Dynamics of protein nitration in cells and mitochondria

被引:148
作者
Aulak, KS
Koeck, T
Crabb, JW
Stuehr, DJ
机构
[1] Cleveland Clin Fdn, Lerner Res Inst, Dept Immunol, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Cole Eye Inst, Cleveland, OH 44195 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2004年 / 286卷 / 01期
关键词
nitrotyrosine; peroxynitrite; inflammation; ischemia reperfusion;
D O I
10.1152/ajpheart.00743.2003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nitric oxide is a precursor of reactive nitrating species such as peroxynitrite and nitrogen dioxide that modify proteins to generate 3- nitrotyrosine. Many diseases are associated with increased levels of protein- bound nitrotyrosine, and this is used as a marker for oxidative damage. However, the regulation of protein nitration and its role in cell function are unclear. We demonstrate that biological protein nitration can be a specific and dynamic process. Proteins were nitrated in distinct temporal patterns in cells undergoing inflammatory activation, and protein denitration and renitration occurred rapidly in respiring mitochondria. The targets of protein nitration varied over time, which may reflect their sensitivity to nitration, expression pattern, or turnover. The dynamic nature of the nitration process was revealed by denitration and renitration of proteins occurring within minutes in mitochondria that were subject to hypoxiaanoxia and reoxygenation. Our results have implications that are particularly important for ischemia- reperfusion injury.
引用
收藏
页码:H30 / H38
页数:9
相关论文
共 65 条
[31]   Histone H1.2 is a substrate for denitrase, an activity that reduces nitrotyrosine immunoreactivity in proteins [J].
Irie, Y ;
Saeki, M ;
Kamisaki, Y ;
Martin, E ;
Murad, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :5634-5639
[32]   Biological tyrosine nitration: A pathophysiological function of nitric oxide and reactive oxygen species [J].
Ischiropoulos, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1998, 356 (01) :1-11
[33]   Comparative anatomy of the aldo-keto reductase superfamily [J].
Jez, JM ;
Bennett, MJ ;
Schlegel, BP ;
Lewis, M ;
Penning, TM .
BIOCHEMICAL JOURNAL, 1997, 326 :625-636
[34]   An activity in rat tissues that modifies nitrotyrosine-containing proteins [J].
Kamisaki, Y ;
Wada, K ;
Bian, K ;
Balabanli, B ;
Davis, K ;
Martin, E ;
Behbod, F ;
Lee, YC ;
Murad, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (20) :11584-11589
[35]   The role of aldose reductase inhibitors in diabetic complications: Recent trends [J].
Kaul, CL ;
Ramarao, P .
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY, 2001, 23 (08) :465-475
[36]  
Keller JN, 1998, J NEUROSCI, V18, P687
[37]   ALDOSE REDUCTASE IN DIABETIC COMPLICATIONS OF THE EYE [J].
KINOSHITA, JH ;
FUKUSHI, S ;
KADOR, P ;
MEROLA, LO .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1979, 28 (04) :462-469
[38]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[39]   Reactive species mechanisms of cellular hypoxia-reoxygenation injury [J].
Li, CY ;
Jackson, RM .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 282 (02) :C227-C241
[40]   INDUCTION OF DNA FRAGMENTATION AFTER 10 TO 120 MINUTES OF FOCAL CEREBRAL-ISCHEMIA IN RATS [J].
LI, Y ;
CHOPP, M ;
JIANG, N ;
ZHANG, ZG ;
ZALOGA, C .
STROKE, 1995, 26 (07) :1252-1257