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. 1973 Jan 31;137(2):511–526. doi: 10.1084/jem.137.2.511

INDEPENDENCE OF H-2K AND H-2D ANTIGENIC DETERMINANTS ON THE SURFACE OF MOUSE LYMPHOCYTES

Catherine Neauport-Sautes 1, Frank Lilly 1, Danielle Silvestre 1, François M Kourilsky 1
PMCID: PMC2139496  PMID: 4119593

Abstract

At 37°C, fluorescein-conjugated anti-H-2 alloantibodies specifically induce, at the surface of living mouse lymphocytes, the redistribution of the corresponding H-2 antigens, which cluster as patches and sometimes single caps at one pole of the cell. This aggregation is inhibited at 0°C and the H-2 antigens, stained by fluorescent antibodies in the cold, appear evenly spread over the cell surface. This phenomenon was used to define the relationships between the membrane structures bearing the antigens coded by the H-2K and the H-2D genes of the H-2 region. Monospecific anti-H-2 antibodies coupled to either tetramethyl rhodamine isothiocyanate or fluorescein isothiocyanate were used to induce the redistribution of H-2D and H-2K antigens of the H-2 b and H-2 k haplotype at the surface of lymph node cells from homozygous and F1 hybrid mice. It was observed that the diffuse distribution of H-2K antigens labeled at 0°C was not affected by the prior antibody-induced aggregation of H-2D antigens and vice versa. The results were the same for H-2 antigens governed by genes located either in cis or in trans position. These data indicate that the H-2K and H-2D antigens migrate independently at the cell surface, and suggest that the gene products from the D and the K end of the H-2 region are expressed on independent molecules or structures at the cell membrane.

