Early onset of puberty and early ovarian failure in CYP7B1 knockout mice

被引:45
作者
Omoto, Y
Lathe, R
Warner, M
Gustafsson, JÅ
机构
[1] Karolinska Inst, Dept Med Nutr, S-14186 Huddinge, Sweden
[2] Karolinska Inst, Dept Biosci, S-14186 Huddinge, Sweden
[3] Pieta Res, Edinburgh EH10 5YW, Midlothian, Scotland
关键词
3 beta Adiol; estrogen receptor; precocious puberty; cytochrome P-450; mammary gland;
D O I
10.1073/pnas.0500198102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CYP7B1 is the enzyme responsible for hydroxylation and termination of the estrogenic actions of the androgen metabolite, 5alpha-androstane-3beta, 17beta-diol (3betaAdiol). 3betaAdiol is estrogenic in ERalpha or ERbeta positive cells only if they do not express CYP7B1. In this study we show that female CYP7B1(-/-) mice experience early onset of growth of the uterus and mammary glands and commence estrus cycles 2 days earlier than their wild-type littermates. Adult mammary glands and uteri appear to be under continuous estrogenic stimulation. We conclude that, by cell-specific regulation of the estrogenicity of 3betaAdiol, CYP7B1 performs two major tasks: (t) it allows 3betaAdiol to have growth inhibitory effects through ERbeta an (it) it permits estradiol-specific activation of estrogen receptors by protection of certain cells from the estrogenic effects of 3betaAdiol. When CYP7B1 is inactivated, 3betaAdiol activates estrogen receptors indiscriminately, and the overall effect is prolonged and inappropriate exposure to estrogen.
引用
收藏
页码:2814 / 2819
页数:6
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