Melanocyte function and its control by melanocortin peptides

被引:169
作者
Tsatmali, M [1 ]
Ancans, J [1 ]
Thody, AJ [1 ]
机构
[1] Univ Bradford, Dept Biomed Sci, Bradford BD7 1DP, W Yorkshire, England
关键词
skin pigmentation; pro-opiomelanocortin peptides; melanocortin receptor 1; nitric oxide;
D O I
10.1177/002215540205000201
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Melanocytes are cells of neural crest origin. In the human epidermis, they form a close association with keratinocytes via their dendrites. Melanocytes are well known for their role in skin pigmentation, and their ability to produce and distribute melanin has been studied extensively. One of the factors that regulates melanocytes and skin pigmentation is the locally produced melanocortin peptide alpha-MSH. The effects of alpha-MSH on melanogenesis are mediated via the MC-IR and tyrosinase, the rate-limiting enzyme in the melanogenesis pathway. Binding of alpha-MSH to its receptor increases tyrosinase activity and eumelanin production, which accounts for the skin-darkening effect of a-MSH. Other alpha-MISH-related melanocortin peptides, such as ACTH1-17 and desacetylated alpha-MSH, are also agonists at the MC-IHR and could regulate melanocyte function. Recent evidence shows that melanocytes have other functions in the skin in addition to their ability to produce melanin. They are able to secrete a wide range of signal molecules, including cytokines, POMC peptides, catecholamines, and NO in response to UV irradiation and other stimuli. Potential targets of these secretory products are keratinocytes, lymphocytes, fibroblasts, mast cells, and endothelial cells, all of which express receptors for these signal molecules. Melanocytes may therefore act as important local regulators of a range of skin cells. It been shown that alpha-MSH regulates NO production from melanocytes, and it is possible that skin pigmentation the melanocortins regulate the release of other signalling molecules from melanocytes. pro-opiomelanocortin peptides Therefore, the melanocortin signaling system is one of the important regulators of skin homeotasis.
引用
收藏
页码:125 / 133
页数:9
相关论文
共 108 条
[21]   THE EXPRESSION OF FUNCTIONAL MSH RECEPTORS ON CULTURED HUMAN MELANOCYTES [J].
DONATIEN, PD ;
HUNT, G ;
PIERON, C ;
LUNEC, J ;
TAIEB, A ;
THODY, AJ .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1992, 284 (07) :424-426
[22]   RECEPTORS FOR MELANOCYTE-STIMULATING HORMONE ON MELANOMA-CELLS [J].
EBERLE, AN ;
SIEGRIST, W ;
BAGUTTI, C ;
CHLUBADETAPIA, J ;
SOLCA, F ;
WIKBERG, JES ;
CHHAJLANI, V .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 680 :320-341
[23]   Inhibition of the mitogen-activated protein kinase pathway triggers B16 melanoma cell differentiation [J].
Englaro, W ;
Bertolotto, C ;
Buscà, R ;
Brunet, A ;
Pagès, G ;
Ortonne, JP ;
Ballotti, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9966-9970
[24]   Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation [J].
Flanagan, N ;
Healy, E ;
Ray, A ;
Philips, S ;
Todd, C ;
Jackson, IJ ;
Birch-Machin, MA ;
Rees, JL .
HUMAN MOLECULAR GENETICS, 2000, 9 (17) :2531-2537
[25]  
FORSTER E, 1991, J INVEST DERMATOL, V96, P608
[26]  
Frändberg PA, 1998, BIOCHEM MOL BIOL INT, V46, P913
[27]   Regulation of the catalytic activity of preexisting tyrosinase in Black and Caucasian human melanocyte cell cultures [J].
Fuller, BB ;
Spaulding, DT ;
Smith, DR .
EXPERIMENTAL CELL RESEARCH, 2001, 262 (02) :197-208
[28]   MAPPING OF THE GENE ENCODING THE MELANOCORTIN-1 (ALPHA-MELANOCYTE-STIMULATING HORMONE) RECEPTOR (MC1R) TO HUMAN-CHROMOSOME 16Q24.3 BY FLUORESCENCE IN-SITU HYBRIDIZATION [J].
GANTZ, I ;
YAMADA, T ;
TASHIRO, T ;
KONDA, Y ;
SHIMOTO, Y ;
MIWA, H ;
TRENT, JM .
GENOMICS, 1994, 19 (02) :394-395
[29]   Agouti protein inhibits the production of eumelanin and phaeomelanin in the presence and absence of alpha-melanocyte stimulating hormone [J].
Graham, A ;
Wakamatsu, K ;
Hunt, G ;
Ito, S ;
Thody, AJ .
PIGMENT CELL RESEARCH, 1997, 10 (05) :298-303
[30]   Kinesin participates in melanosomal movement along melanocyte dendrites [J].
Hara, M ;
Yaar, M ;
Byers, HR ;
Goukassian, D ;
Fine, RE ;
Gonsalves, J ;
Gilchrest, BA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (03) :438-443