Abstract
Transmembrane Ca2+ influx is recognized as a universal second messenger that transduces T-cell activation signals to cytoplasm and nucleus, thereby stimulating transcription and cell division. To examine the role of endogenous factors that regulate mitogenic Ca2+ signalling of T-cells, we measured the concanavalin (Con) A-induced increase in cytoplasmic free calcium ([Ca2+]i) in spleen cells of BALB/c mice, using flow cytometry with an indicator dye, Indo-1 acetoxymethyl ester (Indo-1/AM). Con A is a polyclonal activator of T-cells. Unstimulated splenocytes had a [Ca2+]i of 100 nM. [Ca2+]i increased with Con A in a dose-dependent manner up to a concentration of 50 micrograms/ml. In the presence of 50 micrograms/ml Con A, [Ca2+]i was 350 nM. Natural polyamines (putrescine, spermidine and spermine) inhibited Con-A-induced Ca2+ influx in a dose-dependent manner. Putrescine was the most effective polyamine in desensitizing the Ca2+ signal, and decreased [Ca2+]i from 350 nM in the absence of putrescine to 250 nM in the presence of 100 microM putrescine. This effect was not mimicked by structurally related homologues or inorganic cations, suggesting a specific structural effect of the polyamine. H.p.l.c. analysis showed that polyamines were internalized during incubation of cells in vitro. In experiments using monoclonal anti-CD4 and anti-CD8 antibodies, we found a differential effect of putrescine on Ca2+ influx in CD4 and CD8 subpopulations of T cells. For CD4+ cells, [Ca2+]i decreased from 625 nM to 420 nM in the presence of 500 microM putrescine, whereas [Ca2+]i was not affected by putrescine in CD8+ cells. These data suggest that natural polyamines have cell-specific effects on mitogen-stimulated Ca(2+)-influx in T-cell subsets.
Full text
PDF






Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Alcover A., Weiss M. J., Daley J. F., Reinherz E. L. The T11 glycoprotein is functionally linked to a calcium channel in precursor and mature T-lineage cells. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2614–2618. doi: 10.1073/pnas.83.8.2614. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Altman A., Coggeshall K. M., Mustelin T. Molecular events mediating T cell activation. Adv Immunol. 1990;48:227–360. doi: 10.1016/s0065-2776(08)60756-7. [DOI] [PubMed] [Google Scholar]
- Bowlin T. L., McKown B. J., Sunkara P. S. The effect of alpha-difluoromethylornithine, an inhibitor of polyamine biosynthesis, on mitogen-induced interleukin 2 production. Immunopharmacology. 1987 Apr;13(2):143–147. doi: 10.1016/0162-3109(87)90051-8. [DOI] [PubMed] [Google Scholar]
- Budd R. C., Winslow G., Inokuchi S., Imboden J. B. Intact antigen receptor-mediated generation of inositol phosphates and increased intracellular calcium in CD4 CD8 T lymphocytes from MRL lpr mice. J Immunol. 1990 Nov 1;145(9):2862–2872. [PubMed] [Google Scholar]
- Celano P., Baylin S. B., Casero R. A., Jr Polyamines differentially modulate the transcription of growth-associated genes in human colon carcinoma cells. J Biol Chem. 1989 May 25;264(15):8922–8927. [PubMed] [Google Scholar]
- Chatila T., Silverman L., Miller R., Geha R. Mechanisms of T cell activation by the calcium ionophore ionomycin. J Immunol. 1989 Aug 15;143(4):1283–1289. [PubMed] [Google Scholar]
- Chused T. M., Wilson H. A., Greenblatt D., Ishida Y., Edison L. J., Tsien R. Y., Finkelman F. D. Flow cytometric analysis of murine splenic B lymphocyte cytosolic free calcium response to anti-IgM and anti-IgD. Cytometry. 1987 Jul;8(4):396–404. doi: 10.1002/cyto.990080409. [DOI] [PubMed] [Google Scholar]
- Colombatto S., De Agostini M., Corsi D., Sinicco A. Polyamines in lymphocytes from patients infected by human immunodeficiency virus. Biol Chem Hoppe Seyler. 1989 Jul;370(7):745–748. doi: 10.1515/bchm3.1989.370.2.745. [DOI] [PubMed] [Google Scholar]
- Ehrke M. J., Porter C. W., Eppolito C., Mihich E. Selective modulation by alpha-difluoromethylornithine of T-lymphocyte and antibody-mediated cytotoxic responses to mouse tumor allografts. Cancer Res. 1986 Jun;46(6):2798–2803. [PubMed] [Google Scholar]
