급성 부동 스트레스 후 척수 회색질에서 Peroxiredoxin I 및 III의 발현 변화

Characterization of Peroxiredoxins in the Gray matter in the spinal cord after Acute Immobilization Stress

  • 백남현 (대전선병원 외과학교실) ;
  • 곽승수 (대전선병원 외과학교실) ;
  • 이동석 (강원대학교 동물생명과학부 동물 생명공학과) ;
  • 이영호 (충남대학교 의과대학 해부학실)
  • Paek, Nam-Hyun (Department of Surgery, SUN General Hospital) ;
  • Kwak, Seung-Soo (Department of Surgery, SUN General Hospital) ;
  • Lee, Dong-Seok (College of animal resource science sciences, Kangwon National University) ;
  • Lee, Young-Ho (Department of anatomy, College of Medicine, Chungnam National University)
  • 투고 : 2006.09.13
  • 심사 : 2006.10.31
  • 발행 : 2006.12.30

초록

Purpose: Many stresses produce reactive oxygen species and bring about mechanism of antioxidant reaction. Cytokine and a neurotransmitter through the cell membrane, as well as signal transduction through the cell membrane, are used for various pathological condition of the brain, such as neurodegenerative disease. There are several antioxidant enzymes in cells (superoxcide dismutase, glutathion peroxidasae, peroxiredoxin catalase, etc.) Methods: This study used single- or double-label immunohistochemical techniques to analyze mouse spinal neuron cells expressing Prx I and Prx III after acute mobilization stress. Results: Prx I was observed in dendritic cell of the gray matter of the spinal cord, and Prx III was observed in the cytoplasm of the GM of the spinal cord. Conclusion: The results of this study will help to explain differences of expression in the distributions of the peroxiredoxin enzymes of the spinal cord.

