Antioxidant defence systems and generation of reactive oxygen species in osteosarcoma cells with defective mitochondria: Effect of selenium

被引:23
作者
Wojewoda, Marta [1 ]
Duszynski, Jerzy [1 ]
Szczepanowska, Joanna [1 ]
机构
[1] M Nencki Inst Expt Biol, Dept Biochem, PL-02093 Warsaw, Poland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2010年 / 1797卷 / 6-7期
关键词
Mitochondria; NARP; Selenium; ROS; Antioxidant enzyme; OXIDATIVE STRESS; NARP MUTATION; HUMAN-DISEASE; ATP SYNTHASE; MTDNA; REDUCTASE; GENE; DNA; HYDROETHIDINE; THIOREDOXIN;
D O I
10.1016/j.bbabio.2010.01.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial diseases originate from mutations in mitochondrial or nuclear genes encoding for mitochondrial proteome. Neurogenic muscle weakness, ataxia and retinitis pigmentosa (NARP) syndrome is associated with the T8993G transversion in ATP6 gene which results in substitution at the very conservative site in the subunit 6 of mitochondrial ATP synthase. Defects in the mitochondrial respiratory chain and the ATPase are considered to be accompanied by changes in the generation of reactive oxygen species (ROS). This study aimed to elucidate effects of selenium on ROS and antioxidant system of NARP cybrid cells with 98% of T8993G mutation load. We found that selenium decreased ROS generation and increased the level and activity of antioxidant enzymes such as glutathione peroxidase (GPx) and thioredoxin reductase (TrxR). Therefore, we propose selenium to be a promising therapeutic agent not only in the case of NARP syndrome but also other diseases associated with mitochondrial dysfunctions and oxidative stress. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:890 / 896
页数:7
相关论文
共 34 条
  • [1] The thioredoxin system in cancer
    Arner, Elias S. J.
    Holmgren, Arne
    [J]. SEMINARS IN CANCER BIOLOGY, 2006, 16 (06) : 420 - 426
  • [2] Cytotoxic effects induced by oxidative stress in cultured mammalian cells and protection provided by Hsp27 expression
    Arrigo, AP
    Firdaus, WJJ
    Mellier, G
    Moulin, M
    Paul, C
    Diaz-latoud, C
    Kretz-remy, C
    [J]. METHODS, 2005, 35 (02) : 126 - 138
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] The Nrf2-Keapl defence pathway: Role in protection against drug-induced toxicity
    Copple, Ian M.
    Goldring, Christopher E.
    Kitteringham, Neil R.
    Park, B. Kevin
    [J]. TOXICOLOGY, 2008, 246 (01) : 24 - 33
  • [5] The mtDNA NARP mutation activates the actin-Nrf2 signaling of antioxidant defenses
    Dassa, Emmanuel Philippe
    Paupe, Vincent
    Goncalves, Sergio
    Rustin, Pierre
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 368 (03) : 620 - 624
  • [6] Multisystem manifestations of mitochondrial disorders
    Di Donato, Stefano
    [J]. JOURNAL OF NEUROLOGY, 2009, 256 (05) : 693 - 710
  • [7] Mitochondrial diseases
    DiMauro, S
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1658 (1-2): : 80 - 88
  • [8] A critical approach to the therapy of mitochondrial respiratory chain and oxidative phosphorylation diseases
    DiMauro, Salvatore
    Rustin, Pierre
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2009, 1792 (12): : 1159 - 1167
  • [9] Structure, functioning, and assembly of the ATP synthase in cells from patients with the T8993G mitochondrial DNA mutation -: Comparison with the enzyme in Rho0 cells completely lacking mtDNA
    García, JJ
    Ogilvie, I
    Robinson, BH
    Capaldi, RA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (15) : 11075 - 11081
  • [10] Superoxide-induced massive apoptosis in cultured skin fibroblasts harboring the neurogenic ataxia retinitis pigmentosa (NARP) mutation in the ATPase-6 gene of the mitochondrial DNA
    Geromel, V
    Kadhom, N
    Cebalos-Picot, I
    Ouari, O
    Polidori, A
    Munnich, A
    Rötig, A
    Rustin, P
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (11) : 1221 - 1228