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Superoxide, nitric oxide, peroxynitrite and cytokine combinations all cause functional impairment and morphological changes in rat islets of Langerhans and insulin secreting cell lines, but dictate cell death by different mechanisms

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Abstract

We have shown that nitric oxide treatment for 30–90 min causes inhibition of insulin secretion, DNA damage and disturbs sub-cellular organization in rat and human islets of Langerhans and HIT-T15 cells. Here rat islets and beta-cell lines were treated with various free radical generating systems S-nitrosoglutathione (nitric oxide), xanthine oxidase plus hypoxanthine (reactive oxygen species), 3-morpholinosydnonimine (nitric oxide, super-oxide, peroxynitrite, hydrogen peroxide) and peroxynitrite and their effects over 4 h to 3 days compared with those of the cytokine combination interleukin-1β, tumour necrosis factor-α and interferon-γ. End points examined were de novo protein synthesis, cellular reducing capacity, morphological changes and apoptosis by acridine orange cytochemistry, DNA gel electrophoresis and electron microscopy. Treatment (24–72 h) with nitric oxide, superoxide, peroxynitrite or combined cytokines differentially decreased redox function and inhibited protein synthesis in rat islets of Langerhans and in insulin-containing cell lines; cytokine effects were arginine and nitric oxide dependent. Peroxynitrite gave rare apoptosis in HIT-T15 cells and superoxide gave none in any cell type, but caused the most beta cell-specific damage in islets. S-nitroso-glutathione was the most effective agent at causing DNA laddering or chromatin margination characteristic of apoptotic cell death in insulin-containing cells. Cytokine-induced apoptosis was observed specifically in islet beta cells, combined cytokine effects on islet function and death most resembled those of the mixed radical donor SIN-1.

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References

  1. Appels B, Burkart V, Kantweke-Funke G, et al. Spontaneous cytotoxicity of macrophages against pancreatic islet cells. J Immunol 1989; 142: 3803–3808.

    Google Scholar 

  2. Kröncke KD, Kolb-Bachofen V, Berschick B, Burkart V, Kolb H. Activated macrophages kill pancreatic syngenic islet cells via arginine-dependent nitric oxide generation. Biochem Biophys Res Commun 1991; 175: 752–758.

    Google Scholar 

  3. Mandrup-Poulsen T, Helqvist S, Wogensen LD, et al. Cytokines and free radicals as effector molecules in the destruction of pancreatic β cells. In: Baekkeshov S, Hansen B, eds. Human diabetes — genetic, environmental and autoimmune etiology. Berlin, Germany: Springer, 1990: 166–193.

    Google Scholar 

  4. Southern C, Schulster D, Green IC. Inhibition of insulin secretion by interleukin-1β and tumour necrosis factor-alpha by an L-arginine-dependent nitric oxide generating mechanism. FEBS Lett 1990; 276: 42–44.

    Google Scholar 

  5. Corbett JA, Wang JL, Hughes JH, et al. Nitric oxide and cGMP formation induced by IL-1b in the islets of Langerhans. Biochem J 1992; 287: 229–235.

    Google Scholar 

  6. Corbett JA, Kwon G, Misko TP, Rodi CP, McDaniel ML. Tyrosine kinase involvement in IL-b-induced expression of iNOS by β-cells purified from islets of Langerhans. Am J Physiol 1994; 267: C48–C54.

    Google Scholar 

  7. Eizirik DL, Cagliero E, Björkland A, Welsh N. Interleukin 1β induces the expression of an isoform of nitric oxide synthase in insulin producing cells, which is similar to that observed in activated macrophages. FEBS Lett 1992; 308: 249–252.

    Google Scholar 

  8. Green IC, Cunningham JM, Delaney CA, et al. Effects of cytokines and nitric oxide donors on insulin secretion, cyclic GMP and DNA damage: relation to nitric oxide production. Biochem Soc Trans 1994; 22: 30–37.

    Google Scholar 

  9. Griffith OW, Stuehr DJ. Nitric oxide synthases: Properties and catalytic mechanism. Annu Rev Physiol 1995; 57: 707–736.

    Google Scholar 

  10. Burkart V, Koike T, Brenner H-H, Kolb H. Oxygen radicals generated by the enzyme xanthine oxidase lyse rat pancreatic islet cells in vitro. Diabetologia 1992; 35: 1028–1034.

