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Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease?
The blood-brain barrier is the interface through which the brain interacts with the milieu and consists mainly of a sophisticated network of brain endothelial cells that forms blood vessels and selectively moves molecules inside and outside the brain through multiple mechanisms of transport. Althoug...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358681/ https://www.ncbi.nlm.nih.gov/pubmed/37449594 http://dx.doi.org/10.4103/1673-5374.373672 |
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author | Estudillo, Enrique López-Ornelas, Adolfo Rodríguez-Oviedo, Alejandro Gutiérrez de la Cruz, Neptali Vargas-Hernández, Marco Antonio Jiménez, Adriana |
author_facet | Estudillo, Enrique López-Ornelas, Adolfo Rodríguez-Oviedo, Alejandro Gutiérrez de la Cruz, Neptali Vargas-Hernández, Marco Antonio Jiménez, Adriana |
author_sort | Estudillo, Enrique |
collection | PubMed |
description | The blood-brain barrier is the interface through which the brain interacts with the milieu and consists mainly of a sophisticated network of brain endothelial cells that forms blood vessels and selectively moves molecules inside and outside the brain through multiple mechanisms of transport. Although brain endothelial cell function is crucial for brain homeostasis, their role in neurodegenerative diseases has historically not been considered with the same importance as other brain cells such as microglia, astroglia, neurons, or even molecules such as amyloid beta, Tau, or alpha-synuclein. Alzheimer’s disease is the most common neurodegenerative disease, and brain endothelial cell dysfunction has been reported by several groups. However, its impairment has barely been considered as a potential therapeutic target. Here we review the most recent advances in the relationship between Alzheimer’s disease and brain endothelial cells commitment and analyze the possible mechanisms through which their alterations contribute to this neurodegenerative disease, highlighting their inflammatory phenotype and the possibility of an impaired secretory pattern of brain endothelial cells that could contribute to the progression of this ailment. Finally, we discuss why shall brain endothelial cells be appreciated as a therapeutic target instead of solely an obstacle for delivering treatments to the injured brain in Alzheimer’s disease. |
format | Online Article Text |
id | pubmed-10358681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-103586812023-07-21 Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? Estudillo, Enrique López-Ornelas, Adolfo Rodríguez-Oviedo, Alejandro Gutiérrez de la Cruz, Neptali Vargas-Hernández, Marco Antonio Jiménez, Adriana Neural Regen Res Review The blood-brain barrier is the interface through which the brain interacts with the milieu and consists mainly of a sophisticated network of brain endothelial cells that forms blood vessels and selectively moves molecules inside and outside the brain through multiple mechanisms of transport. Although brain endothelial cell function is crucial for brain homeostasis, their role in neurodegenerative diseases has historically not been considered with the same importance as other brain cells such as microglia, astroglia, neurons, or even molecules such as amyloid beta, Tau, or alpha-synuclein. Alzheimer’s disease is the most common neurodegenerative disease, and brain endothelial cell dysfunction has been reported by several groups. However, its impairment has barely been considered as a potential therapeutic target. Here we review the most recent advances in the relationship between Alzheimer’s disease and brain endothelial cells commitment and analyze the possible mechanisms through which their alterations contribute to this neurodegenerative disease, highlighting their inflammatory phenotype and the possibility of an impaired secretory pattern of brain endothelial cells that could contribute to the progression of this ailment. Finally, we discuss why shall brain endothelial cells be appreciated as a therapeutic target instead of solely an obstacle for delivering treatments to the injured brain in Alzheimer’s disease. Wolters Kluwer - Medknow 2023-04-20 /pmc/articles/PMC10358681/ /pubmed/37449594 http://dx.doi.org/10.4103/1673-5374.373672 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Estudillo, Enrique López-Ornelas, Adolfo Rodríguez-Oviedo, Alejandro Gutiérrez de la Cruz, Neptali Vargas-Hernández, Marco Antonio Jiménez, Adriana Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title | Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title_full | Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title_fullStr | Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title_full_unstemmed | Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title_short | Thinking outside the black box: are the brain endothelial cells the new main target in Alzheimer’s disease? |
title_sort | thinking outside the black box: are the brain endothelial cells the new main target in alzheimer’s disease? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10358681/ https://www.ncbi.nlm.nih.gov/pubmed/37449594 http://dx.doi.org/10.4103/1673-5374.373672 |
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