Skip to main content
Log in

Hydrogen peroxide-induced expression of the proto-oncogenes, c-jun, c-fos and c-myc in rabbit lens epithelial cells

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

The involvement of H2O2 in cataract development has been established inboth human patients and animal models. At the molecular level H2O2 has beenobserved to cause damage to DNA, protein and lipid. To explore the oxidativestress response of the lens system at the gene expression level, we haveexamined the effects of H2O2 on the mRNA change of the proto-oncogenes,c-jun, c-fos and c-myc in a rabbit lens cell line, N/N1003A. H2O2 treatmentof the rabbit lens epithelial cells for 60 min induces quick up-regulationof both c-jun and c-fos mRNAs. The maximal induction is 38 fold for c-jun at150 µM and 72 fold for c-fos at 250 µM H2O2. Treatment ofN/N1003A cells with 50-250 µM H2O2 for 60 min leads to a 2-5 foldincrease of the c-myc mRNA level. H2O2 also induces an up-regulation intransactivity of the activating protein-1 (AP-1) as shown with a reportergene driven by a prolactin gene promoter with 4 copies of AP-1 binding sitesinserted in the upstream of the promoter. Maximal induction occurs with 150µM H2O2. In the same system, the antioxidants, N-acetyl-cysteine (NAC)and pyrrolidine dithiocarbamate (PDTC) at concentrations shown toup-regulate the mRNAs of both c-jun and c-fos, also enhance thetransactivity of AP-1. NAC and PDTC have different effects in modulating theinduction of AP-1 activity by H2O2 and TPA. These results reveal thatoxidative stress regulates expression of various regulatory genes in lenssystems, which likely affects cell proliferation, differentiation andviability and thus affect normal lens functions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Spector A: Oxidative stress-induced cataract: Mechanism of action. FASEB J 9: 1173–1182, 1995

    Google Scholar 

  2. Spector A, Garner WH: Hydrogen peroxide and human cataract. Exp Eye Res 33: 673–681, 1981

    Google Scholar 

  3. Varma SD, Kumar S, Richards RD: Light induced damage to ocular lens pump. Prevention by vitamin C. Proc Natl Acad Sci USA 76: 3504–3506, 1979

    Google Scholar 

  4. Garner WH, Garner MH, Spector, A: H2O2 induced uncoupling of bovine lens Na+, K+-ATPase. Proc Natl Acad Sci USA 77: 1274–1277, 1983

    Google Scholar 

  5. Zigler JS Jr, Jernigan HM, Garland D, Reddy VN: The effect of oxygen radicals generated in the medium on lenses in organ culture, inhibition of damage by chelated iron. Arch Biochem Biophys 241: 163–172, 1985

    Google Scholar 

  6. Giblin FJ, McCready JP, Schrimscher L, Reddy VN: Peroxide-induced effects on lens cation transport following inhibition of glutathione reductase activity in vitro. Exp Eye Res 45: 77–91, 1987

    Google Scholar 

  7. Spector A, Wang GM, Wang RR: Photochemically induced cataract in rat lenses can be prevented by AL-3823A, a glutathione peroxidase mimic. Proc Natl Acad Sci USA 90: 7845–7849, 1993

    Google Scholar 

  8. Li W-C, Kuszak JR, Dunn K, Wang R-R, Ma W-C, Wang G-M, Spector A, Leib M, Cotliar AM, Weiss M, Espy J, Howard G, Farris RL, Auran J, Donn A, Hofeldt A, Mackay C, Merriam J, Mittl R, Smith TR: Lens epithelial cell apoptosis appears to be a common cellular basis for non-congenital cataract formation in humans and animals. J Cell Biol 130: 169–181, 1995

    Google Scholar 

  9. Li W-C, Spector A: Lens epithelial cell apoptosis is an early event during UVB induced cataract formation. Free Radic Biol Med 20: 301–311, 1996

