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Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model

Acquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, ide...

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Autores principales: Dolón, Jorge F., Paniagua, Antonio E., Valle, Vicente, Segurado, Alicia, Arévalo, Rosario, Velasco, Almudena, Lillo, Concepción
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076319/
https://www.ncbi.nlm.nih.gov/pubmed/30076417
http://dx.doi.org/10.1038/s41598-018-30210-5
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author Dolón, Jorge F.
Paniagua, Antonio E.
Valle, Vicente
Segurado, Alicia
Arévalo, Rosario
Velasco, Almudena
Lillo, Concepción
author_facet Dolón, Jorge F.
Paniagua, Antonio E.
Valle, Vicente
Segurado, Alicia
Arévalo, Rosario
Velasco, Almudena
Lillo, Concepción
author_sort Dolón, Jorge F.
collection PubMed
description Acquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, identified in mammals, are expressed in epithelial-derived tissues like brain, kidney and retina. CRB2 has a ubiquitous expression and has been detected in embryonic brain tissue; but currently there is no data regarding its localization in the adult brain. In our study, we characterized the presence of CRB2 in adult mice brain, where it is particularly enriched in cortex, hippocampus, hypothalamus and cerebellum. Double immunofluorescence analysis confirmed that CRB2 is a neuron-specific protein, present in both soma and projections where colocalizes with certain populations of exocytic and endocytic vesicles and with other members of the Crumbs complex. Finally, in the cortex of CRB1(rd8) mutant mice that contain a mutation in the Crb1 gene generating a truncated CRB1 protein, there is an abnormal increase in the expression levels of the CRB2 protein which suggests a possible compensatory mechanism for the malfunction of CRB1 in this mutant background.
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spelling pubmed-60763192018-08-08 Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model Dolón, Jorge F. Paniagua, Antonio E. Valle, Vicente Segurado, Alicia Arévalo, Rosario Velasco, Almudena Lillo, Concepción Sci Rep Article Acquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, identified in mammals, are expressed in epithelial-derived tissues like brain, kidney and retina. CRB2 has a ubiquitous expression and has been detected in embryonic brain tissue; but currently there is no data regarding its localization in the adult brain. In our study, we characterized the presence of CRB2 in adult mice brain, where it is particularly enriched in cortex, hippocampus, hypothalamus and cerebellum. Double immunofluorescence analysis confirmed that CRB2 is a neuron-specific protein, present in both soma and projections where colocalizes with certain populations of exocytic and endocytic vesicles and with other members of the Crumbs complex. Finally, in the cortex of CRB1(rd8) mutant mice that contain a mutation in the Crb1 gene generating a truncated CRB1 protein, there is an abnormal increase in the expression levels of the CRB2 protein which suggests a possible compensatory mechanism for the malfunction of CRB1 in this mutant background. Nature Publishing Group UK 2018-08-03 /pmc/articles/PMC6076319/ /pubmed/30076417 http://dx.doi.org/10.1038/s41598-018-30210-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dolón, Jorge F.
Paniagua, Antonio E.
Valle, Vicente
Segurado, Alicia
Arévalo, Rosario
Velasco, Almudena
Lillo, Concepción
Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title_full Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title_fullStr Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title_full_unstemmed Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title_short Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1(rd8) mutant mouse model
title_sort expression and localization of the polarity protein crb2 in adult mouse brain: a comparison with the crb1(rd8) mutant mouse model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6076319/
https://www.ncbi.nlm.nih.gov/pubmed/30076417
http://dx.doi.org/10.1038/s41598-018-30210-5
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