Melanocyte biology and skin pigmentation

被引:962
作者
Lin, Jennifer Y.
Fisher, David E.
机构
[1] Childrens Hosp Boston, Dana Farber Canc Inst, Melanoma Program, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Harvard Combined Program Dermatol, Boston, MA 02115 USA
[3] Childrens Hosp Boston, Dana Farber Canc Inst, Dept Pediat Hematol & Oncol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature05660
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Melanocytes are phenotypically prominent but histologically inconspicuous skin cells. They are responsible for the pigmentation of skin and hair, and thereby contribute to the appearance of skin and provide protection from damage by ultraviolet radiation. Pigmentation mutants in various species are highly informative about basic genetic and developmental pathways, and provide important clues to the processes of photoprotection, cancer predisposition and even human evolution. Skin is the most common site of cancer in humans. Continued understanding of melanocyte contributions to skin biology will hopefully provide new opportunities for the prevention and treatment of skin diseases.
引用
收藏
页码:843 / 850
页数:8
相关论文
共 102 条
[1]   P-locus is a target for the melanogenic effects of MC-1R signaling - A possible control point for facultative pigmentation [J].
Ancans, J ;
Flanagan, N ;
Hoogduijn, MJ ;
Thody, AJ .
MELANOCORTIN SYSTEM, 2003, 994 :373-377
[2]   MELANOMA AND USE OF SUNSCREENS - AN EORTC CASE-CONTROL STUDY IN GERMANY, BELGIUM AND FRANCE [J].
AUTIER, P ;
DORE, JF ;
SCHIFFLERS, E ;
CESARINI, JP ;
BOLLAERTS, A ;
KOELMEL, KF ;
GEFELLER, O ;
LIABEUF, A ;
LEJEUNE, F ;
LIENARD, D ;
JOARLETTE, M ;
CHEMALY, P ;
KLEEBERG, UR .
INTERNATIONAL JOURNAL OF CANCER, 1995, 61 (06) :749-755
[3]   Divergence of melanocortin pathways in the control of food intake and energy expenditure [J].
Balthasar, N ;
Dalgaard, LT ;
Lee, CE ;
Yu, J ;
Funahashi, H ;
Williams, T ;
Ferreira, M ;
Tang, V ;
McGovern, RA ;
Kenny, CD ;
Christiansen, LM ;
Edelstein, E ;
Choi, B ;
Boss, O ;
Aschkenasi, C ;
Zhang, CY ;
Mountjoy, K ;
Kishi, T ;
Elmquist, JK ;
Lowell, BB .
CELL, 2005, 123 (03) :493-505
[4]   Biochemical and genetic studies of pigment-type switching [J].
Barsh, G ;
Gunn, T ;
He, L ;
Schlossman, S ;
Duke-Cohan, J .
PIGMENT CELL RESEARCH, 2000, 13 :48-53
[5]   Sun exposure and mortality from melanoma [J].
Berwick, M ;
Armstrong, BK ;
Ben-Porat, L ;
Fine, J ;
Kricker, A ;
Eberle, C ;
Barnhill, R .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (03) :195-199
[6]   Melanosome transfer to and translocation in the keratinocyte [J].
Boissy, RE .
EXPERIMENTAL DERMATOLOGY, 2003, 12 :5-12
[7]   Malignant melanoma: genetics and therapeutics in the genomic era [J].
Chin, Lynda ;
Garraway, Levi A. ;
Fisher, David E. .
GENES & DEVELOPMENT, 2006, 20 (16) :2149-2182
[8]   Molecular control of neural crest formation, migration and differentiation [J].
Christiansen, JH ;
Goles, EG ;
Wilkinson, DG .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (06) :719-724
[9]   UV-induced expression of key component of the tanning process, the POMC and MC1R genes, is dependent on the p-38-activated upstream stimulating factor-1 (USF-1) [J].
Corre, S ;
Primot, A ;
Sviderskaya, E ;
Bennett, DC ;
Vaulont, S ;
Goding, CR ;
Galibert, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (49) :51226-51233
[10]   Topical drug rescue strategy and skin protection based on the role of Mc1r in UV-induced tanning [J].
D'Orazio, John A. ;
Nobuhisa, Tetsuji ;
Cui, Rutao ;
Arya, Michelle ;
Spry, Malinda ;
Wakamatsu, Kazumasa ;
Igras, Vivien ;
Kunisada, Takahiro ;
Granter, Scott R. ;
Nishimura, Emi K. ;
Ito, Shosuke ;
Fisher, David E. .
NATURE, 2006, 443 (7109) :340-344