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The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases

Damaged and misfolded proteins accumulate during the aging process, impairing cell function and tissue homeostasis. These perturbations to protein homeostasis (proteostasis) are hallmarks of age-related neurodegenerative disorders such as Alzheimer’s, Parkinson’s or Huntington’s disease. Damaged pro...

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Detalles Bibliográficos
Autores principales: Saez, Isabel, Vilchez, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958958/
https://www.ncbi.nlm.nih.gov/pubmed/24653662
http://dx.doi.org/10.2174/138920291501140306113344
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author Saez, Isabel
Vilchez, David
author_facet Saez, Isabel
Vilchez, David
author_sort Saez, Isabel
collection PubMed
description Damaged and misfolded proteins accumulate during the aging process, impairing cell function and tissue homeostasis. These perturbations to protein homeostasis (proteostasis) are hallmarks of age-related neurodegenerative disorders such as Alzheimer’s, Parkinson’s or Huntington’s disease. Damaged proteins are degraded by cellular clearance mechanisms such as the proteasome, a key component of the proteostasis network. Proteasome activity declines during aging, and proteasomal dysfunction is associated with late-onset disorders. Modulation of proteasome activity extends lifespan and protects organisms from symptoms associated with proteostasis disorders. Here we review the links between proteasome activity, aging and neurodegeneration. Additionally, strategies to modulate proteasome activity and delay the onset of diseases associated to proteasomal dysfunction are discussed herein.
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spelling pubmed-39589582014-08-01 The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases Saez, Isabel Vilchez, David Curr Genomics Article Damaged and misfolded proteins accumulate during the aging process, impairing cell function and tissue homeostasis. These perturbations to protein homeostasis (proteostasis) are hallmarks of age-related neurodegenerative disorders such as Alzheimer’s, Parkinson’s or Huntington’s disease. Damaged proteins are degraded by cellular clearance mechanisms such as the proteasome, a key component of the proteostasis network. Proteasome activity declines during aging, and proteasomal dysfunction is associated with late-onset disorders. Modulation of proteasome activity extends lifespan and protects organisms from symptoms associated with proteostasis disorders. Here we review the links between proteasome activity, aging and neurodegeneration. Additionally, strategies to modulate proteasome activity and delay the onset of diseases associated to proteasomal dysfunction are discussed herein. Bentham Science Publishers 2014-02 2014-02 /pmc/articles/PMC3958958/ /pubmed/24653662 http://dx.doi.org/10.2174/138920291501140306113344 Text en ©2014 Bentham Science Publishers http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Saez, Isabel
Vilchez, David
The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title_full The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title_fullStr The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title_full_unstemmed The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title_short The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases
title_sort mechanistic links between proteasome activity, aging and age-related diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958958/
https://www.ncbi.nlm.nih.gov/pubmed/24653662
http://dx.doi.org/10.2174/138920291501140306113344
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