Reactive Oxygen Species as Mediators of Signal Transduction in Cardiovascular Disease

  • Jun-ichi Abe
  • Bradford C. Berk
Part of the Developments in Cardiovascular Medicine book series (DICM, volume 233)

Abstract

Cells respond to extracellular stimuli by transmitting intracellular messengers to coordinate appropriate responses. The process that transduces the extracellular message across plasma membranes into the intracellular environment is called signal transduction or cell signaling. Recently, reduction-oxidation (redox) reactions that generate reactive oxygen species (ROS) have gained attention as important chemical processes that regulate signal transduction. Accumulating evidence indicates that excessive ROS may be pathogenic for a wide variety of human diseases.

Keywords

Extracellular Signal Regulate Kinase Compensatory Enlargement Kinase Signal Transduction Pathway Growth Factor Signal Transduction Pyridinyl Imidazole 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    Rimm EB, Stampfer MJ, Ascherio A, Giovannucci E, Colditz GA, Willett WC. Vitamin E consumption and the risk of coronary heart disease in men. N Engl J Med 1993;328:1450–6.PubMedCrossRefGoogle Scholar
  2. 2.
    Stephens NG, Parsons A, Schofield PM, Kelly F, Cheeseman K, Mitchinson MJ. Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS). Lancet 1996;347(9004):781–6.PubMedCrossRefGoogle Scholar
  3. 3.
    Starkebaum G, Harlan JM. Endothelial cell injury due to copper-catalyzed hydrogen peroxide generation from homocysteine. J Clin Invest 1986;77(4):1370–6.PubMedCrossRefGoogle Scholar
  4. 4.
    Nygard O, Nordrehaug JE, Refsum H, Ueland PM, Farstad M, Vollset SE. Plasma homocysteine levels and mortality in patients with coronary artery disease. N Engl J Med 1997;337:230–6.PubMedCrossRefGoogle Scholar
  5. 5.
    Nunes GL, Sgoutas DS, Redden RA, Sigman SR, Gravanis MB, King SBr, et al. Combination of vitamins C and E alters the response to coronary balloon injury in the pig. Arterioscler Thromb Vase Biol 1995;15(1):156–65.CrossRefGoogle Scholar
  6. 6.
    Mulvany MJ, Baumbach GL, Aalkjaer C, Heagerty AM, Korsgaard N, Schiffrin EL, et al. Vascular remodeling. Hypertension 1996;28(3):505–6.PubMedGoogle Scholar
  7. 7.
    Nunes GL, Robinson K, Kalynych A, King III SB, Sgoutas DS, Berk BC. Vitamins C and E inhibit O2 production in the pig coronary artery. Circulation 1997;96:3593–601.Google Scholar
  8. 8.
    Abe J, Kusuhara M, Ulevitch RJ, Berk BC, Lee JD. Big mitogen-activated protein kinase 1 (BMK1) is a redox-sensitive kinase. J Biol Chem 1996;271(28):16586–90.PubMedCrossRefGoogle Scholar
  9. 9.
    Baas AS, Berk BC. Differential activation of mitogen-activated protein kinases by H202 and 02invascular smooth muscle cells. Cire Res 1995;77(1):29–36.CrossRefGoogle Scholar
  10. 10.
    Sundaresan M, Yu ZX, Ferrans VJ, Irani K, Finkel T. Requirement for generation of H2O2 for platelet-derived growth factor signal transduction. Science 1995;270(5234):296–9.PubMedCrossRefGoogle Scholar
  11. 11.
    Irani K, Xia Y, Zweier JL, Sollott SJ, Der CJ, Fearon ER, et al. Mitogenic signaling mediated by oxidants in Ras-transformed fibroblasts. Science 1997;275(5306):1649–52.PubMedCrossRefGoogle Scholar
  12. 12.
    Suh YA, Arnold RS, Lassegue B, Shi J, Xu X, Sorescu D, et al. Cell transformation by the superoxide-generating oxidase Moxl. Nature 1999;401(6748):79–82.PubMedCrossRefGoogle Scholar
