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
. 1984 Oct;81(20):6418–6421. doi: 10.1073/pnas.81.20.6418

Phorbol 12-myristate 13-acetate, ionomycin or ouabain, and raised extracellular magnesium induce proliferation of chicken heart mesenchymal cells.

S D Balk, A Morisi, H S Gunther
PMCID: PMC391935  PMID: 6333683

Abstract

Cultured chicken heart mesenchymal cells are proliferatively quiescent at low densities in medium containing plasma at 10%. Mitogenic hormones like epidermal growth factor and insulin-like growth factors cause these cells to proliferate very actively, as does infection with avian sarcoma viruses, erythroblastosis virus, or myelocytomatosis virus. We have found that the combination of phorbol 12-myristate 13-acetate (PMA), ionomycin or ouabain, and raised extracellular magnesium, likewise, causes these cells to proliferate very actively. Although these agents have no significant effect when acting singly, the combination of PMA at 100 ng/ml and 0.5 microM ionomycin induces a 6-fold increase in cell number at 4 days, and the combination of PMA, ionomycin, and 5.6 mM magnesium induces 12-fold multiplication. Likewise, PMA plus 1 microM ouabain induces 3-fold multiplication, whereas the combination of PMA, ouabain, and magnesium induces 6-fold multiplication. The tumor promoter PMA, like diacylglycerol released by breakdown of plasma membrane phosphatidylinositol diphosphate, is known to activate the serine- and threonine-specific intracellular enzyme kinase C. The divalent cation ionophore ionomycin is known to carry calcium into cells down an electrochemical gradient, and the Na+,K+-ATPase inhibitor ouabain appears to elevate intracellular calcium by means of a sodium-mediated exchange mechanism. Magnesium, like calcium, is known to enter cells passively down an electrochemical gradient and to be involved in the regulation of many key intracellular reactions. Our findings with PMA, ionotropes, and magnesium support a hypothesis that diacylglycerol-mediated activation of kinase C plus cellular divalent cation influx and/or mobilization, caused by the action of mitogenic hormones or the protein products of onc genes, are key events in the initiation of cell replication.

