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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.
Afiliación
  • Chen JH; Department of Medical Laboratory Science and Biotechnology, College of Medical Technology, Nursing and Wellbeing, Yuanpei University, No. 306 Yuan-Pei Street, Hsinchu 30015, Taiwan.
  • Chang JL; Department of Pathology & Laboratory Medicine, Taoyuan Armed Forces General Hospital, Taoyuan 32551, Taiwan ; Department of Biomedical Engineering, School of Health, Ming Chuan University, No. 5 De-Ming Road, Gui Shan District, Taoyuan County, Taoyuan 333, Taiwan.
  • Chen PR; Department of Biomedical Engineering, School of Health, Ming Chuan University, No. 5 De-Ming Road, Gui Shan District, Taoyuan County, Taoyuan 333, Taiwan.
  • Chuang YJ; Department of Biomedical Engineering, School of Health, Ming Chuan University, No. 5 De-Ming Road, Gui Shan District, Taoyuan County, Taoyuan 333, Taiwan.
  • Tang ST; Department of Biomedical Engineering, School of Health, Ming Chuan University, No. 5 De-Ming Road, Gui Shan District, Taoyuan County, Taoyuan 333, Taiwan.
  • Pan SF; Department of Biotechnology, School of Health, Ming Chuan University, Taoyuan 333, Taiwan.
  • Lin TB; Department of Physiology, College of Medicine, Taipei Medical University, No. 250 Wuxing Street, Taipei 110, Taiwan.
  • Chen KH; Department of Surgery, Cheng Hsin General Hospital, No. 45 Cheng Hsin Street, Pai Tou, Taipei 112, Taiwan.
  • Chen MJ; Department of Biomedical Engineering, School of Health, Ming Chuan University, No. 5 De-Ming Road, Gui Shan District, Taoyuan County, Taoyuan 333, Taiwan.
Biomed Res Int ; 2014: 695797, 2014.
Article en En | MEDLINE | ID: mdl-25250328
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: PPAR gamma / Carcinogénesis / Anilidas / Melaninas / Melanoma Límite: Animals Idioma: En Revista: Biomed Res Int Año: 2014 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: PPAR gamma / Carcinogénesis / Anilidas / Melaninas / Melanoma Límite: Animals Idioma: En Revista: Biomed Res Int Año: 2014 Tipo del documento: Article País de afiliación: Taiwán Pais de publicación: Estados Unidos