Skip to main content
Log in

Germinal centers and the B-cell system

VII. Complement receptors, antigen receptors, immunoglobulin and alkaline phosphatase in germinal centers of the rabbit appendix and popliteal lymph nodes

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Summary

Germinal centers of the rabbit appendix were studied for the presence of complement receptors, immunoglobulin and alkaline phosphatase. In popliteal lymph nodes, de novo-developing germinal centers were studied with respect to these markers up to 21 days after sheep red blood cell (SRBC)-stimulation. In addition, the possible presence of antigen (SRBC) receptor-bearing cells in these germinal centers was investigated.

The results may be summarized as follows: 1) Germinal centers in the appendix as well as those in popliteal lymph nodes were rich in complement receptor-bearing cells. Complement-receptor density did not significantly change during a germinal-center reaction. 2) Immunoglobulins were present only at very low densities on the surface of lymphoid cells in the densely populated area of germinal centers. In germinal centers of popliteal lymph nodes lymphoid cells in the thinly populated area again showed higher densities. Immunoglobulins possibly complexed with antigen on the surface of follicular dendritic cells were not observed in the initial phase of a germinal center reaction. In contrast, in germinal centers of the appendix, immunoglobulin was present in excessive amounts throughout the thinly populated area, possibly complexed with antigen, which is also abundantly present. 3) Reticular staining patterns of alkaline phosphatase were present in the densely populated area, but absent in the thinly populated area of germinal centers in both appendix and popliteal lymph nodes. Primary follicles and young germinal centers were alkaline phosphatase-negative. 4) Antigen receptor-bearing cells were detected in germinal centers of popliteal lymph nodes as early as 5 days after SRBC-stimulation, reaching a maximum at day 10.

In conclusion, with the present experimental approach, microenvironmental differences were shown between the densely populated area and the thinly populated area of germinal centers. However, no indication was obtained for a postulated maturation event of the lymphocytes within germinal centers, or for functional differences that may exist between germinal centers in the appendix and popliteal lymph nodes.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Allison RT, Slade M, Walker DM (1976) A method for distinguishing sheep erythrocytes adherent to human tissue sections. J Clin Pathol 29:79–80

    Google Scholar 

  • Bos WH (1967) In: Recirculatie en transformatie van lymphocytes. PhD thesis. Van Denderen, Groningen, p 45

    Google Scholar 

  • Brandon DL, Edwards AJ, Parkhouse RME (1979) The response to lipopolysaccharide of mouse spleen lymphocytes fractionated on the basis of surface immunoglobulin and complement receptor using fluorescence-activated cell sorting and rosetting techniques. Immunology 36:865–873

    Google Scholar 

  • Calkins CE, Carboni JM, Waksman BH (1975) B-cells in the appendix and other lymphoid organs of the rabbit: complement receptor lymphocytes. J Immunol 115:1339–1345

    Google Scholar 

  • Culvenor JG, Harris AW, Mandel TE, Whitelaw A, Ferber E (1981) Alkaline phosphatase in hemopoietic tumor cell lines of the mouse: high activity in cells of the B lymphoid lineages. J Immunol 126:1974–1977

    Google Scholar 

  • Gastkemper NA, Wubbena AS, Prop N, Nieuwenhuis P (1980) Possible antigen specificity of germinal centre precursor cells in rat TDL. Fourth International Congress of Immunology (Paris) (abstract)

  • Gomori G (1952) Microscopic histochemistry, principles and practice. University Press, Chigaco

    Google Scholar 

  • Hanaoka M, Williams RM, Waksman BH (1971) Appendix and γm antibody formation. III. Uptake and distribution of soluble or alum-precipitated bovine-globulin injected into the rabbit appendix. Lab Invest 24:31–37

    Google Scholar 

  • Klaus GGB, Humphrey JH, Kunkl A, Dongworth DW (1980) The follicular dendritic cell: its role in antigen presentation in the generation of immunological memory. Immunol Rev 53:3–28

    Google Scholar 

  • Lennert K (1978) Malignant lymphomas. Springer-Verlag, Berlin, pp 58–59

    Google Scholar 

  • Nieuwenhuis P (1971) On the origin and fate of immunologically competent cells. Wolters-Noordhoff Publishing, Groningen

    Google Scholar 

  • Nieuwenhuis P, Keuning FJ (1974b) Germinal centres and the origin of the B-cell system II. Germinal centres in the rabbit spleen and popliteal lymph nodes. Immunology 26:509–519

    Google Scholar 

  • Nieuwenhuis P, Nouhuys CE van, Eggens JH, Keuning FJ (1974a) Germinal centres and the origin of the B-cell system. I. Germinal centres in the rabbit appendix. Immunology 26:497–507

    Google Scholar 

  • Opstelten D, Deenen GJ, Stikker R, Bos L, Nieuwenhuis P (1981) Germinal centers and the B-cell system VIII. Functional characteristics and cell surface markers of germinal center cell subsets differing in density and in sedimentation velocity (submitted)

  • Osmond DG (1979) Generation of B lymphocytes in the bone marrow. In: Cooper MD, Mosier DE,Sher I, Vitetta ES (eds) B lymphocytes in the immune response. Elsevier/North Holland, 63–70

  • Poppema S, Elema JD, Halie MR (1979) Alkaline phosphatase positive lymphomas and lymphocytes. In: Müller-Ruchholtz W, Müller-Hermelink HK (eds) Adv Exp Med Biol Vol 114. Plenum Press, New York, pp 573–577

    Google Scholar 

  • Sainte-Marie G, Peng FS (1980) Thymic cell migration in the subnodular spaces of draining lymph nodes of rats. Cell Immunol 52:211–217

    Google Scholar 

  • Sitia R, Abbott J, Hämmerling U (1979) The ontogeny of B-lymphocytes V. Lipopolysaccharide-induced changes of IgD expression on murine B-lymphocytes. Eur J Immunol 9:859–863

    Google Scholar 

  • Stein H, Tolksdorf G (1980) Development and differentiation of the T-cell and B-cell systems: a perspective. In: Van den Tweel JG (ed) Malignant lymphoproliferative diseases. Leiden University Press, The Hague, 13–29

    Google Scholar 

  • Steven WM (1980) Effects of antigen dosage on early localization of specific antibodies in rat splenic germinal centers. Anat Rec 198:503–511

    Google Scholar 

  • Tew JG, Philips RP, Mandel TE (1980) The maintenance and regulation of the humoral immune response: persisting antigen and the role of follicular antigen-binding dendritic cells as accessory cells. Immunol Rev 53:175–201

    Google Scholar 

  • Tsunoda R, Yaginuma Y, Kojima M (1980) Immunocytochemical studies on the constituent cells of the secondary nodules in human tonsils. Acta Pathol Jpn 30:33–58

    Google Scholar 

  • Waksman BH, Ozer H, Blythman HE (1973) Appendix and γm-antibody formation VI. The functional anatomy of the rabbit appendix. Eab Invest 28:614–626

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Opstelten, D., Stikker, R., Deenen, G.J. et al. Germinal centers and the B-cell system. Cell Tissue Res. 224, 505–516 (1982). https://doi.org/10.1007/BF00213748

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00213748

Key words

Navigation