Skip to main content
Immunology logoLink to Immunology
. 1985 May;55(1):165–172.

Thymus-derived macrophages in long-term culture: release of IL-1, stimulation of MLR and expression of tumoricidal activity.

R Gallily, M Zeira, I Stain
PMCID: PMC1453578  PMID: 3158594

Abstract

The present report examines the behaviour of a slowly proliferating pure population of thymus-derived macrophages in long-term culture, regarding their ability to secrete interleukin-1 (IL-1) and prostaglandin E2 (PGE2), to stimulate a mixed leucocyte reaction (MLR) and to lyse tumour cells in vitro. Following stimulation with LPS, high levels of IL-1 were released to the medium. IL-1 release was significantly augmented by the addition of indomethacin during stimulation. Thymus-derived macrophages constitutively secreted significant levels of PGE2. These cells served as excellent stimulators in a one-way MLR, substantiating the claim that pure populations of macrophages effectively stimulate an allogeneic response in vitro. Thymus-derived macrophages showed tumoricidal activity following activation with either high concentrations of LPS or suboptimal concentrations of LPS and T-cell lymphokine. These findings portray a close interrelationship and reciprocal regulation between thymus-derived macrophages and T lymphocytes.

Full text

PDF
165

Selected References

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

  1. Bach F. H., Bach M. L., Sondel P. M. Differential function of major histocompatibility complex antigens in T-lymphocyte activation. Nature. 1976 Jan 29;259(5541):273–281. doi: 10.1038/259273a0. [DOI] [PubMed] [Google Scholar]
  2. 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]
  3. Beller D. I., Unanue E. R. Regulation of macrophage populations. II. Synthesis and expression of Ia antigens by peritoneal exudate macrophages is a transient event. J Immunol. 1981 Jan;126(1):263–269. [PubMed] [Google Scholar]
  4. Beller D. I., Unanue E. R. Thymic macrophages modulate one stage of T cell differentiation in vitro. J Immunol. 1978 Nov;121(5):1861–1864. [PubMed] [Google Scholar]
  5. Calamai E. G., Beller D. I., Unanue E. R. Regulation of macrophage populations. IV. Modulation of Ia expression in bone marrow-derived macrophages. J Immunol. 1982 Apr;128(4):1692–1694. [PubMed] [Google Scholar]
  6. Farrar W. L., Mizel S. B., Farrar J. J. Participation of lymphocyte activating factor (Interleukin 1) in the induction of cytotoxic T cell responses. J Immunol. 1980 Mar;124(3):1371–1377. [PubMed] [Google Scholar]
  7. Fink P. J., Bevan M. J. H-2 antigens of the thymus determine lymphocyte specificity. J Exp Med. 1978 Sep 1;148(3):766–775. doi: 10.1084/jem.148.3.766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gallily R., Savion N. Cultivation, proliferation and characterization of thymic macrophages. Immunology. 1983 Sep;50(1):139–148. [PMC free article] [PubMed] [Google Scholar]
  9. Gery I., Davies P., Derr J., Krett N., Barranger J. A. Relationship between production and release of lymphocyte-activating factor (interleukin 1) by murine macrophages. 1. Effects of various agents. Cell Immunol. 1981 Nov 1;64(2):293–303. doi: 10.1016/0008-8749(81)90481-0. [DOI] [PubMed] [Google Scholar]
