Apoptotic process in the monkey small intestinal epithelium: 2. Possible role of oxidative stress

Free Radical Biology and Medicine

Volumn 26, Issue 3-4, 1999, Pages 431-438

  Madesh, M ^a   Benard, O ^a   Balasubramanian, K A ^a  

^a Wellcome Trust Research Laboratory   (India)

Author keywords

Apoptosis; Free Radicals; Intestinal epithelium; Monkey; Oxidative stress

Indexed keywords

ANTIOXIDANT; CATALASE; FREE RADICAL; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; SUPEROXIDE DISMUTASE;

ANIMAL CELL; APOPTOSIS; ARTICLE; CELL LEVEL; CELL VIABILITY; ENZYME ACTIVITY; ENZYME ASSAY; LIPID PEROXIDATION; MITOCHONDRIAL RESPIRATION; MONKEY; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; SMALL INTESTINE MUCOSA;

ANIMALS; ANTIOXIDANTS; APOPTOSIS; GLUTATHIONE PEROXIDASE; GLUTATHIONE REDUCTASE; GLUTATHIONE TRANSFERASE; HAPLORHINI; INTESTINAL MUCOSA; INTESTINE, SMALL; OXIDATIVE STRESS; SUPEROXIDE DISMUTASE; VITAMIN E;

ANIMALIA;

EID: 0032898279     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0891-5849(98)00218-4     Document Type: Article

References (52)

