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Antimelanogenesis Effects of Theasinensin A
Theasinensin A (TSA) is a major group of catechin dimers mainly found in oolong tea and black tea. This compound is also manufactured with epigallocatechin gallate (EGCG) as a substrate and is refined after the enzyme reaction. In previous studies, TSA has been reported to be effective against infla...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305159/ https://www.ncbi.nlm.nih.gov/pubmed/34299073 http://dx.doi.org/10.3390/ijms22147453 |
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author | Lim, Hye Yeon Kim, Eunji Park, Sang Hee Hwang, Kyung Hwan Kim, Donghyun Jung, You-Jung Kopalli, Spandana Rajendra Hong, Yong Deog Sung, Gi-Ho Cho, Jae Youl |
author_facet | Lim, Hye Yeon Kim, Eunji Park, Sang Hee Hwang, Kyung Hwan Kim, Donghyun Jung, You-Jung Kopalli, Spandana Rajendra Hong, Yong Deog Sung, Gi-Ho Cho, Jae Youl |
author_sort | Lim, Hye Yeon |
collection | PubMed |
description | Theasinensin A (TSA) is a major group of catechin dimers mainly found in oolong tea and black tea. This compound is also manufactured with epigallocatechin gallate (EGCG) as a substrate and is refined after the enzyme reaction. In previous studies, TSA has been reported to be effective against inflammation. However, the effect of these substances on skin melanin formation remains unknown. In this study, we unraveled the role of TSA in melanogenesis using mouse melanoma B16F10 cells and normal human epidermal melanocytes (NHEMs) through reverse transcription polymerase chain reaction (RT-PCR), Western blotting analysis, luciferase reporter assay, and enzyme-linked immunosorbent assay analysis. TSA inhibited melanin formation and secretion in α-melanocyte stimulating hormone (α-MSH)-induced B16F10 cells and NHEMs. TSA down-regulated the mRNA expression of tyrosinase (Tyr), tyrosinase-related protein 1 (Tyrp1), and Tyrp2, which are all related to melanin formation in these cells. TSA was able to suppress the activities of certain proteins in the melanocortin 1 receptor (MC1R) signaling pathway associated with melanin synthesis in B16F10 cells: cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB), protein kinase A (PKA), tyrosinase, and microphthalmia-associated transcription factor (MITF). We also confirmed α-MSH-mediated CREB activities through a luciferase reporter assay, and that the quantities of cAMP were reduced by TSA in the enzyme linked immunosorbent assay (ELISA) results. Based on these findings, TSA should be considered an effective inhibitor of hyperpigmentation. |
format | Online Article Text |
id | pubmed-8305159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83051592021-07-25 Antimelanogenesis Effects of Theasinensin A Lim, Hye Yeon Kim, Eunji Park, Sang Hee Hwang, Kyung Hwan Kim, Donghyun Jung, You-Jung Kopalli, Spandana Rajendra Hong, Yong Deog Sung, Gi-Ho Cho, Jae Youl Int J Mol Sci Article Theasinensin A (TSA) is a major group of catechin dimers mainly found in oolong tea and black tea. This compound is also manufactured with epigallocatechin gallate (EGCG) as a substrate and is refined after the enzyme reaction. In previous studies, TSA has been reported to be effective against inflammation. However, the effect of these substances on skin melanin formation remains unknown. In this study, we unraveled the role of TSA in melanogenesis using mouse melanoma B16F10 cells and normal human epidermal melanocytes (NHEMs) through reverse transcription polymerase chain reaction (RT-PCR), Western blotting analysis, luciferase reporter assay, and enzyme-linked immunosorbent assay analysis. TSA inhibited melanin formation and secretion in α-melanocyte stimulating hormone (α-MSH)-induced B16F10 cells and NHEMs. TSA down-regulated the mRNA expression of tyrosinase (Tyr), tyrosinase-related protein 1 (Tyrp1), and Tyrp2, which are all related to melanin formation in these cells. TSA was able to suppress the activities of certain proteins in the melanocortin 1 receptor (MC1R) signaling pathway associated with melanin synthesis in B16F10 cells: cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB), protein kinase A (PKA), tyrosinase, and microphthalmia-associated transcription factor (MITF). We also confirmed α-MSH-mediated CREB activities through a luciferase reporter assay, and that the quantities of cAMP were reduced by TSA in the enzyme linked immunosorbent assay (ELISA) results. Based on these findings, TSA should be considered an effective inhibitor of hyperpigmentation. MDPI 2021-07-12 /pmc/articles/PMC8305159/ /pubmed/34299073 http://dx.doi.org/10.3390/ijms22147453 Text en © 2021 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 Lim, Hye Yeon Kim, Eunji Park, Sang Hee Hwang, Kyung Hwan Kim, Donghyun Jung, You-Jung Kopalli, Spandana Rajendra Hong, Yong Deog Sung, Gi-Ho Cho, Jae Youl Antimelanogenesis Effects of Theasinensin A |
title | Antimelanogenesis Effects of Theasinensin A |
title_full | Antimelanogenesis Effects of Theasinensin A |
title_fullStr | Antimelanogenesis Effects of Theasinensin A |
title_full_unstemmed | Antimelanogenesis Effects of Theasinensin A |
title_short | Antimelanogenesis Effects of Theasinensin A |
title_sort | antimelanogenesis effects of theasinensin a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305159/ https://www.ncbi.nlm.nih.gov/pubmed/34299073 http://dx.doi.org/10.3390/ijms22147453 |
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