Aging, graying and loss of melanocyte stem cells

被引:37
作者
Sarin, Kavita Y. [1 ]
Artandi, Steven E. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
来源
STEM CELL REVIEWS | 2007年 / 3卷 / 03期
关键词
stem cells; aging; pigmentation; graying; melanocytes; telomeres; Bcl2; vitiligo; light mutation; HAIR FOLLICLE; NEURAL CREST; SELF-RENEWAL; COAT COLOR; MOUSE; SURVIVAL; NICHE; TELOMERES; KIT; MAINTENANCE;
D O I
10.1007/s12015-007-0028-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hair graying is one of the prototypical signs of human aging. Maintenance of hair pigmentation is dependent on the presence and functionality of melanocytes, neural crest derived cells which synthesize pigment for growing hair. The melanocytes, themselves, are maintained by a small number of stem cells which reside in the bulge region of the hair follicle. The recent characterization of the melanocyte lineage during aging has significantly accelerated our understanding of how age-related changes in the melanocyte stem cell compartment contribute to hair graying. This review will discuss our current understanding of hair graying, drawing on evidence from human and mouse studies, and consider the contribution of melanocyte stem cells to this process. Furthermore, using the melanocyte lineage as an example, it will discuss common theories of tissue and stem cell aging.
引用
收藏
页码:212 / 217
页数:6
相关论文
共 50 条
[1]   Telomerase is required to slow telomere shortening and extend replicative lifespan of HSCs during serial transplantation [J].
Allsopp, RC ;
Morin, GB ;
DePinho, R ;
Harley, CB ;
Weissman, IL .
BLOOD, 2003, 102 (02) :517-520
[2]   Towards a "free radical theory of graying": melanocyte apoptosis in the aging human hair follicle is an indicator of oxidative stress induced tissue damage [J].
Arck, Petra Clara ;
Overall, Rupert ;
Spatz, Katharina ;
Liezman, Christiane ;
Handjiski, Bori ;
Klapp, Burghard F. ;
Birch-Machin, Mark A. ;
Peters, Eva Milena Johanne .
FASEB JOURNAL, 2006, 20 (09) :1567-+
[3]   The emerging role of epigenetics in cellular and organismal aging [J].
Bandyopadhyay, D ;
Medrano, EE .
EXPERIMENTAL GERONTOLOGY, 2003, 38 (11-12) :1299-1307
[4]   The genetics of pigmentation: From fancy genes to complex traits [J].
Barsh, GS .
TRENDS IN GENETICS, 1996, 12 (08) :299-305
[5]   Switching and signaling at the telomere [J].
Blackburn, EH .
CELL, 2001, 106 (06) :661-673
[6]   Self-renewal, multipotency, and the existence of two cell populations within an epithelial stem cell niche [J].
Blanpain, C ;
Lowry, WE ;
Geoghegan, A ;
Polak, L ;
Fuchs, E .
CELL, 2004, 118 (05) :635-648
[7]   Epithelial stem cells: Turning over new leaves [J].
Blanpain, Cedric ;
Horsley, Valerie ;
Fuchs, Elaine .
CELL, 2007, 128 (03) :445-458
[8]   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
[9]   MUTATIONS AT THE W-LOCUS AFFECT SURVIVAL OF NEURAL CREST-DERIVED MELANOCYTES IN THE MOUSE [J].
CABLE, J ;
JACKSON, IJ ;
STEEL, KP .
MECHANISMS OF DEVELOPMENT, 1995, 50 (2-3) :139-150
[10]   Essential role of limiting telomeres in the pathogenesis of Werner syndrome [J].
Chang, S ;
Multani, AS ;
Cabrera, NG ;
Naylor, ML ;
Laud, P ;
Lombard, D ;
Pathak, S ;
Guarente, L ;
DePinho, RA .
NATURE GENETICS, 2004, 36 (08) :877-882