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The Oxidative Function of Diferric Transferrin

There is evidence for an unexpected role of diferric transferrin as a terminal oxidase for the transplasma membrane oxidation of cytosolic NADH. In the original studies which showed the reduction of iron in transferrin by the plasma membranes NADH oxidase, the possible role of the reduction on iron...

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Autores principales: Crane, Frederick L., Löw, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286898/
https://www.ncbi.nlm.nih.gov/pubmed/22400117
http://dx.doi.org/10.1155/2012/592806
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author Crane, Frederick L.
Löw, Hans
author_facet Crane, Frederick L.
Löw, Hans
author_sort Crane, Frederick L.
collection PubMed
description There is evidence for an unexpected role of diferric transferrin as a terminal oxidase for the transplasma membrane oxidation of cytosolic NADH. In the original studies which showed the reduction of iron in transferrin by the plasma membranes NADH oxidase, the possible role of the reduction on iron uptake was emphasized. The rapid reoxidation of transferrin iron under aerobic conditions precludes a role for surface reduction at neutral pH for release of iron for uptake at the plasma membrane. The stimulation of cytosolic NADH oxidation by diferric transferrin indicates that the transferrin can act as a terminal oxidase for the transplasma membrane NADH oxidase or can bind to a site which activates the oxidase. Since plasma membrane NADH oxidases clearly play a role in cell signaling, the relation of ferric transferrin stimulation of NADH oxidase to cell control should be considered, especially in relation to the growth promotion by transferrin not related to iron uptake. The oxidase can also contribute to control of cytosolic NAD concentration, and thereby can activate sirtuins for control of ageing and growth.
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spelling pubmed-32868982012-03-07 The Oxidative Function of Diferric Transferrin Crane, Frederick L. Löw, Hans Biochem Res Int Review Article There is evidence for an unexpected role of diferric transferrin as a terminal oxidase for the transplasma membrane oxidation of cytosolic NADH. In the original studies which showed the reduction of iron in transferrin by the plasma membranes NADH oxidase, the possible role of the reduction on iron uptake was emphasized. The rapid reoxidation of transferrin iron under aerobic conditions precludes a role for surface reduction at neutral pH for release of iron for uptake at the plasma membrane. The stimulation of cytosolic NADH oxidation by diferric transferrin indicates that the transferrin can act as a terminal oxidase for the transplasma membrane NADH oxidase or can bind to a site which activates the oxidase. Since plasma membrane NADH oxidases clearly play a role in cell signaling, the relation of ferric transferrin stimulation of NADH oxidase to cell control should be considered, especially in relation to the growth promotion by transferrin not related to iron uptake. The oxidase can also contribute to control of cytosolic NAD concentration, and thereby can activate sirtuins for control of ageing and growth. Hindawi Publishing Corporation 2012 2012-02-09 /pmc/articles/PMC3286898/ /pubmed/22400117 http://dx.doi.org/10.1155/2012/592806 Text en Copyright © 2012 F. L. Crane and H. Löw. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Crane, Frederick L.
Löw, Hans
The Oxidative Function of Diferric Transferrin
title The Oxidative Function of Diferric Transferrin
title_full The Oxidative Function of Diferric Transferrin
title_fullStr The Oxidative Function of Diferric Transferrin
title_full_unstemmed The Oxidative Function of Diferric Transferrin
title_short The Oxidative Function of Diferric Transferrin
title_sort oxidative function of diferric transferrin
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3286898/
https://www.ncbi.nlm.nih.gov/pubmed/22400117
http://dx.doi.org/10.1155/2012/592806
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