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Original

Retinol and retinoic acid increase MMP-2 activity by different pathways in cultured Sertoli cells

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Pages 1338-1347 | Published online: 07 Jul 2009

References

  • Finkel T. Oxidant signals and oxidative stress. Current Opinion in Cell Biology 2003; 15: 247–254
  • Haddad JJ. Antioxidant and prooxidant mechanisms in the regulation of redox(y)-sensitive transcription factors. Cellular Signalling 2002; 14: 879–897
  • Jackson AL, Loeb LA. The contribution of endogenous sources of DNA damage to the multiple mutations in cancer. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2001; 477: 7–21
  • Visse R, Nagase H. Matrix metalloproteinases and tissue inhibitors of metalloproteinases-Structure, function, and biochemistry. Circulation Research 2003; 92: 827–839
  • Bode W, Maskos K. Structural basis of the matrix metalloproteinases and their physiological inhibitors, the tissue inhibitors of metalloproteinases. Biological Chemistry 2003; 384: 863–872
  • McCawley LJ, Matrisian LM. Matrix metalloproteinases: they're not just for matrix anymore!. Current Opinion in Cell Biology 2001; 13: 534–540
  • Coussens LM, Fingleton B, Matrisian LM. Cancer therapy-Matrix metalloproteinase inhibitors and cancer: Trials and tribulations. Science 2001; 295: 2387–2392
  • Sternlicht MD, Werb Z. How matrix metalloproteinases regulate cell behavior. Annual Review of Cell and Developmental Biology 2001; 17: 463–516
  • Nelson KK, Melendez JA. Mitochondrial redox control of matrix metalloproteinases. Free Radical Biology and Medicine 2004; 37: 768–784
  • Overall CM. Molecular determinants of metalloproteinase substrate specificity-Matrix metalloproteinase substrate binding domains, modules, and exosites. Molecular Biotechnology 2002; 22: 51–86
  • Overall CM, Kleifeld O. Tumour microenvironment-Opinion-Validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy. Nature Reviews Cancer 2006; 6: 227–239
  • El Ramy R, Verot A, Mazaud S, Odet F, Magre S, Magueresse-Battistoni B. Fibroblast growth factor (FGF) 2 and FGF9 mediate mesenchymal-epithelial interactions of peritubular and Sertoli cells in the rat testis. Journal of Endocrinology 2005; 187: 135–147
  • Longin J, Guillaumot P, Chauvin VA, Morera AM, Magueresse-Battistoni B. MT1-MMP in rat testicular development and the control of Sertoli cell proMMP-2 activation. Journal of Cell Science 2001; 114: 2125–2134
  • Longin J, Magueresse-Battistoni B. Evidence that MMP-2 and TIMP-2 are at play in the FSH-induced changes in Sertoli cells. Molecular and Cellular Endocrinology 2002; 189: 25–35
  • Palace VP, Khaper N, Qin QI, Singal PK. Antioxidant potentials of vitamin A and carotenoids and their relevance to heart disease. Free Radical Biology and Medicine 1999; 26: 746–761
  • Dal Pizzol F, Klamt F, Frota MLC, Moraes LF, Moreira JCF, Benfato MS. Retinol supplementation induces DNA damage and modulates iron turnover in rat Sertoli cells. Free Radical Research 2000; 33: 677–687
  • de Oliveira RB, Klamt F, Castro MAA, Polydoro M, Zanotto-Filho A, Gelain DP, Dal Pizzol F, Moreira JCF. Morphological and oxidative alterations on Sertoli cells cytoskeleton due to retinol-induced reactive oxygen species. Molecular and Cellular Biochemistry 2005; 271: 189–196
  • Moreira JCF, Dal Pizzol F, Von Endt D, Bernard EA. Effect of retinol on chromatin structure in Sertoli cells: 1,10-phenanthroline inhibit the increased DNAse I sensitivity induced by retinol. Medical Science Research 1997; 25: 635–638