  10. Gery I., Gershon R. K., Waksman B. H. Potentiation of the T-lymphocyte response to mitogens. I. The responding cell. J Exp Med. 1972 Jul 1;136(1):128–142. doi: 10.1084/jem.136.1.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Gospodarowicz D., Delgado D., Vlodavsky I. Permissive effect of the extracellular matrix on cell proliferation in vitro. Proc Natl Acad Sci U S A. 1980 Jul;77(7):4094–4098. doi: 10.1073/pnas.77.7.4094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Gospodarowicz D., Ill C. Extracellular matrix and control of proliferation of vascular endothelial cells. J Clin Invest. 1980 Jun;65(6):1351–1364. doi: 10.1172/JCI109799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gospodarowicz D., Mescher A. L., Birdwell C. R. Stimulation of corneal endothelial cell proliferations in vitro by fibroblast and epidermal growth factors. Exp Eye Res. 1977 Jul;25(1):75–89. doi: 10.1016/0014-4835(77)90248-2. [DOI] [PubMed] [Google Scholar]
  14. Loewenstein J., Rottem S., Gallily R. Induction of macrophage-mediated cytolysis of neoplastic cells by mycoplasmas. Cell Immunol. 1983 Apr 15;77(2):290–297. doi: 10.1016/0008-8749(83)90029-1. [DOI] [PubMed] [Google Scholar]
  15. Minami M., Shreffler D. C., Cowing C. Characterization of the stimulator cells in the murine primary mixed leukocyte response. J Immunol. 1980 Mar;124(3):1314–1321. [PubMed] [Google Scholar]
  16. Mizel S. B. Interleukin 1 and T cell activation. Immunol Rev. 1982;63:51–72. doi: 10.1111/j.1600-065x.1982.tb00411.x. [DOI] [PubMed] [Google Scholar]
  17. Mosier D. E., Pierce C. W. Functional maturation of thymic lymphocyte populations in vitro. J Exp Med. 1972 Dec 1;136(6):1484–1500. doi: 10.1084/jem.136.6.1484. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Owen J. J., Jordan R. K., Robinson J. H., Singh U., Willcox H. N. In vitro studies on the generation of lymphocyte diversity. Cold Spring Harb Symp Quant Biol. 1977;41(Pt 1):129–137. doi: 10.1101/sqb.1977.041.01.017. [DOI] [PubMed] [Google Scholar]
  19. Papiernik M., Homo-Delarche F. Thymic reticulum in mice. III. Phagocytic cells of the thymic reticulum in culture secrete both prostaglandin E2 and interleukin 1 which regulate thymocyte proliferation. Eur J Immunol. 1983 Aug;13(8):689–692. doi: 10.1002/eji.1830130815. [DOI] [PubMed] [Google Scholar]
  20. Rock K. L., Benacerraf B. The role of Ia molecules in the activation of T lymphocytes. IV. The basis of the thymocyte IL 1 response and its possible role in the generation of the T cell repertoire. J Immunol. 1984 Apr;132(4):1654–1662. [PubMed] [Google Scholar]
  21. Shohami E., Rosenthal J., Lavy S. The effect of incomplete cerebral ischemia on prostaglandin levels in rat brain. Stroke. 1982 Jul-Aug;13(4):494–499. doi: 10.1161/01.str.13.4.494. [DOI] [PubMed] [Google Scholar]
  22. Steinman R. M., Witmer M. D. Lymphoid dendritic cells are potent stimulators of the primary mixed leukocyte reaction in mice. Proc Natl Acad Sci U S A. 1978 Oct;75(10):5132–5136. doi: 10.1073/pnas.75.10.5132. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Van Voorhis W. C., Witmer M. D., Steinman R. M. The phenotype of dendritic cells and macrophages. Fed Proc. 1983 Nov;42(14):3114–3118. [PubMed] [Google Scholar]
  24. Wiener F., Klein G., Harris H. The analysis of malignancy by cell fusion. IV. Hybrid between tumour cells and a malignant L cell derivative. J Cell Sci. 1973 Jan;12(1):253–261. doi: 10.1242/jcs.12.1.253. [DOI] [PubMed] [Google Scholar]
  25. Zinkernagel R. M. Thymus and lymphohemopoietic cells: their role in T cell maturation in selection of T cells' H-2-restriction-specificity and in H-2 linked Ir gene control. Immunol Rev. 1978;42:224–270. doi: 10.1111/j.1600-065x.1978.tb00264.x. [DOI] [PubMed] [Google Scholar]

Articles from Immunology are provided here courtesy of British Society for Immunology

RESOURCES