Protein S-nitrosylation: Role for nitric oxide signaling in neuronal death

被引:38
作者
Shahani, Neelam [1 ]
Sawa, Akira [1 ,2 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21287 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2012年 / 1820卷 / 06期
关键词
Nitric oxide; S-nitrosylation; Apoptosis; Caspase; XIAP; GAPDH; NECROSIS-FACTOR-ALPHA; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE GAPDH; AMYOTROPHIC-LATERAL-SCLEROSIS; UBIQUITIN-LIGASE ACTIVITY; PROGRAMMED CELL-DEATH; ALZHEIMERS-DISEASE; NUCLEAR TRANSLOCATION; PARKINSONS-DISEASE; TYROSINE NITRATION; NEURODEGENERATIVE DISORDERS;
D O I
10.1016/j.bbagen.2011.07.010
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
Background: One of the signaling mechanisms mediated by nitric oxide (NO) is through S-nitrosylation, the reversible redox-based modification of cysteine residues, on target proteins that regulate a myriad of physiological and pathophysiological processes. In particular, an increasing number of studies have identified important roles for S-nitrosylation in regulating cell death. Scope of review: The present review focuses on different targets and functional consequences associated with nitric oxide and protein S-nitrosylation during neuronal cell death. Major conclusions: S-Nitrosylation exhibits double-edged effects dependent on the levels, spatiotemporal distribution, and origins of NO in the brain: in general Snitrosylation resulting from the basal low level of NO in cells exerts anti-cell death effects, whereas S-nitrosylation elicited by induced NO upon stressed conditions is implicated in pro-cell death effects. General Significance: Dysregulated protein S-nitrosylation is implicated in the pathogenesis of several diseases including degenerative diseases of the central nervous system (CNS). Elucidating specific targets of S-nitrosylation as well as their regulatory mechanisms may aid in the development of therapeutic intervention in a wide range of brain diseases. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:736 / 742
页数:7
相关论文
共 113 条
[1]   Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[2]   Regulated protein denitrosylation by cytosolic and mitochondrial thioredoxins [J].
Benhar, Moran ;
Forrester, Michael T. ;
Hess, Douglas T. ;
Stamler, Jonathan S. .
SCIENCE, 2008, 320 (5879) :1050-1054
[3]   Protein denitrosylation: enzymatic mechanisms and cellular functions [J].
Benhar, Moran ;
Forrester, Michael T. ;
Stamler, Jonathan S. .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (10) :721-732
[4]   Nitric oxide and neuronal death [J].
Brown, Guy C. .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2010, 23 (03) :153-165
[5]   Oxidatively Modified Glyceraldehyde-3-Phosphate Dehydrogenase (GAPDH) and Alzheimer's Disease: Many Pathways to Neurodegeneration [J].
Butterfield, D. Allan ;
Hardas, Sarita S. ;
Lange, Miranda L. Bader .
JOURNAL OF ALZHEIMERS DISEASE, 2010, 20 (02) :369-393
[6]  
Calabrese V, 2009, ANTIOXID REDOX SIGN, V11, P2717, DOI [10.1089/ars.2009.2721, 10.1089/ARS.2009.2721]
[7]   Mitochondria: Dynamic organelles in disease, aging, and development [J].
Chan, David C. .
CELL, 2006, 125 (07) :1241-1252
[8]   Phosphatase PTEN in neuronal injury and brain disorders [J].
Chang, Ning ;
El-Hayek, Youssef H. ;
Gomez, Everlyne ;
Wan, Qi .
TRENDS IN NEUROSCIENCES, 2007, 30 (11) :581-586
[9]   Mitochondrial fusion protects against neurodegeneration in the cerebellum [J].
Chen, Hsiuchen ;
McCaffery, J. Michael ;
Chan, David C. .
CELL, 2007, 130 (03) :548-562
[10]   Mitochondrial dynamics in cell death and neurodegeneration [J].
Cho, Dong-Hyung ;
Nakamura, Tomohiro ;
Lipton, Stuart A. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2010, 67 (20) :3435-3447