    Google Scholar 

  10. Kleiman NJ, Wang RR, Spector A: Hydrogen peroxide induced DNA damage in bovine lens epithelial cells. Mutat Res 240: 35–45, 1990

    Google Scholar 

  11. Dische Z, Zil, H: Studies on the oxidation of cysteine to cysteine in lens proteins during cataract formation. Am J Ophthalmol 34: 104–113, 1951

    Google Scholar 

  12. Harding JJ: The nature and origin of the urea-insoluble protein of the human lens. Exp Eye Res 13: 33–40, 1972

    Google Scholar 

  13. Spector A, Garner WH: Glycosylation of lens proteins and its relationship to cataract. In: SK Srivastava (ed). The Red Blood Cell and Lens Metabolism. Elsevier North Holland, New York, 1980, pp 233–236

    Google Scholar 

  14. Bhuyan D K, Bhuyan KC: Regulation of hydrogen peroxide in eye humors: Effects of 3-amino-1H-1,2,4-triazole on catalase and glutathione peroxidase of rabbit eye. Biochem Biophys Acta 497: 641–651, 1977

    Google Scholar 

  15. Zigler JS, Huang QL, Du XY: Oxidative modification of lens crystalline by H2O2 and chelated iron. Free Radicals Biol Med 7: 499–505, 1989

    Google Scholar 

  16. Li W-C, Wang G-M, Wang R-R, Spector A: The redox active components H2O2 and N-acetyl-L-cysteine regulate expression of c-junand c-fosin lens systems. Exp Eye Res 59: 179–190, 1994

    Google Scholar 

  17. Reddan JR, Cheplinsky AB, Dziedzic DC, Piatigorsky J, Goldenberg EM: Retention of lens specificity in long-term cultures of diploid rabbit lens epithelial cells. Differentiation 33: 168–174, 1986

    Google Scholar 

  18. Storz G, Tartaglia LA, Farr SB, Ames BN: Bacterial defences against oxidative stress. Trends Genet 6: 363–368, 1990

    Google Scholar 

  19. Demple B, Amabile-Cuevas CF: Redox Redux: The control of oxidative stress response. Cell 67: 837–839, 1991

    Google Scholar 

  20. Fornace AJ Jr: Mammalian genes induced by radiation; Activation of genes associated with growth control. Annu Rev Genet 26: 507–526, 1992

    Google Scholar 

  21. Schreck R, Albermann K, Baeuerle PA: Nuclear factor ?B: An oxidative stress-responsive transcription factor of eukaryotic cells (areview). Free Radic Res Commun 17: 221–237, 1992

    Google Scholar 

  22. Shibanuma M, Kuroki T, Nose K: (1988). Induction of DNA replication and expression of proto-oncogene c-mycand c-fosin quiescent Balb/3T3 cells by xanthine/xanthine oxidase. Oncogene 3: 17–21, 1988

    Google Scholar 

  23. Crawford D, Zbinden I, Amstad P, Cerutti P: Oxidant stress induces the protooncogenes c-fosand c-mycin mouse epidermal cells. Oncogene 3: 27–32, 1988

    Google Scholar 

  24. Hollander MC, Fornace AJ Jr: Induction of fosRNA by DNA-damaging agents. Cancer Res 49: 1687–1692, 1989

    Google Scholar 

  25. Nose K, Shibanuma M, Kikuchi K, Kageyama H, Sakiyama S, Kuroki T: Transcriptional activation of early-response genes by hydrogen peroxide in a mouse osteoblastic cell line. Eur J Biochem 201: 99–106, 1991

    Google Scholar 

  26. Devary Y, Gottlieb RA, Lau LF, Karin M: Rapid and preferential activation of the c-jungene during the mammalian UV response. Mol Cell Biol 11: 2804–2811, 1991