- Flescher E., Bowlin T. L., Ballester A., Houk R., Talal N. Increased polyamines may downregulate interleukin 2 production in rheumatoid arthritis. J Clin Invest. 1989 Apr;83(4):1356–1362. doi: 10.1172/JCI114023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gardner P. Calcium and T lymphocyte activation. Cell. 1989 Oct 6;59(1):15–20. doi: 10.1016/0092-8674(89)90865-9. [DOI] [PubMed] [Google Scholar]
- Gouy H., Cefai D., Christensen S. B., Debré P., Bismuth G. Ca2+ influx in human T lymphocytes is induced independently of inositol phosphate production by mobilization of intracellular Ca2+ stores. A study with the Ca2+ endoplasmic reticulum-ATPase inhibitor thapsigargin. Eur J Immunol. 1990 Oct;20(10):2269–2275. doi: 10.1002/eji.1830201016. [DOI] [PubMed] [Google Scholar]
- Hawrylko E., Spertus A., Mele C. A., Oster N., Frieri M. Increased interleukin-2 production in response to human type I collagen stimulation in patients with systemic sclerosis. Arthritis Rheum. 1991 May;34(5):580–587. doi: 10.1002/art.1780340510. [DOI] [PubMed] [Google Scholar]
- Heby O., Persson L. Molecular genetics of polyamine synthesis in eukaryotic cells. Trends Biochem Sci. 1990 Apr;15(4):153–158. doi: 10.1016/0968-0004(90)90216-x. [DOI] [PubMed] [Google Scholar]
- Imboden J. B., Stobo J. D. Transmembrane signalling by the T cell antigen receptor. Perturbation of the T3-antigen receptor complex generates inositol phosphates and releases calcium ions from intracellular stores. J Exp Med. 1985 Mar 1;161(3):446–456. doi: 10.1084/jem.161.3.446. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kabra P. M., Lee H. K., Lubich W. P., Marton L. J. Solid-phase extraction and determination of dansyl derivatives of unconjugated and acetylated polyamines by reversed-phase liquid chromatography: improved separation systems for polyamines in cerebrospinal fluid, urine and tissue. J Chromatogr. 1986 Jul 11;380(1):19–32. doi: 10.1016/s0378-4347(00)83621-x. [DOI] [PubMed] [Google Scholar]
- 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]
- Koenig H., Goldstone A., Lu C. Y. Polyamines regulate calcium fluxes in a rapid plasma membrane response. Nature. 1983 Oct 6;305(5934):530–534. doi: 10.1038/305530a0. [DOI] [PubMed] [Google Scholar]
- Lewis R. S., Cahalan M. D. Mitogen-induced oscillations of cytosolic Ca2+ and transmembrane Ca2+ current in human leukemic T cells. Cell Regul. 1989 Nov;1(1):99–112. doi: 10.1091/mbc.1.1.99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lin C. S., Boltz R. C., Siekierka J. J., Sigal N. H. FK-506 and cyclosporin A inhibit highly similar signal transduction pathways in human T lymphocytes. Cell Immunol. 1991 Apr 1;133(2):269–284. doi: 10.1016/0008-8749(91)90103-i. [DOI] [PubMed] [Google Scholar]
- Mills G. B., Cheung R. K., Grinstein S., Gelfand E. W. Increase in cytosolic free calcium concentration is an intracellular messenger for the production of interleukin 2 but not for expression of the interleukin 2 receptor. J Immunol. 1985 Mar;134(3):1640–1643. [PubMed] [Google Scholar]
- Ng J., Fredholm B. B., Jondal M., Andersson T. Regulation of receptor-mediated calcium influx across the plasma membrane in a human leukemic T-cell line: evidence of its dependence on an initial calcium mobilization from intracellular stores. Biochim Biophys Acta. 1988 Sep 16;971(2):207–214. doi: 10.1016/0167-4889(88)90193-0. [DOI] [PubMed] [Google Scholar]
- Nordmann R., Andersen E., Trussardi R., Mazer N. A. Kinetics of interleukin 2 mRNA and protein produced in the human T-cell line Jurkat and effect of cyclosporin A. Biochemistry. 1989 Feb 21;28(4):1791–1797. doi: 10.1021/bi00430a055. [DOI] [PubMed] [Google Scholar]
- Oettgen H. C., Terhorst C., Cantley L. C., Rosoff P. M. Stimulation of the T3-T cell receptor complex induces a membrane-potential-sensitive calcium influx. Cell. 1985 Mar;40(3):583–590. doi: 10.1016/0092-8674(85)90206-5. [DOI] [PubMed] [Google Scholar]
- Oreffo V. I., John R. A., Richards R. J. Diamine uptake by rat lung type II cells in vitro. Biochem Pharmacol. 1991 Apr 15;41(8):1209–1215. doi: 10.1016/0006-2952(91)90660-w. [DOI] [PubMed] [Google Scholar]
- Palade P. Drug-induced Ca2+ release from isolated sarcoplasmic reticulum. III. Block of Ca2+-induced Ca2+ release by organic polyamines. J Biol Chem. 1987 May 5;262(13):6149–6154. [PubMed] [Google Scholar]