  13. 13.
    Dugan LL, Creedon DJ, Johnson EM, Holtzman DM. Rapid suppression of free radical formation by nerve growth factor involves the mitogen-activated protein kinase pathway. Proceedings Of The National Academy Of Sciences Of The United States Of America 1997;94(8):4086–91.PubMedCrossRefGoogle Scholar
  14. 14.
    Nakamura K, Hori T, Sato N, Sugie K, Kawakami T, Yodoi J. Redox regulation of a src family protein tyrosine kinase p561ck in T cells. Oncogene 1993;8(11):3133–9.PubMedGoogle Scholar
  15. 15.
    Schieven GL, Mittler RS, Nadler SG, Kirihara JM, Bolen JB, Kanner SB, et al. ZAP-70 tyrosine kinase, CD45, and T cell receptor involvement in UV- and H202-induced T cell signal transduction. J Biol Chem 1994;269(32):20718–26.PubMedGoogle Scholar
  16. 16.
    Bolen JB, Rowley RB, Spana C, Tsygankov AY. The Src family of tyrosine protein kinases in hemopoietic signal transduction. Faseb J 1992;6(15):3403–9.PubMedGoogle Scholar
  17. 17.
    Pascal SM, Singer AU, Gish G, Yamazaki T, Shoelson SE, Pawson T, et al. Nuclear magnetic resonance structure of an SH2 domain of phospholipase C-gamma 1 complexed with a high affinity binding peptide. Cell 1994;77(3):461–72.PubMedCrossRefGoogle Scholar
  18. 18.
    Klages S, Adam D, Class K, Fargnoli J, Bolen JB, Penhallow RC. Ctk: a protein-tyrosine kinase related to Csk that defines an enzyme family. Proc Natl Acad Sci U S A 1994;91(7):2597–601.PubMedCrossRefGoogle Scholar
  19. 19.
    Cooper JA, Howell B. The when and how of Src regulation. Cell 1993;73(6):1051–4.PubMedCrossRefGoogle Scholar
  20. 20.
    Yu XM, Askalan R, Keil GJ, 2nd, Salter MW. NMDA channel regulation by channel-associated protein tyrosine kinase Src. Science 1997;275(5300):674–8.PubMedCrossRefGoogle Scholar
  21. 21.
    Shalloway D, Bagrodia S, Chackalaparampil I, Shenoy S, Lin PH, Taylor SJ. c-Src and mitosis. Ciba Found Symp 1992;170:248–65.PubMedGoogle Scholar
  22. 22.
    Wary KK, Mariotti A, Zurzolo C, Giancotti FG. A requirement for caveolin-1 and associated kinase Fyn in integrin signaling and anchorage-dependent cell growth. Cell 1998;94(5):625–34.PubMedCrossRefGoogle Scholar
  23. 23.
    Puceat M, Roche S, Vassort G. Src family tyrosine kinase regulates intracellular pH in cardiomyocytes. J Cell Biol 1998;141(7):1637–46.PubMedCrossRefGoogle Scholar
  24. 24.
    Hansen K, Alonso G, Courtneidge SA, Ronnstrand L, Heldin CH. PDGF-induced phosphorylation of Tyr28 in the N-terminus of Fyn affects Fyn activation. Biochem Biophys Res Commun 1997;241(2):355–62.PubMedCrossRefGoogle Scholar
  25. 25.
    Blenis J. Signal transduction via the MAP kinases: proceed at your own RSK. Proc. Natl. Acad. Sci. USA 1993;90:5889–92.PubMedCrossRefGoogle Scholar
  26. 26.
    Cano E, Hazzalin CA, Mahadevan LC. Anisomycin-activated protein kinases p45 and p55 but not mitogen-activated protein kinases ERK-1 and -2 are implicated in the induction of c-fos and c-jun. Mol Cell Biol 1994;14(11):7352–62.PubMedGoogle Scholar
  27. 27.
    Han J, Lee JD, Bibbs L, Ulevitch RI. A MAP kinase targeted by endotoxin and hyperosmolarity in mammalian cells. Science 1994;265(5173):808–11.PubMedCrossRefGoogle Scholar
  28. 28.
