Down-regulation of heme oxygenase-1 by hepatitis C virus infection in vivo and by the in vitro expression of hepatitis C core protein

被引:68
|
作者
Abdalla, MY
Britigan, BE
Wen, F
Icardi, M
McCormick, ML
LaBrecque, DR
Voigt, M
Brown, KE
Schmidt, WN
机构
[1] Vet Adm Med Ctr, Dept Internal Med, Iowa City, IA 52240 USA
[2] Vet Adm Med Ctr, Res Serv, Iowa City, IA 52240 USA
[3] Univ Iowa, Dept Radiat Oncol, Free Rad & Radiat Biol Program, Iowa City, IA USA
[4] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[5] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[6] Univ Iowa, Roy G & Lucille A Carver Coll Med, Dept Pathol, Iowa City, IA USA
关键词
D O I
10.1086/423488
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antioxidant enzymes, including heme oxygenase (HO)-1, are an important line of defense against oxidant-mediated liver injury. Because hepatitis C virus (HCV) infection appears to increase the production of oxidants, we evaluated levels of antioxidant enzymes and HO-1 in liver-biopsy samples from HCV-infected patients by immunoblot and semiquantitative reverse-transcriptase polymerase chain reaction. In HCV-infected liver samples, levels of immunoreactive HO-1 and HO-1 mRNA were >4-fold lower than levels in control samples, but levels of superoxide dismutase and catalase were unaffected. Immunohistochemical results confirmed the decreased expression of HO-1 in hepatocytes from liver samples from HCV-infected patients but not in those from patients with other chronic liver diseases. The expression of HO-1 was also reduced in cell lines that stably express HCV core protein, which suggests that core gene products are capable of regulating the expression of HO-1.
引用
收藏
页码:1109 / 1118
页数:10
相关论文
共 54 条
  • [1] TRANSFECTION OF THE HUMAN HEME OXYGENASE GENE INTO RABBIT CORONARY MICROVESSEL ENDOTHELIAL-CELLS - PROTECTIVE EFFECT AGAINST HEME AND HEMOGLOBIN TOXICITY
    ABRAHAM, NG
    LAVROVSKY, Y
    SCHWARTZMAN, ML
    STOLTZ, RA
    LEVERE, RD
    GERRITSEN, ME
    SHIBAHARA, S
    KAPPAS, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (15) : 6798 - 6802
  • [2] CHRONIC HEPATITIS - AN UPDATE ON TERMINOLOGY AND REPORTING
    BATTS, KP
    LUDWIG, J
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1995, 19 (12) : 1409 - 1417
  • [3] Threshold effect of liver iron content on hepatic inflammation and fibrosis in hepatitis B and C
    Beinker, NK
    Voigt, MD
    Arendse, M
    Smit, J
    Stander, IA
    Kirsch, RE
    [J]. JOURNAL OF HEPATOLOGY, 1996, 25 (05) : 633 - 638
  • [4] CYP2E1-dependent toxicity and oxidative stress in HEPG2 cells
    Cederbaum, AI
    Wu, DF
    Mari, M
    Bai, JX
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2001, 31 (12) : 1539 - 1543
  • [5] Nitric oxide-mediated cytoprotection of hepatocytes from glucose deprivation-induced cytotoxicity: Involvement of heme oxygenase-1
    Choi, BM
    Pae, HO
    Kim, YM
    Chung, HT
    [J]. HEPATOLOGY, 2003, 37 (04) : 810 - 823
  • [6] A DNA chip off the aging block
    Cristofalo, VJ
    [J]. NATURE MEDICINE, 2000, 6 (05) : 507 - 507
  • [7] Association between reactive oxygen species and disease activity in chronic hepatitis C
    DeMaria, N
    Colantoni, A
    Fagiuoli, S
    Liu, GJ
    Rogers, BK
    Farinati, F
    VanThiel, DH
    Floyd, RA
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (03) : 291 - 295
  • [8] DESMET VJ, 1994, HEPATOLOGY, V19, P1513, DOI 10.1002/hep.1840190629
  • [9] EL DW, 1993, CELL, V75, P817
  • [10] ELDEIRY WS, 1994, CANCER RES, V54, P1169