Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1986 Aug 1;164(2):594–604. doi: 10.1084/jem.164.2.594

Interleukin 1 of the central nervous system is produced by ameboid microglia

PMCID: PMC2188228  PMID: 3487617

Abstract

By screening specific populations of rat brain cells, we found that ameboid microglia secrete an 18 kD peptide with IL-1 biological activity. The IL-1 activity released by microglia was found to be identical to rat macrophage IL-1 on fractionation by gel filtration and high pressure liquid anion-exchange chromatography, and it was neutralized by an antiserum specific for murine IL-1. When added to astroglia grown in culture, microglial IL-1 increased the cell number of five- to sevenfold, and increased astroglial incorporation of [3H]thymidine by three- to fivefold. We propose that the proliferation of astroglia in specific brain regions may be regulated by the signaled release of IL-1 from activated microglial cells.

Full Text

The Full Text of this article is available as a PDF (730.9 KB).

Selected References

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

  1. Aguayo A. J., David S., Bray G. M. Influences of the glial environment on the elongation of axons after injury: transplantation studies in adult rodents. J Exp Biol. 1981 Dec;95:231–240. doi: 10.1242/jeb.95.1.231. [DOI] [PubMed] [Google Scholar]
  2. Bottenstein J. E., Sato G. H. Growth of a rat neuroblastoma cell line in serum-free supplemented medium. Proc Natl Acad Sci U S A. 1979 Jan;76(1):514–517. doi: 10.1073/pnas.76.1.514. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dayer J. M., de Rochemonteix B., Burrus B., Demczuk S., Dinarello C. A. Human recombinant interleukin 1 stimulates collagenase and prostaglandin E2 production by human synovial cells. J Clin Invest. 1986 Feb;77(2):645–648. doi: 10.1172/JCI112350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Dinarello C. A. Interleukin-1. Rev Infect Dis. 1984 Jan-Feb;6(1):51–95. doi: 10.1093/clinids/6.1.51. [DOI] [PubMed] [Google Scholar]
  5. Fontana A., Kristensen F., Dubs R., Gemsa D., Weber E. Production of prostaglandin E and an interleukin-1 like factor by cultured astrocytes and C6 glioma cells. J Immunol. 1982 Dec;129(6):2413–2419. [PubMed] [Google Scholar]
  6. Gimenez-Gallego G., Rodkey J., Bennett C., Rios-Candelore M., DiSalvo J., Thomas K. Brain-derived acidic fibroblast growth factor: complete amino acid sequence and homologies. Science. 1985 Dec 20;230(4732):1385–1388. doi: 10.1126/science.4071057. [DOI] [PubMed] [Google Scholar]
  7. Giulian D., Allen R. L., Baker T. J., Tomozawa Y. Brain peptides and glial growth. I. Glia-promoting factors as regulators of gliogenesis in the developing and injured central nervous system. J Cell Biol. 1986 Mar;102(3):803–811. doi: 10.1083/jcb.102.3.803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Giulian D., Baker T. J. Peptides released by ameboid microglia regulate astroglial proliferation. J Cell Biol. 1985 Dec;101(6):2411–2415. doi: 10.1083/jcb.101.6.2411. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Giulian D., Lachman L. B. Interleukin-1 stimulation of astroglial proliferation after brain injury. Science. 1985 Apr 26;228(4698):497–499. doi: 10.1126/science.3872478. [DOI] [PubMed] [Google Scholar]
  10. Giulian D. Peptides from the regenerating central nervous system of goldfish stimulate glia. Proc Natl Acad Sci U S A. 1984 Jun;81(11):3567–3571. doi: 10.1073/pnas.81.11.3567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Giulian D., Tomozawa Y., Hindman H., Allen R. L. Peptides from regenerating central nervous system promote specific populations of macroglia. Proc Natl Acad Sci U S A. 1985 Jun;82(12):4287–4290. doi: 10.1073/pnas.82.12.4287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Kaye J., Gillis S., Mizel S. B., Shevach E. M., Malek T. R., Dinarello C. A., Lachman L. B., Janeway C. A., Jr Growth of a cloned helper T cell line induced by a monoclonal antibody specific for the antigen receptor: interleukin 1 is required for the expression of receptors for interleukin 2. J Immunol. 1984 Sep;133(3):1339–1345. [PubMed] [Google Scholar]
