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Evidence for control of complement receptor rosette-forming cells by α- and β-adrenergic agents

Abstract

PHARMACOLOGICAL agents such as dibutyryl cyclic AMP1,2, cholera toxin3,4 and β-adrenergic stimulants5 have an effect on antibody production which can be inhibitory or enhancing, depending on the dose used and the time of addition of the agent. Such stimulants are known to inhibit the human T-lymphocyte receptor for sheep erythrocytes6,7 and the murine lymphoma Fc receptor8, and it has been shown that the complement receptor on B lymphocytes has an important role in the cellular events leading to antibody production9,10, thus emphasising the need to clarify its nature. We report here that the number of complement receptor rosette-forming cells (EAC–RFC) in suspensions of mouse spleen cells can be decreased by α-adrenergic stimulants and increased by β-adrenergic stimulants, respectively.

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References

  1. Watson, J., Epstein, R. & Cohn, M. Nature 246, 405–409 (1973).

    Article  ADS  CAS  Google Scholar 

  2. Teh, H. S. & Paetkau, V. Nature 250, 505–507 (1974).

    Article  ADS  CAS  Google Scholar 

  3. Cook, R. G., Stavitsky, A. B. & Schoenberg, M. D. J. Immun. 114, 426–434 (1975).

    CAS  PubMed  Google Scholar 

  4. Kateley, J. R., Kasarov, L. & Friedman, H. J. Immun. 114, 81–86 (1975).

    CAS  PubMed  Google Scholar 

  5. Braun, W. Ann. N.Y. Sci. 207, 17–28 (1973).

    Article  ADS  CAS  Google Scholar 

  6. Chisari, F. V. & Edgington, T. S. J. exp. Med. 140, 1122–1126 (1974).

    Article  CAS  Google Scholar 

  7. Galant, S. P. & Remo, R. A. J. Immun. 114, 512–513 (1975).

    CAS  PubMed  Google Scholar 

  8. Zuckerman, S. H. & Douglas, S. D. Nature 255, 410–412 (1975).

    Article  ADS  CAS  Google Scholar 

  9. Dukor, P., Dietrich, F. M., Gisler, R. H., Schuman, G. & Bitter-Suermann, D. Prog. Immun. II 3, 99–109 (1974).

    CAS  Google Scholar 

  10. Arnaiz-Villena, A., Playfair, J. H. L. & Roitt, I. M. Clin. exp. Immun. 20, 375–378 (1975).

    CAS  PubMed  Google Scholar 

  11. Bianco, C., Patrick, R. & Nussenzweig, V. J. exp. Med. 132, 702–720 (1970).

    Article  CAS  Google Scholar 

  12. Butcher, R. W. & Sutherland, E. W. Ann. N.Y. Acad. Sci. 139, 849–859 (1967).

    Article  ADS  CAS  Google Scholar 

  13. Butcher, R. W. & Sutherland, E. W. J. biol. Chem. 237, 1244–1250 (1962).

    CAS  PubMed  Google Scholar 

  14. Roberts, G., Richardson, A. W. & Green, H. D. J. Pharmac. exp. Therap. 105, 466–476 (1952).

    CAS  Google Scholar 

  15. Black, J. W., Crowther, A. F., Shanks, R. G., Smith, L. H. & Dornhorst, A. C. Lancet 1, 1080–1081 (1964).

    Article  CAS  Google Scholar 

  16. Robinson, G. A., Butcher, R. W. & Sutherland, E. W. Ann. N.Y. Acad. Sci. 139, 703–723 (1967).

    Article  ADS  Google Scholar 

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ITO, M., SLESS, F. & PARROTT, D. Evidence for control of complement receptor rosette-forming cells by α- and β-adrenergic agents. Nature 266, 633–635 (1977). https://doi.org/10.1038/266633a0

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