Aquatide Activation of SIRT1 Reduces Cellular Senescence through a SIRT1-FOXO1-Autophagy Axis
Biomolecules & Therapeutics
; : 511-518, 2017.
Article
en En
| WPRIM
| ID: wpr-38706
Biblioteca responsable:
WPRO
ABSTRACT
Ultraviolet (UV) irradiation is a relevant environment factor to induce cellular senescence and photoaging. Both autophagy- and silent information regulator T1 (SIRT1)-dependent pathways are critical cellular processes of not only maintaining normal cellular functions, but also protecting cellular senescence in skin exposed to UV irradiation. In the present studies, we investigated whether modulation of autophagy induction using a novel synthetic SIRT1 activator, heptasodium hexacarboxymethyl dipeptide-12 (named as Aquatide), suppresses the UVB irradiation-induced skin aging. Treatment with Aquatide directly activates SIRT1 and stimulates autophagy induction in cultured human dermal fibroblasts. Next, we found that Aquatide-mediated activation of SIRT1 increases autophagy induction via deacetylation of forkhead box class O (FOXO) 1. Finally, UVB irradiation-induced cellular senescence measured by SA-β-gal staining was significantly decreased in cells treated with Aquatide in parallel to occurring SIRT1 activation-dependent autophagy. Together, Aquatide modulates autophagy through SIRT1 activation, contributing to suppression of skin aging caused by UV irradiation.
Palabras clave
Texto completo:
1
Base de datos:
WPRIM
Asunto principal:
Piel
/
Autofagia
/
Envejecimiento de la Piel
/
Senescencia Celular
/
Fibroblastos
Límite:
Humans
Idioma:
En
Revista:
Biomolecules & Therapeutics
Año:
2017
Tipo del documento:
Article