1. Richter C., Gogvadze V., Laffranchi R., Schlapbach R., Schweizer M., Suter M., Walter P., Yaffee M. Oxidants in mitochondria from physiology to diseases . Biochim. Biophys. Acta. 1271:1995;67-74.
2. Janssen Y.M., Van H.B., Borm P.J., Mossman B.T. Cell and tissue responses to oxidative damage. Lab. Invest. 69:1993;261-274.
3. Ueda N., Shah S.V. Endonuclease-induced DNA damage and cell death in oxidant injury to renal tubular epithelial cells. J. Clin. Invest. 90:1992;2593-2597.
4. Buttke T.M., Sandstrom P.A. Oxidative stress as a mediator of apoptosis. Immunol. Today. 15:1994;7-10.
5. Lennon S.V., Martin S.J., Cotter T.G. Dose-dependent induction of apoptosis in human tumor cell lines by widely diverging stimuli. Cell. Prolif. 24:1991;203-214.
6. Novogrodsky A., Ravid A., Rubin A.L., Stenzel K.H. Hydroxy radical scavengers inhibit lymphocyte mitogenesis. Proc. Natl. Acad .Sci. USA. 79:1982;1171-1174.
7. Murrell G.A.C., Francis M.J.O., Bromley L. Modulation of fibroblast proliferation by oxygen free radicals. Biochem.J. 265:1990;659-665.
8. Sarafian T.A., Bredesen D.E. Invited commentary. Is apoptosis mediated by reactive oxygen species? Free. Radic. Res. 21:1994;1-8.
9. Reid V.C., Hardwick S.J., Mitchinson M.J. Fragmentation of DNA in P388D1 macrophages exposed to oxidised low-density lipoprotein. FEBS Lett. 332:1993;218-220.
10. Halliwell B., Gutteridge M.C. Oxygen toxicity, oxygen radicals, transition metals and disease. Biochem. J. 219:1984;1-14.
11. 2+ from intracellular stores. J. Biol. Chem. 266:1991;4295-4302.
12. Sandstrom P.A., Tebbey P.W., Van Cleave S., Buttke T.M. Lipid peroxides induce apoptosis in T cells displaying a HIV-associated glutathione peroxidase deficiency. J. Biol. Chem. 296:1994;798-801.
13. Hockenbery D.M., Oltvai Z.N., Yin X-M, Milliman C.L., Korsmeyer S.J. Bcl-2 functions in an antioxidant pathway to prevent apoptosis. Cell. 75:1993;241-251.
14. Kane D.J., Sarafian T.A., Anton R., Hahn H., Gralla Valentine J.S., Ord T., Bredesen D.E. Bcl-2 inhibition of neural death decreased generation of reactive oxygen species . Science. 262:1993;1274-1277.
15. Vecchini F., Pringault E., Billiar T.R., Geller A., Hausel P., Felley-Bosco E. Decreased activity of inducible nitric oxide synthease type 2 and modulation of the expression of glutathione S-transferase α, bcl-2, and metallothioneins during the differentiation of CaCo-2 cells. Cell Growth Differ. 8:1997;261-268.
16. Zucker B., Hanusch J., Bauer G. Glutathione depletion in fibroblasts is the basis for apoptosis-induction by endogenous oxygen species. Cell Death Differ. 4:1997;388-395.
17. Zhong L-T, Sarafian R., Kane D.J., Charles A.C., Mah S.P., Edwards R.H., Breseden D.E. Bcl-2 inhibits death of central neural cells by multiple agents. Proc. Natl. Acad. Sci. USA. 90:1993;4533-4537.
18. Lionetti P., Breese E., Braegger C., Murch S.H., Taylor J., MacDonald T.T. T cell activation can induce mucosal destruction or adaptation in cultured human fetal small intestine. Gastroenterology. 105:1993;373-381.
19. Sartor B.R. Cytokines in intestinal inflammation pathophysiological and clinical considerations . Gastroenterology. 106:1994;533-539.
20. Iwanaga T., Hongxia H., Kazuo A., Fujita T. A novel mechanism for disposing of effete epithelial cells in the small intestine of guinea pigs. Gastroenterology. 105:1993;1089-1097.
21. Raff M.C. Social controls on cell survival and cell death. Nature. 356:1992;397-400.
22. Raff M.C., Barres B.A., Burne J.F., Coles H.S., Ishizaki Y., Jacobson M.D. Programmed cell death and control of cell survival lessons from the nervous system . Science. 162:1993;695-700.
23. Smith M.W. Expression of digestive and absorptive function in differentiating enterocytes. Annu. Rev. Physiol. 47:1985;247-260.
24. Gavrieli Y., Sherman Y., Ben-Sasson S.A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J. Cell. Biol. 119:1992;493-501.
25. Merritt A.J., Potten C.S., Watson A.J.M., Loh D.Y., Nakayama K., Hickman J.A. Differential expression of bcl-2 in intestinal epithelia. J. Cell. Sci. 108:1995;2261-2271.
26. Que F. G, Gores G. J. Cell death by apoptosis basic concepts and disease relevance for the gastroenterologist . Gastroenterology. 110:1996;1238-1243.
27. Weiser M.M. Intestinal epithelial cell surface membrane glycoprotein synthesis. J. Biol. Chem. 248:1973;2536-2541.
