非那雄胺
二氢睾酮
睾酮(贴片)
头皮
半胱氨酸蛋白酶3
脱发
体内
医学
细胞凋亡
内分泌学
内科学
体外
雄激素
生物
皮肤病科
前列腺
程序性细胞死亡
激素
生物化学
生物技术
癌症
作者
Juan Pablo de Rivero Vaccari,Marty E. Sawaya,Frank Brand,Bernard P. Nusbaum,Alan J. Bauman,Helen M. Bramlett,Dalton W. Dietrich,Robert W. Keane
出处
期刊:Dermatologic Surgery
[Ovid Technologies (Wolters Kluwer)]
日期:2012-03-08
卷期号:38 (7): 1033-1039
被引量:33
标识
DOI:10.1111/j.1524-4725.2012.02378.x
摘要
Inflammasomes that activate caspase-1 govern the innate immune inflammatory response. Whether hair loss associated with androgenetic alopecia (AGA) involves caspase-1 activation is not known.Immunohistochemical staining for caspase-1 was performed on scalp tissue sections, and protein lysates were analyzed from individuals with AGA (no treatment), and individuals with AGA taking finasteride with apparent hair growth, individuals with AGA taking finasteride without noted hair growth, and normal controls. In vitro studies of human keratinocytes were conducted to establish effects of finasteride, dihydrotestosterone (DHT), and testosterone on caspase-1 levels using immunoblot analysis.Caspase-1 is expressed in normal human adult epidermal keratinocytes. Caspase-1 expression is greater in men with AGA. In contrast, in men taking finasteride, caspase-1 levels were lower and were similar to those in normal controls. In vitro studies showed that keratinocytes treated with finasteride in combination with testosterone or DHT resulted in a significant decrease in caspase-1 expression.In vivo and in vitro finasteride treatment resulted in lower caspase-1 expression, supporting the idea that androgens influence innate immunity involved in the hair cycle in AGA. These findings may provide a basis for development of novel treatments for inflammatory skin and hair diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI