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Spontaneous loss and subsequent stimulation ofH-2 expression in clones of a heterozygous lymphoma cell line

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Abstract

The expression of H-2Kk antigens in a (C3H × DBA/2)F1 lymphoma cell line growing in vitro was investigated with monoclonal antibodies specific for a public antigen of theH-2K k region (H-2.m3) in fluorescence analysis and microcytotoxicity assays and in cell-mediated cytotoxicity with allogeneically stimulated effector cells. Estimates of relative levels of H-2Kk-antigen expression obtained by the different methods were highly correlated. The uncloned, unselected population gradually lost H-2Kk surface antigen expression under culture conditions. This was due to the appearance of H-2Kk negative variants. Fifteen cloned sublines of a population enriched for cells expressing antigen H-2.m3 in the fluorescence activated cell sorter contained either two distinct populations, one consisting of H-2.m3 negative and one of H-2.m3 positive cells, or consisted of H-2.m3 negative cells only. The expression of the H-2.m3 determinant of H-2Kk paralleled that of other serological H-2Kk determinants and of H-2Kk target determinants for cell-mediated cytotoxicity. In nearly all clones where two populations could be detected, the proportion of H-2.m3 negative cells increased with time in culture. The amounts of H-2Kk antigen expressed by the clones appeared not to be correlated to the amounts of H-2Dk antigens on the cell surface as judged by cell-mediated cytotoxicity.

In at least one clone and in the uncloned population, H-2Kk-antigen expression detectable by fluorescence analysis could be stimulated by growing the cells in the peritoneal cavities of (C3H × DBA/2)F1 mice or by adding mouse interferon preparations to the cell cultures. The increase in susceptibility to cell-mediated lympholysis of cells grown in vivo paralleled the increase inH-2 expression detected by fluorescence. In contrast, cells growing in the presence of interferon in vitro showed reduced sensitivity to lysis by alloreactive lymphocytes, although H-2 antigens were strongly expressed as measured by fluorescence.

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References

  • Amos, D. B.: Cytotoxicity testing.In J. G. Ray, D. B. Hare, P. D. Pedersen, and D. E. Kayhoe (eds.):Manual of Tissue Typing Techniques, pp. 23–26, Transplantation and Immunology Branch Collaborative Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, 1974

    Google Scholar 

  • Bevan, M. J. and Cohn, M.: Cytotoxic effect of antigen and mitogen induced T-cells on various targets.J. Immunol. 114: 559–565, 1975

    Google Scholar 

  • Bjaring, B. and Klein, G.: Antigenic characterisation of heterozygous mouse lymphomas after immunoselection in vivo.J. Natl. Cancer, Inst. 41: 1411–1429, 1968

    Google Scholar 

  • Bonner, W. A., Hulett, H. R., Sweet, R. G., and Herzenberg, L. A.: Fluorescence-activated cell sorting.Rev. Sci. Instrum. 43: 404–409, 1972

    PubMed  Google Scholar 

  • Cikes, M., Friberg, S. jr., and Klein, G.: Progressive loss of H-2 antigens with concomitant increase of cell surface antigen(s) determined by Moloney leukemia virus in cultured murine lymphomas.J. Natl. Cancer Inst. 50: 347–362, 1973

    PubMed  Google Scholar 

  • Finn, O. J., Lieberman, M., and Kaplan, H. S.: H-2 antigen expression: Loss in vitro, restoration in vivo, and correlation with cell-mediated cytotoxicity in a mouse lymphoma cell line.Immunogenetics 7: 79–88, 1978

    Google Scholar 

  • Gresser, I.: On the varied biologic effects of interferon.Cell Immunol. 34: 406–415, 1977

    PubMed  Google Scholar 

  • Hellström, K. E.: Studies on isoantigenic variation in mouse lymphomas.J. Natl. Cancer Inst. 25: 237–269, 1960

    PubMed  Google Scholar 

  • Hirt, H. M., Becker, H. and Kirchner, H.: Induction of interferon production in mouse spleen cell cultures by Corynebacterium parvum.Cell. Immunol. 38: 168–175, 1978

    PubMed  Google Scholar 

  • Holtkamp, B.: Expression von Antigenen des Haupthistokompatibilitätslocus auf Lymphomzellen der Maus. Diplomarbeit, University of Cologne, Institute of Genetics, April 1978

  • Hyman, R. and Trowbridge, I.: Analysis of lymphocyte surface antigen expression by the use of variant cell lines.Cold Spring Harbor Symp. Quant. Biol. 41: 407–415, 1976

    Google Scholar 

  • Killander, D., Lindahl, P., Lundin, L., Leary, P., and Gresser, I.: Relationship between the enhanced expression of histocompatibility antigens on interferon-treated L 1210 cells and their position in the cell cycle.Eur. J. Immunol. 6: 56–59, 1976

    PubMed  Google Scholar 

  • Klein, G. and Klein, E.: Histocompatibility changes in tumors.J. Cell. Physiol. 52: 125–168, 1958

    PubMed  Google Scholar 

  • Klein, J., Huang, H.-J. S., Lemke, H., Hämmerling, G. J., and Hämmerling, U.: Serological analysis of H-2 and Ia molecules with monoclonal antibodies,Immunogenetics 8: 419–432, 1979