28. Thambidurai D., Bachawat B.K. Purification and properties of brain alkaline phosphatase. J. Neurochem. 29:1979;503-512.
29. Reeves W.J., Fimognari G. L-lactic dehydrogenase Heart (H4) . Methods Enzymol. 9:1966;288-294.
30. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the Folin-phenol regeant. J. Biol. Chem. 193:1951;265-275.
31. Madesh M., Lakshmi B., Balasubramanian K.A. Enterocyte viability and mitochondrial function after graded intestinal ischemia and reperfusion in rats. Mol. Cell. Biochem. 167:1997;81-87.
32. Bligh E.G., Dyer W.J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37:1959;911-917.
33. Chan H.W.S., Levett G. Autoxidation of methyl linoleate separation and analysis of isomeric mixtures of methyl linoleate hydroperoxides and methyl hydrolinoleates. Lipids. 12:1977;99-104.
34. Vatassery G.T. Oxidation of vitamin E in red cell membranes by fatty acids, hydroperoxides and selected oxidants. Lipids. 24:1989;299-304.
35. Madesh M., Balasubramanian K.A. Microtiter plate assay for superoxide dismutase using MTT reduction by superoxide. Ind. J. Biochem. Biophys. 35:1998;184-188.
36. Aebi H. Catalase in vitro. Methods Enzymol. 105:1984;121-126.
37. Awasthi Y.C., Dao D.D., Saneto R.P. Interrelationship between anionic and cationic forms of glutathione S-transferase of human liver. Biochem. J. 191:1980;1-10.
38. Nakamura W., Hosoda S., Havashi K. Purification and properties of rat liver glutathione peroxidase. Biochim. Biophys. Acta. 358:1974;251-261.
39. Racker E. Glutathione reductase (liver and yeast). Methods Enzymol. 2:1955;722-725.
40. White E. Death-defying acts a meeting reviews on apoptosis . Genes & Dev. 7:1993;2277-2284.
41. Oberhammer F., Pavelka M., Sharma S., Tiefenbacher R., Purchio A.F., Bursch W., Schutle-Hermann R. Induction of apoptosis in cultured hepatocytes and in regressing liver by transforming growth factor β1. Proc. Natl. Acad. Sci. USA. 89:1992;5408-5412.
42. Fukuda K., Kojiro M., Chiu J.F. Induction of apoptosis by transforming growth factor-beta 1 in the rat hepatoma cell line McA-RH7777 a possible association with tissue transglutaminase expression . Hepatology. 18:1993;945-953.
43. Albrecht H., Tschopp J., Jongeneel C.V. Bcl-2 protects from oxidative damage and apoptotic cell death without interfering with activation of NF-kappa B by TNF. FEBS Lett. 351:1994;45-48.
44. Forrest V.J., Kang Y.H., McClain D.E., Robinson D.H., Ramakrishnan N. Oxidative stress-induced apoptosis prevented by Trolox. Free Radic. Biol. Med. 16:1994;675-684.
45. Slater A.F., Nobel C.S., Orrenius S. The role of intracellular oxidants in apoptosis. Biochim. Biophys. Acta. 1271:1995;59-62.
46. Jones G.R. Cancer desturction in vivo through disrupted energy metabolism. Part I. The endogenous mechanism of self-destruction within the malignant cell, and the roles of endotoxin, certain hormones and drugs, and active oxygen in causing cellular injury and death. Physiol. Chem. Phys. Med. NMR. 24:1992;169-179.
47. Zamzami N., Marchetti P., Castedo M., Decaudin D., Macho A., Hirsch T., Susin S.A., Petit P.X., Mignotte B., Kroemer G. Sequential reduction of mitochndrial transmembrane potential and generation of reactive oxygen species in early programmed cell death. J. Exp. Med. 182:1995;367-377.
48. Merritt A.J., Potten C.S., Kemp C.J., Hickman J.A., Ballmain A., Lane D.P., Hall P.A. The role of p53 in spontaneous and radiation-induced apoptosis in the gastrointestinal tract of normal and p53-deficient mice. Cancer Res. 54:1994;614-617.
49. Moss S.F., Attia L., Scholes J.V., Walters J.R.F., Holt P.R. Increased small intestinal apoptosis in coeliac disease. Gut. 39:1996;811-817.
50. Flomerfelt F.A., Briehl M.M., Dowd D.R., Dieken E.S., Miesfeld R.L. Elevated glutathione S-transferase gene expression is an early event during steroid-induced lymphocyte apoptosis. J. Cell. Physiol. 154:1993;573-581.
51. Petit P.X., Susin S-A, Zamzami N., Mignotte B., Kroemer G. Mitochndria and programmed cell death back to the future . FEBS Lett. 396:1996;7-13.
52. Zamzami N., Hirsch T., Dallaporta B., Petit P.X., Kroemer G. Mitochondrial implication in accidental and programmed cell death apoptosis and necrosis . J. Bioenerg. Biomemb. 29:1997;185-193.