Mechanism of cell death induced by an antioxidant extract of Cratoxylum cochinchinense (YCT) in Jurkat T cells: The role of reactive oxygen species and calcium

Free Radical Biology and Medicine

Volumn 36, Issue 12, 2004, Pages 1588-1611

  Tang, Soon Yew ^a   Whiteman, Matthew ^a   Jenner, Andrew ^a   Peng, Zhao Feng ^a   Halliwell, Barry ^a  

^a NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

Author keywords

balcalein monohydrate; BHT; BL; BM; bromoenol lactone; butylated hydroxytoluene; Ca2+ influx; DMEM; Dulbecco's modified Eagle's medium; Free radicals; Mitochondrial depolarization; Oxidative stress; Plasma membrane redox system; Potassium ferricyanide

Indexed keywords

ADENOSINE TRIPHOSPHATE; ANTIOXIDANT; CALCIUM; CASPASE 3; CASPASE 9; CRATOXYLUM COCHINCHINENSE EXTRACT; CYTOCHROME C; MANGIFERIN; PLANT EXTRACT; POTASSIUM FERRICYANIDE; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG;

ANTIOXIDANT ACTIVITY; APOPTOSIS; ARTICLE; CELL DEATH; CONTROLLED STUDY; CRATOXYLUM COCHINCHINENSE; CYTOTOXICITY; DNA DEGRADATION; DRUG MECHANISM; ENZYME ACTIVITY; FLOW CYTOMETRY; HUMAN; HUMAN CELL; LEUKEMIA CELL LINE; MEDICINAL PLANT; MITOCHONDRION; OXIDATIVE STRESS; PRIORITY JOURNAL;

ADENOSINE TRIPHOSPHATE; ANIMALS; ANTIOXIDANTS; APOPTOSIS; BLOTTING, WESTERN; CALCIUM; CASPASE 3; CASPASE 9; CASPASES; CELL ADHESION; CELL LINE; CELL MEMBRANE; CELL SURVIVAL; CLUSIACEAE; COLORING AGENTS; CYTOCHROMES C; DNA FRAGMENTATION; DOGS; FERRICYANIDES; FLOW CYTOMETRY; GLUTATHIONE; HL-60 CELLS; HUMANS; JURKAT CELLS; LYMPHOCYTES; MEMBRANE POTENTIALS; MITOCHONDRIA; MODELS, BIOLOGICAL; NUCLEOSOMES; OXIDATION-REDUCTION; OXIDATIVE STRESS; PC12 CELLS; PHOSPHATIDYLSERINES; PLANT EXTRACTS; RATS; REACTIVE OXYGEN SPECIES; TETRAZOLIUM SALTS; THIAZOLES; TIME FACTORS; TRYPAN BLUE;

CICONIIFORMES; CRATOXYLUM; CRATOXYLUM COCHINCHINENSE;

EID: 2942532593     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2004.03.018     Document Type: Article

References (72)

