EPR detection of glutathionyl and protein-tyrosyl radicals during the interaction of peroxynitrite with macrophages (J774)

被引:43
作者
de Menezes, SL [1 ]
Augusto, O [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Bioquim, BR-05513970 Sao Paulo, Brazil
关键词
D O I
10.1074/jbc.M104012200
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
Peroxynitrite is one of the biological oxidants whose addition to cells has been shown to either activate signaling pathways or lead to cell injury, depending on cell type and oxidant concentration. The intermediacy of free radicals in these processes has been directly demonstrated only during the interaction of peroxynitrite with erythrocytes, a particular cell type, due to its high hemoglobin content. Here, we demonstrate that the addition of peroxynitrite to a macrophage cell line (J774) led to the production of glutathionyl and protein-tyrosyl radicals. The glutathionyl radical was characterized by EPR spin-trapping experiments with 5,5-dimethyl-1-pyrroline-N-oxide. Protein-tyrosyl radical formation was suggested by direct EPR spectroscopy and confirmed by EPR spin-trapping experiments with 3,5-dibromo-4-nitrosobenzenesulfonic acid and Western blot analysis of nitrated proteins in treated macrophages. Time dependence studies of free radical formation indicate that intracellular glutathione and unidentified proteins are the initial peroxynitrite targets in macrophages and that their derived radicals trigger radical chain reactions. The results are likely to be relevant to the understanding of the bioregulatory and biodamaging effects of peroxynitrite.
引用
收藏
页码:39879 / 39884
页数:6
相关论文
共 54 条
[1]  
Akerboom T P, 1981, Methods Enzymol, V77, P373
[2]   Bridge over troubled waters:: Sensing stress by disulfide bond formation [J].
Åslund, F ;
Beckwith, J .
CELL, 1999, 96 (06) :751-753
[3]   SPIN-TRAPPING STUDIES OF PEROXYNITRITE DECOMPOSITION AND OF 3-MORPHOLINOSYDNONIMINE N-ETHYLCARBAMIDE AUTOOXIDATION - DIRECT EVIDENCE FOR METAL-INDEPENDENT FORMATION OF FREE-RADICAL INTERMEDIATES [J].
AUGUSTO, O ;
GATTI, RM ;
RADI, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1994, 310 (01) :118-125
[4]   ESR spin-trapping of a protein-derived tyrosyl radical from the reaction of cytochrome c with hydrogen peroxide [J].
Barr, DP ;
Gunther, MR ;
Deterding, LJ ;
Tomer, KB ;
Mason, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (26) :15498-15503
[5]   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
[6]  
BOLANOS JP, 1995, J NEUROCHEM, V64, P1965
[7]   Carbon dioxide stimulates the production of thiyl, sulfinyl, and disulfide radical anion from thiol oxidation by peroxynitrite [J].
Bonini, MG ;
Augusto, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :9749-9754
[8]   Direct EPR detection of the carbonate radical anion produced from peroxynitrite and carbon dioxide [J].
Bonini, MG ;
Radi, R ;
Ferrer-Sueta, G ;
Ferreira, AMD ;
Augusto, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :10802-10806
[9]   Nitric oxide and peroxynitrite-dependent aconitase inactivation and iron-regulatory protein-1 activation in mammalian fibroblasts [J].
Castro, LA ;
Robalinho, RL ;
Cayota, A ;
Meneghini, R ;
Radi, R .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 359 (02) :215-224
[10]   Hydroxyl radical formation during peroxynitrous acid decomposition [J].
Coddington, JW ;
Hurst, JK ;
Lymar, SV .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (11) :2438-2443