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Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease
Amyloid-β (Aβ) is the predominant pathologic protein in Alzheimer’s disease (AD). The production and deposition of Aβ are important factors affecting AD progression and prognosis. The deposition of neurotoxic Aβ contributes to damage of the blood–brain barrier. However, the BBB is also crucial in ma...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326917/ https://www.ncbi.nlm.nih.gov/pubmed/34349624 http://dx.doi.org/10.3389/fncel.2021.695479 |
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author | Wang, Dong Chen, Fanglian Han, Zhaoli Yin, Zhenyu Ge, Xintong Lei, Ping |
author_facet | Wang, Dong Chen, Fanglian Han, Zhaoli Yin, Zhenyu Ge, Xintong Lei, Ping |
author_sort | Wang, Dong |
collection | PubMed |
description | Amyloid-β (Aβ) is the predominant pathologic protein in Alzheimer’s disease (AD). The production and deposition of Aβ are important factors affecting AD progression and prognosis. The deposition of neurotoxic Aβ contributes to damage of the blood–brain barrier. However, the BBB is also crucial in maintaining the normal metabolism of Aβ, and dysfunction of the BBB aggravates Aβ deposition. This review characterizes Aβ deposition and BBB damage in AD, summarizes their interactions, and details their respective mechanisms. |
format | Online Article Text |
id | pubmed-8326917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83269172021-08-03 Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease Wang, Dong Chen, Fanglian Han, Zhaoli Yin, Zhenyu Ge, Xintong Lei, Ping Front Cell Neurosci Neuroscience Amyloid-β (Aβ) is the predominant pathologic protein in Alzheimer’s disease (AD). The production and deposition of Aβ are important factors affecting AD progression and prognosis. The deposition of neurotoxic Aβ contributes to damage of the blood–brain barrier. However, the BBB is also crucial in maintaining the normal metabolism of Aβ, and dysfunction of the BBB aggravates Aβ deposition. This review characterizes Aβ deposition and BBB damage in AD, summarizes their interactions, and details their respective mechanisms. Frontiers Media S.A. 2021-07-19 /pmc/articles/PMC8326917/ /pubmed/34349624 http://dx.doi.org/10.3389/fncel.2021.695479 Text en Copyright © 2021 Wang, Chen, Han, Yin, Ge and Lei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Wang, Dong Chen, Fanglian Han, Zhaoli Yin, Zhenyu Ge, Xintong Lei, Ping Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title | Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title_full | Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title_fullStr | Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title_full_unstemmed | Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title_short | Relationship Between Amyloid-β Deposition and Blood–Brain Barrier Dysfunction in Alzheimer’s Disease |
title_sort | relationship between amyloid-β deposition and blood–brain barrier dysfunction in alzheimer’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326917/ https://www.ncbi.nlm.nih.gov/pubmed/34349624 http://dx.doi.org/10.3389/fncel.2021.695479 |
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