Mitochondria-targeted redox probes as tools in the study of oxidative damage and ageing

被引:75
作者
James, AM [1 ]
Cochemé, HM [1 ]
Murphy, MP [1 ]
机构
[1] MRC, Dunn Human Nutr Unit, Cambridge CB2 2XY, England
关键词
coenzyme Q; mitochondria; reactive oxygen species; antioxidants; oxidative stress; lipophilic cations; redox signalling;
D O I
10.1016/j.mad.2005.03.026
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial reactive oxygen species (ROS) and oxidative damage are associated with a range of age-related human pathologies. It is also likely that mitochondrial ROS generation is a factor in stress response and signal transduction pathways. However, current methods for measuring and influencing mitochondrial ROS production in vivo often lack the desired specificity. To help elucidate the potential role of mitochondrial ROS production in ageing, we have developed a range of mitochondria-targeted ROS probes that may be useful in vivo. This was achieved by covalently attaching a lipophilic cation to a ROS-reactive moiety causing its membrane potential-dependent accumulation within mitochondria. Mitochondria-targeted molecules developed so far include antioxidants that detoxify mitochondrial ROS, probes that react with mitochondrial ROS, and reagents that specifically label mitochondrial protein thiols. Here, we outline how the formation and consequences of mitochondrial ROS production can be investigated using these probes. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:982 / 986
页数:5
相关论文
共 47 条
[1]   Lipid peroxidation in mitochondrial inner membranes .1. An integrative kinetic model [J].
Antunes, F ;
Salvador, A ;
Marinho, HS ;
Alves, R ;
Pinto, RE .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 21 (07) :917-943
[2]   USE OF ACETYLATED FERRICYTOCHROME-C FOR DETECTION OF SUPEROXIDE RADICALS PRODUCED IN BIOLOGICAL-MEMBRANES [J].
AZZI, A ;
MONTECUCCO, C ;
RICHTER, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1975, 65 (02) :597-603
[3]   Oxidative damage to mitochondrial DNA is inversely related to maximum life span in the heart and brain of mammals [J].
Barja, G ;
Herrero, A .
FASEB JOURNAL, 2000, 14 (02) :312-318
[4]   Aging in vertebrates, and the effect of caloric restriction: a mitochondrial free radical production-DNA damage mechanism? [J].
Barja, G .
BIOLOGICAL REVIEWS, 2004, 79 (02) :235-251
[5]   Free radicals and aging [J].
Barja, G .
TRENDS IN NEUROSCIENCES, 2004, 27 (10) :595-600
[6]  
Beal MF, 2003, ANN NY ACAD SCI, V991, P120
[7]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[8]   Redox regulation of cAMP-responsive element-binding protein and induction of manganous superoxide dismutase in nerve growth factor-dependent cell survival [J].
Bedogni, B ;
Pani, G ;
Colavitti, R ;
Riccio, A ;
Borrello, S ;
Murphy, M ;
Smith, R ;
Eboli, ML ;
Galeotti, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (19) :16510-16519
[9]   Glutaredoxin 2 catalyzes the reversible oxidation and glutathionylation of mitochondrial membrane thiol proteins - Implications for mitochondrial redox regulation and antioxidant defense [J].
Beer, SM ;
Taylor, ER ;
Brown, SE ;
Dahm, CC ;
Costa, NJ ;
Runswick, MJ ;
Murphy, MP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (46) :47939-47951
[10]   The role of oxidative damage and stress in aging [J].
Bokov, A ;
Chaudhuri, A ;
Richardson, A .
MECHANISMS OF AGEING AND DEVELOPMENT, 2004, 125 (10-11) :811-826