1. Bennett G.J., Lee H.H. Xanthones from Guttiferae. Phytochemistry. 28:1989;967-998
2. Bremness L. Eyewitness handbook: herbs. 1994;Dorling Kindersley, London
3. Tang S.Y., Whiteman M., Peng Z.F., Jenner A., Yong E.L., Halliwell B. Characterization of antioxidant and antiglycation properties and isolation of active ingredients from Traditional Chinese Medicines. Free Radic. Biol. Med. 2004
4. Nuñez Selles A.J., Velez Castro H.T., Aguero-Aguero J., Gonzalez-Gonzalez J., Naddeo F., De Simone F., Rastelli L. Isolation and quantitative analysis of phenolic antioxidants, free sugars, and polyols from mango (Mangifera indica L.) stem bark aqueous decoction used in Cuba as a nutritional supplement. J. Agric. Food Chem. 50:2002;762-766
5. Sato T., Kawamoto A., Tamura A., Tatsumi Y., Fujii T. Mechanism of antioxidant action of pueraria glycoside (PG)-1 (an isoflavonoid) and mangiferin (a xanthonoid). Chem. Pharm. Bull. 40:1992;721-724
6. Chattopadhyay U., Das S., Guha S., Ghosal S. Activation of lymphocytes of normal and tumor bearing mice by mangiferin, a naturally occurring glucosylxanthone. Cancer Lett. 37:1987;293-299
7. Guha S., Ghosal S., Chattopadhyay U. Antitumor, immunomodulatory and anti-HIV effect of mangiferin, a naturally occurring glucosylxanthone. Chemotherapy. 42:1996;443-451
8. Leiro J.M., Alvarez E., Arranz J.A., Siso I.G., Orallo F. In vitro effects of mangiferin on superoxide concentrations and expression of the inducible nitric oxide synthase, tumour necrosis factor-alpha and transforming growth factor-beta genes. Biochem. Pharmacol. 65:2003;1361-1371
9. Vasant C., Balamurugan K., Rajaram R., Ramasami T. Apoptosis of lymphocytes in the presence of Cr(V) complexes: Roles in Cr(VI)-induced toxicity. Biochem. Biophys. Res. Commun. 285:2001;1354-1360
10. Hansen M.B., Nielsen S.E., Berg K. Re-examination and further development of a precise and rapid dye method for measuring cell growth/cell kill. J. Immunol. Methods. 119:1989;203-210
11. 2+ and slow release of reactive oxygen species are two cross-talked events important in tumour necrosis factor-alpha-mediated apoptosis. Free Radic. Res. 33:2000;295-304
12. Weis M., Schlegel J., Kass G.E.N., Holmstrom T.H., Peters I., Eriksson J., Orrenius S., Chow S.C. Cellular events in Fas/APO-1-mediated apoptosis in JURKAT T lymphocytes. Exp. Cell Res. 219:1995;699-708
13. Zhivotovsky B., Samali A., Gahm A., Orrenius S. Caspases: their intracellular localization and translocation during apoptosis. Cell Death Differ. 6:1999;644-651
14. Spencer J.P.E., Whiteman M., Jenner A., Halliwell B. Nitrite-induced deamination and hypochlorite-induced oxidation of DNA in intact human respiratory tract epithelial cells. Free Radic. Biol. Med. 28:2000;1039-1050
15. Frisch S.M., Francis H. Disruption of epithelial cell-matrix interactions induces apoptosis. J. Cell Biol. 124:1994;619-626
16. 2+ levels through the activation of non-selective cation channels induced by oxidative stress causes mitochondrial depolarization leading to apoptosis-like death in Leishmania donovani promastigotes. J. Biol. Chem. 27:2002;24717-24727
17. Macho A., Hirsch T., Marzo I., Marchetti P., Dallaporta B., Susin S.A., Zamzami N., Kroemer G. Glutathione depletion is an early and calcium elevation is a late event of thymocyte apoptosis. J. Immunol. 158:1997;4612-4619
18. Pap E.H.W., Drummen G.P.C., Winter V.J., Kooij T.W.A., Rijken P., Wirtz K.W.A., Op Den Kamp J.A.F., Hage W.J., Post J.A. Ratio-fluorescence microscopy of lipid oxidation in living cells using C11-BODIPY(581/591). FEBS Lett. 453:1999;278-282
19. Wong A., Cortopassi G.A. High-throughput measurement of mitochondrial membrane potential in a neural cell line using a fluorescence plate reader. Biochem. Biophys. Res. Commun. 298:2002;750-754
20. Bestwick C.S., Milne L. Quercetin modifies reactive oxygen levels but exerts only partial protection against oxidative stress within HL-60 cells. Biochim. Biophys. Acta. 1528:2001;49-59
21. 2+ network. J. Cell Biol. 136:1997;833-844
22. McCarthy J.V., Cotter T.G. Cell shrinkage and apoptosis: a role for potassium and sodium ion efflux. Cell Death Differ. 4:1997;756-770
23. Tiku M.L., Shah R., Allison G.T. Evidence linking chondrocyte lipid peroxidation to cartilage matrix protein degradation. J. Biol. Chem. 275:2000;20069-20076
