4.7 Article

The Skin-Whitening Effects of Ectoine via the Suppression of α-MSH-Stimulated Melanogenesis and the Activation of Antioxidant Nrf2 Pathways in UVA-Irradiated Keratinocytes

Journal

ANTIOXIDANTS
Volume 9, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/antiox9010063

Keywords

Ectoine; keratinocytes; melanogenesis; tyrosinase; alpha-MSH; Nrf2

Funding

  1. Ministry of Science and Technology
  2. Asia University
  3. China Medical University, Taiwan [MOST-106-2320-B-039-054-MY3, MOST-107-2320-B-039-013-MY3, CMU 107-ASIA-15, CMU106-ASIA-19]
  4. Chinese Medicine Research Center, China Medical University from The Featured Areas Research Center Program within Ministry of Education (MOE) in Taiwan [CMRC-CHM-8]

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Ultraviolet A (UVA)-irradiation induced reactive oxygen species (ROS) production mediates excessive melanogenesis in skin cells leading to pigmentation. We demonstrated the depigmenting and anti-melanogenic effects of Ectoine, a natural bacterial osmolyte, in UVA-irradiated human (HaCaT) keratinocytes, and the underlying molecular mechanisms were elucidated. HaCaT cells were pre-treated with low concentrations of Ectoine (0.5-1.5 mu M) and assayed for various depigmenting and anti-melanogenic parameters. This pre-treatment significantly downregulated ROS generation, alpha-melanocyte-stimulating hormone (alpha-MSH) production, and proopiomelanocortin (POMC) expression in UVA-irradiated HaCaT cells. Also, antioxidant heme oxygenase-1 (HO-1), NAD(P)H dehydrogenase [quinone 1] (NQO-1), and gamma-glutamate-cysteine ligase catalytic subunit (gamma-GCLC) protein expressions were mediated via the nuclear translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) whose knockdown indeed impaired this effect signifying the importance of the Nrf2 pathway. Ectoine was mediating the activation of Nrf2 via the p38, protein kinase B (also known as AKT), protein kinase C (PKC), and casein kinase II protein kinase (CKII) pathways. The conditioned medium obtained from the Ectoine pre-treated and UVA-irradiated HaCaT cells downregulated the tyrosinase, tyrosinase-related protein-1 and -2 (TRP-1/-2), cyclic AMP (c-AMP) protein kinase, c-AMP response element-binding protein (CREB), and microphthalmia-associated transcription factor (MITF) expressions leading to melanoma B16F10 cells having inhibited melanin synthesis. Interestingly, this anti-melanogenic effect in alpha-MSH-stimulated B16F10 cells was observable only at 50-400 mu M concentrations of Ectoine, signifying the key role played by Ectoine (0.5-1 mu M)-treated keratinocytes in skin whitening effects. We concluded that Ectoine could be used as an effective topical natural cosmetic agent with depigmenting and anti-melanogenic efficacy.

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