The Hair Follicle: A Paradoxical Androgen Target Organ

绒毛 毛乳头 毛囊 雄激素 生物 内分泌学 雄激素受体 内科学 真皮 旁分泌信号 二氢睾酮 细胞生物学 受体 头皮 激素 解剖 医学 癌症 前列腺癌
作者
Valerie A. Randall,Nigel A. Hibberts,M. Julie Thornton,Kazuto Hamada,Alison Merrick,Shoji Kato,Tracey J. Jenner,Isobel De Oliveira,Andrew G. Messenger
出处
期刊:Hormone Research in Paediatrics [Karger Publishers]
卷期号:54 (5-6): 243-250 被引量:91
标识
DOI:10.1159/000053266
摘要

Androgens are the main regulator of normal human hair growth. After puberty, they promote transformation of vellus follicles, producing tiny, unpigmented hairs, to terminal ones, forming larger pigmented hairs, in many areas, e.g. the axilla. However, they have no apparent effect on the eyelashes, but can cause the opposite transformation on the scalp leading to the replacement of terminal hairs by vellus ones and the gradual onset of androgenetic alopecia. This paradox appears to be an unique hormonal effect. Hair follicles are mainly epithelial tissues, continuous with the epidermis, which project into the dermis. A mesenchyme-derived dermal papilla enclosed within the hair bulb at the base controls many aspects of follicle function. In the current hypothesis for androgen regulation, the dermal papilla is also considered the main site of androgen action with androgens from the blood binding to receptors in dermal papilla cells of androgen-sensitive follicles and causing an alteration of their production of paracrine factors for target cells e.g. keratinocytes. Studies of cultured dermal papilla cells from sites with different responses to androgens in vivo have confirmed the paradoxical responses. All dermal papilla cells from androgen-sensitive sites contain low capacity, high affinity androgen receptors. However, only some cells formed 5alpha-dihydrotestosterone, e.g. beard but not axillary cells, in line with hair growth in 5alpha-reductase deficiency. Incubation with androgens also stimulated the mitogenic capacity of beard cell media, but inhibited that produced by scalp cells. This suggests that the paradoxical differences are due to differential gene expression within hair follicles, presumably caused during embryogenesis.
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