Mitochondrial thioredoxin in regulation of oxidant-induced cell death

被引:80
作者
Chen, Yan
Cai, Jiyang
Jones, Dean P.
机构
[1] Vanderbilt Univ, Vanderbilt Eye Inst, Nashville, TN 37232 USA
[2] Emory Univ, Sch Med, Dept Med, Div Pulm Allergy & Crit Care Med, Atlanta, GA 30322 USA
关键词
thioredoxin; mitochondria; oxidative stress; redox; thioredoxin reductase;
D O I
10.1016/j.febslet.2006.11.007
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 thioredoxin (mtTrx) can be oxidized in response to inducers of oxidative stress; yet the functional consequences of the oxidation have not been determined. This study evaluated the redox status of mtTrx and its association to oxidant-induced apoptosis. Results showed that mtTrx was oxidized after exposure to peroxides and diamide. Overexpression of mtTrx protected against diamide-induced oxidation and cytotoxicity. Oxidation of mtTrx was also achieved by knocking down its reductase; and lead to increased susceptibility to cell death. The data indicate that the redox status of mtTrx is a regulatory mechanism underlying the vulnerability of mitochondria to oxidative injury. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:6596 / 6602
页数:7
相关论文
共 23 条
[1]   Mitochondrial free radical generation, oxidative stress, and aging [J].
Cadenas, E ;
Davies, KJA .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (3-4) :222-230
[2]   Overexpressed human mitochondrial thioredoxin confers resistance to oxidant-induced apoptosis in human osteosarcoma cells [J].
Chen, Y ;
Cai, JY ;
Murphy, TJ ;
Jones, DP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (36) :33242-33248
[3]   Protection against oxidant-induced apoptosis by mitochondrial thioredoxin in SH-SY5Y neuroblastoma cells [J].
Chen, Yan ;
Yu, Min ;
Jones, Dean P. ;
Greenamyre, J. Timothy ;
Cai, Jiyang .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2006, 216 (02) :256-262
[4]  
Chiarugi Paola, 2003, Ital J Biochem, V52, P28
[5]   Reactive oxygen species and signal transduction [J].
Finkel, T .
IUBMB LIFE, 2001, 52 (1-2) :3-6
[6]   Differential oxidation of thioredoxin-1, thioredoxin-2, and glutathione by metal ions [J].
Hansen, JM ;
Zhang, H ;
Jones, DP .
FREE RADICAL BIOLOGY AND MEDICINE, 2006, 40 (01) :138-145
[7]   Regulation of cell function by methionine oxidation and reduction [J].
Hoshi, T ;
Heinemann, SH .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (01) :1-11
[8]   Protection from inactivation of the adenine nucleotide translocator during hypoglycaemia-induced apoptosis by mitochondrial phospholipid hydroperoxide glutathione peroxidase [J].
Imai, H ;
Koumura, T ;
Nakajima, R ;
Nomura, K ;
Nakagawa, Y .
BIOCHEMICAL JOURNAL, 2003, 371 :799-809
[9]   Molecular cloning and characterization of a mitochondrial selenocysteine-containing thioredoxin reductase from rat liver [J].
Lee, SR ;
Kim, JR ;
Kwon, KS ;
Yoon, HW ;
Levine, RL ;
Ginsburg, A ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (08) :4722-4734
[10]   Role of mitochondria in oxidative stress and ageing [J].
Lenaz, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1998, 1366 (1-2) :53-67