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Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling

Excessive increase in melanin pigment in the skin can be caused by a variety of environmental factors, including UV radiation, and can result in spots, freckles, and skin cancer. Therefore, it is important to develop functional whitening cosmetic reagents that regulate melanogenesis. In this study,...

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Autores principales: Choi, Mi Ran, Lee, Heejin, Kim, Hyoung Kyu, Han, Jin, Seol, Jung Eun, Vasileva, Elena A., Mishchenko, Natalia P., Fedoreyev, Sergey A., Stonik, Valentin A., Ju, Won Seok, Kim, Dai-Jin, Lee, Sang-Rae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502928/
https://www.ncbi.nlm.nih.gov/pubmed/36135744
http://dx.doi.org/10.3390/md20090555
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author Choi, Mi Ran
Lee, Heejin
Kim, Hyoung Kyu
Han, Jin
Seol, Jung Eun
Vasileva, Elena A.
Mishchenko, Natalia P.
Fedoreyev, Sergey A.
Stonik, Valentin A.
Ju, Won Seok
Kim, Dai-Jin
Lee, Sang-Rae
author_facet Choi, Mi Ran
Lee, Heejin
Kim, Hyoung Kyu
Han, Jin
Seol, Jung Eun
Vasileva, Elena A.
Mishchenko, Natalia P.
Fedoreyev, Sergey A.
Stonik, Valentin A.
Ju, Won Seok
Kim, Dai-Jin
Lee, Sang-Rae
author_sort Choi, Mi Ran
collection PubMed
description Excessive increase in melanin pigment in the skin can be caused by a variety of environmental factors, including UV radiation, and can result in spots, freckles, and skin cancer. Therefore, it is important to develop functional whitening cosmetic reagents that regulate melanogenesis. In this study, we investigated the effects of echinochrome A (Ech A) on melanogenesis in the B16F10 murine melanoma cell line. We triggered B16F10 cells using α-MSH under Ech A treatment to observe melanin synthesis and analyze expression changes in melanogenesis-related enzymes (tyrosinase, tyrosinase-related protein 1 (TYRP1), and tyrosinase-related protein 2 (TYRP2)) at the mRNA and protein levels. Furthermore, we measured expression changes in the microphthalmia-associated transcription factor (MITF), CREB, and pCREB proteins. Melanin synthesis in the cells stimulated by α-MSH was significantly reduced by Ech A. The expression of the tyrosinase, TYRP1, and TYRP2 mRNA and proteins was significantly decreased by Ech A, as was that of the MITF, CREB, and pCREB proteins. These results show that Ech A suppresses melanin synthesis by regulating melanogenesis-related enzymes through the CREB signaling pathway and suggest the potential of Ech A as a functional agent to prevent pigmentation and promote skin whitening.
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spelling pubmed-95029282022-09-24 Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling Choi, Mi Ran Lee, Heejin Kim, Hyoung Kyu Han, Jin Seol, Jung Eun Vasileva, Elena A. Mishchenko, Natalia P. Fedoreyev, Sergey A. Stonik, Valentin A. Ju, Won Seok Kim, Dai-Jin Lee, Sang-Rae Mar Drugs Article Excessive increase in melanin pigment in the skin can be caused by a variety of environmental factors, including UV radiation, and can result in spots, freckles, and skin cancer. Therefore, it is important to develop functional whitening cosmetic reagents that regulate melanogenesis. In this study, we investigated the effects of echinochrome A (Ech A) on melanogenesis in the B16F10 murine melanoma cell line. We triggered B16F10 cells using α-MSH under Ech A treatment to observe melanin synthesis and analyze expression changes in melanogenesis-related enzymes (tyrosinase, tyrosinase-related protein 1 (TYRP1), and tyrosinase-related protein 2 (TYRP2)) at the mRNA and protein levels. Furthermore, we measured expression changes in the microphthalmia-associated transcription factor (MITF), CREB, and pCREB proteins. Melanin synthesis in the cells stimulated by α-MSH was significantly reduced by Ech A. The expression of the tyrosinase, TYRP1, and TYRP2 mRNA and proteins was significantly decreased by Ech A, as was that of the MITF, CREB, and pCREB proteins. These results show that Ech A suppresses melanin synthesis by regulating melanogenesis-related enzymes through the CREB signaling pathway and suggest the potential of Ech A as a functional agent to prevent pigmentation and promote skin whitening. MDPI 2022-08-29 /pmc/articles/PMC9502928/ /pubmed/36135744 http://dx.doi.org/10.3390/md20090555 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Choi, Mi Ran
Lee, Heejin
Kim, Hyoung Kyu
Han, Jin
Seol, Jung Eun
Vasileva, Elena A.
Mishchenko, Natalia P.
Fedoreyev, Sergey A.
Stonik, Valentin A.
Ju, Won Seok
Kim, Dai-Jin
Lee, Sang-Rae
Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title_full Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title_fullStr Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title_full_unstemmed Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title_short Echinochrome A Inhibits Melanogenesis in B16F10 Cells by Downregulating CREB Signaling
title_sort echinochrome a inhibits melanogenesis in b16f10 cells by downregulating creb signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502928/
https://www.ncbi.nlm.nih.gov/pubmed/36135744
http://dx.doi.org/10.3390/md20090555
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