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Age‐associated alterations in murine dermis through inflammatory response with mitochondrial DNA deletions
Author(s) -
Kawaguchi Koichiro,
Kim SangEun,
Sugiyama Daijiro,
Sugimoto Masataka,
Maruyama Mitsuo
Publication year - 2019
Publication title -
geriatrics and gerontology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.823
H-Index - 57
eISSN - 1447-0594
pISSN - 1444-1586
DOI - 10.1111/ggi.13635
Subject(s) - senescence , mitochondrial dna , dermis , reactive oxygen species , polymerase chain reaction , phenotype , skin aging , inflammation , real time polymerase chain reaction , dna damage , mitochondrion , microbiology and biotechnology , gene , biology , pathology , dna , medicine , immunology , genetics , dermatology
Aim Skin aging is caused by intrinsic and extrinsic mechanisms. Because it is difficult to distinguish intrinsic mechanisms from extrinsic skin aging, the mechanisms of intrinsic skin aging remain unclear. The present study aimed to characterize age‐associated alterations in murine skin and investigate the mechanisms of intrinsic skin aging. Methods We measured morphological changes in dorsal skin from young (aged 2 months) and old (aged 22–24 months) mice by histological analysis. Age‐associated alteration of gene expression patterns was determined by quantitative polymerase chain reaction and immunohistochemistry. Reactive oxygen species production in mouse dorsal skin was detected by confocal laser scanning microscopy. Mitochondrial DNA deletions were detected by conventional polymerase chain reaction and quantitative polymerase chain reaction analyses. Results Chronologically aged skin had dermal atrophy caused by increased matrix‐degrading enzymes and decreased collagen synthesis. Chronologically aged skin samples also had increased senescence‐associated secretory phenotype factors, elevated reactive oxygen species production and a higher frequency of the mitochondrial DNA common deletion. Conclusions These observations suggest that chronological skin aging is associated with increased frequency of the mitochondrial DNA common deletion and chronic inflammation through the reactive oxygen species–senescence‐associated secretory phenotype axis. Geriatr Gerontol Int 2019; 19: 451–457 .