키워드

참고문헌

  1. Wisemen H, Halliwell B. Damage to DNA by reactive oxygen and mitrogen species : role in inflamatory disease and progression to cancer. J Biochem 1996;313:17-29 https://doi.org/10.1042/bj3130017
  2. Henle ES, Linn S. Formation, prevention, and repair of DNA damage by iron/hydorgen peroxide. J Biol Chem 1997;272:9095-8
  3. Norberg J, Arner ES. Reactive oxygen species, anioxidants, and the mammalian thioredoxin system. Free Radic Biol Med 2001;31:1287-312 https://doi.org/10.1016/S0891-5849(01)00724-9
  4. Zaidi SM, Al-Qirim TM, Hoda N, Banu N. Modulation of restraint stress induced oxidative changes in rats by antioxidant vitamins. J Nutr Biochem 2003;14:633-6 https://doi.org/10.1016/S0955-2863(03)00117-7
  5. Hofmann B, Hecht HJ, Flohe L. Peroxiredoxins. Biol Chem 2002;383:347-64 https://doi.org/10.1515/BC.2002.040
  6. Jin DY, Jeang KT. Peroxiredoxins in cell signaling and HIV infection. In: C.K. Sen et al. Antioxidant and Redox Regulation of Genes. Academic Press 2000. p. 381-407
  7. Link AJ, Robison K, Church GM. Comparing the predicted and observed properties of proteins encoded in the genome of Escherichia coli K-12. Electrophoresis 1997;18:1259-313 https://doi.org/10.1002/elps.1150180807
  8. Moore RB, Mankad MV, Shriver SK, Mankad VN, Plishker GA. Reconstitution of Ca2+-dependent K+ transport in erythrocyte membrane vesicles requires a cytoplasmic protein. J Biol Chem 1991;266:18964-8
  9. Chae HZ, Kim HJ, Kang SW, Rhee SG. Characterization of three isoforms of mammalian peroxiredoxin that reduce peroxides in the presence of thioredoxin Diabetes Res. Clin. Pract 1999;45: 101-12 https://doi.org/10.1016/S0168-8227(99)00037-6
  10. Netto LES, Chae HZ, Kang SW, Rhee SG, Stadtman ER. Removal of hydrogen peroxide by thiol-specific antioxidant enzyme (TSA) is involved with its antioxidant properties. TSA possesses thiol peroxidase activity. J Biol Chem 1996;271:15315-21 https://doi.org/10.1074/jbc.271.26.15315
  11. Poole LB. Flavin-dependent alkyl hydroperoxide reductase from Salmonella typhimurium. 2. Cystine disulfides involved in catalysis of peroxide reduction. Biochem 1996;35:65-75 https://doi.org/10.1021/bi951888k
  12. Bruchhaus I, Richter S, Tannich E. Removal of hydrogen peroxide by the 29 kDa protein of Entamoeba histolytica. J Biochem 1997;326:785-9 https://doi.org/10.1042/bj3260785
  13. Manevich Y, Sweitzer T, Pak JH, Feinstein SI, Muzykantov V, Fisher AB. 1-Cys peroxiredoxin overexpression protects cells against phospholipid peroxidation-mediated membrane damage. Proc Natl Acad. Sci USA 2002;99:11599-604 https://doi.org/10.1073/pnas.182384499
  14. Pak JH, Manevich Y, Kim HS, Feinstein SI, Fisher AB. An antisense oligonucleotide to 1-cys peroxiredoxin causes lipid peroxidation and apoptosis in lung epithelial cells. J Biol Chem 2002;277:49927-34 https://doi.org/10.1074/jbc.M204222200
  15. Bryk R, Griffin P, Nathan C. Peroxynitrite reductase activity of bacterial peroxiredoxins. Nature 2000;407:211-5 https://doi.org/10.1038/35025109
  16. Kim HS, Pak JH, Gonzales LW, Feinstein SI, Fisher AB. Regulation of 1-cys peroxiredoxin expression in lung epithelial cells. Am J Respir Cell Mol Biol 2002;27:227-33 https://doi.org/10.1165/ajrcmb.27.2.20010009oc
  17. Chen JW, Dodia C, Feinstein SI, Jain MK, Fisher AB. 1-Cys peroxiredoxin, a bifunctional enzyme with glutathione peroxidase and phospholipase A2 activities. J Biol Chem 2000;275:28421-7 https://doi.org/10.1074/jbc.M005073200
  18. Chang TS, Jeong W, Choi SY, Yu S, Kang SW, Rhee SG. Regulation of peroxiredoxin I activity by Cdc2-mediated phosphorylation. J Biol Chem 2002;277:25370-6 https://doi.org/10.1074/jbc.M110432200
  19. Jin DY, Chae HZ, Rhee SG, Jeang KT. Regulatory role for a novel human thioredoxin peroxidase in NFkappaB activation. J Biol Chem 1997;272:30952-61 https://doi.org/10.1074/jbc.272.49.30952
  20. Zhang P, Liu B, Kang,SW, Seo MS. Thioredoxin peroxidase is a novel inhibitor of apoptosis with a mechanism distinct from that of Bcl-2. J Biol Chem 1997;272:30615-8 https://doi.org/10.1074/jbc.272.49.30615
  21. Fujii J, Ikeda Y. Advances in our understanding of peroxiredoxin, a multifunctional, mammalian redox protein. Redox Rep 2002;7:123-30 https://doi.org/10.1179/135100002125000352
  22. Kim H, Lee JH, Park ES, Suh JM, Park SJ, Chung HK, et al. Role of peroxiredoxins in regulating intracellular hydrogen peroxide and hydrogen peroxide-induced apoptosis in thyroid cells. J Biol Chem 2000;275:18266-70 https://doi.org/10.1074/jbc.275.24.18266
  23. Isermann K, Liebau E, Roeder T. Bruchhaus IA. peroxiredoxin specifically expressed in two types of pharyngeal neurons is required for normal growth and egg production in Caenorhabditis elegans. J Mol Biol 2004;338:745-55 https://doi.org/10.1016/j.jmb.2004.03.021
  24. Kvetnansky R, Gewirtz GP, Weise VK, Kopin IJ. Effect of hypophysectomy on immobilization-induced elevation of tyrosine hydroxylase and phenyletha nolamine-N-methyl transferase in the rat adrenal. Endocrinology 1997;87:1323-9 https://doi.org/10.1210/endo-87-6-1323
  25. Park EM, Park JS, Kim YJ. Role of oxidative stress in the radiation-induced lung pathogenesis in mice. J Biochem Mol Biol 2001;34:544-50
  26. Ishii T, Yamada M, Sato H, Matsue M, Taketani S, Nakamura K, Sugita Y, Bannai S. Cloning and characterization of a 23-kDa stress-induced mouse peritoneal macrophage protein. J Biol Chem 1993;268:18633-6
  27. Mitsumoto A, Takanezawa Y, Okawa K, Iwamatsu A, Nakagawa Y. Variants of peroxiredoxins expression in response to hydroperoxide stress. Free Radic Biol Med 2001;30:625-35 https://doi.org/10.1016/S0891-5849(00)00503-7
  28. Yamamoto T, Matsui Y, Natori S, Obinata M, Cloning of a housekeeping-type gene (MER5) preferentially expressed in murine erythroleukemia cells. Gene 1989;80:337-43 https://doi.org/10.1016/0378-1119(89)90297-7
  29. Kim SH, Fountoulakis M, Cairns N, Lubec G. Protein levels of human peroxiredoxin subtypes in brains of patients with Alzheimer's disease and Down syndrome. J Neural Transm Suppl 2001; 61:223-35
  30. Shibata E, Nanri H, Ejima K, Araki M, Fukuda J, Yoshimura K, Toki N, Ikeda M, Kashimura M. Enhancement of mitochondrial oxidative stress and up-regulation of antioxidant protein peroxiredoxin III/SP-22 in the mitochondria of human pre-eclamptic placentae. Placenta 2003;24:698-705 https://doi.org/10.1016/S0143-4004(03)00083-3
  31. Van Schaick HS, Smidt MP, Rovescalli AC, Luijten M, van der Kleij AA, Asoh S, Kozak CA, Nirenberg M, Burbach JP. Homeobox gene Prx3 expression in rodent brain and extraneural tissues. Proc Natl Acad Sci USA 1997;94:12993-8
  32. Choi JH, Kim TN, Kim S, Baek SH, Kim JH, Lee SR, Kim JR. Overexpression of mitochondrial thioredoxin reductase and peroxiredoxin III in hepatocellular carcinomas. Anticancer Res 2002;22:3331-5
  33. Chang TS, Cho CS, Park S, Yu S, Kang SW, Rhee SG. Peroxiredoxin III, a Mitochondrion-specific Peroxidase, Regulates Apoptotic Signaling by Mitochondria. J Biol Chem 2004;279:41975-84 https://doi.org/10.1074/jbc.M407707200
  34. Miaskowski C, Ong GL, Lukic D, Haldar J. Immobilization stress affects oxytocin and vasopressin levels in hypothalamic and extrahypothalamic sites. Brain Res 1988;458:137-41 https://doi.org/10.1016/0006-8993(88)90505-7