    Google Scholar 

  11. Kröncke K-D, Brenner H-H, Rodriguez M-L, et al. Pancreatic islet cells are highly susceptible towards the cytotoxic effects of chemically generated nitric oxide. Biochim Biophys Acta 1993; 1182: 221–229.

    Google Scholar 

  12. Delaney CA, Green MHL, Lowe JE, Green IC. Endogenous nitric oxide induced by interleukin-1b in rat islets of Langerhans and HIT-T15 cells causes significant DNA damage as measured by the ‘comet’ assay. FEBS Lett 1993; 333: 291–295.

    Google Scholar 

  13. Fehsel K, Jalowy A, Qi S, et al. Islet cell DNA is a target of inflammatory attack by nitric oxide. Diabetes 1993; 42: 496–500.

    Google Scholar 

  14. Cunningham JM, Mabley JG, Delaney CA, Green IC. The effect of nitric oxide donors on insulin secretion, cyclic GMP and cyclic AMP in rat islets of Langerhans and the insulin secreting lines HIT-T15 and RINm5F. Mol Cell Endocrinol 1994; 102: 23–29.

    Google Scholar 

  15. Di Matteo M, MacArthur D, Delaney CA, Cunningham J, Green IC. Effects of nitric oxide donors on DNA synthesis and cell viability in RINm5F cells [Abstract]. Diabetologia 1994; 37: 200.

    Google Scholar 

  16. Dunger AM, Cunningham J, Delaney CA, et al. Nitric oxide induced by tumour necrosis factor-alpha and interferon-gamma inhibits insulin secretion and causes DNA damage in unweaned rat islets. Diabetes 1996; 45: 183–189.

    Google Scholar 

  17. Suarez-Pinzon WL, Strynadka K, Schulz R, Rabinovitch A. Mechanisms of cytokine-induced destruction of rat insulinoma cells: the role of nitric oxide. Endocrinology 1994; 134: 1006–1010.

    Google Scholar 

  18. Panagiotidis G, Åkesson B, Rydell EL, Lundquist I. Influence of nitric oxide synthase inhibition, nitric oxide and hydroperoxide on insulin release induced by various secretagogues. Br J Pharmacol 1995; 114: 289–296.

    Google Scholar 

  19. Rabinovitch A, Suarez WL, Thomas PD, Strynadka K, Simpson I. Cytotoxic effects of cytokines on rat islets: evidence for involvement of free radicals and lipid peroxidation. Diabetologia 1992; 35: 409–413.

    Google Scholar 

  20. Beckman JS, Beckman TW, Chen J, Marshall PA, Freeman BA. Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide. Proc Natl Acad Sci USA 1990; 87: 1620–1624.

    Google Scholar 

  21. Ródenas J, Mitjavila MT, Carbonell T. Simultaneous generation of nitric oxide and superoxide by inflammatory cells in rats. Free Radic Biol Med 1995; 18: 869–875.

    Google Scholar 

  22. Thomas S, Delaney CA, Lowe J, Green MHL, Green IC. Free radical and scavenging enzyme effects on HIT-T15 cells. Diabetologia 1995; 38: A253.

    Google Scholar 

  23. Delaney CA, Tyrberg B, Bouwens L, et al. Sensitivity of human pancreatic islets to peroxynitrite-induced cell dysfunction and death. FEBS Lett 1996; 394: 300–306.

    Google Scholar 

  24. Albina JE, Cui S, Mateo RB, Reichner JS. Nitric oxide-mediated apoptosis in murine peritoneal macrophages. J Immunol 1993; 150: 5080–5085.

    Google Scholar 

  25. Nishio E, Fukushima K, Shiozaki M, Watanabe Y. Nitric oxide donor SNAP induces apoptosis in smooth muscle cells through cGMP-independent mechanism. Biochem Biophys Res Commun 1996; 221: 163–168.

    Google Scholar 

  26. Fehsel K, Kröncke K-D, Meyer KL, et al. Nitric oxide induces apoptosis in mouse thymocytes. J Immunol 1995; 155: 2858–2865.

    Google Scholar 

  27. Beauvais F, Michel L, Dubertret L. The nitric oxide donors, azide and hydoxylamine, inhibit the programmed cell death of cytokine-deprived human eosinophils. FEBS Lett 1995; 361: 229–232.

    Google Scholar 

  28. Mannick JB, Asano K, Izumi K, Kieff E, Stamler JS. Nitric oxide produced by human B lymphocytes inhibits apoptosis and Epstein-Barr virus reactivation. Cell 1994; 79: 1137–1146.

