| Literature DB >> 32910336 |
Su-Jeong Kim1, Brendan Miller2, Hiroshi Kumagai2,3, Ana R Silverstein2, Melanie Flores2, Kelvin Yen2.
Abstract
A decline in mitochondrial quality and activity has been associated with normal aging and correlated with the development of a wide range of age-related diseases. Here, we review the evidence that a decline in the levels of mitochondrial-derived peptides contributes to aging and age-related diseases. In particular, we discuss how mitochondrial-derived peptides, humanin and MOTS-c, contribute to specific aspects of the aging process, including cellular senescence, chronic inflammation, and cognitive decline. Genetic variations in the coding region of humanin and MOTS-c that are associated with age-related diseases are also reviewed, with particular emphasis placed on how mitochondrial variants might, in turn, regulate MDP expression and age-related phenotypes. Taken together, these observations suggest that mitochondrial-derived peptides influence or regulate a number of key aspects of aging and that strategies directed at increasing mitochondrial-derived peptide levels might have broad beneficial effects.Entities:
Keywords: Age-related diseases; Aging; Humanin; MOTS-c; Mitochondria; Mitochondrial-derived peptides
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Year: 2020 PMID: 32910336 PMCID: PMC8190245 DOI: 10.1007/s11357-020-00262-5
Source DB: PubMed Journal: Geroscience ISSN: 2509-2723 Impact factor: 7.713