Estrogen Hormone Biology

被引:221
作者
Hamilton, Katherine J. [1 ]
Hewitt, Sylvia C. [1 ]
Arao, Yukitomo [1 ]
Korach, Kenneth S. [1 ]
机构
[1] NIEHS, Reprod & Dev Biol Lab, NIH, POB 12233, Res Triangle Pk, NC 27709 USA
来源
NUCLEAR RECEPTORS IN DEVELOPMENT AND DISEASE | 2017年 / 125卷
关键词
RECEPTOR-MEDIATED TRANSCRIPTION; EPITHELIAL-CELL PROLIFERATION; MUTATION PROVIDES EVIDENCE; ALPHA-KNOCKOUT MOUSE; BETA ER-BETA; IN-VIVO; NULL MICE; TARGETED DISRUPTION; REPRODUCTIVE PHENOTYPES; OVARIAN PHENOTYPE;
D O I
10.1016/bs.ctdb.2016.12.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The hormone estrogen is involved in both female and male reproduction, as well as numerous other biological systems including the neuroendocrine, vascular, skeletal, and immune systems. Therefore, it is also implicated in many different diseases and conditions such as infertility, obesity, osteoporosis, endometriosis, and a variety of cancers. Estrogen works through its two distinct nuclear receptors, estrogen receptor alpha (ER alpha) and estrogen receptor beta (ER beta). Various transcriptional regulation mechanisms have been identified as the mode of action for estrogen, mainly the classical mechanism with direct DNA binding but also a nongenomic mode of action and one using tethered or indirect binding. The expression profiles of ER alpha and ER beta are unique with the primary sites of ER alpha expression being the uterus and pituitary gland and the main site of ER beta expression being the granulosa cells of the ovary. Mouse models with knockout or mutation of Esr1 and Esr2 have furthered our understanding of the role of each individual receptor plays in physiology. From these studies, it is known that the primary roles for ER alpha are in the uterus and neuroendocrine system, as female mice lacking ER alpha are infertile due to impaired ovarian and uterine function, whereas female mice lacking ER beta are subfertile due to ovarian defects. The development of effective therapies for estrogen-related diseases has relied on an understanding of the physiological roles and mechanistic functionalities of ER alpha and ER beta in human health and disease.
引用
收藏
页码:109 / 146
页数:38
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