698. doi: 10.1084/jem.144.3.685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Redelman D., Scott C. B., Sheppard H. W., Jr, Sell S. In vitro studies of the rabbit immune system. V. Suppressor T cells activated by concanavalin A block the proliferation, not the induction of antierythrocyte plaque-forming cells. J Exp Med. 1976 Apr 1;143(4):919–936. doi: 10.1084/jem.143.4.919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Rich R. R., Pierce C. W. Biological expressions of lymphocyte activation. II. Generation of a population of thymus-derived suppressor lymphocytes. J Exp Med. 1973 Mar 1;137(3):649–659. doi: 10.1084/jem.137.3.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Roszman T. L. Suppression of the in vitro secondary antibody response of rabbit lymphoid cells by Concanavalin A. Proc Soc Exp Biol Med. 1975 Jun;149(2):407–412. doi: 10.3181/00379727-149-38817. [DOI] [PubMed] [Google Scholar]
  17. Scavulli J., Dutton R. W. Competition between concanavalin A-induced stimulatory and inhibitory effects in the in vitro immune response to antigen. J Exp Med. 1975 Feb 1;141(2):524–529. doi: 10.1084/jem.141.2.524. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Stout R. D., Herzenberg L. A. The Fc receptor on thymus-derived lymphocytes. I. Detection of a subpopulation of murine T lymphocytes bearing the Fc receptor. J Exp Med. 1975 Sep 1;142(3):611–621. doi: 10.1084/jem.142.3.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Stout R. D., Herzenberg L. A. The Fc receptor on thymus-derived lymphocytes: II. Mitogen responsiveness of T lymphocytes bearing the Fc receptor. J Exp Med. 1975 Nov 1;142(5):1041–1051. doi: 10.1084/jem.142.5.1041. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Stout R. D., Waksal S. D., Herzenberg L. A. The Fc receptor on thymus-derived lymphocytes. III. Mixed lymphocyte reactivity and cell-mediated lympholytic activity of Fc- and Fc+ T lymphocytes. J Exp Med. 1976 Jul 1;144(1):54–68. doi: 10.1084/jem.144.1.54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Swain S. L., Trefts P. E., Tse H. Y., Dutton R. W. The significance of T-B collaboration across haplotype barriers. Cold Spring Harb Symp Quant Biol. 1977;41(Pt 2):597–609. doi: 10.1101/sqb.1977.041.01.069. [DOI] [PubMed] [Google Scholar]
  22. Tada T., Taniguchi M., David C. S. Properties of the antigen-specific suppressive T-cell factor in the regulation of antibody response of the mouse. IV. Special subregion assignment of the gene(s) that codes for the suppressive T-cell factor in the H-2 histocompatibility complex. J Exp Med. 1976 Sep 1;144(3):713–725. doi: 10.1084/jem.144.3.713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tse H., Dutton R. W. Separation of helper and suppressor T lymphocytes on a ficoll velocity sedimentation gradient. J Exp Med. 1976 May 1;143(5):1199–1210. doi: 10.1084/jem.143.5.1199. [DOI] [PMC free article] [PubMed] [Google Scholar]

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