    Google Scholar 

  27. Datta R, Hallahan DE, Kharbanda SM, Rubin E, Sherman ML, Huberman E, Weichselbaum RR, Kufe DW: Involvement of reactive oxygen intermediates in the induction of c-jungene transcription by ionizing radiation. Biochemistry 31: 8300–8306, 1992

    Google Scholar 

  28. Maki A, Berezesky IK, Fargnoli J, Holbrook NJ, Trump BF: Role of [Ca2+] in induction of fos, junand c-mycmRNA in rat PTE after oxidative stress. FASEB J 6: 919–924, 1992

    Google Scholar 

  29. Meyer M; Schreck R, Baeuerle PA: H2O2 and antioxidants have opposite effects on activation of NF-?B and AP-1 in intact cells: AP-1 As a secondary antioxidant-responsive factor. EMBO J 12: 2005–2115, 1993

    Google Scholar 

  30. Angel P, Karin M: The role of Jun, Fos and the AP-1 complex in cellproliferation and Transformation. Biochem Biophys Acta 1072, 129–157, 1991

    Google Scholar 

  31. Curran T, Vogt PK: Dangerous liaisons: Fos and Jun, oncogenic transcription factors. In: SL Mcknight and KR Yamamoto (eds). Transcriptional Regulation. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1992, pp 797–831

    Google Scholar 

  32. Marcu KB, Bossone SA, Patel AJ: Mycfunction and regulation. Ann Rev Biochem 61: 809–860, 1992

    Google Scholar 

  33. Evan GI, Brown L, Whyte M, Harrington E: Apoptosis and the cell cycle. Curr Opin Cell Biol 7: 825–834, 1995

    Google Scholar 

  34. Evan GI, Littlewood TD: The role of c-mycin cell growth. Curr Opin Genet Dev 3: 44–49, 1993

    Google Scholar 

  35. Depinho RA, Schreiber-Agus N, Alt FW: Myc family oncogenes in the development of normal and neoplastic cells. Adv Cancer Res 57: 1–46, 1991

    Google Scholar 

  36. Kelly K, Cochran BH, Stiles CD, Leder P: Cell-specific regulation of the c-mycgene by lymphocyte mitogens and platelet-derived growth factor. Cell 35: 603–610, 1983

    Google Scholar 

  37. Rao GN, Church RL: Regulation of expression of c-mycprotooncogene in a clonal line of mouse lens epithelial cells by serum growth factors. Exp Cell Res 183: 140–148, 1989

    Google Scholar 

  38. Reuse S, Maenhaut C, Dumont JE: Regulation of expression of c-mycprotooncogenes c-fosand c-mycexpression by protein tyrosine kinase, protein kinase C, and cyclic AMP mitogenic pathways in dog primary thymocites: A positive and negative control by cyclic AMP on c-mycexpression. Exp Cell Res 189: 33–44

  39. Rinaudo JAS, Zelenka PS: Expression of c-fosand c-junmRNA in the developing chicken lens: Relationship to cell proliferation, quiescence, and differentiation. Exp Cell Res 199: 147–153, 1992

    Google Scholar 

  40. Rinaudo JAS, Vachiano E, Zelenka PS: Effects of c-junand a negative dominant mutation of c jun on differentiation and gene expression in lens epithelial cell cells. J Cell Biochem 58: 237–247, 1995

    Google Scholar 

  41. Nath P, Getzenberg R, Beebe D, Pallansch L, Zelenka P: c-mycmRNA is elevated as differentiating lens cells withdraw from cell cycle. Exp Cell Res. 169: 215–222, 1987

    Google Scholar 

  42. Harris LL, Talian JC, Zelenka PZ: Contrasting pattern of c-mycand N-mycexpression in proliferating, quiescent, and differentiating cells of the embryonic chicken lens. Development 115: 813–820, 1992

    Google Scholar 

  43. Wen Y, Shu S, Unakar NJ, Bekhor I: Expression of c-mycprotooncogene in rat lens cells during development, maturation and reversal of galactose cataracts. Mol Cell Biochem 112: 73–79, 1992

