Resveratrol inhibition of human keratinocyte proliferation via SIRT1/ARNT/ERK dependent downregulation of aquaporin 3

• Published in: Journal of dermatological science Vol. 75; no. 1; pp. 16 - 23
• Main Authors: Wu, Zhouwei, Uchi, Hiroshi, Morino-Koga, Saori, Shi, Weimin, Furue, Masutaka
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Ireland Ltd 01.07.2014
• Subjects: Aquaporin 3; Aquaporin 3 - genetics; Aquaporin 3 - metabolism; ARNT; Aryl Hydrocarbon Receptor Nuclear Translocator - genetics; Aryl Hydrocarbon Receptor Nuclear Translocator - metabolism; Cell Proliferation - drug effects; Cells, Cultured; Dermatology; Dose-Response Relationship, Drug; Down-Regulation; Enzyme Activation; ERK; Extracellular Signal-Regulated MAP Kinases - metabolism; Fibroblasts - drug effects; Fibroblasts - enzymology; Humans; Keratinocytes; Phosphorylation; Resveratrol; RNA Interference; Signal Transduction - drug effects; SIRT1; Sirtuin 1 - genetics; Sirtuin 1 - metabolism; Stilbenes - pharmacology; Transfection; Keratinocytes; ARNT; SIRT1; Resveratrol; Aquaporin 3; ERK
• ISSN: 0923-1811; 1873-569X
• DOI: 10.1016/j.jdermsci.2014.03.004

Abstract Background Aquaporin 3 (AQP3) is the predominant aquaporin in the skin and is overexpressed in hyperplastic epidermal disorders. Upregulation of AQP3 contributes to keratinocyte proliferation and epidermal hyperplasia. Resveratrol, a natural polyphenol, has an anti-proliferative effect on normal human epidermal keratinocytes (NHEKs), but its exact mechanism remains largely unknown. Objective To investigate the ability and mechanism of resveratrol to affect the proliferation and the AQP3 expression in NHEKs. Methods NHEKs treated with resveratrol were analyzed. BrdU incorporation assay, real-time PCR, Western blotting and RNA interference using small interfering RNA were employed. Results At non-toxic concentrations (less than 40 μM), resveratrol inhibited the proliferation of NHEKs. Resveratrol inhibited the ERK phosphorylation and the AQP3 expression with reciprocal upregulation of ARNT expression in a concentration-dependent manner. The inhibitory effects of resveratrol on the ERK phosphorylation and the AQP3 expression were canceled by transfection of siRNA for ARNT, but not by that for AhR. Furthermore, the induction effect of resveratrol on ARNT expression was canceled after SIRT1 was knocked down in NHEKs. Conclusion Resveratrol inhibited NHEK proliferation by downregulating the expression of AQP3 in an SIRT1/ARNT/ERK dependent fashion. This novel mechanism may facilitate drug innovation for hyperplastic skin disorders.