Abstract
The purine nucleoside guanosine, when derivatized at the C-8 position to give 8-bromoguanosine (8-BrGuo), acquires the capacity to stimulate high-level lymphocyte proliferation in the presence or absence of serum. Direct comparisons were undertaken to determine whether this activity is exerted only by virtue of the structural resemblance of 8-BrGuo to 8-bromo cyclic GMP (8-BrcGMP) (a known intracellular lymphocyte mitogen). They showed that, of the brominated guanosine derivatives studied, 8-BrGuo is the primary activator because (i) it is a far more potent lymphocyte activator than 8-BrcGMP, the order of mitogenic potency being 8-BrGuo greater than 8-bromo GMP (8-BrGMP) greater than 8-BrcGMP; (ii) it acts much more rapidly than 8-BrcGMP; (iii) it is not metabolized to 8-BrcGMP or cGMP; and (iv) it does not elevate intracellular cGMP content. cGMP is not likely to be the second messenger serving to activate B cells because (i) it does not induce significant proliferation unless brominated at the C-8 position; (ii) the brominated form is much less efficient than 8-BrGuo or 8-BrGMP; (iii) 8-BrGuo and many other mitogens do not increase intracellular cGMP; (iv) many agents that increase cGMP fail to initiate lymphocyte activation; (v) certain agents that increase cGMP (i.e., 15-hydroperoxyarachidonic acid, azide) inhibit lymphocyte activation; and (vi) addition of unbrominated cGMP to cultures stimulated with 8-BrGuo actually diminished stimulation. These data (i) indicate that, by interaction with cellular components, 8-BrGuo triggers high level lymphocyte activation and (ii) cast significant doubt on the role of cGMP as an intracellular second messenger in lymphocyte proliferation.
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Selected References
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- Bleich H. L., Boro E. S. Control of lymphocyte function. N Engl J Med. 1976 Nov 18;295(21):1180–1186. doi: 10.1056/NEJM197611182952110. [DOI] [PubMed] [Google Scholar]
- Burleson D. G., Sage H. J. Effect of lectins on the levels of cAMP and cGMP in guinea pig lymphocytes: early responses of lymph node cells to mitogenic and non-mitogenic lectins. J Immunol. 1976 Mar;116(3):696–703. [PubMed] [Google Scholar]
- Böhme E., Schultz G. Separation of cyclic nucleotides by thin-layer chromatography on polyethyleneimine cellulose. Methods Enzymol. 1974;38:27–38. doi: 10.1016/0076-6879(74)38007-x. [DOI] [PubMed] [Google Scholar]
- Chaplin D. D., Wedner H. J., Parker C. W. Protein phosphorylation in human peripheral blood lymphocytes: mitogen-induced increases in protein phosphorylation in intact lymphocytes. J Immunol. 1980 May;124(5):2390–2398. [PubMed] [Google Scholar]
- Coffey R. G., Hadden E. M., Hadden J. W. Evidence for cyclic GMP and calcium mediation of lymphocyte activation by mitogens. J Immunol. 1977 Oct;119(4):1387–1394. [PubMed] [Google Scholar]
- Diamantstein T., Ulmer A. Stimulation by cyclic GMP of lymphocytes mediated by soluble factor released from adherent cells. Nature. 1975 Jul 31;256(5516):418–419. doi: 10.1038/256418a0. [DOI] [PubMed] [Google Scholar]
- Diamantstein T., Ulmer A. The antagonistic action of cyclic GMP and cyclic AMP on proliferation of B and T lymphocytes. Immunology. 1975 Jan;28(1):113–119. [PMC free article] [PubMed] [Google Scholar]
- Glass W. F., 2nd, Moore J. B., Jr Inhibition of human lung cyclic GMP and cyclic AMP phosphodiesterases by certain nucleosides, nucleotides, and pharmacological phosphodiesterase inhibitors. Biochem Pharmacol. 1979 Apr 1;28(7):1107–1112. doi: 10.1016/0006-2952(79)90313-7. [DOI] [PubMed] [Google Scholar]
- Goodman M. G., Brunton L. L., Weigle W. O. Modulation of lymphocyte activation. II. Alteration of intracellular cyclic nucleotide concentrations by an oxidation product of arachidonic acid. Cell Immunol. 1981 Feb;58(1):85–96. doi: 10.1016/0008-8749(81)90151-9. [DOI] [PubMed] [Google Scholar]
