Citric acid promoted melanin synthesis in B16F10 mouse melanoma cells, but inhibited it in human epidermal melanocytes and HMV-II melanoma cells via the GSK3β/β-catenin signaling pathway

PLoS One. 2020 Dec 17;15(12):e0243565. doi: 10.1371/journal.pone.0243565. eCollection 2020.

Abstract

Melanin, a pigment synthesized by melanocytes in the skin, resists the damage caused by ultraviolet rays to cells. Citric acid, a well-known food additive, is commonly used as an antioxidant and is an important part of the tricarboxylic acid (TCA) cycle for energy production during cellular metabolism. Here, we aimed to investigate whether the addition of excess citric acid regulates melanin synthesis, and to delineate the underlying mechanism. First, we observed that citric acid exerts opposite redox effects on mouse and human cells. Interestingly, treatment with excess citric acid increased the melanin content in mouse cells but decreased it in human cells. Furthermore, the expression of factors important for melanin synthesis, such as microphthalmia-associated transcription factor (MITF), was also regulated by citric acid treatment-it was promoted in mouse cells and suppressed in human cells. Citric acid also impacted the upstream regulators of MITF, glycogen synthase kinase 3β (GSK3β), and β-catenin. Second, we determined the importance of GSK3β in the citric acid-mediated regulation of melanin synthesis, using a GSK3β inhibitor (BIO). To the best of our knowledge, this is the first study to show that citric acid regulates melanin synthesis via the GSK3β/β-catenin signaling pathway, and that equal amounts of exogenous citric acid exert opposing effects on mouse and human cells.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Citric Acid / metabolism
  • Citric Acid / pharmacology*
  • Epidermal Cells / metabolism
  • Epidermis / metabolism
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Humans
  • Melanins / metabolism*
  • Melanocytes / drug effects
  • Melanocytes / metabolism*
  • Melanoma / drug therapy
  • Melanoma / metabolism
  • Melanoma, Experimental / metabolism
  • Mice
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Oxidation-Reduction / drug effects
  • Phosphorylation / drug effects
  • Pigmentation / drug effects
  • Signal Transduction / drug effects
  • beta Catenin / metabolism

Substances

  • Melanins
  • Microphthalmia-Associated Transcription Factor
  • beta Catenin
  • Citric Acid
  • Glycogen Synthase Kinase 3 beta

Grants and funding

The author(s) received no specific funding for this work.