Cargando…

L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy

Iron is essential in the retina because the heme-containing enzyme guanylate cyclase modulates phototransduction in rods and cones. Transferrin endocytosis is the classical pathway for obtaining iron from the blood circulation in the retina. However, the iron storage protein ferritin has been also r...

Descripción completa

Detalles Bibliográficos
Autores principales: Mendes-Jorge, Luísa, Ramos, David, Valença, Andreia, López-Luppo, Mariana, Pires, Virgínia Maria Rico, Catita, Joana, Nacher, Victor, Navarro, Marc, Carretero, Ana, Rodriguez-Baeza, Alfonso, Ruberte, Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178024/
https://www.ncbi.nlm.nih.gov/pubmed/25259650
http://dx.doi.org/10.1371/journal.pone.0106974
_version_ 1782336880555065344
author Mendes-Jorge, Luísa
Ramos, David
Valença, Andreia
López-Luppo, Mariana
Pires, Virgínia Maria Rico
Catita, Joana
Nacher, Victor
Navarro, Marc
Carretero, Ana
Rodriguez-Baeza, Alfonso
Ruberte, Jesús
author_facet Mendes-Jorge, Luísa
Ramos, David
Valença, Andreia
López-Luppo, Mariana
Pires, Virgínia Maria Rico
Catita, Joana
Nacher, Victor
Navarro, Marc
Carretero, Ana
Rodriguez-Baeza, Alfonso
Ruberte, Jesús
author_sort Mendes-Jorge, Luísa
collection PubMed
description Iron is essential in the retina because the heme-containing enzyme guanylate cyclase modulates phototransduction in rods and cones. Transferrin endocytosis is the classical pathway for obtaining iron from the blood circulation in the retina. However, the iron storage protein ferritin has been also recently proposed as an iron carrier. In this study, the presence of Scara5 and its binding to L-ferritin was investigated in the retina. Our results showed that Scara5, the specific receptor for L-ferritin, was expressed in mouse and human retinas in many cell types, including endothelial cells. Furthermore, we showed that intravenously injected ferritin crossed the blood retinal barrier through L-ferritin binding to Scara5 in endothelial cells. Thus, suggesting the existence of a new pathway for iron delivery and trafficking in the retina. In a murine model of photoreceptor degeneration, Scara5 was downregulated, pointing out this receptor as a potential player implicated in retinopathy and also as a possible therapeutic target.
format Online
Article
Text
id pubmed-4178024
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41780242014-10-02 L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy Mendes-Jorge, Luísa Ramos, David Valença, Andreia López-Luppo, Mariana Pires, Virgínia Maria Rico Catita, Joana Nacher, Victor Navarro, Marc Carretero, Ana Rodriguez-Baeza, Alfonso Ruberte, Jesús PLoS One Research Article Iron is essential in the retina because the heme-containing enzyme guanylate cyclase modulates phototransduction in rods and cones. Transferrin endocytosis is the classical pathway for obtaining iron from the blood circulation in the retina. However, the iron storage protein ferritin has been also recently proposed as an iron carrier. In this study, the presence of Scara5 and its binding to L-ferritin was investigated in the retina. Our results showed that Scara5, the specific receptor for L-ferritin, was expressed in mouse and human retinas in many cell types, including endothelial cells. Furthermore, we showed that intravenously injected ferritin crossed the blood retinal barrier through L-ferritin binding to Scara5 in endothelial cells. Thus, suggesting the existence of a new pathway for iron delivery and trafficking in the retina. In a murine model of photoreceptor degeneration, Scara5 was downregulated, pointing out this receptor as a potential player implicated in retinopathy and also as a possible therapeutic target. Public Library of Science 2014-09-26 /pmc/articles/PMC4178024/ /pubmed/25259650 http://dx.doi.org/10.1371/journal.pone.0106974 Text en © 2014 Mendes-Jorge et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mendes-Jorge, Luísa
Ramos, David
Valença, Andreia
López-Luppo, Mariana
Pires, Virgínia Maria Rico
Catita, Joana
Nacher, Victor
Navarro, Marc
Carretero, Ana
Rodriguez-Baeza, Alfonso
Ruberte, Jesús
L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title_full L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title_fullStr L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title_full_unstemmed L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title_short L-Ferritin Binding to Scara5: A New Iron Traffic Pathway Potentially Implicated in Retinopathy
title_sort l-ferritin binding to scara5: a new iron traffic pathway potentially implicated in retinopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4178024/
https://www.ncbi.nlm.nih.gov/pubmed/25259650
http://dx.doi.org/10.1371/journal.pone.0106974
work_keys_str_mv AT mendesjorgeluisa lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT ramosdavid lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT valencaandreia lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT lopezluppomariana lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT piresvirginiamariarico lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT catitajoana lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT nachervictor lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT navarromarc lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT carreteroana lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT rodriguezbaezaalfonso lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy
AT rubertejesus lferritinbindingtoscara5anewirontrafficpathwaypotentiallyimplicatedinretinopathy