- Goodman M. G., Fidler J. M., Weigle W. O. Nonspecific activation of murine lymphocytes. IV. Proliferation of a distinct, late maturing lymphocyte subpopulation induced by 2-mercaptoethanol. J Immunol. 1978 Nov;121(5):1905–1913. [PubMed] [Google Scholar]
- Hadden J. W., Coffey R. G., Hadden E. M., Lopez-Corrales E., Sunshine G. H. Effects of levamisole and imidazole on lymphocyte proliferation and cyclic nucleotide levels. Cell Immunol. 1975 Nov;20(1):98–103. doi: 10.1016/0008-8749(75)90088-x. [DOI] [PubMed] [Google Scholar]
- Ismail N. A., Montague W. Effects of guanosine on insulin secretion and adenylyl and guanylyl cyclase activities of isolated rat islets of Langerhans. Biochim Biophys Acta. 1977 Jul 21;498(1):325–330. doi: 10.1016/0304-4165(77)90270-7. [DOI] [PubMed] [Google Scholar]
- Johnson E. M., Hadden J. W. Phosphorylation of lymphocyte nuclear acidic proteins: regulation by cyclic nucleotides. Science. 1975 Mar 28;187(4182):1198–1200. doi: 10.1126/science.163491. [DOI] [PubMed] [Google Scholar]
- Lacour F., Harel L., Friend C., Huynh T., Holland J. G. Induction of differentiation of murine erythroleukemia cells by aminonucleoside of puromycin and inhibition of this induction by purines and purine derivatives. Proc Natl Acad Sci U S A. 1980 May;77(5):2740–2742. doi: 10.1073/pnas.77.5.2740. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Londos C., Cooper D. M., Wolff J. Subclasses of external adenosine receptors. Proc Natl Acad Sci U S A. 1980 May;77(5):2551–2554. doi: 10.1073/pnas.77.5.2551. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mishell R. I., Dutton R. W. Immunization of dissociated spleen cell cultures from normal mice. J Exp Med. 1967 Sep 1;126(3):423–442. doi: 10.1084/jem.126.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schacter L. P., Burke P. J. Nicotinamide adenine dinucleotide (NAD) stimulation of DNA synthesis by human bone marrow cells. Biochem Biophys Res Commun. 1978 Feb 14;80(3):504–510. doi: 10.1016/0006-291x(78)91597-8. [DOI] [PubMed] [Google Scholar]
- Smith J. W., Steiner A. L., Parker C. W. Human lymphocytic metabolism. Effects of cyclic and noncyclic nucleotides on stimulation by phytohemagglutinin. J Clin Invest. 1971 Feb;50(2):442–448. doi: 10.1172/JCI106511. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stollar B. D., Borel Y. Nucleoside specificity in the carrier IgG-dependent induction of tolerance. J Immunol. 1976 Oct;117(4):1308–1313. [PubMed] [Google Scholar]
- Watson J. Cyclic nucleotides as intracellular mediators of B cell activation. Transplant Rev. 1975;23:223–249. doi: 10.1111/j.1600-065x.1975.tb00161.x. [DOI] [PubMed] [Google Scholar]
- Watson J., Epstein R., Cohn M. Cyclic nucleotides as intracellular mediators of the expression of antigen-sensitive cells. Nature. 1973 Dec 14;246(5433):405–409. doi: 10.1038/246405a0. [DOI] [PubMed] [Google Scholar]
- Watson J. The influence of intracellular levels of cyclic nucleotides on cell proliferation and the induction of antibody synthesis. J Exp Med. 1975 Jan 1;141(1):97–111. doi: 10.1084/jem.141.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson J. The involvement of cyclic nucleotide metabolism in the initiation of lymphocyte proliferation induced by mitogens. J Immunol. 1976 Nov;117(5 Pt 1):1656–1663. [PubMed] [Google Scholar]
- Weber T. H., Goldberg M. L. Effect of leukoagglutinating phytohemagglutinin on cAMP and cGMP levels in lymphocytes. Exp Cell Res. 1976 Feb;97(2):432–435. doi: 10.1016/0014-4827(76)90637-6. [DOI] [PubMed] [Google Scholar]
- Wedner H. J., Dankner R., Parker C. W. Cyclic GMP and lectin-induced lymphocyte activation. J Immunol. 1975 Dec;115(6):1682–1687. [PubMed] [Google Scholar]
- Weinstein Y., Chambers D. A., Bourne H. R., Melmon K. L. Cyclic GMP stimulates lymphocyte nucleic acid synthesis. Nature. 1974 Sep 27;251(5473):352–353. doi: 10.1038/251352a0. [DOI] [PubMed] [Google Scholar]
- Weinstein Y., Segal S., Melmon K. L. Specific mitogenic activity of 8-Br-guanosine 3',5'-monophosphate (Br-cyclic GMP) on B lymphocytes. J Immunol. 1975 Jul;115(1):112–117. [PubMed] [Google Scholar]