    Google Scholar 

  • Lemke, H., Hämmerling, G. J., Höhmann, C., and Rajewsky, K.: Hybrid cell lines secreting monoclonal antibody specific for major histocompatibility antigens of the mouse.Nature 271: 249–251, 1978

    PubMed  Google Scholar 

  • Lesley, J., Hyman, R., and Dennert, G.: Effect of antigen density on complement-mediated lysis, T-cell-mediated killing and antigenic modulation.J. Natl. Cancer. Inst. 53: 1759–1765, 1974

    PubMed  Google Scholar 

  • Liesegang, B., Radbruch, A., and Rajewsky, K.: Isolation of myeloma variants with predefined variant surface immunoglobulin by cell sorting.Proc. Natl. Acad. Sci. USA 75: 3901–3905, 1978

    PubMed  Google Scholar 

  • Lindahl, K. F., Peck, A. B., and Bach, F. H.: Specificity of cell-mediated lympholysis for public and private H-2 determinants.Scand. J. Immunol. 4: 541–553, 1975

    PubMed  Google Scholar 

  • Lindahl, K. F. and Lemke, H.: Inhibition of killer-target cell interaction by monoclonal anti-H-2 antibodies.Eur. J. Immunol., in press, 1979

  • Lonai, P. and Steinman, L.: Physiological regulation of antigen binding to T-cells: Role of a soluble macrophage factor and of interferon.Proc. Natl. Acad. Sci. USA 74: 5662–5666, 1977

    PubMed  Google Scholar 

  • McMahon Pratt, D., Strominger, J., Parkman, R., Kaplan, D., Schwaber, J., Rosenberg, N., Scher, C. D.: Abelson virus-transformed lymphocytes: Null cells that modulate H-2.Cell 12: 683–690, 1977

    PubMed  Google Scholar 

  • Moller, G.: Demonstration of mouse isoantigens at the cellular level by the fluorescent antibody technique.J. Exp. Med. 114: 415–434, 1961

    Google Scholar 

  • Nabholz, M., Vives, J., Young, H. M., Meo, T., Miggiano, V., Rijnbeek, A., and Shreffler, D. C.: Cell-mediated cell lysis in vitro: Genetic control of killer cell production and target specificities in the mouse.Eur. J. Immunol. 4: 378–387, 1974

    PubMed  Google Scholar 

  • Ogburn, C. A., Berg, K., and Paucker, K.: Purification of mouse interferon by affinity chromatography on anti-interferon globulin-sepharose.J. Immunol. 111: 1206–1218, 1973

    PubMed  Google Scholar 

  • Papermaster, B. W. and Herzenberg, L. A.: Isolation and characterization of an isoantigenic variant from a heterozygous mouse lymphoma in culture.J. Cell Physiol. 67: 407–420, 1966

    PubMed  Google Scholar 

  • Rajan, T. V., Nathenson, S. G., and Scharff, M.: Regulatory variants for the expression of H-2 antigens. I. Isolation and characterization.J. Natl. Cancer Inst. 56: 1221–1227, 1976

    PubMed  Google Scholar 

  • Rajan, T. V.: H-2 antigen variants in a cultured heterozygous leukemia cell line.Immunogenetics 4: 105–115, 1977

    Google Scholar 

  • Russel, J. H., Hale, A. H., Ginns, L. C., and Eisen, H. N.: Periodic loss of reactivity of a myeloma tumor with cytotoxic thymus-derived lymphocytes.Proc. Natl. Acad. Sci. USA 75: 441–445, 1978

    PubMed  Google Scholar 

  • Schendel, D. J. and Bach, F. H.: H-2 and non H-2 determinants in the genetic control of cell-mediated lympholysis.Eur. J. Immunol. 5: 880–882, 1975

    Google Scholar 

  • Sibley, C. H. and Tomkins, G. M.: Isolation of lymphoma cell variants resistant to killing by glucocorticoids.Cell 2: 213–220, 1974

    PubMed  Google Scholar 

  • Snedecor, G. W. and Cochran, W. G.:Statistical Methods, Sixth Edition, The Iowa State University Press, Ames, Iowa, U.S.A., 1967

    Google Scholar 

  • Ting, C. C. and Herberman, R. B.: Inverse relationship of polyoma tumour specific cell surface antigen to H-2 histocompatibility antigens.Nature New Biol. 232: 118–120, 1971

    PubMed  Google Scholar 

  • Trinchieri, G. and Santoli, D.: Anti-viral activity induced by culturing lymphocytes with tumor-derived or virus-transformed cells. Enhancement of human natural killer cell activity by interferon and antagonistic inhibition of suspectibility of target cells to lysis.J. Exp. Med. 147:1314–1333, 1978

    Google Scholar 

  • Vignaux, F. and Gresser, I.: Differential effects of inferferon on the expression of H-2K, H-2D and Ia antigens on mouse lymphocytes.J. Immunol. 118:721–723, 1977

    PubMed  Google Scholar 

  • Wood, B. T., Thompson, S. H., and Goldstein, G.: Fluorescent antibody staining. III. Preparation of Fluorescein-Isothiocyanate-labelled antibodies.J. Immunol. 95:225–229, 1965

    PubMed  Google Scholar 

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Holtkamp, B., Lindahl, K.F., Segall, M. et al. Spontaneous loss and subsequent stimulation ofH-2 expression in clones of a heterozygous lymphoma cell line. Immunogenetics 9, 405–421 (1979). https://doi.org/10.1007/BF01570434

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