  • Dal Pizzol F, Klamt F, Benfato MS, Bernard EA, Moreira JCF. Retinol supplementation induces oxidative stress and modulates antioxidant enzyme activities in rat sertoli cells. Free Radical Research 2001; 34: 395–404
  • de Oliveira RB, Pasquali MAB, Zanotto-Filho A, Dalmolin RJS, Gelain DP, Gottfried C, Rodrigues JL, Klamt F, Moreira JCF. Can electrons travel through actin microfilaments and generate oxidative stress in retinol treated Sertoli cell?. Molecular and Cellular Biochemistry 2007; 301: 33–45
  • Klamt F, Dal Pizzol F, Roehrs R, de Oliveira RB, Dalmolin RJS, Henriques JAP, de Andrades HHR, Ramos ALLD, Saffi J, Moreira JCF. Genotoxicity, recombinogenicity and cellular preneoplasic transformation induced by Vitamin A supplementation. Mutation Research-Genetic Toxicology and Environmental Mutagenesis 2003; 539: 117–125
  • Gelain DP, Cammarota M, Zanotto-Filho A, de Oliveira RB, Dal Pizzol F, Izquierdo I, Bevilaqua LRM, Moreira JCF. Retinol induces the ERK 1/2-dependent phosphorylation of CREB through a pathway involving the generation of reactive oxygen species in cultured Sertoli cells. Cellular Signalling 2006; 18: 1685–1694
  • Lebel CP, Ischiropoulos H, Bondy SC. Evaluation of the Probe 2′,7′-Dichlorofluorescin As An Indicator of Reactive Oxygen Species Formation and Oxidative Stress. Chemical Research in Toxicology 1992; 5: 227–231
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein Measurement with the Folin Phenol Reagent. Journal of Biological Chemistry 1951; 193: 265–275
  • Roux PP, Blenis J. ERK and p38 MAPK-Activated Protein Kinases: a Family of Protein Kinases with Diverse Biological Functions. Microbiology and Molecular Biology Reviews 2004; 68: 320–344
  • Newton R, Cambridge L, Hart LA, Stevens DA, Lindsay MA, Barnes PJ. The MAP kinase inhibitors, PD098059, UO126 and SB203580, inhibit IL-1β-dependent PGE 2 release via mechanistically distinct processes. British Journal of Pharmacology 2000; 130: 1353–1361
  • Favata MF, Horiuchi KY, Manos EJ, Daulerio AJ, Stradley DA, Feeser WS, Van Dyk DE, Pitts WJ, Earl RA, Hobbs F, Copeland RA, Magolda RL, Scherle PA, Trzaskos JM. Identification of a novel inhibitor of mitogen-activated protein kinase kinase. Journal of Biological Chemistry 1998; 273: 18623–18632
  • Morgunova E, Tuuttila A, Bergmann U, Isupov M, Lindqvist Y, Schneider G, Tryggvason K. Structure of human pro-matrix metalloproteinase-2: Activation mechanism revealed. Science 1999; 284: 1667–1670
  • Murata M, Kawanishi S. Oxidative DNA Damage by Vitamin A and Its Derivative via Superoxide Generation. Journal of Biological Chemistry 2000; 275: 2003–2008
  • Klamt F, Dal Pizzol F, Ribeiro NC, Barnard EA, Benfato MS, Moreira JCF. Retinol-induced elevation of ornithine decarboxylase activity in cultured rat Sertoli cells is attenuated by free radical scavenger and by iron chelator. Molecular and Cellular Biochemistry 2000;208:71–76.
  • Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature 2000; 408: 239–247
  • Kamata H, Hirata H. Redox regulation of cellular signalling. Cellular Signalling 1999; 11: 1–14
  • Aikawa R, Komuro I, Yamazaki T, Zou YZ, Kudoh S., Tanaka M, Shiojima I, Hiroi Y, Yazaki Y. Oxidative stress activates extracellular signal-regulated kinases through Src and ras in cultured cardiac myocytes of neonatal rats. Journal of Clinical Investigation 1997; 100: 1813–1821
  • Biswas S, Chida AS, Rahman I. Redox modifications of protein-thiols: Emerging roles in cell signaling. Biochemical Pharmacology 2006; 71: 551–564