    Google Scholar 

  44. Yamada S, Ikeda M, Eto K: Differential expression of c-mycand Nmycduring oral organogenesis of the mouse embryo. Dev Growth Differ 34: 239–251, 1992

    Google Scholar 

  45. Morgenbesser SD, Schreiber-Agus N, Bidder M, Mahon KA, Overbeek PA, Homer J, Depinho RA: Contrasting roles for c-Myc and L-Myc in the regulation of cellular growth and differentiation in vivo. EMBO J 14: 743–756, 1995

    Google Scholar 

  46. Hildebrandt AG, Root I, Tjoe M, Heinemeyer G: Hydrogen peroxide in hepatic microsome. Meth Enzymol LII: 342–350, 1978

    Google Scholar 

  47. Curran T, Gordon MB, Rubino KL, Sambucetti LC: Isolation and characterization of the c-fos(rat) cDNA and analysis of post-translational modification in vitro. Oncogene 2: 79–84, 1987

    Google Scholar 

  48. Macgregor PF, Abate C, Curran T: Direct cloning of leucine zipper proteins: Jun binds cooperatively to the CRE with CRE-BP1. Oncogene 5: 451–458, 1990

    Google Scholar 

  49. Stanton LW, Fahrlander PD, Tesser PM, Marcu KB: Nucleotide sequence comparison of normal and translocated murine c-mycgenes. Nature 310: 423–425, 1984

    Google Scholar 

  50. Tso JY, Sun XH, Kao TH, Reece KS, Wu R: Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: Genomic complexity and molecular evolution of the gene. Nucleic Acids Res 13: 2485–2502, 1985

    Google Scholar 

  51. Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JE, Smith JA, Struhl K: Current Protocols in Molecular Biology. John Wiley and Sons, New York, 1995

    Google Scholar 

  52. Feinberg AP, Vogelstein B: A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132: 6–13, 1983

    Google Scholar 

  53. Chomczynski P, Sacchi N: Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162, 156–159, 1987

    Google Scholar 

  54. Thomas PS: Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc Natl Acad Sci USA 77: 5201–5205, 1980

    Google Scholar 

  55. Li W-C, Riddiford LM: The two duplicated insecticyanin genes, insaand ins-bare differentially expressed in the tobacco hornworm, Manduca sexta. Nucl Acids Res 22: 2945–2950, 1994

    Google Scholar 

  56. Borras T, Peterson CA, Piatigorsky J: Evidence for positive and negative regulation in the promoter of the chicken ?-crystallin gene. DevBiol 127, 209–219, 1988

    Google Scholar 

  57. Chen C, Okayama H: High efficiency transformation of mammalian cells by plasmid DNA. Mol Cell Biol 7: 2745–2752, 1987

    Google Scholar 

  58. Brasier AR, Tate JE, Habener JF: Optimized use of the firefly luciferase assay as a reporter gene in mammalian cell lines. BioTechniques 7: 1116–1122, 1989

    Google Scholar 

  59. Nielsen DA, Chou J, MacKrell AJ, Casadaban MJ, Steiner DF: Expression of a preproinsulin-?-galactosidasegene fusion in mammalian cells. Proc Natl Acad Sci USA 80: 5198–5202, 1983

    Google Scholar 

  60. Cheplinsky AB, Sommer B, Piatigorsky J: Interaction between two different regulatory elements activates the murine ?A-crystallin gene promoter in explanted lens epithelia. Mol Cell Biol 7: 1807–1814, 1987

    Google Scholar 

  61. Meister A: Glutathione deficiency produced by inhibition of its synthesis and its reversal, applications in research and therapy. Pharmacol Therap 51: 155–194, 1991

    Google Scholar 

  62. Keyse SM, Tyrrell RM: Heme oxygenase is the major 32-kDa stress protein induced in human skin fibroblasts by UVA-radiation, hydrogen peroxide and sodium arsenate. Proc Natl Acad Sci USA 86: 99–103, 1989