Full text

PDF
6418

Selected References

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

  1. Balk S. D. Active proliferation of Rous sarcoma virus-infected, but not normal, chicken heart mesenchymal cells in culture medium of physiological composition. Proc Natl Acad Sci U S A. 1980 Nov;77(11):6606–6610. doi: 10.1073/pnas.77.11.6606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Balk S. D. Calcium as a regulator of the proliferation of normal, but not of transformed, chicken fibroblasts in a plasma-containing medium. Proc Natl Acad Sci U S A. 1971 Feb;68(2):271–275. doi: 10.1073/pnas.68.2.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Balk S. D., Gunther H. S., Morisi A. Morphological transformation, autonomous proliferation and colony formation by chicken heart mesenchymal cells infected with avian sarcoma, erythroblastosis and myelocytomatosis viruses. Life Sci. 1984 Sep 10;35(11):1157–1171. doi: 10.1016/0024-3205(84)90186-3. [DOI] [PubMed] [Google Scholar]
  4. Balk S. D., Levine S. P., Young L. L., LaFleur M. M., Raymond N. M. Mitogenic factors present in serum but not in plasma. Proc Natl Acad Sci U S A. 1981 Sep;78(9):5656–5660. doi: 10.1073/pnas.78.9.5656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Balk S. D., Morisi A., Gunther H. S., Svoboda M. F., Van Wyk J. J., Nissley S. P., Scanes C. G. Somatomedins (insulin-like growth factors), but not growth hormone, are mitogenic for chicken heart mesenchymal cells and act synergistically with epidermal growth factor and brain fibroblast growth factor. Life Sci. 1984 Jul 23;35(4):335–346. doi: 10.1016/0024-3205(84)90643-x. [DOI] [PubMed] [Google Scholar]
  6. Balk S. D., Polimeni P. I., Hoon B. S., LeStourgeon D. N., Mitchell R. S. Proliferation of Rous sarcoma virus-infected, but not of normal, chicken fibroblasts in a medium of reduced calcium and magnesium concentration. Proc Natl Acad Sci U S A. 1979 Aug;76(8):3913–3916. doi: 10.1073/pnas.76.8.3913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Balk S. D. Precipitates and particulates cause proliferative activity of density-inhibited cultured cells by disturbing the diffusion boundary layer: an artefact superimposed upon an artefact? Life Sci. 1980 Nov 24;27(21):1917–1920. doi: 10.1016/0024-3205(80)90409-9. [DOI] [PubMed] [Google Scholar]
  8. Balk S. D., Shiu R. P., LaFleur M. M., Young L. L. Epidermal growth factor and insulin cause normal chicken heart mesenchymal cells to proliferate like their Rous sarcoma virus-infected counterparts. Proc Natl Acad Sci U S A. 1982 Feb;79(4):1154–1157. doi: 10.1073/pnas.79.4.1154. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Balk S. D., Whitfield J. F., Youdale T., Braun A. C. Roles of calcium, serum, plasma, and folic acid in the control of proliferation of normal and Rous sarcoma virus-infected chicken fibroblasts. Proc Natl Acad Sci U S A. 1973 Mar;70(3):675–679. doi: 10.1073/pnas.70.3.675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Berridge M. J. Rapid accumulation of inositol trisphosphate reveals that agonists hydrolyse polyphosphoinositides instead of phosphatidylinositol. Biochem J. 1983 Jun 15;212(3):849–858. doi: 10.1042/bj2120849. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Bishop J. M. Cellular oncogenes and retroviruses. Annu Rev Biochem. 1983;52:301–354. doi: 10.1146/annurev.bi.52.070183.001505. [DOI] [PubMed] [Google Scholar]
  12. Bourguignon L. Y., Pressman B. C. Stimulation of lymphocyte receptor capping by the ionophore monensin. J Membr Biol. 1983;73(1):91–93. doi: 10.1007/BF01870343. [DOI] [PubMed] [Google Scholar]
  13. Deuel T. F., Huang J. S., Huang S. S., Stroobant P., Waterfield M. D. Expression of a platelet-derived growth factor-like protein in simian sarcoma virus transformed cells. Science. 1983 Sep 30;221(4618):1348–1350. doi: 10.1126/science.6310754. [DOI] [PubMed] [Google Scholar]
  14. Downward J., Yarden Y., Mayes E., Scrace G., Totty N., Stockwell P., Ullrich A., Schlessinger J., Waterfield M. D. Close similarity of epidermal growth factor receptor and v-erb-B oncogene protein sequences. Nature. 1984 Feb 9;307(5951):521–527. doi: 10.1038/307521a0. [DOI] [PubMed] [Google Scholar]
  15. Durham A. C., Walton J. M. Calcium ions and the control of proliferation in normal and cancer cells. Biosci Rep. 1982 Jan;2(1):15–30. doi: 10.1007/BF01142195. [DOI] [PubMed] [Google Scholar]
  16. Koenig H., Goldstone A. D., Lu C. Y. Beta-adrenergic stimulation of Ca2+ fluxes, endocytosis, hexose transport, and amino acid transport in mouse kidney cortex is mediated by polyamine synthesis. Proc Natl Acad Sci U S A. 1983 Dec;80(23):7210–7214. doi: 10.1073/pnas.80.23.7210. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Levine B. S., Coburn J. W. Magnesium, the mimic/antagonist to calcium. N Engl J Med. 1984 May 10;310(19):1253–1255. doi: 10.1056/NEJM198405103101910. [DOI] [PubMed] [Google Scholar]
  18. Liu C., Hermann T. E. Characterization of ionomycin as a calcium ionophore. J Biol Chem. 1978 Sep 10;253(17):5892–5894. [PubMed] [Google Scholar]
  19. Mastro A. M., Smith M. C. Calcium-dependent activation of lymphocytes by ionophore, A23187, and a phorbol ester tumor promoter. J Cell Physiol. 1983 Jul;116(1):51–56. doi: 10.1002/jcp.1041160109. [DOI] [PubMed] [Google Scholar]
  20. Nishizuka Y. The role of protein kinase C in cell surface signal transduction and tumour promotion. Nature. 1984 Apr 19;308(5961):693–698. doi: 10.1038/308693a0. [DOI] [PubMed] [Google Scholar]
  21. Owen N. E., Villereal M. L. Efflux of 45Ca2+ from human fibroblasts in response to serum or growth factors. J Cell Physiol. 1983 Oct;117(1):23–29. doi: 10.1002/jcp.1041170105. [DOI] [PubMed] [Google Scholar]
  22. Rubin H. Central role for magnesium in coordinate control of metabolism and growth in animal cells. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3551–3555. doi: 10.1073/pnas.72.9.3551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Sawyer S. T., Cohen S. Enhancement of calcium uptake and phosphatidylinositol turnover by epidermal growth factor in A-431 cells. Biochemistry. 1981 Oct 13;20(21):6280–6286. doi: 10.1021/bi00524a057. [DOI] [PubMed] [Google Scholar]
  24. Siess W., Siegel F. L., Lapetina E. G. Arachidonic acid stimulates the formation of 1,2-diacylglycerol and phosphatidic acid in human platelets. Degree of phospholipase C activation correlates with protein phosphorylation, platelet shape change, serotonin release, and aggregation. J Biol Chem. 1983 Sep 25;258(18):11236–11242. [PubMed] [Google Scholar]
  25. Sugimoto Y., Whitman M., Cantley L. C., Erikson R. L. Evidence that the Rous sarcoma virus transforming gene product phosphorylates phosphatidylinositol and diacylglycerol. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2117–2121. doi: 10.1073/pnas.81.7.2117. [DOI] [PMC free article] [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