  13. Lachman L. B., Shih L. C., Brown D. C. Interleukin 1 from human leukemic monocytes. Methods Enzymol. 1985;116:467–479. doi: 10.1016/s0076-6879(85)16038-6. [DOI] [PubMed] [Google Scholar]
  14. Lomedico P. T., Gubler U., Hellmann C. P., Dukovich M., Giri J. G., Pan Y. C., Collier K., Semionow R., Chua A. O., Mizel S. B. Cloning and expression of murine interleukin-1 cDNA in Escherichia coli. 1984 Nov 29-Dec 5Nature. 312(5993):458–462. doi: 10.1038/312458a0. [DOI] [PubMed] [Google Scholar]
  15. Manthorpe M., Varon S., Adler R. Neurite-promoting factor in conditioned medium from RN22 Schwannoma cultures: bioassay, fractionation, and properties. J Neurochem. 1981 Sep;37(3):759–767. doi: 10.1111/j.1471-4159.1982.tb12552.x. [DOI] [PubMed] [Google Scholar]
  16. Merrill J. E., Kutsunai S., Mohlstrom C., Hofman F., Groopman J., Golde D. W. Proliferation of astroglia and oligodendroglia in response to human T cell-derived factors. Science. 1984 Jun 29;224(4656):1428–1430. doi: 10.1126/science.6610212. [DOI] [PubMed] [Google Scholar]
  17. Mizel S. B., Dukovich M., Rothstein J. Preparation of goat antibodies against interleukin 1: use of an immunoadsorbent to purify interleukin 1. J Immunol. 1983 Oct;131(4):1834–1837. [PubMed] [Google Scholar]
  18. Neuman D., Yerushalmi A., Schwartz M. Inhibition of non-neuronal cell proliferation in the goldfish visual pathway affects the regenerative capacity of the retina. Brain Res. 1983 Aug 8;272(2):237–245. doi: 10.1016/0006-8993(83)90569-3. [DOI] [PubMed] [Google Scholar]
  19. Paré M., Levine R. L. Long-term degeneration renders central tracts refractory to penetration by regenerating optic fibers. Brain Res. 1982 Jul 15;243(2):360–362. doi: 10.1016/0006-8993(82)90261-x. [DOI] [PubMed] [Google Scholar]
  20. Pitas R. E., Innerarity T. L., Weinstein J. N., Mahley R. W. Acetoacetylated lipoproteins used to distinguish fibroblasts from macrophages in vitro by fluorescence microscopy. Arteriosclerosis. 1981 May-Jun;1(3):177–185. doi: 10.1161/01.atv.1.3.177. [DOI] [PubMed] [Google Scholar]
  21. Postlethwaite A. E., Lachman L. B., Kang A. H. Induction of fibroblast proliferation by interleukin-1 derived from human monocytic leukemia cells. Arthritis Rheum. 1984 Sep;27(9):995–1001. doi: 10.1002/art.1780270905. [DOI] [PubMed] [Google Scholar]
  22. Raff M. C., Fields K. L., Hakomori S. I., Mirsky R., Pruss R. M., Winter J. Cell-type-specific markers for distinguishing and studying neurons and the major classes of glial cells in culture. Brain Res. 1979 Oct 5;174(2):283–308. doi: 10.1016/0006-8993(79)90851-5. [DOI] [PubMed] [Google Scholar]
  23. Schmitt C., Ballet J. J. A microcomputer program for the calculation of interleukin 2 activity. Lymphokine Res. 1983;2(4):145–150. [PubMed] [Google Scholar]
  24. Schwartz M., Mizrachi Y., Eshhar N. Factor(s) from goldfish brain induce neuritic outgrowth from explanted regenerating retinas. Brain Res. 1982 Jan;255(1):29–35. doi: 10.1016/0165-3806(82)90073-6. [DOI] [PubMed] [Google Scholar]
  25. Silver J., Lorenz S. E., Wahlsten D., Coughlin J. Axonal guidance during development of the great cerebral commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways. J Comp Neurol. 1982 Sep 1;210(1):10–29. doi: 10.1002/cne.902100103. [DOI] [PubMed] [Google Scholar]
  26. Smith K. A., Lachman L. B., Oppenheim J. J., Favata M. F. The functional relationship of the interleukins. J Exp Med. 1980 Jun 1;151(6):1551–1556. doi: 10.1084/jem.151.6.1551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Thiele D. L., Kurosaka M., Lipsky P. E. Phenotype of the accessory cell necessary for mitogen-stimulated T and B cell responses in human peripheral blood: delineation by its sensitivity to the lysosomotropic agent, L-leucine methyl ester. J Immunol. 1983 Nov;131(5):2282–2290. [PubMed] [Google Scholar]
  28. Zeller N. K., Behar T. N., Dubois-Dalcq M. E., Lazzarini R. A. The timely expression of myelin basic protein gene in cultured rat brain oligodendrocytes is independent of continuous neuronal influences. J Neurosci. 1985 Nov;5(11):2955–2962. doi: 10.1523/JNEUROSCI.05-11-02955.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES