Hair follicle pigmentation

被引:407
作者
Slominski, A
Wortsman, J
Plonka, PM
Schallreuter, KU
Paus, R
Tobin, DJ
机构
[1] Univ Tennessee, Dept Pathol, Memphis, TN USA
[2] So Illinois Univ, Dept Med, Springfield, IL USA
[3] Jagiellonian Univ, Fac Biotechnol, Dept Biophys, Krakow, Poland
[4] Univ Bradford, Dept Biomed Sci, Bradford BD7 1DP, W Yorkshire, England
[5] Ernst Moritz Arndt Univ Greifswald, Inst Pigmentary Disorders, Greifswald, Germany
[6] Univ Hosp Hamburg Eppendorf, Dept Dermatol, Hamburg, Germany
关键词
follicular melanocytes; hair pigmentation; melanin; melanogenesis;
D O I
10.1111/j.0022-202X.2004.23528.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Hair shaft melanin components (eu- or/and pheomelanin) are a long-lived record of precise interactions in the hair follicle pigmentary unit, e.g., between follicular melanocytes, keratinocytes, and dermal papilla fibroblasts. Follicular melanogenesis (FM) involves sequentially the melanogenic activity of follicular melanocytes, the transfer of melanin granules into cortical and medulla keratinocytes, and the formation of pigmented hair shafts. This activity is in turn regulated by an array of enzymes, structural and regulatory proteins, transporters, and receptors and their ligands, acting on the developmental stages, cellular, and hair follicle levels. FM is stringently coupled to the anagen stage of the hair cycle, being switched-off in catagen to remain absent through telogen. At the organ level FM is precisely coupled to the life cycle of melanocytes with changes in their compartmental distribution and accelerated melanoblast/melanocyte differentiation with enhanced secretory activity. The melanocyte compartments in the upper hair follicle also provides a reservoir for the repigmentation of epidermis and, for the cyclic formation of new anagen hair bulbs. Melanin synthesis and pigment transfer to bulb keratinocytes are dependent on the availability of melanin precursors, and regulation by signal transduction pathways intrinsic to skin and hair follicle, which are both receptor dependent and independent, act through auto-, para- or intracrine mechanisms and can be modified by hormonal signals. The important regulators are MC1 receptor its and adrenocorticotropic hormone, melanocyte stimulating hormone, agouti protein ligands (in rodents), c-Kit, and the endothelin receptors with their ligands. Melanin itself has a wide range of bioactivities that extend far beyond its determination of hair color.
引用
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页码:13 / 21
页数:9
相关论文
共 65 条
[1]
Melanosomal pH controls rate of melanogenesis, eumelanin/phaeomelanin ratio and melanosome maturation in melanocytes and melanoma cells [J].
Ancans, J ;
Tobin, DJ ;
Hoogduijn, MJ ;
Smit, NP ;
Wakamatsu, K ;
Thody, AJ .
EXPERIMENTAL CELL RESEARCH, 2001, 268 (01) :26-35
[2]
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
[3]
BELL M, 1967, ADV BIOL SKIN
[4]
Proprotein convertase cleavage liberates a fibrillogenic fragment of a resident glycoprotein to initiate melanosome biogenesis [J].
Berson, JF ;
Theos, AC ;
Harper, DC ;
Tenza, D ;
Raposo, G ;
Marks, MS .
JOURNAL OF CELL BIOLOGY, 2003, 161 (03) :521-533
[5]
SCF/c-kit signaling is required for cyclic regeneration of the hair pigmentation unit [J].
Botchkareva, NV ;
Khlgatian, M ;
Longley, BJ ;
Botchkarev, VA ;
Gilchrest, BA .
FASEB JOURNAL, 2001, 15 (03) :645-658
[6]
Pink-eyed dilution protein controls the processing of tyrosinase [J].
Chen, K ;
Manga, P ;
Orlow, SJ .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (06) :1953-1964
[7]
Human hair greying is linked to a specific depletion of hair follicle melanocytes affecting both the bulb and the outer root sheath [J].
Commo, S ;
Gaillard, O ;
Bernard, BA .
BRITISH JOURNAL OF DERMATOLOGY, 2004, 150 (03) :435-443
[8]
Melanocyte subpopulation turnover during the human hair cycle: An immunohistochemical study [J].
Commo, S ;
Bernard, BA .
PIGMENT CELL RESEARCH, 2000, 13 (04) :253-259
[9]
FREE RADICALS IN BIOLOGICAL MATERIALS [J].
COMMONER, B ;
TOWNSEND, J ;
PAKE, GE .
NATURE, 1954, 174 (4432) :689-691
[10]
Evidence of the indirect formation of the catecholic intermediate substrate responsible for the autoactivation kinetics of tyrosinase [J].
Cooksey, CJ ;
Garratt, PJ ;
Land, EJ ;
Pavel, S ;
Ramsden, CA ;
Riley, PA ;
Smit, NPM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26226-26235