Abstract
This study shows that human lymphocytes markedly decrease chloramines (long-lived oxidants) generated by polymorphonuclear neutrophils (PMN) after stimulation by phorbol-myristate-acetate or opsonized zymosan. In a cell-free model, reduced glutathione (GSH) scavenged chloramines, giving rise to oxidized glutathione (GSSG). In the cell system, treatment of lymphocytes with autologous PMN-derived chloramines induced a profound decrease in their total and reduced glutathione (GSH) content and markedly inhibited their proliferate responses to concanavalin-A and, to a lesser extent, phytohaemagglutinin. It is concluded that (i) lymphocytes may play a defensive role against phagocyte-derived oxidative stress by scavenging chloramines, and (ii) as this effect which is mediated by GSH affects lymphocyte proliferative responses, it may help to elucidate the still obscure mechanisms of oxidative stress associated immunodeficiency.
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Selected References
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- Anderson M. E. Determination of glutathione and glutathione disulfide in biological samples. Methods Enzymol. 1985;113:548–555. doi: 10.1016/s0076-6879(85)13073-9. [DOI] [PubMed] [Google Scholar]
- Babior B. M. Oxygen-dependent microbial killing by phagocytes (first of two parts). N Engl J Med. 1978 Mar 23;298(12):659–668. doi: 10.1056/NEJM197803232981205. [DOI] [PubMed] [Google Scholar]
- Bilzer M., Lauterburg B. H. Effects of hypochlorous acid and chloramines on vascular resistance, cell integrity, and biliary glutathione disulfide in the perfused rat liver: modulation by glutathione. J Hepatol. 1991 Jul;13(1):84–89. doi: 10.1016/0168-8278(91)90868-c. [DOI] [PubMed] [Google Scholar]
- Burchill B. R., Oliver J. M., Pearson C. B., Leinbach E. D., Berlin R. D. Microtubule dynamics and glutathione metabolism in phagocytizing human polymorphonuclear leukocytes. J Cell Biol. 1978 Feb;76(2):439–447. doi: 10.1083/jcb.76.2.439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Farber J. L., Kyle M. E., Coleman J. B. Mechanisms of cell injury by activated oxygen species. Lab Invest. 1990 Jun;62(6):670–679. [PubMed] [Google Scholar]
- Hamilos D. L., Zelarney P., Mascali J. J. Lymphocyte proliferation in glutathione-depleted lymphocytes: direct relationship between glutathione availability and the proliferative response. Immunopharmacology. 1989 Nov-Dec;18(3):223–235. doi: 10.1016/0162-3109(89)90020-9. [DOI] [PubMed] [Google Scholar]
- Harlan J. M., Levine J. D., Callahan K. S., Schwartz B. R., Harker L. A. Glutathione redox cycle protects cultured endothelial cells against lysis by extracellularly generated hydrogen peroxide. J Clin Invest. 1984 Mar;73(3):706–713. doi: 10.1172/JCI111263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ishii Y., Partridge C. A., Del Vecchio P. J., Malik A. B. Tumor necrosis factor-alpha-mediated decrease in glutathione increases the sensitivity of pulmonary vascular endothelial cells to H2O2. J Clin Invest. 1992 Mar;89(3):794–802. doi: 10.1172/JCI115658. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liang C. M., Lee N., Cattell D., Liang S. M. Glutathione regulates interleukin-2 activity on cytotoxic T-cells. J Biol Chem. 1989 Aug 15;264(23):13519–13523. [PubMed] [Google Scholar]
- Liang S. M., Lee N., Finbloom D. S., Liang C. M. Regulation by glutathione of interleukin-4 activity on cytotoxic T cells. Immunology. 1992 Mar;75(3):435–440. [PMC free article] [PubMed] [Google Scholar]
- Messina J. P., Lawrence D. A. Cell cycle progression of glutathione-depleted human peripheral blood mononuclear cells is inhibited at S phase. J Immunol. 1989 Sep 15;143(6):1974–1981. [PubMed] [Google Scholar]
- Nathan C. F. Neutrophil activation on biological surfaces. Massive secretion of hydrogen peroxide in response to products of macrophages and lymphocytes. J Clin Invest. 1987 Dec;80(6):1550–1560. doi: 10.1172/JCI113241. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nguyen A. T., Golub R., Feuillet-Fieux M. N., Descamps-Latscha B. Modulation of human granulocyte and monocyte chemiluminescence responses: evidence for distinct free radical generating systems. J Clin Lab Immunol. 1983 Sep;12(1):47–55. [PubMed] [Google Scholar]
- Smyth M. J. Glutathione modulates activation-dependent proliferation of human peripheral blood lymphocyte populations without regulating their activated function. J Immunol. 1991 Mar 15;146(6):1921–1927. [PubMed] [Google Scholar]
- Swaim M. W., Pizzo S. V. Methionine sulfoxide and the oxidative regulation of plasma proteinase inhibitors. J Leukoc Biol. 1988 Apr;43(4):365–379. doi: 10.1002/jlb.43.4.365. [DOI] [PubMed] [Google Scholar]
- Wasil M., Halliwell B., Hutchison D. C., Baum H. The antioxidant action of human extracellular fluids. Effect of human serum and its protein components on the inactivation of alpha 1-antiproteinase by hypochlorous acid and by hydrogen peroxide. Biochem J. 1987 Apr 1;243(1):219–223. doi: 10.1042/bj2430219. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weiss S. J., Lampert M. B., Test S. T. Long-lived oxidants generated by human neutrophils: characterization and bioactivity. Science. 1983 Nov 11;222(4624):625–628. doi: 10.1126/science.6635660. [DOI] [PubMed] [Google Scholar]
- Weiss S. J. Tissue destruction by neutrophils. N Engl J Med. 1989 Feb 9;320(6):365–376. doi: 10.1056/NEJM198902093200606. [DOI] [PubMed] [Google Scholar]
- Witko V., Nguyen A. T., Descamps-Latscha B. Microtiter plate assay for phagocyte-derived taurine-chloramines. J Clin Lab Anal. 1992;6(1):47–53. doi: 10.1002/jcla.1860060110. [DOI] [PubMed] [Google Scholar]
