Estrogen actions in the ovary revisited

被引:133
作者
Britt, KL [1 ]
Findlay, JK [1 ]
机构
[1] Prince Henrys Inst Med Res, Clayton, Vic 3168, Australia
关键词
D O I
10.1677/joe.0.1750269
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Estrogens are synonymous with fertility and infertility in mammals. Our knowledge of the biological actions of estrogens, however, is incomplete. Three recent developments have thrown new light on the actions of estrogens in mammalian reproduction that will lead to a greater understanding of their functions. They are (a) the identification of a second estrogen receptor, called ERbeta, (b) the identification of ligand-specific ER coactivators and (c) mouse models with targeted disruption of the genes encoding both ER and the aromatase enzyme. These models provide for the first time animals which are either unable to respond to endogenous or exogenous estrogens (ER 'knockouts'), or can respond to exogenous estrogen but do not make endogenous estrogen (aromatase 'knockout' or ArKO). Furthermore, the ArKO mouse has provided a model to study the effects on the ovary of exogenous estrogens of plant and synthetic origin that are of clinical relevance. The data show that estrogens are essential for fertility but not for survival after birth or for the formation of the reproductive tract. This commentary focuses on the roles of estrogen in folliculogenesis and in the maintenance of the ovarian somatic cell phenotype in the mouse. We also hypothesize that the ERalpha and ERbeta may subserve the proliferative and differentiative actions of estrogen, respectively, within a follicle. In summary, estrogen is obligatory for normal folliculogenesis beyond the antral stage and for the maintenance of the female phenotype of the somatic cells within the ovaries. This clearly demonstrates a major role for sex steroids in somatic cell differentiation in the gonads of eutherian mammals and challenges the central paradigm that the ovary is the default gonad, arising due to the absence of testicular defining signals. Evidence is also provided for the plasticity of the adult female gonad. Understanding the mechanisms of estrogen actions will provide an insight into the regulation of reproductive disorders afflicting women today, notably ovarian dysfunction and the menopause.
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页码:269 / 276
页数:8
相关论文
共 72 条
[11]  
Capel B, 1996, CURR TOP DEV BIOL, V32, P1, DOI 10.1016/S0070-2153(08)60423-8
[12]   ESTRADIOL, TESTOSTERONE, AND ANDROSTENEDIONE IN OVINE FOLLICULAR-FLUID DURING GROWTH AND ATRESIA OF OVARIAN FOLLICLES [J].
CARSON, RS ;
FINDLAY, JK ;
CLARKE, IJ ;
BURGER, HG .
BIOLOGY OF REPRODUCTION, 1981, 24 (01) :105-113
[13]  
Charpentier AH, 2000, CANCER RES, V60, P5977
[14]   A role for the androgen receptor in follicular atresia of estrogen receptor beta knockout mouse ovary [J].
Cheng, GJ ;
Zhang, WH ;
Mäkinen, S ;
Saji, S ;
Warner, M ;
Gustafsson, JÅ ;
Hovatta, O .
BIOLOGY OF REPRODUCTION, 2002, 66 (01) :77-84
[15]   Stromal estrogen receptors mediate mitogenic effects of estradiol on uterine epithelium [J].
Cooke, PS ;
Buchanan, DL ;
Young, P ;
Setiawan, T ;
Brody, J ;
Korach, KS ;
Taylor, J ;
Lubahn, DB ;
Cunha, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6535-6540
[16]   Postnatal sex reversal of the ovaries in mice lacking estrogen receptors α and β [J].
Couse, JF ;
Hewitt, SC ;
Bunch, DO ;
Sar, M ;
Walker, VR ;
Davis, BJ ;
Korach, KS .
SCIENCE, 1999, 286 (5448) :2328-2331
[17]   Estrogen receptor null mice: What have we learned and where will they lead us? [J].
Couse, JF ;
Korach, KS .
ENDOCRINE REVIEWS, 1999, 20 (03) :358-417
[18]  
Couse JF, 1999, ANN ENDOCRINOL-PARIS, V60, P143
[19]   LIGHT AND ELECTRON-MICROSCOPY OF OVARIAN INTERSTITIAL-TISSUE IN SENILE RAT - NORMAL ASPECT AND RESPONSE TO HCG OF DEFICIENCY CELLS AND EPITHELIAL CORDS [J].
CRUMEYROLLEARIAS, M ;
SCHEIB, D ;
ASCHHEIM, P .
GERONTOLOGY, 1976, 22 (03) :185-204
[20]   AROMATASE-ACTIVITY IN GONADS OF TURTLE EMBRYOS AS A FUNCTION OF THE INCUBATION-TEMPERATURE OF EGGS [J].
DESVAGES, G ;
PIEAU, C .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :851-853