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The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite

While investigating peroxynitrite-dependent oxidation in murine RAW 264.7 macrophage cells, we observed that removal of the Labile Iron Pool (LIP) by chelation increases the intracellular oxidation of the fluorescent indicator H(2)DCF, so we concluded that the LIP reacts with peroxynitrite and decre...

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Autores principales: Condeles, André Luís, Toledo Junior, José Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466499/
https://www.ncbi.nlm.nih.gov/pubmed/34572543
http://dx.doi.org/10.3390/biom11091331
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author Condeles, André Luís
Toledo Junior, José Carlos
author_facet Condeles, André Luís
Toledo Junior, José Carlos
author_sort Condeles, André Luís
collection PubMed
description While investigating peroxynitrite-dependent oxidation in murine RAW 264.7 macrophage cells, we observed that removal of the Labile Iron Pool (LIP) by chelation increases the intracellular oxidation of the fluorescent indicator H(2)DCF, so we concluded that the LIP reacts with peroxynitrite and decreases the yield of peroxynitrite-derived oxidants. This was a paradigm-shifting finding in LIP biochemistry and raised many questions. In this follow-up study, we address fundamental properties of the interaction between the LIP and peroxynitrite by using the same cellular model and fluorescence methodology. We have identified that the reaction between the LIP and peroxynitrite has catalytic characteristics, and we have estimated that the rate constant of the reaction is in the range of 10(6) to 10(7) M(−1)s(−1). Together, these observations suggest that the LIP represents a constitutive peroxynitrite reductase system in RAW 264.7 cells.
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spelling pubmed-84664992021-09-27 The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite Condeles, André Luís Toledo Junior, José Carlos Biomolecules Article While investigating peroxynitrite-dependent oxidation in murine RAW 264.7 macrophage cells, we observed that removal of the Labile Iron Pool (LIP) by chelation increases the intracellular oxidation of the fluorescent indicator H(2)DCF, so we concluded that the LIP reacts with peroxynitrite and decreases the yield of peroxynitrite-derived oxidants. This was a paradigm-shifting finding in LIP biochemistry and raised many questions. In this follow-up study, we address fundamental properties of the interaction between the LIP and peroxynitrite by using the same cellular model and fluorescence methodology. We have identified that the reaction between the LIP and peroxynitrite has catalytic characteristics, and we have estimated that the rate constant of the reaction is in the range of 10(6) to 10(7) M(−1)s(−1). Together, these observations suggest that the LIP represents a constitutive peroxynitrite reductase system in RAW 264.7 cells. MDPI 2021-09-09 /pmc/articles/PMC8466499/ /pubmed/34572543 http://dx.doi.org/10.3390/biom11091331 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Condeles, André Luís
Toledo Junior, José Carlos
The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title_full The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title_fullStr The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title_full_unstemmed The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title_short The Labile Iron Pool Reacts Rapidly and Catalytically with Peroxynitrite
title_sort labile iron pool reacts rapidly and catalytically with peroxynitrite
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466499/
https://www.ncbi.nlm.nih.gov/pubmed/34572543
http://dx.doi.org/10.3390/biom11091331
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