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Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease
Blood-brain barrier (BBB) breakdown, due to the concomitant disruption of the tight junctions (TJs), normally required for the maintenance of BBB function, and to the altered transport of molecules between blood and brain and vice-versa, has been suggested to significantly contribute to the developm...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259798/ https://www.ncbi.nlm.nih.gov/pubmed/28117381 http://dx.doi.org/10.1038/srep41316 |
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author | Di Pardo, Alba Amico, Enrico Scalabrì, Francesco Pepe, Giuseppe Castaldo, Salvatore Elifani, Francesca Capocci, Luca De Sanctis, Claudia Comerci, Laura Pompeo, Francesco D’Esposito, Maurizio Filosa, Stefania Crispi, Stefania Maglione, Vittorio |
author_facet | Di Pardo, Alba Amico, Enrico Scalabrì, Francesco Pepe, Giuseppe Castaldo, Salvatore Elifani, Francesca Capocci, Luca De Sanctis, Claudia Comerci, Laura Pompeo, Francesco D’Esposito, Maurizio Filosa, Stefania Crispi, Stefania Maglione, Vittorio |
author_sort | Di Pardo, Alba |
collection | PubMed |
description | Blood-brain barrier (BBB) breakdown, due to the concomitant disruption of the tight junctions (TJs), normally required for the maintenance of BBB function, and to the altered transport of molecules between blood and brain and vice-versa, has been suggested to significantly contribute to the development and progression of different brain disorders including Huntington’s disease (HD). Although the detrimental consequence the BBB breakdown may have in the clinical settings, the timing of its alteration remains elusive for many neurodegenerative diseases. In this study we demonstrate for the first time that BBB disruption in HD is not confined to established symptoms, but occurs early in the disease progression. Despite the obvious signs of impaired BBB permeability were only detectable in concomitance with the onset of the disease, signs of deranged TJs integrity occur precociously in the disease and precede the onset of overt symptoms. To our perspective this finding may add a new dimension to the horizons of pathological mechanisms underlying this devastating disease, however much remains to be elucidated for understanding how specific BBB drug targets can be approached in the future. |
format | Online Article Text |
id | pubmed-5259798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52597982017-01-25 Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease Di Pardo, Alba Amico, Enrico Scalabrì, Francesco Pepe, Giuseppe Castaldo, Salvatore Elifani, Francesca Capocci, Luca De Sanctis, Claudia Comerci, Laura Pompeo, Francesco D’Esposito, Maurizio Filosa, Stefania Crispi, Stefania Maglione, Vittorio Sci Rep Article Blood-brain barrier (BBB) breakdown, due to the concomitant disruption of the tight junctions (TJs), normally required for the maintenance of BBB function, and to the altered transport of molecules between blood and brain and vice-versa, has been suggested to significantly contribute to the development and progression of different brain disorders including Huntington’s disease (HD). Although the detrimental consequence the BBB breakdown may have in the clinical settings, the timing of its alteration remains elusive for many neurodegenerative diseases. In this study we demonstrate for the first time that BBB disruption in HD is not confined to established symptoms, but occurs early in the disease progression. Despite the obvious signs of impaired BBB permeability were only detectable in concomitance with the onset of the disease, signs of deranged TJs integrity occur precociously in the disease and precede the onset of overt symptoms. To our perspective this finding may add a new dimension to the horizons of pathological mechanisms underlying this devastating disease, however much remains to be elucidated for understanding how specific BBB drug targets can be approached in the future. Nature Publishing Group 2017-01-24 /pmc/articles/PMC5259798/ /pubmed/28117381 http://dx.doi.org/10.1038/srep41316 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Di Pardo, Alba Amico, Enrico Scalabrì, Francesco Pepe, Giuseppe Castaldo, Salvatore Elifani, Francesca Capocci, Luca De Sanctis, Claudia Comerci, Laura Pompeo, Francesco D’Esposito, Maurizio Filosa, Stefania Crispi, Stefania Maglione, Vittorio Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title | Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title_full | Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title_fullStr | Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title_full_unstemmed | Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title_short | Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease |
title_sort | impairment of blood-brain barrier is an early event in r6/2 mouse model of huntington disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259798/ https://www.ncbi.nlm.nih.gov/pubmed/28117381 http://dx.doi.org/10.1038/srep41316 |
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