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Selected References

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

  1. Amos D. B., Cohen I., Klein W. J., Jr Mechanisms of immunologic enhancement. Transplant Proc. 1970 Mar;2(1):68–75. [PubMed] [Google Scholar]
  2. Aoki T., Hämmerling U., De Harven E., Boyse E. A., Old L. J. Antigenic structure of cell surfaces. An immunoferritin study of the occurrence and topography of H-2' theta, and TL alloantigens on mouse cells. J Exp Med. 1969 Nov 1;130(5):979–1001. doi: 10.1084/jem.130.5.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Boyse E. A., Old L. J., Stockert E. An approach to the mapping of antigens on the cell surface. Proc Natl Acad Sci U S A. 1968 Jul;60(3):886–893. doi: 10.1073/pnas.60.3.886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Boyse E. A., Stockert E., Old L. J. Modification of the antigenic structure of the cell membrane by thymus-leukemia (TL) antibody. Proc Natl Acad Sci U S A. 1967 Sep;58(3):954–957. doi: 10.1073/pnas.58.3.954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chang S., Stockert E., Boyse E. A., Hämmerling U., Old L. J. Spontaneous release of cytotoxic alloantibody from viable cells sensitized in excess antibody. Immunology. 1971 Nov;21(5):829–838. [PMC free article] [PubMed] [Google Scholar]
  6. Cresswell P., Sanderson A. R. Spatial arrangement of H-2 specificities: evidence from antibody adsorption and kinetic studies. Transplantation. 1968 Dec;6(9):996–1004. doi: 10.1097/00007890-196812000-00006. [DOI] [PubMed] [Google Scholar]
  7. Cullen S. E., Schwartz B. D., Nathenson S. G., Cherry M. The molecular basis of codominant expression of the histocompatibility-2 genetic region. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1394–1397. doi: 10.1073/pnas.69.6.1394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Davis W. C. H-2 antigen on cell membranes: an explanation for the alteration of distribution by indirect labeling techniques. Science. 1972 Mar 3;175(4025):1006–1008. doi: 10.1126/science.175.4025.1006. [DOI] [PubMed] [Google Scholar]
  9. Frye L. D., Edidin M. The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons. J Cell Sci. 1970 Sep;7(2):319–335. doi: 10.1242/jcs.7.2.319. [DOI] [PubMed] [Google Scholar]
  10. Karnovsky M. J., Unanue E. R., Leventhal M. Ligand-induced movement of lymphocyte membrane macromolecules. II. Mapping of surface moieties. J Exp Med. 1972 Oct 1;136(4):907–930. doi: 10.1084/jem.136.4.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Klein J., Shreffler D. C. Evidence supporting a two-gene model for the H-2 histocompatibility system of the mouse. J Exp Med. 1972 Apr 1;135(4):924–937. doi: 10.1084/jem.135.4.924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Klein J., Shreffler D. C. The H-2 model for the major histocompatibility systems. Transplant Rev. 1971;6:3–29. doi: 10.1111/j.1600-065x.1971.tb00457.x. [DOI] [PubMed] [Google Scholar]
  13. Kourilsky F. M., Silvestre D., Neauport-Sautes C., Loosfelt Y., Dausset J. Antibody-induced redistribution of HL-A antigens at the cell surface. Eur J Immunol. 1972 Jun;2(3):249–257. doi: 10.1002/eji.1830020311. [DOI] [PubMed] [Google Scholar]
  14. Lamm M. E., Boyse E. A., Old L. J., Lisowska-Bernstein B., Stockert E. Modulation of TL (thymus-leukemia) antigens by Fab-fragments of TL antibody. J Immunol. 1968 Jul;101(1):99–103. [PubMed] [Google Scholar]
  15. Lilly F. The role of genetics in Gross virus leukemogenesis. Bibl Haematol. 1970;(36):213–220. doi: 10.1159/000391710. [DOI] [PubMed] [Google Scholar]
  16. Loor F., Forni L., Pernis B. The dynamic state of the lymphocyte membrane. Factors affecting the distribution and turnover of surface immunoglobulins. Eur J Immunol. 1972 Jun;2(3):203–212. doi: 10.1002/eji.1830020304. [DOI] [PubMed] [Google Scholar]
  17. McDevitt H. O., Deak B. D., Shreffler D. C., Klein J., Stimpfling J. H., Snell G. D. Genetic control of the immune response. Mapping of the Ir-1 locus. J Exp Med. 1972 Jun 1;135(6):1259–1278. doi: 10.1084/jem.135.6.1259. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Passmore H. C., Shreffler D. C. A sex-limited serum protein variant in the mouse: inheritance and association with the H-2 region. Biochem Genet. 1970 Jun;4(3):351–365. doi: 10.1007/BF00485752. [DOI] [PubMed] [Google Scholar]
  19. Preud'homme J. L., Neauport-Sautes C., Piat S., Silvestre D., Kourilsky F. M. Independence of HL-A antigens and immunoglobulin determinants on the surface of human lymphoid cells. Eur J Immunol. 1972 Jun;2(3):297–300. doi: 10.1002/eji.1830020323. [DOI] [PubMed] [Google Scholar]
  20. STIMPFLING J. H., RICHARDSON A. RECOMBINATION WITHIN THE HISTOCOMPATIBILITY LOCUS OF THE MOUSE. Genetics. 1965 May;51:831–846. doi: 10.1093/genetics/51.5.831. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Singer S. J., Nicolson G. L. The fluid mosaic model of the structure of cell membranes. Science. 1972 Feb 18;175(4023):720–731. doi: 10.1126/science.175.4023.720. [DOI] [PubMed] [Google Scholar]
  22. Unanue E. R., Perkins W. D., Karnovsky M. J. Endocytosis by lymphocytes of complexes of anti-Ig with membrane-bound Ig. J Immunol. 1972 Feb;108(2):569–572. [PubMed] [Google Scholar]
  23. Unanue E. R., Perkins W. D., Karnovsky M. J. Ligand-induced movement of lymphocyte membrane macromolecules. I. Analysis by immunofluorescence and ultrastructural radioautography. J Exp Med. 1972 Oct 1;136(4):885–906. doi: 10.1084/jem.136.4.885. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. WIGZELL H. QUANTITATIVE TITRATIONS OF MOUSE H-2 ANTIBODIES USING CR-51-LABELLED TARGET CELLS. Transplantation. 1965 May;3:423–431. doi: 10.1097/00007890-196505000-00011. [DOI] [PubMed] [Google Scholar]

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