24. Qu B., Li Q.T., Wong K.P., Tan T., Theresa M.C., Halliwell B. Mitochondrial damage by the "pro-oxidant" peroxisomal proliferator clofibrate. Free Radic. Biol. Med. 31:2001;659-669
25. Kalbhem D.D., Koch H.J. Methodologic studies of the quantitative microdetermination of ATP in biological materials with the firefly enzyme system. Z. Klin. Chem, Klin. Biochem. 5:1967;299-394
26. Hissin P.J., Hilf R. A fluorometric method for determination of oxidized and reduced glutathione in tissues. Anal. Biochem. 74:1976;214-226
27. 2+-ATPase inhibitor thapsigargin. Exp. Cell Res. 212:1994;84-92
28. Wiseman H., Halliwell B. Carcinogenic antioxidants: diethylstilboestrol, hexoestrol and 17α-ethynyloestradiol. FEBS Lett. 332:1993;159-163
29. Martin S.J., Reutelingsperger C.P., McGahon A.J., Rader J.A., van Schie R.C., LaFace D.M., Green D.R. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl. J. Exp. Med. 182:1995;1545-1556
30. Halliwell B., Whiteman M. Measuring reactive species and oxidative damage in vivo and cell culture. How should you do it and what do the results mean? Br. J. Pharmacol. 2004;. in press
31. Long L.H., Clement M.V., Halliwell B. Artifacts in cell culture: rapid generation of hydrogen peroxide on addition of (-)-epigallocatechin, (-)-epigallocatechin gallate, (+)-catechin, and quercetin to commonly used cell culture media. Biochem. Biophys. Res. Commun. 273:2000;50-53
32. Halliwell B. Oxidative stress in cell culture: an under-appreciated problem? FEBS Lett. 540:2003;3-6
33. Martinus R.D., Linnane A.W., Nagley P. Growth of rho 0 human Namalwa cells lacking oxidative phosphorylation can be sustained by redox compounds potassium ferricyanide or coenzyme Q10 putatively acting through the plasma membrane oxidase. Biochem. Mol. Biol. Int. 31:1993;997-1005
34. Li N., Ragheb K., Lawler G., Sturgis J., Rajwa B., Melendez J.A., Robinson J.P. Mitochondrial complex I inhibitor rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production. J. Biol. Chem. 278:2003;8516-8525
35. Laneuville O., Breuer D.K., Dewitt D.L., Hla T., Funk D.D., Smith W.L. Differential inhibition of human prostaglandin endoperoxide H synthases-1 and -2 by nonsteroidal anti-inflammatory drugs. J. Pharmacol. Exp. Ther. 271:1994;927-934
36. Hampton M.B., Winterbourn C.C. Modification of neutrophil oxidant production with diphenyliodonium and its effect on bacterial killing. Free Radic. Biol. Med. 18:1995;633-639
37. Carriere A., Fernandez Y., Rigoulet M., Penicaud L., Casteilla L. Inhibition of proliferation by mitochondrial reactive oxygen species. FEBS Lett. 550:2003;163-167
38. Zhao H., Kalivendi S., Zhang H., Joseph J., Nithipatikom K., Vasquez-Vivar J., Kalyanaraman B. Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: potential implications in intracellular fluorescence detection of superoxide. Free Radic. Biol. Med. 34:2003;1359-1368
39. Halliwell B., Gutteridge J.M.C. Free radicals in biology and medicine. 3rd ed. 1999;Oxford Univ. Press, Oxford
40. Maier O., Oberle V., Hoekstra D. Fluorescent lipid probes: some properties and applications (a review). Chem. Phys. Lipids. 116:2002;3-18
41. Hedley D., Chow S. Flow cytometric measurement of lipid peroxidation in vital cells using parinaric acid. Cytometry. 13:1992;686-692
42. Tithof P.K., Elgayyar M., Cho Y., Guan W., Fisher A.B., Peters-Golden M. Polycyclic aromatic hydrocarbons present in cigarette smoke cause endothelial cell apoptosis by a phospholipase A2-dependent mechanism. FASEB J. 16:2002;1463-1464
43. Lu X.R., Ong W.Y., Halliwell B., Horrocks L.A., Farooqui A.A. Differential effects of calcium-dependent and calcium-independent phospholipase A(2) inhibitors on kainate-induced neuronal injury in rat hippocampal slices. Free Radic. Biol. Med. 30:2001;1263-1273
44. Gao D., Sakurai K., Katoh M., Chen J., Ogiso T. Inhibition of microsomal lipid peroxidation by baicalein: a possible formation of an iron-baicalein complex. Biochem. Mol. Biol. Int. 39:1996;215-225
45. Hogaboam C.M., Donigi-Gale D., Shoupe T.S., Bissonnette E.Y., Befus A.D., Wallace J.L. Platelet-activating factor synthesis by peritoneal mast cells and its inhibition by two quinoline-based compounds. Br. J. Pharmacol. 105:1992;87-92
46. Vanderhoek J.Y., Lands W.E.M. Acetylenic inhibitors of sheep vesicular gland oxygenase. Biochim. Biophys. Acta. 296:1973;374-381
47. Scaduto R.C., Grotyohann L.W. Measurement of mitochondrial membrane potential using fluorescent rhodamine derivatives. Biophys. J. 76:1999;469-477
