FoxO3a is an antimelanogenic factor that mediates antioxidant-induced depigmentation

J Invest Dermatol. 2014 May;134(5):1378-1388. doi: 10.1038/jid.2013.510. Epub 2013 Nov 27.

Abstract

Forkhead box-O (FoxO) family transcriptional factors control the expression of many genes involved in a variety of cellular processes. Melanogenesis is an oxidizing process; therefore, many antioxidants are used to inhibit melanin production. However, their mechanism of action is poorly understood. In this study, we investigated the role of FoxO3a, which is a key factor in oxidative stress-related cellular responses in melanogenesis. When FoxO3a expression was inhibited, the expression of melanogenic genes and melanin levels increased. In contrast, the overexpression of wild-type FoxO3a and the increased nuclear translocation induced by the phosphoinositide 3-kinase inhibitors or by Akt inhibition reversed these phenomena. This effect was not observed when FoxO3a harbored a deletion in the nuclear localization signal, indicating that its nuclear translocation is important for the regulation of melanogenesis. When antioxidants such as vitamin C, N-acetylcysteine, and Trolox were applied to MNT1 cells, melanin levels decreased in parallel with FoxO3a nuclear translocation, and this effect disappeared with FoxO3a-directed small interfering RNA treatment. Because FoxO3a orchestrates the expression of many genes in order to regulate cellular phenotypes in a variety of environmental states, this gene, a factor involved in melanogenesis regulation, may represent a good target for studying antimelanogenic signaling pathways and for designing pharmacological or antimelanogenic agents that regulate melanin synthesis.

MeSH terms

  • Aging / physiology
  • Animals
  • Antioxidants / metabolism*
  • Antioxidants / pharmacology
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins / metabolism
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism*
  • Humans
  • Hypopigmentation / genetics
  • Hypopigmentation / metabolism*
  • Melanins / biosynthesis
  • Melanins / metabolism
  • Melanocytes / cytology
  • Melanocytes / physiology*
  • Melanoma
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology*
  • Phenotype
  • Phosphatidylinositol 3-Kinases / metabolism
  • Primary Cell Culture
  • RNA, Small Interfering / genetics
  • Skin Neoplasms

Substances

  • Antioxidants
  • Caenorhabditis elegans Proteins
  • FOXO3 protein, human
  • FOXO3a protein, C elegans
  • Forkhead Box Protein O3
  • Forkhead Transcription Factors
  • Melanins
  • RNA, Small Interfering
  • Phosphatidylinositol 3-Kinases