Nitric oxide, S-nitrosylation and neurodegeneration

被引:61
作者
Chung, KKK
Dawson, TM
Dawson, VL
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Dept Neurol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Dept Neurosci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Dept Physiol, Baltimore, MD 21205 USA
关键词
nitric oxide; S-nitrosylation; oxidative stress; nitrosative stress; parkin; Parkinson's disease; neurodegeneration;
D O I
10.1170/T625
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
Nitric oxide is a critically important signaling molecule, controlling a wide range of pathways and biological processes. Highly reactive nitric oxide mediates its function through reaction with different molecules directly or indirectly. One of these modifications is the S-nitrosylation of cysteine residues in proteins. S-nitrosylation is emerging as an important redox signaling mechanism and has been found to regulate a broad range of biologic, physiologic and cellular functions. One of the major findings in this area recently is the linkage of nitrosative stress to various neurodegenerative disorders. Oxidative stress has long been regarded as a prime mediator in the development of neurodegeneration as various indices of oxidative stress are readily observed in postmortem studies. A causitive role for nitrosative stress in neurodegeneration is just now being appreciated. The direct connection of S-nitrosylation to the pathogenesis of Parkinson's disease in recent studies further provide insights into how imbalance in nitric oxide metabolism can contribute to the development of selective injury and disease.
引用
收藏
页码:247 / 254
页数:8
相关论文
共 79 条
[1]   Detection of S-Nitrosothiols and other nitric oxide derivatives by photolysis-chemiluminescence spectrometry [J].
Alpert, C ;
Ramdev, N ;
George, D ;
Loscalzo, J .
ANALYTICAL BIOCHEMISTRY, 1997, 245 (01) :1-7
[2]   Oxidative stress in neurodegeneration: cause or consequence? [J].
Andersen, JK .
NATURE MEDICINE, 2004, 10 (07) :S18-S25
[3]   Neurodegenerative diseases and oxidative stress [J].
Barnham, KJ ;
Masters, CL ;
Bush, AI .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (03) :205-214
[4]   The mechanisms of vesicle budding and fusion [J].
Bonifacino, JS ;
Glick, BS .
CELL, 2004, 116 (02) :153-166
[5]   Nitric oxide:: NO apoptosis or turning it ON? [J].
Brüne, B .
CELL DEATH AND DIFFERENTIATION, 2003, 10 (08) :864-869
[6]   Structure of the C-terminal RING finger from a RING-IBR-RING/TRIAD motif reveals a novel zinc-binding domain distinct from a RING [J].
Capili, AD ;
Edghill, EL ;
Wu, K ;
Borden, KLB .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (05) :1117-1129
[7]   Molecular basis of NMDA receptor-coupled ion channel modulation by S-nitrosylation [J].
Choi, YB ;
Tenneti, L ;
Le, DA ;
Ortiz, J ;
Bai, G ;
Chen, HSV ;
Lipton, SA .
NATURE NEUROSCIENCE, 2000, 3 (01) :15-21
[8]  
CHUNG KK, 2004, NEURON, V44, P1
[9]   S-nitrosylation of Parkin regulates ubiquitination and compromises Parkin's protective function [J].
Chung, KKK ;
Thomas, B ;
Li, XJ ;
Pletnikova, O ;
Troncoso, JC ;
Marsh, L ;
Dawson, VL ;
Dawson, TM .
SCIENCE, 2004, 304 (5675) :1328-1331
[10]   New insights into Parkinson's disease [J].
Chung, KKK ;
Dawson, VL ;
Dawson, TM .
JOURNAL OF NEUROLOGY, 2003, 250 (Suppl 3) :15-24