Effect of Hydrogen Peroxide on Interleukin-8 Synthesis and Death of Caco-2 Cells

REFERENCES

• Malago J.J., Koninkx J.F.J.G., Tooten P.C.J., van Liere E., van Dijk J.E. Anti-inflammatory properties of Hsp70 and butyrate on Salmonella-induced IL-8 secretion in enterocyte-like Caco-2 cells. Clin. Exp. Immunol. 2005; 141(1)62–71
   PubMed Web of Science ®Google Scholar
• Yamamoto K., Kushima R., Kisaki O., Fujiyama Y., Okabe H. Combined effect of hydrogen peroxide-induced oxidative stress and IL-1β on IL-8 production in Caco-2 cells (a human colon carcinoma cell line) and normal intestinal epithelial cells. Inflammation 2003; 27(3)123–128
   PubMedGoogle Scholar
• Ebert E.C. Tumour necrosis factor-α enhances intra-epithelial lymphocyte proliferation and migration. Gut 1998; 42: 650–655
   PubMedGoogle Scholar
• O'Farelly C. Just how inflamed is the normal gut?. Gut 1998; 42: 613–606
   Google Scholar
• Baggiolini M., Loetscher P., Moser B. Interleukin-8 and the chemokine family. Int. J. Immunopharmacol. 1995; 17: 103–108
   PubMed Web of Science ®Google Scholar
• Huber A.R., Kunkel S.L., Todd R.F., Weiss S.J. Regulation of transendothelial neutrophil migration by endogenous interleukin-8. Science 1991; 254: 99–102
   PubMed Web of Science ®Google Scholar
• Gerard C., Rollins B.J. Chemokines and diseases. Nat. Immunol. 2001; 2: 108–115
   PubMed Web of Science ®Google Scholar
• Seitz M., Dewald B., Ceska M., Gerber N., Baggioloni M. Interleukin-8 in inflammatory rheumatic diseases: synovial fluid levels, relation to rheumatoid factors, production by mononuclear cells, and effects of gold sodium thiomalate and methotrexate. Rheumatol. Int. 1992; 12: 159–164
   PubMedGoogle Scholar
• Mahida Y.R., Ceska M., Effenberger F., Kurlak L., Lindley I., Hawkey C.J. Enhanced synthesis of neutrophil-activating peptide-1/interleukin-8 in active ulcerative colitis. Clin. Sci. 1992; 82: 273–275
   Web of Science ®Google Scholar
• Josse C., Boelaert J.R., Best-Belpomme M., Piette J. Importance of post-transcriptional regulation of chemokine genes by oxidative stress. Biochem. J. 2001; 360: 321–333
   PubMed Web of Science ®Google Scholar
• Mukaida N., Okamoto S., Ishikawa Y., Matsushima K. Molecular mechanism of interleukin-8 gene expression. J. Leukoc. Biol. 1994; 56: 554–558
   PubMed Web of Science ®Google Scholar
• Li Q., Verma I.M. NF-kappaB regulation in the immune system. Nat. Rev. Immunol. 2002; 2: 725–734
   PubMed Web of Science ®Google Scholar
• Sies H. Oxidative stress: introductory remarks. Oxidative Stress, H. Sies. Academic Press, London 1985; 1–7
   Google Scholar
• Chandra J., Samali A., Orrenius S. Triggering and modulation of apoptosis by oxidative stress. Free Rad. Biol. Med. 2000; 29: 323–333
   PubMed Web of Science ®Google Scholar
• Slater T.F. Free-radical mechanisms in tissue injury. Biochem. J. 1984; 222: 1–15
   PubMed Web of Science ®Google Scholar
• Caporossi D., Ciafre S.A., Pittaluga M., Savini I., Farace M.G. Cellular responses to H2O2 and bleomycin-induced oxidative stress in L6C5 rat myoblasts. Free Radical. Biol. Med. 2003; 35: 1355–1364
   PubMed Web of Science ®Google Scholar
• Stocker R., Keaney J.F., Jr. Role of oxidative modifications in atherosclerosis. Physiol. Rev. 2004; 84: 1381–1478
