Mannosylerythritol lipids inhibit melanogenesis via suppressing ERK-CREB-MiTF-tyrosinase signalling in normal human melanocytes and a three-dimensional human skin equivalent

被引:32
作者
Bae, Il-Hong [1 ,2 ]
Lee, Eun Soo [1 ]
Yoo, Jae Won [1 ]
Lee, Sung Hoon [1 ]
Ko, Jae Young [1 ]
Kim, Yong Jin [1 ]
Lee, Tae Ryong [1 ]
Kim, Dae-Yong [2 ]
Lee, Chang Seok [3 ]
机构
[1] Amorepacific Corp R&D Ctr, Yongin, South Korea
[2] Seoul Natl Univ, Dept Vet Pathol, Coll Vet Med, Seoul, South Korea
[3] Eulji Univ, Dept Beauty & Cosmet Sci, Seongnam Si, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
3-dimensional human skin equivalent; mannosylerythritol lipid; melanogenesis;
D O I
10.1111/exd.13836
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Hyperpigmentation is caused by excessive production of melanin in melanocytes. Mannosylerythritol lipids (MELs) are glycolipid biosurfactants that are abundantly produced by yeasts and used commercially in cosmetics. However, the potential depigmenting efficacy of MELs has not been evaluated. In this study, the depigmentary effect of MELs was tested in primary normal human melanocytes (NHMs), alpha-melanocyte-stimulating hormone (MSH)-stimulated B16 cells (murine melanoma cells) and a human skin equivalent (MelanoDerm) using photography, Fontana-Masson (F&M) staining and two-photon microscopy. Mannosylerythritol lipids significantly decreased the melanin contents in NHMs and alpha-MSH-stimulated B16 cells. Consistent with these findings, MELs treatment had a clear whitening effect in a human skin equivalent, brightening the tissue colour and reducing the melanin content. The molecular mechanism underlying the anti-melanogenic effect of MELs treatment was examined by real-time PCR and Western blotting. Mechanistically, MELs clearly suppressed the gene expression levels of representative melanogenic enzymes, including tyrosinase, Tyrp-1 and Tyrp-2, by inhibiting the ERK/CREB/MiTF signalling pathway in NHMs. This work demonstrates for the first time that MELs exert whitening effects on human melanocytes and skin equivalent. Thus, we suggest that MELs could be developed as a potent anti-melanogenic agent for effective whitening, beyond their use as a biosurfactant in cosmetics.
引用
收藏
页码:738 / 741
页数:4
相关论文
共 10 条
[1]   Chemical and instrumental approaches to treat hyperpigmentation [J].
Briganti, S ;
Camera, E ;
Picardo, M .
PIGMENT CELL RESEARCH, 2003, 16 (02) :101-110
[2]   Calcium and cAMP signals differentially regulate cAMP-responsive element-binding protein function via a Rap1-extracellular signal-regulated kinase pathway [J].
Grewal, SS ;
Fass, DM ;
Yao, H ;
Ellig, CL ;
Goodman, RH ;
Stork, PJS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (44) :34433-34441
[3]   Inhibitors of Intracellular Signaling Pathways that Lead to Stimulated Epidermal Pigmentation: Perspective of Anti-Pigmenting Agents [J].
Imokawa, Genji ;
Ishida, Koichi .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (05) :8293-8315
[4]   Sphingosine-1-phosphate decreases melanin synthesis via sustained ERK activation and subsequent MITF degradation [J].
Kim, DS ;
Hwang, ES ;
Lee, JE ;
Kim, SY ;
Kwon, SB ;
Park, KC .
JOURNAL OF CELL SCIENCE, 2003, 116 (09) :1699-1706
[5]   A novel adamantyl benzylbenzamide derivative, AP736, suppresses melanogenesis through the inhibition of cAMP-PKA-CREB-activated microphthalmia-associated transcription factor and tyrosinase expression [J].
Lee, Chang Seok ;
Jang, Won-Hee ;
Park, Miyoung ;
Jung, Kyoungmi ;
Baek, Heung Soo ;
Joo, Yung Hyup ;
Park, Young-Ho ;
Lim, Kyung-Min .
EXPERIMENTAL DERMATOLOGY, 2013, 22 (11) :762-764
[6]   Antimelanogenic Efficacy of Melasolv (3,4,5-Trimethoxycinnamate Thymol Ester) in Melanocytes and Three-Dimensional Human Skin Equivalent [J].
Lee, John Hwan ;
Lee, Eun-Soo ;
Bae, Il-Hong ;
Hwang, Jeong-Ah ;
Kim, Se-Hwa ;
Kim, Dae-Yong ;
Park, Nok-Hyun ;
Rho, Ho Sik ;
Kim, Yong Jin ;
Oh, Seong-Geun ;
Lee, Chang Seok .
SKIN PHARMACOLOGY AND PHYSIOLOGY, 2017, 30 (04) :190-196
[7]   Production of mannosylerythritol lipids and their application in cosmetics [J].
Morita, Tomotake ;
Fukuoka, Tokuma ;
Imura, Tomohiro ;
Kitamoto, Dai .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2013, 97 (11) :4691-4700
[8]   Oral zinc sulphate causes murine hair hypopigmentation and is a potent inhibitor of eumelanogenesis in vivo [J].
Plonka, P. M. ;
Handjiski, B. ;
Michalczyk, D. ;
Popik, M. ;
Paus, R. .
BRITISH JOURNAL OF DERMATOLOGY, 2006, 155 (01) :39-49
[9]  
Yasumoto K., 1833, MOL CELL BIOL, V1995, P15
[10]  
Zhao XX, 1999, CANCER RES, V59, P482