  • Rhee SG, Kang SW, Jeong W, Chang TS, Yang KS, Woo HA. Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins. Current Opinion in Cell Biology 2005; 17: 183–189
  • Cheng FC, Jen JF, Tsai TH. Hydroxyl radical in living systems and its separation methods. Journal of Chromatography B 2002; 781: 481–496
  • Goldstein S, Czapski G. Mannitol as an OH Scavenger in Aqueous Solutions and in Biological Systems. International Journal of Radiation Biology 1984; 46: 725–729
  • Davis RJ. Mapks-New Jnk Expands the Group. Trends in Biochemical Sciences 1994; 19: 470–473
  • Robinson MJ, Cobb MH. Mitogen-activated protein kinase pathways. Current Opinion in Cell Biology 1997; 9: 180–186
  • Westermarck J, Li SP, Kallunki T, Han JH, Kahari VM. p38 mitogen-activated protein kinase-dependent activation of protein phosphatases 1 and 2A inhibits MEK1 and MEK2 activity and collagenase 1 (MMP-1) gene expression. Molecular and Cellular Biology 2001; 21: 2373–2383
  • Overall CM, Lopez-Otin C. Strategies for MMP inhibition in cancer: Innovations for the post-trial era. Nature Reviews Cancer 2002; 2: 657–672
  • Clerk A, Michael A, Sugden PH. Stimulation of multiple mitogen-activated protein kinase sub-families by oxidative stress and phosphorylation of the small heat shock protein, HSP25/27, in neonatal ventricular myocytes. Biochemical Journal 1998; 333: 581–589
  • Kefaloyianni E, Gaitanaki C, Beis I. ERK1/2 and p38-MAPK signalling pathways, through MSK1, are involved in NF-kappa B transactivation during oxidative stress in skeletal myoblasts. Cellular Signalling 2006; 18: 2238–2251
  • Klamt F, de Oliveira MR, Moreira JCF. Retinol induces permeability transition and cytochrome c release from rat liver mitochondria. Biochimica et Biophysica Acta-General Subjects 2005; 1726: 14–20
  • Napoli JL. Interactions of retinoid binding proteins and enzymes in retinoid metabolism. Biochimica et Biophysica Acta-Molecular and Cell Biology of Lipids 1999; 1440: 139–162
  • Bost L, Caron L, Marchetti I, Dani C, Marchand-Brustel Y, Binetruy B. Retinoic acid activation of the ERK pathway is required for embryonic stem cell commitment into the adipocyte lineage. Biochemical Journal 2002; 361: 621–627
  • Yen A, Roberson MS, Varvayanis S, Lee AT. Retinoic acid induced mitogen-activated protein (MAP) extracellular signal-regulated kinase (ERK) kinase-dependent MAP kinase activation needed to elicit HL-60 cell differentiation and growth arrest. Cancer Research 1998; 58: 3163–3172
  • Canon E, Cosgaya JM, Scsucova S, Aranda A. Rapid effects of retinoic acid on CREB and ERK phosphorylation in neuronal cells. Molecular Biology of the Cell 2004; 15: 5583–5592
  • Watson REB, Ratnayaka JA, Brooke RCC, Yee-Sit-Yu S, Ancian P, Griffiths CEM. Retinoic acid receptor alpha expression and cutaneous ageing. Mechanisms of Ageing and Development 2004; 125: 465–473
  • Ulisse S, Rucci N, Piersanti D, Carosa E, Graziano FM, Pavan A, Ceddia P, Arizzi M, Muzi P, Cironi L, Gnessi L, D'Armiento M, Jannini EA. Regulation by thyroid hormone of the expression of basement membrane components in rat prepubertal Sertoli cells. Endocrinology 1998; 139: 741–747
  • Klamt F, Dal-Pizzol F, Gelain DP, Dalmolin RJS, de Oliveira RB, Bastiani M, Horn F, Moreira JCF. Vitamin A treatment induces apoptosis through an oxidant-dependent activation of the mitochondrial pathway. Cell Biology International 2007; In press.
  • Dal Pizzol F, Klamt F, Dalmolin RJS, Bernard EA, Moreira JCF. Mitogenic signaling mediated by oxidants in retinol treated sertoli cells. Free Radical Research 2001; 35: 749–755

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