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Agephagy – Adapting Autophagy for Health During Aging
Autophagy is a major cellular recycling process that delivers cellular material and entire organelles to lysosomes for degradation, in a selective or non-selective manner. This process is essential for the maintenance of cellular energy levels, components, and metabolites, as well as the elimination...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892982/ https://www.ncbi.nlm.nih.gov/pubmed/31850344 http://dx.doi.org/10.3389/fcell.2019.00308 |
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author | Stead, Eleanor R. Castillo-Quan, Jorge I. Miguel, Victoria Eugenia Martinez Lujan, Celia Ketteler, Robin Kinghorn, Kerri J. Bjedov, Ivana |
author_facet | Stead, Eleanor R. Castillo-Quan, Jorge I. Miguel, Victoria Eugenia Martinez Lujan, Celia Ketteler, Robin Kinghorn, Kerri J. Bjedov, Ivana |
author_sort | Stead, Eleanor R. |
collection | PubMed |
description | Autophagy is a major cellular recycling process that delivers cellular material and entire organelles to lysosomes for degradation, in a selective or non-selective manner. This process is essential for the maintenance of cellular energy levels, components, and metabolites, as well as the elimination of cellular molecular damage, thereby playing an important role in numerous cellular activities. An important function of autophagy is to enable survival under starvation conditions and other stresses. The majority of factors implicated in aging are modifiable through the process of autophagy, including the accumulation of oxidative damage and loss of proteostasis, genomic instability and epigenetic alteration. These primary causes of damage could lead to mitochondrial dysfunction, deregulation of nutrient sensing pathways and cellular senescence, finally causing a variety of aging phenotypes. Remarkably, advances in the biology of aging have revealed that aging is a malleable process: a mild decrease in signaling through nutrient-sensing pathways can improve health and extend lifespan in all model organisms tested. Consequently, autophagy is implicated in both aging and age-related disease. Enhancement of the autophagy process is a common characteristic of all principal, evolutionary conserved anti-aging interventions, including dietary restriction, as well as inhibition of target of rapamycin (TOR) and insulin/IGF-1 signaling (IIS). As an emerging and critical process in aging, this review will highlight how autophagy can be modulated for health improvement. |
format | Online Article Text |
id | pubmed-6892982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68929822019-12-17 Agephagy – Adapting Autophagy for Health During Aging Stead, Eleanor R. Castillo-Quan, Jorge I. Miguel, Victoria Eugenia Martinez Lujan, Celia Ketteler, Robin Kinghorn, Kerri J. Bjedov, Ivana Front Cell Dev Biol Cell and Developmental Biology Autophagy is a major cellular recycling process that delivers cellular material and entire organelles to lysosomes for degradation, in a selective or non-selective manner. This process is essential for the maintenance of cellular energy levels, components, and metabolites, as well as the elimination of cellular molecular damage, thereby playing an important role in numerous cellular activities. An important function of autophagy is to enable survival under starvation conditions and other stresses. The majority of factors implicated in aging are modifiable through the process of autophagy, including the accumulation of oxidative damage and loss of proteostasis, genomic instability and epigenetic alteration. These primary causes of damage could lead to mitochondrial dysfunction, deregulation of nutrient sensing pathways and cellular senescence, finally causing a variety of aging phenotypes. Remarkably, advances in the biology of aging have revealed that aging is a malleable process: a mild decrease in signaling through nutrient-sensing pathways can improve health and extend lifespan in all model organisms tested. Consequently, autophagy is implicated in both aging and age-related disease. Enhancement of the autophagy process is a common characteristic of all principal, evolutionary conserved anti-aging interventions, including dietary restriction, as well as inhibition of target of rapamycin (TOR) and insulin/IGF-1 signaling (IIS). As an emerging and critical process in aging, this review will highlight how autophagy can be modulated for health improvement. Frontiers Media S.A. 2019-11-28 /pmc/articles/PMC6892982/ /pubmed/31850344 http://dx.doi.org/10.3389/fcell.2019.00308 Text en Copyright © 2019 Stead, Castillo-Quan, Martinez Miguel, Lujan, Ketteler, Kinghorn and Bjedov. http://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 | Cell and Developmental Biology Stead, Eleanor R. Castillo-Quan, Jorge I. Miguel, Victoria Eugenia Martinez Lujan, Celia Ketteler, Robin Kinghorn, Kerri J. Bjedov, Ivana Agephagy – Adapting Autophagy for Health During Aging |
title | Agephagy – Adapting Autophagy for Health During Aging |
title_full | Agephagy – Adapting Autophagy for Health During Aging |
title_fullStr | Agephagy – Adapting Autophagy for Health During Aging |
title_full_unstemmed | Agephagy – Adapting Autophagy for Health During Aging |
title_short | Agephagy – Adapting Autophagy for Health During Aging |
title_sort | agephagy – adapting autophagy for health during aging |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892982/ https://www.ncbi.nlm.nih.gov/pubmed/31850344 http://dx.doi.org/10.3389/fcell.2019.00308 |
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