7 Regulation of androgen receptor and 5α-reductase in the skin of normal and hirsute women

Pierre Mauvais-Jarvis
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引用次数: 35

Abstract

The hormonal activity of androgens is mediated in target cells, particularly in human skin, by two kinds of proteins: the androgen receptor and the enzyme 5α-reductase. In well differentiated androgen target cells, 5α-reductase achieves the transformation of testosterone (T) into dihydrotestosterone (DHT), a more active androgen than T, because of its higher affinity for the receptor. In other words, 5α-reductase acts as an amplifier of the androgen signal but is not absolutely required for androgen action. Regarding the regulation of the androgen receptor, minimal information is available. However, in genital skin, the receptor seems to be predominantly localized in the cytosolic compartment before puberty in males and in the nuclear compartment after puberty. In hirsute patients, recent data on genital skin fibroblasts do not show significant differences between the binding capacity of fibroblasts from normal and hirsute women whereas there is no difference between normal men and women.

5α-Reductase activity seems to be a very important step in the processes involved in androgen action. While 5α-reductase activity present in the skin of external genitalia does not seem to be androgen dependent, this is not the case for the enzyme located in pubic skin. In this area, a sex difference between males and females may be observed both in skin homogenates and in cultured fibroblasts. In addition DHT added to a medium of pubic skin fibroblasts is capable of increasing 5α-reductase activity. This increase is not observed when cyproterone acetate is added to the medium and in patients with testicular feminization syndrome without receptors. Pubic 5α-reductase activity is an androgen receptor mediated phenomenon. In patients with hirsutism, and particularly idiopathic hirsutism, 5α-reductase activity is high without an increase in circulating androgens. This may be observed both in pubic skin homogenates and in cultured fibroblasts. Thus, an excess of skin 5α-reductase activity may be considered as a cause of hirsutism but both the exact level of the abnormality in the regulation of the enzyme and its genetic control remain to be elucidated.

正常和多毛女性皮肤中雄激素受体和5α-还原酶的调节
雄激素的激素活性在靶细胞中,特别是在人体皮肤中,由两种蛋白质介导:雄激素受体和5α-还原酶。在分化良好的雄激素靶细胞中,5α-还原酶可将睾酮(T)转化为比睾酮更活跃的二氢睾酮(DHT),因为它对受体具有更高的亲和力。换句话说,5α-还原酶作为雄激素信号的放大器,但不是雄激素作用所必需的。关于雄激素受体的调控,目前所知甚少。然而,在生殖器皮肤中,受体似乎主要定位于男性青春期前的细胞质室和青春期后的核室。在多毛患者中,最近关于生殖器皮肤成纤维细胞的数据显示,正常多毛女性和正常多毛女性成纤维细胞的结合能力没有显著差异,而正常男性和女性之间没有差异。5α-还原酶活性似乎是参与雄激素作用过程的一个非常重要的步骤。虽然外生殖器皮肤中的5α-还原酶活性似乎不依赖于雄激素,但位于阴部皮肤的酶却不是如此。在这个区域,男性和女性在皮肤匀浆和培养成纤维细胞中都可以观察到性别差异。此外,DHT添加到耻皮成纤维细胞培养基中能够增加5α-还原酶活性。当在培养基中加入醋酸环丙孕酮和没有受体的睾丸女性化综合征患者时,没有观察到这种增加。耻骨5α-还原酶活性是雄激素受体介导的现象。在多毛症患者,特别是特发性多毛症患者中,5α-还原酶活性高,但循环雄激素不增加。这可以在阴皮匀浆和培养成纤维细胞中观察到。因此,皮肤5α-还原酶活性的过剩可能被认为是多毛症的原因,但酶调节异常的确切水平及其遗传控制仍有待阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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