    Duff JL, Berk BC, Corson MA. Angiotensin 11 stimulates the pp44 and pp42 mitogen-activated protein kinases in cultured rat aortic smooth muscle cells. Biochem Biophys Res Commun 1992;188(1):257–64.PubMedCrossRefGoogle Scholar
  29. 29.
    Rao GN, Baas AS, Glasgow WC, Eling TE, Runge MS, Alexander RW. Activation of mitogenactivated protein kinases by arachidonic acid and its metabolites in vascular smooth muscle cells. J Biol Chem 1994;269(51):32586–91.PubMedGoogle Scholar
  30. 30.
    Marais R, Wynne J, Treisman R. The SRF accessory protein Elk-1 contains a growth factor-regulated transcriptional activation domain. Cell 1993;73(2):381–93.PubMedCrossRefGoogle Scholar
  31. 31.
    Kyriakis JM, Banerjee P, Nikolakaki E, Dai T, Rubie EA, Ahmad MF, et al. The stress-activated protein kinase subfamily of c-Jun kinases. Nature 1994;369(6476):156–60.PubMedCrossRefGoogle Scholar
  32. 32.
    Gupta S, Campbell D, D’Erijard B, Davis RJ. Transcription factor ATF2 regulation by the JNK signal transduction pathway. Science 1995;267(5196):389–93.PubMedCrossRefGoogle Scholar
  33. 33.
    Raingeaud J, Gupta S, Rogers JS, Dickens M, Han J, Ulevitch RJ, et al. Pro-inflammatory cytokines and environmental stress cause p38 mitogen-activated protein kinase activation by dual phosphorylation on tyrosine and threonine. J Biol Chem 1995;270(13):7420–6.PubMedCrossRefGoogle Scholar
  34. 34.
    Kato Y, Kravchenko VV, Tapping RI, Han J, Ulevitch RJ, Lee JD. BMK1/ERK5 regulates serum-induced early gene expression through transcription factor MEF2C. Embo J 1997;16(23):7054–66.PubMedCrossRefGoogle Scholar
  35. 35.
    Cowley S, Paterson H, Kemp P, Marshall CJ. Activation of MAP kinase kinase is necessary and sufficient for PC12 differentiation and for transformation of NIH 3T3 cells. Cell 1994;77:841–52.PubMedCrossRefGoogle Scholar
  36. 36.
    Weber JD, Raben DM, Phillips PJ, Baldassare JJ. Sustained activation of extracellular-signalregulated kinase 1 (ERKI) is required for the continued expression of cyclin DI in GI phase. Biochem J 1997;326(Pt I):61–8.PubMedGoogle Scholar
  37. 37.
    Fukui T, Rajagopalan S, Harrison D, Lassegue B, Griendling K. NADPH oxidase activity and cytochrome 6558 a-subunit mRNA expression are increased in aortas from hypertensive rats. Circulation 1995;92:1–231.CrossRefGoogle Scholar
  38. 38.
    Griendling KK, Ushio-Fukai M. Redox control of vascular smooth muscle proliferation. J Lab Clin Med 1998;132(1):9–15.PubMedCrossRefGoogle Scholar
  39. 39.
    Ushio-Fukai M, Alexander RW, Akers M, Griendling KK. p38 Mitogen-activated protein kinase is a critical component of the redox-sensitive signaling pathways activated by angiotensin II. Role in vascular smooth muscle cell hypertrophy. J Biol Chem 1998;273(24):15022–9.PubMedCrossRefGoogle Scholar
  40. 40.
    Chien KR, Knowlton KU, Zhu H, Chien S. Regulation of cardiac gene expression during myocardial growth and hypertrophy: molecular studies of an adaptive physiologic response. Faseb J 1991;5(15):3037–46.PubMedGoogle Scholar
  41. 41.
    Clerk A, Fuller SJ, Michael A, Sugden PH. Stimulation of “stress-regulated” mitogen-activated protein kinases (stress-activated protein kinases/c-Jun N-terminal kinases and p38- mitogen-activated protein kinases) in perfused rat hearts by oxidative and other stresses. J Biol Chem 1998;273(13):7228–34.PubMedCrossRefGoogle Scholar
  42. 42.
