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The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy

Autophagy is a lysosomal degradation pathway and the main clearance route of many toxic protein aggregates. The molecular pathology of Alzheimer's disease (AD) manifests in the form of protein aggregates—extracellular amyloid-β depositions and intracellular tau neurofibrillary tangles. Perturba...

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Autores principales: Festa, Beatrice Paola, Barbosa, Antonio Daniel, Rob, Matea, Rubinsztein, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519395/
https://www.ncbi.nlm.nih.gov/pubmed/34419832
http://dx.doi.org/10.1016/j.coph.2021.07.011
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author Festa, Beatrice Paola
Barbosa, Antonio Daniel
Rob, Matea
Rubinsztein, David C.
author_facet Festa, Beatrice Paola
Barbosa, Antonio Daniel
Rob, Matea
Rubinsztein, David C.
author_sort Festa, Beatrice Paola
collection PubMed
description Autophagy is a lysosomal degradation pathway and the main clearance route of many toxic protein aggregates. The molecular pathology of Alzheimer's disease (AD) manifests in the form of protein aggregates—extracellular amyloid-β depositions and intracellular tau neurofibrillary tangles. Perturbations at different steps of the autophagy pathway observed in cellular and animal models of AD might contribute to amyloid-β and tau accumulation. Increased levels of autophagosomes detected in patients' brains suggest an alteration of autophagy in human disease. Autophagy is also involved in the fine-tuning of inflammation, which increases in the early stages of AD and possibly drives its pathogenesis. Mounting evidence of a causal link between impaired autophagy and AD pathology uncovers an exciting opportunity for the development of autophagy-based therapeutics.
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spelling pubmed-85193952021-10-21 The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy Festa, Beatrice Paola Barbosa, Antonio Daniel Rob, Matea Rubinsztein, David C. Curr Opin Pharmacol Article Autophagy is a lysosomal degradation pathway and the main clearance route of many toxic protein aggregates. The molecular pathology of Alzheimer's disease (AD) manifests in the form of protein aggregates—extracellular amyloid-β depositions and intracellular tau neurofibrillary tangles. Perturbations at different steps of the autophagy pathway observed in cellular and animal models of AD might contribute to amyloid-β and tau accumulation. Increased levels of autophagosomes detected in patients' brains suggest an alteration of autophagy in human disease. Autophagy is also involved in the fine-tuning of inflammation, which increases in the early stages of AD and possibly drives its pathogenesis. Mounting evidence of a causal link between impaired autophagy and AD pathology uncovers an exciting opportunity for the development of autophagy-based therapeutics. Elsevier Science Ltd 2021-10 /pmc/articles/PMC8519395/ /pubmed/34419832 http://dx.doi.org/10.1016/j.coph.2021.07.011 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Festa, Beatrice Paola
Barbosa, Antonio Daniel
Rob, Matea
Rubinsztein, David C.
The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title_full The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title_fullStr The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title_full_unstemmed The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title_short The pleiotropic roles of autophagy in Alzheimer's disease: From pathophysiology to therapy
title_sort pleiotropic roles of autophagy in alzheimer's disease: from pathophysiology to therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519395/
https://www.ncbi.nlm.nih.gov/pubmed/34419832
http://dx.doi.org/10.1016/j.coph.2021.07.011
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