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. 1982 Dec 1;156(6):1780–1793. doi: 10.1084/jem.156.6.1780

Regulation of murine macrophage Ia antigen expression by a lymphokine with immune interferon activity

PMCID: PMC2186868  PMID: 6816896

Abstract

A culture supernatant of concanavalin A-activated spleen cells (Con A supernatant) induced murine macrophages to express Ia antigens in vitro. Biochemical characterization of the Con A supernatant indicated that the macrophage Ia antigen regulatory activity shares molecular weight, pI, and hydrophobic and affinity characteristics with immune interferon (IFN-gamma). Antiserum to mouse IFN-gamma neutralized both the macrophage Ia antigen regulatory and IFN-gamma bioactivities of the Con A supernatant. Furthermore, both partially purified murine IFN- gamma (10(7) U/mg protein sp act) and IFN-containing culture supernatants of the murine BFS T cell line-induced macrophage Ia antigen expression in vitro. Culture supernatants containing colony- stimulating factor, interleukin 1, interleukin 2, macrophage migration inhibitory factor, and a macrophage-activating activity that were distinct from IFN-gamma did not induce macrophage Ia antigen expression. Taken together, the data indicate that the in vitro expression of Ia antigens on macrophages is regulated by an activity that has the characteristics of interferon.

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Selected References

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

  1. Beller D. I., Unanue E. R. IA antigens and antigen-presenting function of thymic macrophages. J Immunol. 1980 Mar;124(3):1433–1440. [PubMed] [Google Scholar]
  2. Benjamin W. R., Steeg P. S., Farrar J. J. Production of immune interferon by an interleukin 2-independent murine T cell line. Proc Natl Acad Sci U S A. 1982 Sep;79(17):5379–5383. doi: 10.1073/pnas.79.17.5379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Birmingham J. R., Chesnut R. W., Kappler J. W., Marrack P., Kubo R., Grey H. M. Antigen presentation to T cell hybridomas by a macrophage cell line: an inducible function. J Immunol. 1982 Mar;128(3):1491–1492. [PubMed] [Google Scholar]
  4. Cowing C., Pincus S. H., Sachs D. H., Dickler H. B. A subpopulation of adherent accessory cells bearing both I-A and I-E or C subregion antigens is required for antigen-specific murine T lymphocyte proliferation. J Immunol. 1978 Nov;121(5):1680–1686. [PubMed] [Google Scholar]
  5. Cowing C., Schwartz B. D., Dickler H. B. Macrophage Ia antigens. I. macrophage populations differ in their expression of Ia antigens. J Immunol. 1978 Feb;120(2):378–384. [PubMed] [Google Scholar]
  6. De Maeyer-Guignard J., Thang M. N., De Maeyer E. Binding of mouse interferon to polynucleotides. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3787–3790. doi: 10.1073/pnas.74.9.3787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Farrar W. L., Johnson H. M., Farrar J. J. Regulation of the production of immune interferon and cytotoxic T lymphocytes by interleukin 2. J Immunol. 1981 Mar;126(3):1120–1125. [PubMed] [Google Scholar]
  8. Hilfiker M. L., Moore R. N., Farrar J. J. Biologic properties of chromatographically separated murine thymoma-derived Interleukin 2 and colony-stimulating factor. J Immunol. 1981 Nov;127(5):1983–1987. [PubMed] [Google Scholar]
  9. Hodes R. J., Ahmann G. B., Hathcock K. S., Dickler H. B., Singer A. Cellular and genetic control of antibody responses in vitro. IV. Expression of Ia antigens on accessory cells required for responses to soluble antigens including a response under Ir gene control. J Immunol. 1978 Oct;121(4):1501–1509. [PubMed] [Google Scholar]
  10. Koren H. S., Handwerger B. S., Wunderlich J. R. Identification of macrophage-like characteristics in a cultured murine tumor line. J Immunol. 1975 Feb;114(2 Pt 2):894–897. [PubMed] [Google Scholar]
  11. Luger T. A., Stadler B. M., Katz S. I., Oppenheim J. J. Epidermal cell (keratinocyte)-derived thymocyte-activating factor (ETAF). J Immunol. 1981 Oct;127(4):1493–1498. [PubMed] [Google Scholar]
  12. Mogensen K. E., Pyhälä L., Törmä E., Cantell K. No evidence for a carbohydrate moiety affecting the clearance of circulating human leukocyte interferon in rabbits. Acta Pathol Microbiol Scand B Microbiol Immunol. 1974 Jun;82(3):305–310. doi: 10.1111/j.1699-0463.1974.tb02331.x. [DOI] [PubMed] [Google Scholar]
  13. Nussenzweig M. C., Steinman R. M., Unkeless J. C., Witmer M. D., Gutchinov B., Cohn Z. A. Studies of the cell surface of mouse dendritic cells and other leukocytes. J Exp Med. 1981 Jul 1;154(1):168–187. doi: 10.1084/jem.154.1.168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Pike B. L., Robinson W. A. Human bone marrow colony growth in agar-gel. J Cell Physiol. 1970 Aug;76(1):77–84. doi: 10.1002/jcp.1040760111. [DOI] [PubMed] [Google Scholar]
  15. Preble O. T., Black R. J., Friedman R. M., Klippel J. H., Vilcek J. Systemic lupus erythematosus: presence in human serum of an unusual acid-labile leukocyte interferon. Science. 1982 Apr 23;216(4544):429–431. doi: 10.1126/science.6176024. [DOI] [PubMed] [Google Scholar]
  16. Richman L. K., Klingenstein R. J., Richman J. A., Strober W., Berzofsky J. A. The murine Kupffer cell. I. Characterization of the cell serving accessory function in antigen-specific T cell proliferation. J Immunol. 1979 Dec;123(6):2602–2609. [PubMed] [Google Scholar]
  17. Scher M. G., Beller D. I., Unanue E. R. Demonstration of a soluble mediator that induces exudates rich in Ia-positive macrophages. J Exp Med. 1980 Dec 1;152(6):1684–1698. doi: 10.1084/jem.152.6.1684. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Steeg P. S., Moore R. N., Oppenheim J. J. Regulation of murine macrophage Ia-antigen expression by products of activated spleen cells. J Exp Med. 1980 Dec 1;152(6):1734–1744. doi: 10.1084/jem.152.6.1734. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Steinman R. M., Nogueira N., Witmer M. D., Tydings J. D., Mellman I. S. Lymphokine enhances the expression and synthesis of Ia antigens on cultured mouse peritoneal macrophages. J Exp Med. 1980 Nov 1;152(5):1248–1261. doi: 10.1084/jem.152.5.1248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. WAGNER R. R. Biological studies of interferon. I. Suppression of cellular infection with eastern equine encephalomyelitis virus. Virology. 1961 Mar;13:323–337. doi: 10.1016/0042-6822(61)90152-0. [DOI] [PubMed] [Google Scholar]
  21. Walker E. B., Lanier L. L., Warner N. L. Concomitant induction of the cell surface expression of Ia determinants and accessory cell function by a murine macrophage tumor cell line. J Exp Med. 1982 Feb 1;155(2):629–634. doi: 10.1084/jem.155.2.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Wiranowska-Stewart M., Lin L. S., Braude I. A., Stewart W. E., 2nd Production, partial purification and characterization of human and murine interferons--type II. Mol Immunol. 1980 May;17(5):625–633. doi: 10.1016/0161-5890(80)90160-1. [DOI] [PubMed] [Google Scholar]

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