    Ramirez MT, Sah VP, Zhao XL, Hunter JJ, Chien KR, Brown JH. The MEKK-JNK pathway is stimulated by alphal-adrenergic receptor and ras activation and is associated with in vitro and in vivo cardiac hypertrophy. J Biol Chem 1997;272(22):14057–61.PubMedCrossRefGoogle Scholar
  43. 43.
    Zechner D, Thuerauf DJ, Hanford DS, McDonough PM, Glembotski CC. A role for the p38 mitogenactivated protein kinase pathway in myocardial cell growth, sarcomeric organization, and cardiac-specific gene expression. J Cell Biol 1997;139(1):115–27.PubMedCrossRefGoogle Scholar
  44. 44.
    Tournier C, Whitmarsh AJ, Cavanagh J, Barrett T, Davis RJ. Mitogen-activated protein kinase kinase 7 is an activator of the c-Jun NH2-terminal kinase. Proc Natl Acad Sci U S A 1997;94(14):7337–42.PubMedCrossRefGoogle Scholar
  45. 45.
    Wang Y, Su B, Sah VP, Brown JH, Han J, Chien KR. Cardiac hypertrophy induced by mitogenactivated protein kinase kinase 7, a specific activator for c-Jun NH2-terminal kinase in ventricular muscle cells. J Biol Chem 1998;273(10):5423–6.PubMedCrossRefGoogle Scholar
  46. 46.
    Sugden PH, Clerk A. “Stress-responsive” mitogen-activated protein kinases (c-Jun N-terminal kinases and p38 mitogen-activated protein kinases) in the myocardium. Cire Res 1998;83(4):345–52.CrossRefGoogle Scholar
  47. 47.
    Kumar S, McDonnell PC, Gum RJ, Hand AT, Lee JC, Young PR. Novel homologues of CSBP/p38 MAP kinase: activation, substrate specificity and sensitivity to inhibition by pyridinyl imidazoles. Biochem Biophys Res Commun 1997;235(3):533–8.PubMedCrossRefGoogle Scholar
  48. 48.
    Clifton AD, Young PR, Cohen P. A comparison of the substrate specificity of MAPKAP kinase-2 and MAPKAP kinase-3 and their activation by cytokines and cellular stress. FEBS Lett 1996;392(3):209–14.PubMedCrossRefGoogle Scholar
  49. 49.
    Abe J, Takahashi M, Ishida M, Lee J-D, Berk BC. c-Src is required for oxidative stress-mediated activation of big mitogen-activated protein kinase (BMK1). J Biol Chem 1997;272(August 15th):pp. 20389–94.PubMedCrossRefGoogle Scholar
  50. 50.
    Kato Y, Tapping RI, Huang S, Watson MH, Ulevitch RJ, Lee JD. Bmkl/Erk5 is required for cell proliferation induced by epidermal growth factor. Nature 1998;395(6703):713–6.PubMedCrossRefGoogle Scholar
  51. 51.
    Zhou G, Bao ZQ, Dixon JE. Components of a new human protein kinase signal transduction pathway. J Biol Chem 1995;270(21):12665–9.PubMedGoogle Scholar
  52. 52.
    McDermott JC, Cardoso MC, Yu YT, Andres V, Leifer D, Kraine D, et al. hMEF2C gene encodes skeletal muscle-and brain-specific transcription factors. Mol Cell Biol 1993;13(4):2564–77.PubMedGoogle Scholar
  53. 53.
    Sturgill TW, Ray BL, Erikson E, Mailer JL. Insulin-stimulated MAP-2 kinase phosphorylates protein S6 kinase II. Nature 1988;334:715–8.PubMedCrossRefGoogle Scholar
  54. 54.
    Takahashi E, Abe J, Berk BC. Angiotensin II stimulates p90rsk in vascular smooth muscle cells. A potential Na+/H+ exchanger kinase. Circ Res 1997;81:268–73.PubMedCrossRefGoogle Scholar
  55. 55.
    Phan V, Kusuhara M, Lucchesi PA, Berk BC. A 90 kD Na+/H+ exchanger kinase has increased activity in spontaneously hypertensive rat vascular smooth muscle cells. Hypertension 1997;29:126572.Google Scholar
  56. 56.
    Takahashi E, Abe J, Gallis B, Aebersold R, Spring DJ, Krebs EG, et al. p90RSK is a serum-stimulated NHE1 kinase: regulatory phosphorylation of serine 703 of Na+/H+ exchanger isoform-1. J Biol Chem 1999;274(29):20206–14.PubMedCrossRefGoogle Scholar