   PubMed Web of Science ®Google Scholar
• Storz P. Reactive oxygen species in tumor progression. Front. Biosci. 2005; 10: 1881–1896
   PubMed Web of Science ®Google Scholar
• Fink S.L., Cookson B.T. Apoptosis, pyrptosis, and necrosis: mechanistic description of dead and dying eukaryotic cells. Infect. Immun. 2005; 74(4)1907–1916
   Google Scholar
• Majno G., Joris I. Apoptosis, oncosis, and necrosis. An overview of cell death. Am. J. Pathol. 1995; 146: 3–15
   PubMed Web of Science ®Google Scholar
• Suzuki T., Fujikura K., Higashiyama T., Takata K. DNA staining for fluorescence and laser confocal microscopy. J. Hist. Cytochem. 1997; 45(1)49–53
   PubMedGoogle Scholar
• McConkey D.J., Hartzell P., Nicotera P., Wyllie A.H., Orrenius S. Stimulation of endogenous endonuclease activity in hepatocytes exposed to oxidative stress. Toxicol. Lett. 1988; 42: 123–130
   PubMed Web of Science ®Google Scholar
• Wang T.G., Gotoh Y., Yennings M.H., Rhoads C A., Aw T.Y. Lipid hydroperoxide-induced apoptosis in human colonic CaCo-2 cells is associated with an early loss of cellular redox balance. FASEB J. 2000; 14(11)1567–1576
   PubMedGoogle Scholar
• Gumbiner B., Lowenkopf T., Apatira D. Identification of a 160-kDa polypeptide that binds to the tight junction protein ZO-1. Proc. Natl. Acad. Sci. USA 1991; 88: 3460–3464
   PubMed Web of Science ®Google Scholar
• Anderson J.M., Van Itallie C.M. Tight junctions and the molacular basis for regulation of paracellular permeability. Am. J. Physiol. 1995; 269: G467–475
   PubMed Web of Science ®Google Scholar
• Chen Y., Lu Q., Schneeberg E.E., Goodenough D.A. Restoration of tight junction structure and barrier function by down-regulation of the mitogen-activated protein kinase pathway in Ras- transformed Madin-Darby canine kidney cells. Mol. Biol. Cell. 2000; 11: 849–862
   PubMed Web of Science ®Google Scholar
• McCarthy K.M., Skare I.B., Stankewich M.C., Furuse M., Tsukita S., et al. Occludin is a functional component of the tight junction. J. Cell Sci. 1996; 109: 2287–2298
   PubMed Web of Science ®Google Scholar
• McNeill-Blue C., Wetmore B.A., Sanchez J.F., Freed W.J., Merrick B.A. Apoptosis mediated by p53 in rat neural AF5 cells following treatment with hydrogen peroxide and staurosporine. Brain Res. 2006; 1112(1)1–5
   PubMedGoogle Scholar
• Verhasselt V., Goldman M., Willems F. Oxidative stress upregulates IL-8 and TNF-α synthesis by human dendritic cells. Eur. J. Immunol. 1998; 28: 3886–3890
   PubMed Web of Science ®Google Scholar
• Rao R., Baker R.D., Baker S.S. Inhibition of oxidant-induced barrier disruption and protein tyrosine phosphorylation in Caco-2 cell monolayers by epidermal growth factor. Biochem. Pharmacol. 1999; 5: 685–695
   Google Scholar
• Manna C., Galletti P., Cucciolla V., Moltedo O., Leone A., Zappia V. The protective effect of the olive oil polyphenol (3,4-dihydroxyphenyl) ethanol counteracts reactive oxygen metabolite-induced cytotoxicity in Caco-2 cells. J. Nutr. 1997; 127: 286–292
   PubMed Web of Science ®Google Scholar
• Liu L.-N., Mei Q.-B., Liu L., Zhang F., Liu Z.-G., et al. Protective effects of Rheum tanguticum polysaccharide against hydrogen-peroxide–induced intestinal epithelial cell injury. World J. Gastroenterol. 2005; 11: 1503–1507
   PubMed Web of Science ®Google Scholar