Biology and Genetics of Hair

被引:66
作者
Shimomura, Yutaka [1 ]
Christiano, Angela M. [1 ,2 ]
机构
[1] Columbia Univ, Dept Dermatol, New York, NY 10032 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
来源
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS, VOL 11 | 2010年 / 11卷
关键词
hair follicle; hair cycle; stem cells; hereditary hair diseases; genodermatoses; dermis; epithelium; VITAMIN-D-RECEPTOR; HYPOHIDROTIC ECTODERMAL DYSPLASIA; AUTOSOMAL RECESSIVE HYPOTRICHOSIS; RIGHT-VENTRICULAR CARDIOMYOPATHY; CADHERIN ADHESION MOLECULES; PROTEIN-COUPLED RECEPTOR; MALE-PATTERN BALDNESS; WOOLLY HAIR; STEM-CELLS; FOLLICLE MORPHOGENESIS;
D O I
10.1146/annurev-genom-021610-131501
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The mammalian hair follicle (HF) is a complex structure composed of several distinct cell layers. The HF is an ectodermal appendage that resides in the skin, and unlike other tissues and organs, it possesses the remarkable ability to self-renew and undergoes a hair cycle that persists in adult life. Stem cells in the bulge region of the HF, as well as dermal papilla cells, play key roles in the regulation of successive hair cycles. Recent advances in molecular genetics have enabled the identification of many genes and pathways that are involved in HF morphogenesis and cycling. Furthermore, mutations in some of these genes are associated with hereditary hair diseases in humans. Identification of causative genes for hair diseases has provided a better understanding of the crucial roles of these genes in HF morphogenesis, development, and hair growth in humans.
引用
收藏
页码:109 / 132
页数:24
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