Tyrosine-induced melanogenesis shows differences in morphologic and melanogenic preferences of melanosomes from light and dark skin types

被引:27
作者
van Nieuwpoort, F
Smit, NPM
Kolb, R
van der Meulen, H
Koerten, H
Pavel, S
机构
[1] Leiden Univ, Med Ctr, Dept Dermatol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Clin Chem, Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Ctr Electron Microscopy, Leiden, Netherlands
关键词
eumelanin; HPLC; melanosome; pheomelanin; X-ray microanalysis;
D O I
10.1111/j.0022-202X.2004.22533.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The quality, quantity and distribution of melanosomes in epidermis play a crucial role in the determination of skin color and its sensitivity to UV radiation. Melanocyte cultures originating from individuals with light and dark skin types were grown in media with varying concentration of L-tyrosine. Melanosomal melanin content and the size of the organelles were measured after subcellular fractionation. In light-skin type cells, increased melanin production resulted in a more elliptical shape of melanosomes. In melanosomes that constitutively produce more melanin, the tyrosine-induced melanogenesis caused enlargement in all dimensions. X-ray microanalysis provided evidence that the increase in sulfur content induced by high tyrosine concentration was more prominent in the melanosomes from light skin types. A ratio between pheomelanin and eumelanin found in light-skin type melanosomes by HPLC was increased more markedly than that in melanosomes from dark skin melanocytes. These findings suggest that the melanocytes of light-skinned individuals exhibit a preference for pheomelanogenesis. Pheomelanin production is a thiol-consuming process and that might increase the risk of oxidation stress in these cells. This fact, together with the limited ability of pheomelanin to absorb UV radiation may lead to an elevated skin cancer risk among light-skinned individuals.
引用
收藏
页码:1251 / 1255
页数:5
相关论文
共 26 条
[11]   MICROANALYSIS OF EUMELANIN AND PHEOMELANIN IN HAIR AND MELANOMAS BY CHEMICAL DEGRADATION AND LIQUID-CHROMATOGRAPHY [J].
ITO, S ;
FUJITA, K .
ANALYTICAL BIOCHEMISTRY, 1985, 144 (02) :527-536
[12]   COMBINED CHEMICAL AND ELECTRON-MICROSCOPIC STUDIES OF PHEOMELANOSOMES IN HUMAN RED HAIR [J].
JIMBOW, K ;
ISHIDA, O ;
ITO, S ;
HORI, Y ;
WITKOP, CJ ;
KING, RA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (06) :506-511
[13]   COMPARISON OF EUMELANOGENESIS AND PHEOMELANOGENESIS IN RETINAL AND FOLLICULAR MELANOCYTES - ROLE OF VESICULO-GLOBULAR BODIES IN MELANOSOME DIFFERENTIATION [J].
JIMBOW, K ;
OIKAWA, O ;
SUGIYAMA, S ;
TAKEUCHI, T .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1979, 73 (04) :278-284
[14]  
KLUG H, 1982, ARCH GESCHWULSTFORSC, V52, P379
[15]   Determination of pheomelanin by measurement of aminohydroxyphenylalanine isomers with high-performance liquid chromatography [J].
Kolb, AM ;
Lentjes, EGWM ;
Smit, NPM ;
Schothorst, A ;
Vermeer, BJ ;
Pavel, S .
ANALYTICAL BIOCHEMISTRY, 1997, 252 (02) :293-298
[16]   USEFUL EQUATIONS FOR BIOLOGICAL STUDIES [J].
LANDSBERG, JJ .
EXPERIMENTAL AGRICULTURE, 1977, 13 (03) :273-286
[17]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[18]   MELANIN PIGMENTATION IN MAMMALS [J].
PROTA, G ;
THOMSON, RH .
ENDEAVOUR, 1976, 35 (124) :32-38
[19]   DEVELOPMENTAL BIOLOGY OF MAMMALIAN MELANOCYTES [J].
QUEVEDO, WC ;
FLEISCHMANN, RD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1980, 75 (01) :116-120
[20]   The melanosome: Dark pigment granule shines bright light on vesicle biogenesis and more [J].
Setaluri, V .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :650-660