Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1991 Oct 15;88(20):9302–9306. doi: 10.1073/pnas.88.20.9302

Interleukin 1 expression is inducible by nerve growth factor in PC12 pheochromocytoma cells.

K Alheim 1, C Andersson 1, S Tingsborg 1, M Ziolkowska 1, M Schultzberg 1, T Bartfai 1
PMCID: PMC52702  PMID: 1924394

Abstract

Expression of the cytokine interleukin 1 alpha (IL-1 alpha) was demonstrated in the rat PC12 pheochromocytoma cell line by (i) immunohistochemistry using rabbit polyclonal antisera raised against the recombinant murine IL-1 alpha, (ii) an ELISA, and (iii) a specific cell conversion bioassay based on the use of LBRM33-1A5 cells. IL-1 alpha mRNA was demonstrated in the PC12 cells, by PCR amplification. Constitutive expression of IL-1 alpha in PC12 cells was demonstrated in all experiments, although the cellular levels of IL-1 alpha-like immunoreactivity varied. The expression of IL-1 alpha, as studied at the mRNA level, was inducible by mouse nerve growth factor (7S NGF), and the gene product level was inducible in a dose- and time-dependent fashion by 7S NGF. The maximum induction corresponds to a 600% increase in IL-1 alpha-like immunoreactivity above the expression level found in noninduced cells and occurred after a 3-day incubation of the cells with NGF at 0.75 micrograms/ml of culture medium. The significance of the ability of NGF to induce IL-1 expression lies in the fact that IL-1 itself also acts as a growth factor that promotes glial proliferation and, even more importantly, IL-1 itself induces the expression of NGF at peripheral nerve injury [Lindholm, D., Heumann, R., Meyer, M. & Thoenen, H. (1987) Nature (London) 330, 658-659].

