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. 1976 Mar 1;143(3):511–528. doi: 10.1084/jem.143.3.511

Antigen-induced aggregation and modulation of receptors on hapten- specific B lymphocytes

PMCID: PMC2190134  PMID: 55458

Abstract

Mouse spleen cells were subjected to a fractionation procedure designed to enrich for 4-hydroxy-3-iodo-5-nitro-phenylacetyl (NIP)- or DNP- specific B lymphocytes, which depended on adherence of specific cells to a layer of hapten-gelatin at 4 degrees C, recovery of bound cells by melting, and digestion of adherent antigen by collagenase. A population of cells resulted which contained 90% typical B cells and 37% of cells capable of binding a fluorescent, haptenated polymeric protein. Fractionated cells were reacted in vitro with fluorescent conjugates of the specific haptens with polymerized flagellin [NIP-polymerized flagellin (POL)-tetramethylrhodamine isothiocyanate conjugate or DNP- POL-fluorescein isothiocyanate conjugate] under a variety of conditions, with the aim of investigating the behavior of Ig receptors on B lymphocytes after exposure to antigen; Experiments were performed with immunogenic and tolerogenic concentrations of antigen. Furthermore, four experimental designs were used, namely: (a) brief labeling with fluorescent antigen followed by culture without antigen (pulse design); (b) culture in the continuous presence of fluorescent antigen (continuous-labeling design); (c) culture in the continuous presence of nonlabeled antigen followed by labeling of unoccupied receptors by fluorescent antigen (receptor status design); and (d) culture with nonlabeled antigen for 2 h followed by incubation without further antigen for 20 h and labeling with fluorescent antigen (modulation design). Further insight into receptor occupancy and distribution was gained by the use of fluorescent antihapten and antiglobulin reagents. It was found that both immunogenic and tolerogenic antigen concentrations caused rapid patching and capping of the receptors to which they attached, followed by endocytosis and probably some shedding of Ig receptors. However, a proportion of cells continued to bear some cell surface antigen for 24 h. The immunogenic antigen concentration failed to completely remove the receptor coat from the cell surface. At all stages of immunogenesis, plentiful unoccupied receptors could be demonstrated. The tolerogenic concentration nearly saturated available receptors, and in its continuous presence, only few unoccupied or antigen-occupied surface receptors could be detected after 24 h of culture. Experiments of the modulation design showed that brief incubation with the tolerogenic concentration appeared to suppress receptor resynthesis, as few new receptors could be demonstrated after 20 h of further culture without antigen. Experiments were performed to determine whether fractionated cells prepared from spleens of 8-day-old mice showed an unusual tendency for modulation, even with immunogenic antigen concentrations. They were found to behave essentially like adult fractionated cells. The results are discussed in the framework of current theories of B- lymphocyte activation and tolerization.

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Selected References

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  1. Ault K. A., Unanue E. R. Events after the binding of antigen to lymphocytes: removal and regeneration of the antigen receptor. J Exp Med. 1974 May 1;139(5):1110–1124. doi: 10.1084/jem.139.5.1110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ault K. A., Unanue E. R., Katz D. H., Benacerraf B. Failure of lymphocytes to reexpress antigen receptors after brief interaction with a tolerogenic D-amino acid copolymer. Proc Natl Acad Sci U S A. 1974 Aug;71(8):3111–3114. doi: 10.1073/pnas.71.8.3111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bergquist N. R., Nilsson P. The conjugation of immunoglobulins with tetramethylrhodamine isothiocyanate by utilization of dimethylsulfoxide (DMSO) as a solvent. J Immunol Methods. 1974 Jul;5(2):189–198. doi: 10.1016/0022-1759(74)90009-x. [DOI] [PubMed] [Google Scholar]
  4. Brownstone A., Mitchison N. A., Pitt-Rivers R. Chemical and serological studies with an iodine-containing synthetic immunological determinant 4-hydroxy-3-iodo-5-nitrophenylacetic acid (NIP) and related compounds. Immunology. 1966 May;10(5):465–479. [PMC free article] [PubMed] [Google Scholar]
  5. Catt K. J., Dufau M. L. Interactions of LH and hCG with testicular gonadotropin receptors. Adv Exp Med Biol. 1973;36(0):379–418. doi: 10.1007/978-1-4684-3237-4_18. [DOI] [PubMed] [Google Scholar]
  6. DeLuca D., Miller A., Sercarz E. Antigen binding to lymphoid cells from unimmunized mice. IV. Shedding and reappearance of multiple antigen binding Ig receptors of T- and B-lymphocytes. Cell Immunol. 1975 Aug;18(2):286–303. doi: 10.1016/0008-8749(75)90058-1. [DOI] [PubMed] [Google Scholar]
  7. Diener E., Armstrong W. D. Immunological tolerance in vitro: kinetic studies at the cellular level. J Exp Med. 1969 Mar 1;129(3):591–603. doi: 10.1084/jem.129.3.591. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Diener E., Paetkau V. H. Antigen recognition: early surface-receptor phenomena induced by binding of a tritium-labeled antigen. Proc Natl Acad Sci U S A. 1972 Sep;69(9):2364–2368. doi: 10.1073/pnas.69.9.2364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Feldmann M. Induction of immunity and tolerance in vitro by hapten protein conjugates. I. The relationship between the degree of hapten conjugation and the immunogenicity of dinitrophenylated polymerized flagellin. J Exp Med. 1972 Apr 1;135(4):735–753. doi: 10.1084/jem.135.4.735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Haas W., Layton J. E. Separation of antigen-specific lymphocytes. I. Enrichment of antigen-binding cells. J Exp Med. 1975 May 1;141(5):1004–1014. doi: 10.1084/jem.141.5.1004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Haas W. Separation of antigen-specific lymphocytes. II. Enrichment of hapten-specific antibody-forming cell precursors. J Exp Med. 1975 May 1;141(5):1015–1029. doi: 10.1084/jem.141.5.1015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Joniau M., Grossberg A. L., Pressman D. Importance of the phenolate form of the 3-nitro-4-hydroxy-5-iodophenylacetyl (NIP) group for binding to anti-NIP antibody. Immunochemistry. 1971 Jun;8(6):457–470. doi: 10.1016/0019-2791(71)90397-1. [DOI] [PubMed] [Google Scholar]
  13. 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]
  14. Nossal G. J., Pike B. L. Evidence for the clonal abortion theory of B-lymphocyte tolerance. J Exp Med. 1975 Apr 1;141(4):904–917. [PMC free article] [PubMed] [Google Scholar]
  15. Raff M. C., Feldmann M., De Petris S. Monospecificity of bone marrow-derived lymphocytes. J Exp Med. 1973 Apr 1;137(4):1024–1030. doi: 10.1084/jem.137.4.1024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Raff M. C., Owen J. J., Cooper M. D., Lawton A. R., 3rd, Megson M., Gathings W. E. Differences in susceptibility of mature and immature mouse B lymphocytes to anti-immunoglobulin-induced immunoglobulin suppression in vitro. Possible implications for B-cell tolerance to self. J Exp Med. 1975 Nov 1;142(5):1052–1064. doi: 10.1084/jem.142.5.1052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Raff M. C., Sternberg M., Taylor R. B. Immunoglobulin determinants on the surface of mouse lymphoid cells. Nature. 1970 Feb 7;225(5232):553–554. doi: 10.1038/225553a0. [DOI] [PubMed] [Google Scholar]
  18. Sidman C. L., Unanue E. R. Receptor-mediated inactivation of early B lymphocytes. Nature. 1975 Sep 11;257(5522):149–151. doi: 10.1038/257149a0. [DOI] [PubMed] [Google Scholar]
  19. 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]
  20. Yahara I., Edelman G. M. Restriction of the mobility of lymphocyte immunoglobulin receptors by concanavalin A. Proc Natl Acad Sci U S A. 1972 Mar;69(3):608–612. doi: 10.1073/pnas.69.3.608. [DOI] [PMC free article] [PubMed] [Google Scholar]

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