Cell signalling and the glutathione redox system

被引:272
作者
Filomeni, G
Rotilio, G
Ciriolo, MR
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00173 Rome, Italy
[2] Univ Chieti G Dannunzio, Dept Biomed Sci, I-66100 Chieti, Italy
关键词
glutathione; thiols; redox regulation; glutathione-S-thiolation; cell signalling; redox transcription factors;
D O I
10.1016/S0006-2952(02)01176-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The reduction/oxidation (redox) state of the cell is a consequence of the balance between the levels of oxidising and reducing equivalents. A reducing intracellular environment is often associated with cell survival; however, redox unbalance is necessary since it represents a regulatory sensor for several nuclear transcription factors. Activator protein I (AP-1), nuclear factor-kappaB (NF-kappaB) and protein tyrosine phosphatases 1-B (PTP-1B)are some of the well-known molecular factors for which a redox modulation of their activity has been demonstrated. The glutathione buffer system modulates cell response to redox changes induced by either external or intracellular stimuli. This paper summarises recent knowledge on the role played by several redox modulators in inducing signalling events that finally regulate cell cycle progression. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1057 / 1064
页数:8
相关论文
共 64 条
[1]   Role of redox potential and reactive oxygen species in stress signaling [J].
Adler, V ;
Yin, ZM ;
Tew, KD ;
Ronai, Z .
ONCOGENE, 1999, 18 (45) :6104-6111
[2]   Regulation of JNK signaling by GSTp [J].
Adler, V ;
Yin, ZM ;
Fuchs, SY ;
Benezra, M ;
Rosario, L ;
Tew, KD ;
Pincus, MR ;
Sardana, M ;
Henderson, CJ ;
Wolf, CR ;
Davis, RJ ;
Ronai, Z .
EMBO JOURNAL, 1999, 18 (05) :1321-1334
[3]   Conformation-dependent phosphorylation of p53 [J].
Adler, V ;
Pincus, MR ;
Minamoto, T ;
Fuchs, SY ;
Bluth, MJ ;
BrandtRauf, PW ;
Friedman, FK ;
Robinson, RC ;
Chen, JM ;
Wang, XW ;
Harris, CC ;
Ronai, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1686-1691
[4]   Antigen-presenting dendritic cells provide the reducing extracellular microenvironment required for T lymphocyte activation [J].
Angelini, G ;
Gardella, S ;
Ardy, M ;
Ciriolo, MR ;
Filomeni, G ;
Di Trapani, G ;
Clarke, F ;
Sitia, R ;
Rubartelli, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1491-1496
[5]   The neutrophil NADPH oxidase [J].
Babior, BM ;
Lambeth, JD ;
Nauseef, W .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 397 (02) :342-344
[6]   Regulation of PTP1B via glutathionylation of the active site cysteine 215 [J].
Barrett, WC ;
DeGnore, JP ;
König, S ;
Fales, HM ;
Keng, YF ;
Zhang, ZY ;
Yim, MB ;
Chock, PB .
BIOCHEMISTRY, 1999, 38 (20) :6699-6705
[7]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[8]  
Chae HZ, 1999, METHOD ENZYMOL, V300, P219
[9]   TRANSDUCTION OF REDUCING POWER ACROSS THE PLASMA-MEMBRANE BY REDUCED GLUTATHIONE - A H-1-NMR SPIN-ECHO STUDY OF INTACT HUMAN ERYTHROCYTES [J].
CIRIOLO, MR ;
PACI, M ;
SETTE, M ;
DEMARTINO, A ;
BOZZI, A ;
ROTILIO, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 215 (03) :711-718
[10]  
CIRIOLO MR, 1990, J BIOL CHEM, V265, P11030