    Google Scholar 

  29. Mitrovic B, Ignarro LJ, Vinters HV, et al. Nitric oxide induces necrotic but not apoptotic cell death in oligodendrocytes. Neuroscience 1995; 65: 531–539.

    Google Scholar 

  30. Bonfoco E, Krainc D, Ankarcrona M, Nicotera P, Lipton SA. Apoptosis and necrosis — Two distinct events induced respectively by mild and intense insults with N-methyl-D-aspartate or nitric-oxide superoxide in cortical cell cultures. PNAS 1995; 92: 7162–7166.

    Google Scholar 

  31. Morgan NG, Cable HC, Newcombe NR, Williams GT. Treatment of cultured pancreatic β-cells with streptozotocin induces cell death by apoptosis. Biosc Rep 1994; 14: 243–250.

    Google Scholar 

  32. Kröncke K-D, Fehsel K, Sommer A, Rodriguez M-L, Kolb-Bachofen V. Nitric oxide generation during cellular metabolization of the diabetogenic N-methyl-nitroso-urea streptozotozin contributes to islet cell DNA damage. Biol Chem 1995; 376: 179–185.

    Google Scholar 

  33. Delaney CA, Dunger AM, Di Matteo M, et al. Comparison of inhibition of glucose-stimulated insulin secretion in rat islets of Langerhans by streptozotocin and methyl and ethyl nitrosoureas and methanesulphonates: lack of correlation with nitric oxide-releasing or O6-alkylating ability. Biochem Pharmacol 1995; 50: 2015–2020.

    Google Scholar 

  34. Ankarcrona M, Dypbukt J, Brüne B, Nicotera P. Interleukin-1β-induced nitric oxide production activates apoptosis in pancreatic RINm5F cells. Exp Cell Res 1994; 213: 172–177.

    Google Scholar 

  35. Meßmer UK, Ankarcrona M, Nicotera P. Brüne B. p53 expression in nitric oxide-induced apoptosis. FEBS Lett 1994; 355: 23–26.

    Google Scholar 

  36. Iwahashi H, Hanafusa T, Eguchi Y, et al. Cytokine-induced apoptotic cell death in a mouse pancreatic beta cell line: inhibition by Bcl-2. Diabetologia 1996; 39: 530–536.

    Google Scholar 

  37. Kaneto H, Fujii J, Seo HG, et al. Apoptotic cell death triggered by nitric oxide in pancreatic B-cells. Diabetes 1995; 44: 733–738.

    Google Scholar 

  38. Green IC, Delaney CA, Cunningham JM, Karmiris V, Southern C. Interleukin-1β effects on cyclic GMP and cyclic AMP in cultured rat islets of Langerhans-arginine-dependence and relationship to insulin secretion. Diabetologia 1993; 36: 9–16.

    Google Scholar 

  39. Pryor WA, Cueto R, Jin X, et al. A practical method for preparing peroxynitrite solutions of low ionic strength and free of hydrogen peroxide. Free Rad Biol Med 1995; 18: 75–83.

    Google Scholar 

  40. Blough NV, Zafiriou OC. Reaction of superoxide with nitric oxide to form peroxynitrite in alkaline aqueous solution. Inorg Chem 1985; 24: 3502–3504.

    Google Scholar 

  41. Mosmann TJ. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxic assays. J Immunol Meth 1983; 65: 55–63.

    Google Scholar 

  42. Eizirik DL, Delaney CA, Green MHL, et al. Nitric oxide donors decrease the function and survival of human pancreatic islets. Mol Cell Endocrinol 1996; 118: 71–83.

    Google Scholar 

  43. Sekine N, Cirulli V, Regazzi R, et al. Low lactate dehydrogenase and high mitochondrial glycerol phosphate dehydrogenase in pancreatic b cells. J Biol Chem 1994; 269: 4895–4902.

    Google Scholar 

  44. Stamler JS. Redox signaling: nitrosylation and related target interactions of nitric oxide. Cell 1994; 78: 931–936.

    Google Scholar 

  45. Lancaster JR, Hibbs JBJ. EPR demonstration of iron-nitrosyl complex formation by cytotoxic activated macrophages. Proc Natl Acad Sci USA 1990; 87: 1223–1227.

    Google Scholar 

  46. Welsh N, Eizirik DL, Bendtzen K, Sandler S. Interleukin-1β-induced nitric oxide production in isolated rat pancreatic islets requires gene transcription and may lead to inhibition of the Krebs cycle enzyme aconitase. Endocrinology 1991; 129: 3167–3173.

