Autophagy and aging: The importance of maintaining "clean" cells
Open accessAbstract
A decrease in the turnover of cellular components and the intracellular accumulation of altered macromolecules and organelles are features common to all aged cells. Diminished autophagic activity plays a major role in these age-related manifestations. In this work we review the molecular defects responsible for the malfunctioning of two forms of autophagy, macroautophagy and chaperone-mediated autophagy, in old mammals, and highlight general and cell-type specific consequences of dysfunction of the autophagic system with age. Dietary caloric restriction and antilipolytic agents have been proven to efficiently stimulate autophagy in old rodents. These and other possible experimental restorative efforts are discussed.
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Decreased macroautophagic activity with age has been described in different mammalian tissues.
“Decreased macroautophagic activity with age has been described in different mammalian tissues (Cuervo, 2008; Cuervo et al., 2005).”
From Protein Homeostasis and Aging: the importance of exquisite quality control (2011) · cites this paper as Cuervo et al., 2005
Mechanisms of lysosomal degradation and autophagy are crucial to remove potentially toxic and protective fatty acids against ER stress-induced cell death.
“The mechanisms of lysosomal degradation and autophagy are crucial to remove potentially toxic and protective fatty acids against ER stress-induced cell death [129,130,131].”
From GLP-1 Receptor Agonists in Non-Alcoholic Fatty Liver Disease: Current Evidence and Future Perspectives (2023) · cites this paper as [130]
The decline in autophagy with age contributes to a number of age-related diseases.
“Recent studies have suggested that the decline in autophagy with age contributes to a number of age-related diseases (Cuervo et al., 2005; Rubinsztein et al., 2011)”
From Noncanonical autophagy promotes the visual cycle (2013) · cites this paper as Cuervo et al., 2005
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Self-citation
- Authors
- Cuervo, A. M., Bergamini, E., Brunk, U. T., Dröge, W., Ffrench, M., & Terman, A.
- Affiliations
- University of Pisa (IT)
- Yeshiva University (US)
- German Cancer Research Center (DE)
- Lyon 1 Université (FR)
- Venue
- Autophagy
- Publisher
- Informa UK Limited
- Published
- 2005-10-11
- Volume
- 1
- Issue
- 3
- Pages
- 131-140
- ISSN
- 1554-8627 (ISSN-L)
- 1554-8635
- OpenAlex
- W2139425230
- Cited by
- 792
- References
- 137
- Citations by year
- 2026: 14 · 2025: 11 · 2024: 26 · 2023: 23 · 2022: 26 · 2021: 39 · 2020: 54 · 2019: 55 · 2018: 53 · 2017: 49 · 2016: 51 · 2015: 55 · 2014: 44 · 2013: 44 · 2012: 50
- FWCI
- 3.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Autophagy (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministero dell’Istruzione, dell’Università e della Ricerca
- National Institutes of Health
- National Institute on Aging (R03AG019834, AG19834, AG-021904)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- aging, macroautophagy, chaperone-mediated autophagy, cellular senescence, age-related diseases, caloric restriction, antilipolytic agents
- MeSH terms
- Aging, Animals, Autophagy, Cytosol, Humans, Lysosomes, Mitochondria, Cellular Senescence
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