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Biochem Biophys Res Commun. 2014 Jan 3;443(1):167-72. doi: 10.1016/j.bbrc.2013.11.066. Epub 2013 Nov 25.

Age-related disruption of autophagy in dermal fibroblasts modulates extracellular matrix components.

Author information

1
Skin Research Department, POLA Chemical Industries, Inc., Yokohama, Japan; Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
2
Skin Research Department, POLA Chemical Industries, Inc., Yokohama, Japan.
3
Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan; Organelle Homeostasis Research Center, Kyushu University, Fukuoka, Japan.
4
Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
5
Division of Pharmaceutical Cell Biology, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan; Organelle Homeostasis Research Center, Kyushu University, Fukuoka, Japan. Electronic address: tanakay@bioc.phar.kyushu-u.ac.jp.

Abstract

Autophagy is an intracellular degradative system that is believed to be involved in the aging process. The contribution of autophagy to age-related changes in the human skin is unclear. In this study, we examined the relationship between autophagy and skin aging. Transmission electron microscopy and immunofluorescence microscopy analyses of skin tissue and cultured dermal fibroblasts derived from women of different ages revealed an increase in the number of nascent double-membrane autophagosomes with age. Western blot analysis showed that the amount of LC3-II, a form associated with autophagic vacuolar membranes, was significantly increased in aged dermal fibroblasts compared with that in young dermal fibroblasts. Aged dermal fibroblasts were minimally affected by inhibition of autophagic activity. Although lipofuscin autofluorescence was elevated in aged dermal fibroblasts, the expression of Beclin-1 and Atg5-genes essential for autophagosome formation-was similar between young and aged dermal fibroblasts, suggesting that the increase of autophagosomes in aged dermal fibroblasts was due to impaired autophagic flux rather than an increase in autophagosome formation. Treatment of young dermal fibroblasts with lysosomal protease inhibitors, which mimic the condition of aged dermal fibroblasts with reduced autophagic activity, altered the fibroblast content of type I procollagen, hyaluronan and elastin, and caused a breakdown of collagen fibrils. Collectively, these findings suggest that the autophagy pathway is impaired in aged dermal fibroblasts, which leads to deterioration of dermal integrity and skin fragility.

KEYWORDS:

Autophagosome; Autophagy; CMA; Dermal fibroblast; Extracellular matrix; LAMP-2A; LC3; MMP-1; chaperone-mediated autophagy; leu; leupeptin; lysosome-associated receptor protein type 2A; matrix metalloproteinase-1; microtubule-associated protein 1 light chain 3; pep; pepstatin A

PMID:
24287182
DOI:
10.1016/j.bbrc.2013.11.066
[Indexed for MEDLINE]

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