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Autophagy and Longevity
Autophagy is an evolutionally conserved cytoplasmic degradation system in which varieties of materials are sequestered by a double membrane structure, autophagosome, and delivered to the lysosomes for the degradation. Due to the wide varieties of targets, autophagic activity is essential for cellula...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for Molecular and Cellular Biology
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792715/ https://www.ncbi.nlm.nih.gov/pubmed/29370695 http://dx.doi.org/10.14348/molcells.2018.2333 |
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author | Nakamura, Shuhei Yoshimori, Tamotsu |
author_facet | Nakamura, Shuhei Yoshimori, Tamotsu |
author_sort | Nakamura, Shuhei |
collection | PubMed |
description | Autophagy is an evolutionally conserved cytoplasmic degradation system in which varieties of materials are sequestered by a double membrane structure, autophagosome, and delivered to the lysosomes for the degradation. Due to the wide varieties of targets, autophagic activity is essential for cellular homeostasis. Recent genetic evidence indicates that autophagy has a crucial role in the regulation of animal lifespan. Basal level of autophagic activity is elevated in many longevity paradigms and the activity is required for lifespan extension. In most cases, genes involved in autophagy and lysosomal function are induced by several transcription factors including HLH-30/TFEB, PHA-4/FOXA and MML-1/Mondo in long-lived animals. Pharmacological treatments have been shown to extend lifespan through activation of autophagy, indicating autophagy could be a potential and promising target to modulate animal lifespan. Here we summarize recent progress regarding the role of autophagy in lifespan regulation. |
format | Online Article Text |
id | pubmed-5792715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-57927152018-02-14 Autophagy and Longevity Nakamura, Shuhei Yoshimori, Tamotsu Mol Cells Minireview Autophagy is an evolutionally conserved cytoplasmic degradation system in which varieties of materials are sequestered by a double membrane structure, autophagosome, and delivered to the lysosomes for the degradation. Due to the wide varieties of targets, autophagic activity is essential for cellular homeostasis. Recent genetic evidence indicates that autophagy has a crucial role in the regulation of animal lifespan. Basal level of autophagic activity is elevated in many longevity paradigms and the activity is required for lifespan extension. In most cases, genes involved in autophagy and lysosomal function are induced by several transcription factors including HLH-30/TFEB, PHA-4/FOXA and MML-1/Mondo in long-lived animals. Pharmacological treatments have been shown to extend lifespan through activation of autophagy, indicating autophagy could be a potential and promising target to modulate animal lifespan. Here we summarize recent progress regarding the role of autophagy in lifespan regulation. Korean Society for Molecular and Cellular Biology 2018-01-31 2018-01-23 /pmc/articles/PMC5792715/ /pubmed/29370695 http://dx.doi.org/10.14348/molcells.2018.2333 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Minireview Nakamura, Shuhei Yoshimori, Tamotsu Autophagy and Longevity |
title | Autophagy and Longevity |
title_full | Autophagy and Longevity |
title_fullStr | Autophagy and Longevity |
title_full_unstemmed | Autophagy and Longevity |
title_short | Autophagy and Longevity |
title_sort | autophagy and longevity |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792715/ https://www.ncbi.nlm.nih.gov/pubmed/29370695 http://dx.doi.org/10.14348/molcells.2018.2333 |
work_keys_str_mv | AT nakamurashuhei autophagyandlongevity AT yoshimoritamotsu autophagyandlongevity |