  57. 57.
    Abe J, Berk BC. Fyn-dependent activation of p90 ribosomal S6 kinase (RSK) by H202: a new redox sensitive pathway. Circulation (abstract) 1998;98(17):1–220.Google Scholar
  58. 58.
    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 1995;270(36):21195–8.PubMedCrossRefGoogle Scholar
  59. 59.
    Sundaresan M, Yu ZX, Ferrans VJ, Sulciner DJ, Gutkind JS, Irani K, et al. Regulation of reactiveoxygen-species generation in fibroblasts by Racl. Biochem J 1996;318(Pt 2):379–82.PubMedGoogle Scholar
  60. 60.
    Abe J, Berk BC. Fyn and JAK2 mediate Ras Activation by Reactive Oxygen Species. in press.Google Scholar
  61. 61.
    Kunsch C, Medford RM. Oxidative stress as a regulator of gene expression in the vasculature [In Process Citation]. Circ Res 1999;85(8):753–66.PubMedCrossRefGoogle Scholar
  62. 62.
    Liao F, Andalibi A, Qiao JH, Allayee H, Fogelman AM, Lusis AJ. Genetic evidence for a common pathway mediating oxidative stress, inflammatory gene induction, and aortic fatty streak formation in mice. J Clin Invest 1994;94(2):877–84.PubMedCrossRefGoogle Scholar
  63. 63.
    Glagov S, Weisenberg E, Zarins CK, Stankunavicius R, Kolettis G.T. Compensatory enlargement of human atherosclerotic coronary arteries. N Engl J Med 1987;316(22):1371–5.PubMedCrossRefGoogle Scholar
  64. 64.
    Losordo DW, Rosenfield K, Kaufman J, Pieczek A. Isner JM. Focal compensatory enlargement of human arteries in response to progressive atherosclerosis. In vivo documentation using intravascular ultrasound. Circulation 1994;89(6):2570–7.PubMedCrossRefGoogle Scholar
  65. 65.
    Kakuta T, Currier JW, Horten K, Faxon DP. Failure of compensatory enlargement, not neointimal formation, acounts for lumen narrowing after angioplasty in the atherosclerotic rabbit. Circulation 1993;88:1–619.Google Scholar
  66. 66.
    Lafont A, Guzman LA, Whitlow PL, Goormastic M, Cornhill JF, Chisolm GM. Restenosis after experimental angioplasty. Intimai, medial, and adventitial changes associated with constrictive remodeling. Circ Res 1995;76(6):996–1002.PubMedCrossRefGoogle Scholar
  67. 67.
    Mintz G, Popma J, Pichard A, Kent K. Satter L, Painter J et al. Mechanisms of late arterial responses to transcatheter therapy: A serial quantitative angiographie and intravascular ultrasound study. Circulation 1994;90:1–24.CrossRefGoogle Scholar
  68. 68.
    Mintz GS, Kovach JA, Javier SP, Ditrano CJ, Leon MB. Geometric remodeling is the predominant mechanism of late lumen loss after coronary angioplasty. Circulation 1993;88:1–654.Google Scholar
  69. 69.
    Mintz GS, Popma JJ, Pichard AD, Kent KM, Satler LF, Wong C, et al. Arterial remodeling after coronary angioplasty: a serial intravascular ultrasound study. Circulation 1996;94(1):35–43.PubMedCrossRefGoogle Scholar
  70. 70.
    Javier SP, Mintz GS, Popma JJ, Pichard AD, Kent KM, Satler LF, et al. Intravascular ultrasound assessment of the magnitude and mechanism of coronary artery and lumen tapering. Am J Cardiol 1995;75(2):177–80.PubMedCrossRefGoogle Scholar

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© Springer Science+Business Media Dordrecht 2000

Authors and Affiliations

  • Jun-ichi Abe
  • Bradford C. Berk

There are no affiliations available

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