scholarly journals Estrogen Receptor β, But Not Estrogen Receptor α, Is Present in the Vascular Endothelium of the Human and Nonhuman Primate Endometrium1

2001 ◽  
Vol 86 (3) ◽  
pp. 1370-1378 ◽  
Author(s):  
Hilary O. D. Critchley ◽  
Robert M. Brenner ◽  
Teresa A. Henderson ◽  
Karin Williams ◽  
Nihar R. Nayak ◽  
...  

Estrogen action is dependent upon the presence of specific ligand-activated receptors in target tissues. The aim of the present experiments was to compare the spatial and temporal pattern of expression of estrogen receptor β (ERβ) with that of ERα in full thickness endometrial samples (from the superficial to the basal zone) obtained from both women and rhesus macaques. Immunohistochemical localization with specific antibodies revealed that ERα and ERβ were both expressed in nuclei of the glands and stroma. Consistent with previous studies, expression of ERα declined in the glands and stroma of the functionalis during the secretory phase. The luminal epithelium also displayed positive immunoreactivity for ERβ. Expression of ERβ declined in glandular cell nuclei, but not stroma, within the functionalis during the late secretory phase. Levels of expression of ERα and ERβ in all cellular compartments remained unchanged in the basalis. Both receptor subtypes were detected on Western blots using proteins extracted from uterine samples obtained throughout the menstrual cycle. There was a striking contrast between the pattern of expression of ERα and ERβ in the vascular endothelium and the perivascular cells surrounding endometrial blood vessels; only ERβ was present in the endothelial cell population, although both forms of ER were expressed in perivascular cells. We conclude that estrogen action(s) within the vascular endothelium in the endometrium may be mediated via direct binding to the ERβ isoform and that these cells could therefore be a target for agonists or antagonists that selectively target the β form of the ER.

2010 ◽  
Vol 24 (9) ◽  
pp. 1703-1714 ◽  
Author(s):  
Bonnie J. Deroo ◽  
Adrian V. Buensuceso

Abstract The discovery of estrogen receptor-β (ERβ) in 1996 stimulated great interest in the physiological roles and molecular mechanisms of ERβ action. We now know that ERβ plays a major role in mediating estrogen action in several tissues and organ systems, including the ovary, cardiovascular system, brain, and the immune system, and that ERβ and ERα generally play distinct physiological roles in the body. Although significant progress has been made toward understanding the molecular mechanisms of ERβ action, particularly in vitro, there remains a large gap in our understanding of the mechanisms by which ERβ elicits its biological functions in a true physiological context.


1998 ◽  
Vol 19 (4) ◽  
pp. 253-286 ◽  
Author(s):  
George G.J.M. Kuiper ◽  
Paul J. Shughrue ◽  
Istvan Merchenthaler ◽  
Jan-Åke Gustafsson

2005 ◽  
Vol 288 (2) ◽  
pp. H469-H476 ◽  
Author(s):  
Maryanne Skavdahl ◽  
Charles Steenbergen ◽  
James Clark ◽  
Page Myers ◽  
Tracy Demianenko ◽  
...  

The goal of this study was to determine the role of estrogen receptor subtypes in the development of pressure overload hypertrophy in mice. Epidemiological studies have suggested gender differences in the development of hypertrophy and heart disease, but the mechanism and the role of estrogen receptor subtypes are not established. We performed transverse aortic constriction (TAC) and sham operations in male and female wild-type (WT) mice and mice lacking functional estrogen receptor-α [α-estrogen receptor knockout (α-ERKO)] and mice lacking estrogen receptor-β (β-ERKO). Body, heart, and lung weights were measured 2 wk postsurgery. WT male mice subjected to TAC showed a 64% increase in the heart weight-to-body weight ratio (HW/BW) compared with sham, and WT males have increased lung weight at 2 wk. WT female mice subjected to TAC showed a 31% increase in HW/BW compared with sham, which was significantly less than their male counterparts and with no evidence of heart failure. α-ERKO females developed HW/BW nearly identical to that seen in WT littermate females in response to TAC, indicating that estrogen receptor-α is not essential for the attenuation of hypertrophy observed in WT females. In contrast, β-ERKO females responded to TAC with a significantly greater increase in HW/BW than WT littermate females. β-ERKO females have lower expression of lipoprotein lipase at baseline than WT or α-ERKO females. These data suggest an important role for estrogen receptor-β in attenuating the hypertrophic response to pressure overload in females.


2017 ◽  
Vol 292 (44) ◽  
pp. 18178-18191 ◽  
Author(s):  
Francesca Fortini ◽  
Francesco Vieceli Dalla Sega ◽  
Cristiana Caliceti ◽  
Giorgio Aquila ◽  
Micaela Pannella ◽  
...  

2004 ◽  
Vol 171 (4S) ◽  
pp. 429-429
Author(s):  
Masayoshi Nomura ◽  
Naohiro Fujimoto ◽  
Donald W. Pfaff ◽  
Sonoko Ogawa ◽  
Tetsuro Matsumoto

2004 ◽  
Vol 171 (4S) ◽  
pp. 348-348
Author(s):  
Ellen Shapiro ◽  
Hongying Huang ◽  
Rachael R. Mash ◽  
Eliza Ng ◽  
Deborah E. McFadden ◽  
...  

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