    Google Scholar 

  63. Keyse SM, Applegate LA, Tromvoukis Y, Tyrrell RM: Oxidant stress leads to transcriptional activation of the human heme oxygenase gene in cultured skin fibroblasts. Mol Cell Biol 10: 4967–4868, 1990

    Google Scholar 

  64. Shull S, Heintz NH, Periasamy M, Manohar M, Janssen YMW, Marsh JP Mossman BT: Differential regulation of antioxidant enzymes in response to oxidants. J Biol Chem 266: 24398–24403, 1991

    Google Scholar 

  65. Schreck R, Albermann K, Baeuerle PA: Reactive oxygen intermediates as apparently widely used messengers in the activation of the NF-?B transcription factor and HIV-1. EMBO J 10: 2247–2258, 1991

    Google Scholar 

  66. Bhuyan DK, Li W-C, Kuriakose G, Spector A, Bhuyan KC: Up-regulation of antioxidative gene expression in the lenses of emory mice subjected to oxidative stress. Invest Ophthalmol Vis Sci 36: S409, 1995

    Google Scholar 

  67. Piatigorsky J, Zelenka PS: Transcription regulation of crystallin genes: Cis elements, trans-factors, and signal transduction systems in the lens. Adv Dev Biochem 1: 211–256, 1992

    Google Scholar 

  68. McDermott JB, Paterson CA, Piatigorsky J: Structure and lens expression of the gene encoding chicken ?A3/A1-crystallin. Gene 117: 193–200, 1992

    Google Scholar 

  69. Thompson MA, Hawkins JW, Piatigorsky J: Complete nucleotide sequence of the chicken ?A-crystallin gene and its 5??flank sequence Gene 56: 173–184, 1987

    Google Scholar 

  70. Cvekl A, Sax CM, Brensnick EH, Piatigorsky J: A complex array of positive and negative elements regulates the chicken ?A-crystallin gene: Involvement of Pax-6, USF, CREB and/or CREM, and AP-1 proteins. Mol Cell Biol 14: 7363–7376, 1994

    Google Scholar 

  71. Evan GI, Wyllie AH, Gibert CS, Littlewood TD, Land H, Brooks M, Waters CM, Penn LZ, Hancock DC: Induction of apoptosis in fibroblasts by c-mycprotein. Cell 69: 119–128, 1992

    Google Scholar 

  72. Abate C, Patel L, Rauscher III FJ, Curran T: Redox regulation of Fos and Jun DNA binding activity in vitro. Science 249: 1157–1161, 1990

    Google Scholar 

  73. Xanthoudakis S, Miao G, Wang F, Pan YC, Curran T: Redox-activation of Fos-Jun DNA binding activity is mediated by a DNA repair enzyme. EMBO J 11: 3323–3335, 1992

    Google Scholar 

  74. Walker L J, Robson CN, Black E, Gillespie D, Hickson ID: Identification of residues in the human DNA repair enzyme HAP1 (Ref. [1]) that are essential for redox regulation of Jun DNA binding. Mol Cell Biol 13: 5370–5376, 1993

    Google Scholar 

  75. Barone MV, Courtneidge SA: Myc but not Fos rescue of PDGF signaling blockage caused by kinase-inactive Src. Nature 378: 509–512, 1995

    Google Scholar 

  76. Lander HM, Ogiste JS, Teng KK, Novogrodsky A: p21ras as a common signaling target of reactive free radicals and cellular redox stress. J Biol Chem 270: 21195–21198, 1995

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Li, D.WC., Spector, A. Hydrogen peroxide-induced expression of the proto-oncogenes, c-jun, c-fos and c-myc in rabbit lens epithelial cells. Mol Cell Biochem 173, 59–69 (1997). https://doi.org/10.1023/A:1006828402225

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006828402225

Navigation