Reactive oxygen species and α,β-unsaturated aldehydes as second messengers in signal transduction

被引:75
作者
Forman, Henry Jay [1 ]
机构
[1] Univ Calif, Sch Nat Sci, Merced, CA USA
来源
OXIDATIVE/NITROSATIVE STRESS AND DISEASE | 2010年 / 1203卷
关键词
hydrogen peroxide; superoxide; 4-hydroxynonenal; thiol; thiolate; protein tyrosine phosphatase; glutathionylation; thioredoxin; PROTEIN-TYROSINE-PHOSPHATASE; GAMMA-GLUTAMYLCYSTEINE SYNTHETASE; MITOCHONDRIAL HYDROGEN-PEROXIDE; GLUTAMATE CYSTEINE LIGASE; INDUCED OXIDATIVE STRESS; LOW-DENSITY-LIPOPROTEIN; ACTIVE-SITE CYSTEINE; LIPID-PEROXIDATION; REDOX REGULATION; REVERSIBLE INACTIVATION;
D O I
10.1111/j.1749-6632.2010.05551.x
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
Signaling by H(2)O(2), alpha,beta-unsaturated aldehydes, such as 4-hydroxy-2-nonenal (HNE) and related chemical species, is thought to differ from signaling by other second messengers because the oxidants and other electrophiles can readily undergo nonenzymatic reactions and are therefore classified as "reactive." This brief review will describe how and when the chemistry of signaling is similar or differs from classic second messengers, such as cyclic AMP, or posttranslational signaling, such as farnesylation or ubiquitination. The chemistry of cysteine provides a common factor that underlies signaling by H(2)O(2) and HNE. Nonetheless, as H(2)O(2) and HNE are rapidly metabolized in vivo, spatial considerations are extremely important in their actions. Therefore, the locations of sources of H(2)O(2) and alpha,beta-unsaturated aldehydes, the NADPH oxidases, mitochondria, membrane lipids, and redox cycling toxicants, as well as their targets, are key factors. The activation of the JNK pathway by HNE and endogenously generated H(2)O(2) illustrates these principles.
引用
收藏
页码:35 / 44
页数:10
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