Cargando…
APOE-amyloid interaction: Therapeutic targets
Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118587/ https://www.ncbi.nlm.nih.gov/pubmed/32027932 http://dx.doi.org/10.1016/j.nbd.2020.104784 |
_version_ | 1783514591214436352 |
---|---|
author | Wisniewski, Thomas Drummond, Eleanor |
author_facet | Wisniewski, Thomas Drummond, Eleanor |
author_sort | Wisniewski, Thomas |
collection | PubMed |
description | Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest genetic risk factor for late-onset AD. The interaction between APOE and amyloid β (Aβ) plays a key role in AD pathogenesis. The APOE-Aβ interaction regulates Aβ aggregation and clearance and therefore directly influences the development of amyloid plaques, congophilic amyloid angiopathy and subsequent tau related pathology. Relatively few AD therapeutic approaches have directly targeted the APOE-Aβ interaction thus far. Here we review the critical role of APOE in the pathogenesis of AD and some of the most promising therapeutic approaches that focus on the APOE-Aβ interaction. |
format | Online Article Text |
id | pubmed-7118587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71185872021-05-01 APOE-amyloid interaction: Therapeutic targets Wisniewski, Thomas Drummond, Eleanor Neurobiol Dis Article Alzheimer’s disease (AD) is a devastating neurodegenerative disorder that is growing in prevalence globally. It is the only major cause of death without any effective pharmacological means to treat or slow progression. Inheritance of the ε4 allele of the Apolipoprotein (APO) E gene is the strongest genetic risk factor for late-onset AD. The interaction between APOE and amyloid β (Aβ) plays a key role in AD pathogenesis. The APOE-Aβ interaction regulates Aβ aggregation and clearance and therefore directly influences the development of amyloid plaques, congophilic amyloid angiopathy and subsequent tau related pathology. Relatively few AD therapeutic approaches have directly targeted the APOE-Aβ interaction thus far. Here we review the critical role of APOE in the pathogenesis of AD and some of the most promising therapeutic approaches that focus on the APOE-Aβ interaction. 2020-02-04 2020-05 /pmc/articles/PMC7118587/ /pubmed/32027932 http://dx.doi.org/10.1016/j.nbd.2020.104784 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Wisniewski, Thomas Drummond, Eleanor APOE-amyloid interaction: Therapeutic targets |
title | APOE-amyloid interaction: Therapeutic targets |
title_full | APOE-amyloid interaction: Therapeutic targets |
title_fullStr | APOE-amyloid interaction: Therapeutic targets |
title_full_unstemmed | APOE-amyloid interaction: Therapeutic targets |
title_short | APOE-amyloid interaction: Therapeutic targets |
title_sort | apoe-amyloid interaction: therapeutic targets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118587/ https://www.ncbi.nlm.nih.gov/pubmed/32027932 http://dx.doi.org/10.1016/j.nbd.2020.104784 |
work_keys_str_mv | AT wisniewskithomas apoeamyloidinteractiontherapeutictargets AT drummondeleanor apoeamyloidinteractiontherapeutictargets |