48. Reers M., Smith T.W., Chen L.B. J-aggregate formation of a carbocyanine as quantitative fluorescent indicator of membrane potential. Biochemistry. 30:1991;4480-4486
49. Gunter T.E., Buntinas L., Sparagna G., Eliseev R., Gunter K. Mitochondrial calcium transport: mechanisms and functions. Cell Calcium. 28:2000;285-296
50. Ghamari-Langroudi M., Bourque C.W. Flufenamic acid blocks depolarizing afterpotentials and phasic firing in rat supraoptic neurones. J. Physiol. 545:2002;537-542
51. Petit P.X., LeCoeur H., Zorn E., Dauguet C., Mignotte B., Gougeon M.L. Alterations in mitochondrial structure and function are early events of dexamethasone-induced thymocyte apoptosis. J. Cell. Biol. 130:1995;157-167
52. Jambrina E., Alonso R., Alcalde M., Rodriguez M.d.C., Serrano A., Martinez-A C., Garcia-Sancho J., Izquierdo M. Calcium influx through receptor-operated channel induces mitochondria-triggered paraptotic cell death. J. Biol. Chem. 278:2003;14134-14145
53. Sperandio S., de Belle I., Bredesen D.E. An alternative, nonapoptotic form of programmed cell death. Proc. Natl. Acad. Sci. USA. 97:2000;14376-14381
54. Chandra J.S., Samali A., Orrenius S. Triggering and modulation of apoptosis by oxidative stress. Free Radic. Biol. Med. 29:2000;323-333
55. Nicholson D.W., Ali A., Thornberry N.A., Vaillancourt J.P., Ding C.K., Gallant M., Gareau Y., Griffin P.R., Labelle M., Lazebnik Y.A., Munday N.A., Raju S.M., Smulson M.E., Yamin T.-T., Yu V.L., Miller D.K. Identification and inhibition of the ICE/CED-3 protease necessary for mammalian apoptosis. Nature. 376:1995;37-43
56. Nobel C.S., Burgess D.H., Zhivotovsky B., Burkitt M.J., Orrenius S., Slater A.F. Mechanism of dithiocarbamate inhibition of apoptosis: thiol oxidation by dithiocarbamate disulfides directly inhibits processing of the caspase-3 proenzyme. Chem. Res. Toxicol. 10:1997;636-643
57. Hampton M.B., Orrenius S. Dual regulation of caspase activity by hydrogen peroxide: implications for apoptosis. FEBS Lett. 414:1997;552-556
58. Finkel T., Holbrook N.J. Oxidants, oxidative stress and the biology of ageing. Nature. 408:2000;239-247
59. Macho A., Calzado M.A., Muñoz-Blanco J., Gómez-Díaz C., Gajate C., Mollinedo F., Navas P., Muñoz E. Selective induction of apoptosis by capsaicin in transformed cells: the role of reactive oxygen species and calcium. Cell Death Differ. 6:1999;155-165
60. Dirsch V.M., Gerbes A.L., Vollmar A.M. Ajoene, a compound of garlic, induces apoptosis in human promyeloleukemic cells, accompanied by generation of reactive oxygen species and activation of nuclear factor kappaB. Mol. Pharmacol. 53:1998;402-407
61. Macho A., Sancho R., Minassi A., Appendino G., Lawen A., Muñoz E. Involvement of reactive oxygen species in capsaicinoid-induced apoptosis in transformed cells. Free Radic. Res. 37:2003;611-619
62. de Grey A.D.N.J. A hypothesis for the minimal overall structure of the mammalian plasma membrane redox system. Protoplasma. 221:2003;3-9
63. Larm J.A., Vaillant F., Linnane A.W., Lawen A. Up-regulation of the plasma membrane oxidoreductase as a prerequisite for the viability of human Namalwa rho 0 cells. J. Biol. Chem. 269:1994;30097-30100
64. Crane F.L., Morré D.J., Low H. Oxidoreduction at the plasma membrane: relation to growth and transport. 1990;CRC Press, Boca Raton, FL
65. Crane F.L., Sun I.L., Sun E.E., Crowe R.A. Plasma membrane redox and regulation of cell growth. Protoplasma. 184:1995;3-7
66. Morré D.J. Asard H., Bérczi A., Caubergs R. Plasma membrane redox systems and their role in biological stress and disease. 1998;Kluwer Academic, Dordrecht
67. Morré D.J., Chueh P.J., Pletcher J., Tang X., Wu L.Y., Morré D.M. Biochemical basis for the biological clock. Biochemistry. 41:2002;11941-11945
68. Wang S., Pogue R., Morré D.M., Morré D.J. NADH oxidase activity (NOX) and enlargement of HeLa cells oscillate with two different temperature-compensated period lengths of 22 and 24 minutes corresponding to different NOX forms. Biochim. Biophys. Acta. 1539:2001;192-204
69. 2+ signalling and apoptosis. J. Bioenerg. Biomembr. 32:2000;35-46
70. Kroemer G., Reed J.C. Mitochondrial control of cell death. Nat. Med. 6:2000;513-519
71. Cai J., Jones D.P. Mitochondrial redox signaling during apoptosis. J. Bioenerg. Biomembr. 31:1999;327-334
72. Lewis R.S., Cahalan M.D. Potassium and calcium channels in lymphocytes. Annu. Rev. Immunol. 13:1995;623-653