    Google Scholar 

  47. Loweth AC, Williams GT, Scarpello JHB, Morgan NG. Heterotrimeric G-proteins are implicated in the regulation of apoptosis in pancreatic β-cells. Exp Cell Res 1996; 229: 69–76.

    Google Scholar 

  48. Willmott NJ, Galione A, Smith PA. Nitric oxide induces intracellular Ca2+ mobilization and increases secretion of incorporated 5-hydroxytryptamine in rat pancreatic β-cells. FEBS Lett 1995; 371: 99–104.

    Google Scholar 

  49. Hale AJ, Smith CA, Sutherland LC, et al. Apoptosis: molecular regulation of cell death. Eur J Biochem 1996; 236: 1–26.

    Google Scholar 

  50. Pfeilschifter J, Huwiler A. Nitric oxide stimulates stress-activated protein kinases in glomerular endothelial and mesangial cells. FEBS Lett 1996; 396: 67–70.

    Google Scholar 

  51. Loweth AC, Williams GT, Scarpello JHB, Morgan NG. Evidence for the involvement of cGMP and protein kinase G in nitric oxide-induced apoptosis in the pancreatic B cell line HIT-T15. FEBS Lett 1997; 400: 285–288.

    Google Scholar 

  52. Fawthrop DJ, Boobis AR, Davies DS. Mechanisms of cell death. Arch Toxicol 1991; 65: 437–444.

    Google Scholar 

  53. Loweth AC, Scarpello JH, Williams GT, Morgan NG. Evidence for the involvement of cGMP in nitric oxide-induced apoptosis in HIT-T15 cells. Diabetologia 1996; 39: A 104.

    Google Scholar 

  54. Pryor WA, Squadrito GL. The chemistry of peroxynitrite: a product from the reaction of nitric oxide with superoxide. Am J Physiol 1995; 268: L699–L722.

    Google Scholar 

  55. Castro L, Rodriguez M, Radi R. Aconitase is readily inactivated by peroxynitrite, but not by its precursor, nitric oxide. J Biol Chem 1994; 269: 29409–29415.

    Google Scholar 

  56. Hausladen A, Fridovich I. Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not. J Biol Chem 1994; 269: 29405–29408.

    Google Scholar 

  57. Welsh N, Sandler S. Interleukin-1β induces nitric oxide production and inhibits the activity of aconitase without decreasing glucose oxidation rates in isolated mouse pancreatic islets. Biochem Biophys Res Commun 1992; 182: 333–340.

    Google Scholar 

  58. Horton R. An investigation into the role of nitric oxide in the inhibition of hepatic gluconeogenesis by bacterial endotoxin. University of Sussex, 1995.

  59. Yamada K, Takane-Gyotoku N, Yuan X, et al. Mouse islet cell lysis mediated by interleukin-1-induced Fas. Diabetologia 1996; 39: 1306–1312.

    Google Scholar 

  60. Walker R, Bone AJ, Cooke A, Baird JD. Distinct macrophage subpopulations in pancreas of prediabetic BB/E rats. Diabetes 1988; 37: 1301–1304.

    Google Scholar 

  61. Lindsay RM, Smith W, Rossiter SP, et al. NW-nitro-L-arginine methyl ester reduces the incidence of IDDM in BB/E rats. Diabetes 1995; 44: 365–368.

    Google Scholar 

  62. Kleemann R, Rothe H, Kolb-Bachofen V, et al. Transcription and translation of inducible nitric oxide synthase in pancreas of prediabetic BB rats. FEBS Lett 1993; 328: 9–12.

    Google Scholar 

  63. Rabinovitch A, Suarez-Pinzon WL, Sorenson O, Bleackley RC. Inducible nitric oxide synthase (iNOS) in pancreatic islets of nonobese diabetic mice: Identification of iNOS-expressing cells and relationships to cytokines expressed in the islets. Endocrinology 1996; 137: 2093–2099.

    Google Scholar 

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Di Matteo, M.A., Loweth, A.C., Thomas, S. et al. Superoxide, nitric oxide, peroxynitrite and cytokine combinations all cause functional impairment and morphological changes in rat islets of Langerhans and insulin secreting cell lines, but dictate cell death by different mechanisms. Apoptosis 2, 164–177 (1997). https://doi.org/10.1023/A:1026412414666

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