Cellular redox signalling is mediated by the post-translational modification of proteins in signal-transduction pathways by ROS/RNS (reactive oxygen species/reactive nitrogen species) or the products derived from their reactions. NO is perhaps the best understood in this regard with two important modifications of proteins known to induce conformational changes leading to modulation of function. The first is the addition of NO to haem groups as shown for soluble guanylate cyclase and the newly discovered NO/cytochrome c oxidase signalling pathway in mitochondria. The second mechanism is through the modification of thiols by NO to form an S-nitrosated species. Other ROS/RNS can also modify signalling proteins although the mechanisms are not as clearly defined. For example, electrophilic lipids, formed as the reaction products of oxidation reactions, orchestrate adaptive responses in the vasculature by reacting with nucleophilic cysteine residues. In modifying signalling proteins ROS/RNS appear to change the overall activity of signalling pathways in a process that we have termed 'redox tone'. In this review, we discuss these different mechanisms of redox cell signalling, and give specific examples of ROS/RNS participation in signal transduction.
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March 2004
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March 01 2004
Redox signalling: from nitric oxide to oxidized lipids
Sruti Shiva
;
Sruti Shiva
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Doug Moellering
;
Doug Moellering
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Anup Ramachandran
;
Anup Ramachandran
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Anna-Liisa Levonen
;
Anna-Liisa Levonen
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Aimee Landar
;
Aimee Landar
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Aparna Venkatraman
;
Aparna Venkatraman
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Erin Ceaser
;
Erin Ceaser
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Elena Ulasova
;
Elena Ulasova
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Jack H. Crawford
;
Jack H. Crawford
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Paul S. Brookes
;
Paul S. Brookes
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Rakesh P. Patel
;
Rakesh P. Patel
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
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Victor M. Darley-Usmar
Victor M. Darley-Usmar
1
1Department of Pathology, Center for Free Radical Biology, University of Alabama at Birmingham, 901 19th Street South, Birmingham, AL 35294-32180, U.S.A.
1To whom correspondence should be addressed (e-mail Darley@path.uab.edu)
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Biochem Soc Symp (2004) 71: 107–120.
Citation
Chris Cooper, Mike Wilson, Victor Darley-Usmar, Sruti Shiva, Doug Moellering, Anup Ramachandran, Anna-Liisa Levonen, Aimee Landar, Aparna Venkatraman, Erin Ceaser, Elena Ulasova, Jack H. Crawford, Paul S. Brookes, Rakesh P. Patel, Victor M. Darley-Usmar; Redox signalling: from nitric oxide to oxidized lipids. Biochem Soc Symp 1 March 2004; 71 107–120. doi: https://doi.org/10.1042/bss0710107
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