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Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp

The ceruloplasmin mutant R701W, that causes a dramatic phenotype in the young heterozygous patient carrying this mutation, has been shown to have profound effects also in cell culture models. Here we show that Golgi rearrangement and degradation of the iron exporter ferroportin, that follow transfec...

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Autores principales: Persichini, Tiziana, De Francesco, Giovanni, Capone, Caterina, Cutone, Antimo, Bonaccorsi di Patti, Maria Carmela, Colasanti, Marco, Musci, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314996/
https://www.ncbi.nlm.nih.gov/pubmed/22281056
http://dx.doi.org/10.1016/j.neuint.2012.01.010
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author Persichini, Tiziana
De Francesco, Giovanni
Capone, Caterina
Cutone, Antimo
Bonaccorsi di Patti, Maria Carmela
Colasanti, Marco
Musci, Giovanni
author_facet Persichini, Tiziana
De Francesco, Giovanni
Capone, Caterina
Cutone, Antimo
Bonaccorsi di Patti, Maria Carmela
Colasanti, Marco
Musci, Giovanni
author_sort Persichini, Tiziana
collection PubMed
description The ceruloplasmin mutant R701W, that causes a dramatic phenotype in the young heterozygous patient carrying this mutation, has been shown to have profound effects also in cell culture models. Here we show that Golgi rearrangement and degradation of the iron exporter ferroportin, that follow transfection of cells with this mutant, are accompanied by the massive production of reactive oxygen species (ROS) in the cell. Scavenging ROS production with different antioxidants, including reduced glutathione and zinc, restores Golgi morphology and rescues ferroportin on the cell membrane.
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spelling pubmed-33149962012-04-11 Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp Persichini, Tiziana De Francesco, Giovanni Capone, Caterina Cutone, Antimo Bonaccorsi di Patti, Maria Carmela Colasanti, Marco Musci, Giovanni Neurochem Int Article The ceruloplasmin mutant R701W, that causes a dramatic phenotype in the young heterozygous patient carrying this mutation, has been shown to have profound effects also in cell culture models. Here we show that Golgi rearrangement and degradation of the iron exporter ferroportin, that follow transfection of cells with this mutant, are accompanied by the massive production of reactive oxygen species (ROS) in the cell. Scavenging ROS production with different antioxidants, including reduced glutathione and zinc, restores Golgi morphology and rescues ferroportin on the cell membrane. Pergamon Press 2012-03 /pmc/articles/PMC3314996/ /pubmed/22281056 http://dx.doi.org/10.1016/j.neuint.2012.01.010 Text en © 2012 Elsevier Ltd. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Article
Persichini, Tiziana
De Francesco, Giovanni
Capone, Caterina
Cutone, Antimo
Bonaccorsi di Patti, Maria Carmela
Colasanti, Marco
Musci, Giovanni
Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title_full Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title_fullStr Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title_full_unstemmed Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title_short Reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant Arg701Trp
title_sort reactive oxygen species are involved in ferroportin degradation induced by ceruloplasmin mutant arg701trp
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314996/
https://www.ncbi.nlm.nih.gov/pubmed/22281056
http://dx.doi.org/10.1016/j.neuint.2012.01.010
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