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Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells

The purpose of this study was to investigate if PPARγ plays a role in the melanogenesis. B16/F10 cells were divided into five groups: control, melanin stimulating hormone (α-MSH), α-MSH+retinol, α-MSH+GW9662 (PPARγ antagonist), and GW9662. Cells in the control group were cultured in the Dulbecco...

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Autores principales: Chen, Jiun-Han, Chang, Junn-Liang, Chen, Pei-Ru, Chuang, Yun-Ju, Tang, Shih-Tsang, Pan, Shwu-Fen, Lin, Tzer-Bin, Chen, Kang-Hua, Chen, Mei-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164518/
https://www.ncbi.nlm.nih.gov/pubmed/25250328
http://dx.doi.org/10.1155/2014/695797
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author Chen, Jiun-Han
Chang, Junn-Liang
Chen, Pei-Ru
Chuang, Yun-Ju
Tang, Shih-Tsang
Pan, Shwu-Fen
Lin, Tzer-Bin
Chen, Kang-Hua
Chen, Mei-Jung
author_facet Chen, Jiun-Han
Chang, Junn-Liang
Chen, Pei-Ru
Chuang, Yun-Ju
Tang, Shih-Tsang
Pan, Shwu-Fen
Lin, Tzer-Bin
Chen, Kang-Hua
Chen, Mei-Jung
author_sort Chen, Jiun-Han
collection PubMed
description The purpose of this study was to investigate if PPARγ plays a role in the melanogenesis. B16/F10 cells were divided into five groups: control, melanin stimulating hormone (α-MSH), α-MSH+retinol, α-MSH+GW9662 (PPARγ antagonist), and GW9662. Cells in the control group were cultured in the Dulbecco's modified Eagle's medium (DMEM) for 48 hrs. To initiate the melanogenesis, cells in all α-MSH groups were cultured in medium containing α-MSH (10 nM) for 48 hrs. Cells were treated simultaneously with retinol (5 μM) in the α-MSH+retinol group. Instead of retinol, GW9662 (10 μM) was cocultured in the α-MSH+GW9662 group. Cells in the final group were cultured in the DMEM with GW9662. All the analyses were carried out 48 hours after treatments. The α-MSH was able to increase cell number, melanin production, and the activity of tyrosinase, the limiting enzyme in melanogenesis. These α-MSH-induced changes were prevented either by retinol or by GW9662. Further analyses of the activities of antioxidant enzymes including glutathione, catalase, and the superoxide dismutase (SOD) showed that α-MSH treatment raised the activity of SOD which was dependent on PPARγ level. According to our results, the α-MSH-induced melanogenesis was PPARγ dependent, which also modulated the expression of SOD.
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spelling pubmed-41645182014-09-23 Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells Chen, Jiun-Han Chang, Junn-Liang Chen, Pei-Ru Chuang, Yun-Ju Tang, Shih-Tsang Pan, Shwu-Fen Lin, Tzer-Bin Chen, Kang-Hua Chen, Mei-Jung Biomed Res Int Research Article The purpose of this study was to investigate if PPARγ plays a role in the melanogenesis. B16/F10 cells were divided into five groups: control, melanin stimulating hormone (α-MSH), α-MSH+retinol, α-MSH+GW9662 (PPARγ antagonist), and GW9662. Cells in the control group were cultured in the Dulbecco's modified Eagle's medium (DMEM) for 48 hrs. To initiate the melanogenesis, cells in all α-MSH groups were cultured in medium containing α-MSH (10 nM) for 48 hrs. Cells were treated simultaneously with retinol (5 μM) in the α-MSH+retinol group. Instead of retinol, GW9662 (10 μM) was cocultured in the α-MSH+GW9662 group. Cells in the final group were cultured in the DMEM with GW9662. All the analyses were carried out 48 hours after treatments. The α-MSH was able to increase cell number, melanin production, and the activity of tyrosinase, the limiting enzyme in melanogenesis. These α-MSH-induced changes were prevented either by retinol or by GW9662. Further analyses of the activities of antioxidant enzymes including glutathione, catalase, and the superoxide dismutase (SOD) showed that α-MSH treatment raised the activity of SOD which was dependent on PPARγ level. According to our results, the α-MSH-induced melanogenesis was PPARγ dependent, which also modulated the expression of SOD. Hindawi Publishing Corporation 2014 2014-08-28 /pmc/articles/PMC4164518/ /pubmed/25250328 http://dx.doi.org/10.1155/2014/695797 Text en Copyright © 2014 Jiun-Han Chen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Jiun-Han
Chang, Junn-Liang
Chen, Pei-Ru
Chuang, Yun-Ju
Tang, Shih-Tsang
Pan, Shwu-Fen
Lin, Tzer-Bin
Chen, Kang-Hua
Chen, Mei-Jung
Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title_full Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title_fullStr Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title_full_unstemmed Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title_short Inhibition of Peroxisome Proliferator-Activated Receptor Gamma Prevents the Melanogenesis in Murine B16/F10 Melanoma Cells
title_sort inhibition of peroxisome proliferator-activated receptor gamma prevents the melanogenesis in murine b16/f10 melanoma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4164518/
https://www.ncbi.nlm.nih.gov/pubmed/25250328
http://dx.doi.org/10.1155/2014/695797
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