- Pegg A. E. Polyamine metabolism and its importance in neoplastic growth and a target for chemotherapy. Cancer Res. 1988 Feb 15;48(4):759–774. [PubMed] [Google Scholar]
- Pegg A. E. Recent advances in the biochemistry of polyamines in eukaryotes. Biochem J. 1986 Mar 1;234(2):249–262. doi: 10.1042/bj2340249. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rabinovitch P. S., June C. H., Grossmann A., Ledbetter J. A. Heterogeneity among T cells in intracellular free calcium responses after mitogen stimulation with PHA or anti-CD3. Simultaneous use of indo-1 and immunofluorescence with flow cytometry. J Immunol. 1986 Aug 1;137(3):952–961. [PubMed] [Google Scholar]
- Rosoff P. M., Burakoff S. J., Greenstein J. L. The role of the L3T4 molecule in mitogen and antigen-activated signal transduction. Cell. 1987 Jun 19;49(6):845–853. doi: 10.1016/0092-8674(87)90622-2. [DOI] [PubMed] [Google Scholar]
- Russell D. H. Ornithine decarboxylase: a key regulatory enzyme in normal and neoplastic growth. Drug Metab Rev. 1985;16(1-2):1–88. doi: 10.3109/03602538508991430. [DOI] [PubMed] [Google Scholar]
- Schacht J. Inhibition by neomycin of polyphosphoinositide turnover in subcellular fractions of guinea-pig cerebral cortex in vitro. J Neurochem. 1976 Nov;27(5):1119–1124. doi: 10.1111/j.1471-4159.1976.tb00318.x. [DOI] [PubMed] [Google Scholar]
- Schuber F. Influence of polyamines on membrane functions. Biochem J. 1989 May 15;260(1):1–10. doi: 10.1042/bj2600001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sei Y., McIntyre T., Fride E., Yoshimoto K., Skolnick P., Arora P. K. Inhibition of calcium mobilization is an early event in opiate-induced immunosuppression. FASEB J. 1991 May;5(8):2194–2199. doi: 10.1096/fasebj.5.8.2022315. [DOI] [PubMed] [Google Scholar]
- Seyfred M. A., Farrell L. E., Wells W. W. Characterization of D-myo-inositol 1,4,5-trisphosphate phosphatase in rat liver plasma membranes. J Biol Chem. 1984 Nov 10;259(21):13204–13208. [PubMed] [Google Scholar]
- Singh A. B., Thomas T. J., Thomas T., Singh M., Mann R. A. Differential effects of polyamine homologues on the prevention of DL-alpha-difluoromethylornithine-mediated inhibition of malignant cell growth and normal immune response. Cancer Res. 1992 Apr 1;52(7):1840–1847. [PubMed] [Google Scholar]
- Tabor C. W., Tabor H. Polyamines. Annu Rev Biochem. 1984;53:749–790. doi: 10.1146/annurev.bi.53.070184.003533. [DOI] [PubMed] [Google Scholar]
- Tadolini B., Varani E. Interaction of spermine with polyphosphoinositides containing liposomes and myo-inositol 1,4,5 triphosphate. Biochem Biophys Res Commun. 1986 Feb 26;135(1):58–64. doi: 10.1016/0006-291x(86)90942-3. [DOI] [PubMed] [Google Scholar]
- Tamura T., Mizuguchi J., Nariuchi H. Regulatory role of CD4/L3T4 molecules in IL-2 production by affecting intracellular Ca2+ concentration of T cell clone stimulated with soluble anti-CD3. J Immunol. 1990 Jul 1;145(1):78–84. [PubMed] [Google Scholar]
- Thomas T. J., Messner R. P. Structural specificity of polyamines in left-handed Z-DNA formation. Immunological and spectroscopic studies. J Mol Biol. 1988 May 20;201(2):463–467. doi: 10.1016/0022-2836(88)90155-6. [DOI] [PubMed] [Google Scholar]
- Truneh A., Albert F., Golstein P., Schmitt-Verhulst A. M. Early steps of lymphocyte activation bypassed by synergy between calcium ionophores and phorbol ester. Nature. 1985 Jan 24;313(6000):318–320. doi: 10.1038/313318a0. [DOI] [PubMed] [Google Scholar]
- Tsien R. Y., Pozzan T., Rink T. J. T-cell mitogens cause early changes in cytoplasmic free Ca2+ and membrane potential in lymphocytes. Nature. 1982 Jan 7;295(5844):68–71. doi: 10.1038/295068a0. [DOI] [PubMed] [Google Scholar]
- Vergara J., Tsien R. Y., Delay M. Inositol 1,4,5-trisphosphate: a possible chemical link in excitation-contraction coupling in muscle. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6352–6356. doi: 10.1073/pnas.82.18.6352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xu Z. C., Kirchberger M. A. Modulation by polyelectrolytes of canine cardiac microsomal calcium uptake and the possible relationship to phospholamban. J Biol Chem. 1989 Oct 5;264(28):16644–16651. [PubMed] [Google Scholar]
- de Meis L. Fast efflux of Ca2+ mediated by the sarcoplasmic reticulum Ca2(+)-ATPase. J Biol Chem. 1991 Mar 25;266(9):5736–5742. [PubMed] [Google Scholar]