Full text

PDF
9302

Images in this article

Selected References

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

  1. Alonso S., Minty A., Bourlet Y., Buckingham M. Comparison of three actin-coding sequences in the mouse; evolutionary relationships between the actin genes of warm-blooded vertebrates. J Mol Evol. 1986;23(1):11–22. doi: 10.1007/BF02100994. [DOI] [PubMed] [Google Scholar]
  2. Anderson D. J., Axel R. Molecular probes for the development and plasticity of neural crest derivatives. Cell. 1985 Sep;42(2):649–662. doi: 10.1016/0092-8674(85)90122-9. [DOI] [PubMed] [Google Scholar]
  3. Bandtlow C. E., Meyer M., Lindholm D., Spranger M., Heumann R., Thoenen H. Regional and cellular codistribution of interleukin 1 beta and nerve growth factor mRNA in the adult rat brain: possible relationship to the regulation of nerve growth factor synthesis. J Cell Biol. 1990 Oct;111(4):1701–1711. doi: 10.1083/jcb.111.4.1701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blenis J., Erikson R. L. Regulation of protein kinase activities in PC12 pheochromocytoma cells. EMBO J. 1986 Dec 20;5(13):3441–3447. doi: 10.1002/j.1460-2075.1986.tb04667.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Breder C. D., Dinarello C. A., Saper C. B. Interleukin-1 immunoreactive innervation of the human hypothalamus. Science. 1988 Apr 15;240(4850):321–324. doi: 10.1126/science.3258444. [DOI] [PubMed] [Google Scholar]
  6. Cremins J., Wagner J. A., Halegoua S. Nerve growth factor action is mediated by cyclic AMP- and Ca+2/phospholipid-dependent protein kinases. J Cell Biol. 1986 Sep;103(3):887–893. doi: 10.1083/jcb.103.3.887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dinarello C. A. Interleukin-1 and its biologically related cytokines. Adv Immunol. 1989;44:153–205. doi: 10.1016/s0065-2776(08)60642-2. [DOI] [PubMed] [Google Scholar]
  8. 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]
  9. Giulian D., Vaca K., Johnson B. Secreted peptides as regulators of neuron-glia and glia-glia interactions in the developing nervous system. J Neurosci Res. 1988 Oct-Dec;21(2-4):487–500. doi: 10.1002/jnr.490210240. [DOI] [PubMed] [Google Scholar]
  10. Giulian D., Young D. G., Woodward J., Brown D. C., Lachman L. B. Interleukin-1 is an astroglial growth factor in the developing brain. J Neurosci. 1988 Feb;8(2):709–714. doi: 10.1523/JNEUROSCI.08-02-00709.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Greene L. A., Shooter E. M. The nerve growth factor: biochemistry, synthesis, and mechanism of action. Annu Rev Neurosci. 1980;3:353–402. doi: 10.1146/annurev.ne.03.030180.002033. [DOI] [PubMed] [Google Scholar]
  12. Greene L. A., Tischler A. S. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2424–2428. doi: 10.1073/pnas.73.7.2424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Lechan R. M., Toni R., Clark B. D., Cannon J. G., Shaw A. R., Dinarello C. A., Reichlin S. Immunoreactive interleukin-1 beta localization in the rat forebrain. Brain Res. 1990 Apr 23;514(1):135–140. doi: 10.1016/0006-8993(90)90445-h. [DOI] [PubMed] [Google Scholar]
  14. Lindholm D., Heumann R., Meyer M., Thoenen H. Interleukin-1 regulates synthesis of nerve growth factor in non-neuronal cells of rat sciatic nerve. Nature. 1987 Dec 17;330(6149):658–659. doi: 10.1038/330658a0. [DOI] [PubMed] [Google Scholar]
  15. Livett B. G. Adrenal medullary chromaffin cells in vitro. Physiol Rev. 1984 Oct;64(4):1103–1161. doi: 10.1152/physrev.1984.64.4.1103. [DOI] [PubMed] [Google Scholar]
  16. Mandel G., Cooperman S. S., Maue R. A., Goodman R. H., Brehm P. Selective induction of brain type II Na+ channels by nerve growth factor. Proc Natl Acad Sci U S A. 1988 Feb;85(3):924–928. doi: 10.1073/pnas.85.3.924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Minami M., Kuraishi Y., Yamaguchi T., Nakai S., Hirai Y., Satoh M. Convulsants induce interleukin-1 beta messenger RNA in rat brain. Biochem Biophys Res Commun. 1990 Sep 14;171(2):832–837. doi: 10.1016/0006-291x(90)91221-d. [DOI] [PubMed] [Google Scholar]
  18. Nishida T., Nishino N., Takano M., Sekiguchi Y., Kawai K., Mizuno K., Nakai S., Masui Y., Hirai Y. Molecular cloning and expression of rat interleukin-1 alpha cDNA. J Biochem. 1989 Mar;105(3):351–357. doi: 10.1093/oxfordjournals.jbchem.a122667. [DOI] [PubMed] [Google Scholar]
  19. Saiki R. K., Gelfand D. H., Stoffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988 Jan 29;239(4839):487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
  20. Schultzberg M., Andersson C., Undén A., Troye-Blomberg M., Svenson S. B., Bartfai T. Interleukin-1 in adrenal chromaffin cells. Neuroscience. 1989;30(3):805–810. doi: 10.1016/0306-4522(89)90171-1. [DOI] [PubMed] [Google Scholar]
  21. Schultzberg M., Svenson S. B., Unden A., Bartfai T. Interleukin-1-like immunoreactivity in peripheral tissues. J Neurosci Res. 1987;18(1):184–189. doi: 10.1002/jnr.490180126. [DOI] [PubMed] [Google Scholar]
  22. Shoham S., Davenne D., Cady A. B., Dinarello C. A., Krueger J. M. Recombinant tumor necrosis factor and interleukin 1 enhance slow-wave sleep. Am J Physiol. 1987 Jul;253(1 Pt 2):R142–R149. doi: 10.1152/ajpregu.1987.253.1.R142. [DOI] [PubMed] [Google Scholar]
  23. Zlotnik A., Daine B. Activation of IL 1-dependent and IL 1-independent T cell lines by calcium ionophore and phorbol ester. J Immunol. 1986 Feb 1;136(3):1033–1037. [PubMed] [Google Scholar]
  24. di Giovine F. S., Duff G. W. Interleukin 1: the first interleukin. Immunol Today. 1990 Jan;11(1):13–20. doi: 10.1016/0167-5699(90)90005-t. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES