Nitrosative Stress in the ER: A New Role for S-Nitrosylation in Neurodegenerative Diseases

S-Nitrosylation, the covalent addition of a nitrogen monoxide group to a cysteine thiol, has been shown to modify the function of a broad spectrum of mammalian, plant, and microbial proteins and thereby to convey the ubiquitous influence of nitric oxide on cellular signal transduction and host defen...

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Published inACS chemical biology Vol. 1; no. 6; pp. 355 - 358
Main Authors Forrester, Michael T, Benhar, Moran, Stamler, Jonathan S
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 21.07.2006
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Abstract S-Nitrosylation, the covalent addition of a nitrogen monoxide group to a cysteine thiol, has been shown to modify the function of a broad spectrum of mammalian, plant, and microbial proteins and thereby to convey the ubiquitous influence of nitric oxide on cellular signal transduction and host defense. Accumulating evidence indicates that dysregulated, diminished, or excessive S-nitrosylation may be implicated in a wide range of pathophysiological conditions. A recent study establishes a functional relationship between inhibitory S-nitrosylation of the redox enzyme protein disulfide isomerase (PDI), defects in regulation of protein folding within the endoplasmic reticulum (ER), and neurodegeneration. Further, an examination of human brains afflicted with Parkinson’s or Alzheimer’s disease supports a causal role for the S-nitrosylation of PDI and consequent ER stress in these prevalent neurodegenerative disorders.
AbstractList S-Nitrosylation, the covalent addition of a nitrogen monoxide group to a cysteine thiol, has been shown to modify the function of a broad spectrum of mammalian, plant, and microbial proteins and thereby to convey the ubiquitous influence of nitric oxide on cellular signal transduction and host defense. Accumulating evidence indicates that dysregulated, diminished, or excessive S-nitrosylation may be implicated in a wide range of pathophysiological conditions. A recent study establishes a functional relationship between inhibitory S-nitrosylation of the redox enzyme protein disulfide isomerase (PDI), defects in regulation of protein folding within the endoplasmic reticulum (ER), and neurodegeneration. Further, an examination of human brains afflicted with Parkinson’s or Alzheimer’s disease supports a causal role for the S-nitrosylation of PDI and consequent ER stress in these prevalent neurodegenerative disorders.
Author Benhar, Moran
Forrester, Michael T
Stamler, Jonathan S
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Snippet S-Nitrosylation, the covalent addition of a nitrogen monoxide group to a cysteine thiol, has been shown to modify the function of a broad spectrum of...
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SubjectTerms Animals
Endoplasmic Reticulum - chemistry
Endoplasmic Reticulum - metabolism
Humans
Neurodegenerative Diseases - metabolism
Nitric Oxide - chemistry
Nitric Oxide - physiology
Nitrosation
Protein Folding
Title Nitrosative Stress in the ER: A New Role for S-Nitrosylation in Neurodegenerative Diseases
URI http://dx.doi.org/10.1021/cb600244c
https://www.ncbi.nlm.nih.gov/pubmed/17163772
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