Estrogen receptor expression in developing epididymis, efferent ductules, and other male reproductive organs
- PMID: 2036967
- DOI: 10.1210/endo-128-6-2874
Estrogen receptor expression in developing epididymis, efferent ductules, and other male reproductive organs
Abstract
The distribution of estrogen receptors (ER) in developing reproductive organs of male BALB/c mice was determined by 3H-estradiol steroid autoradiography. Efferent ductules, urogenital sinus and Wolffian ducts, and their derivatives, the epididymis, ductus deferens, seminal vesicles, coagulating glands, prostate, and bulbouretheral glands (BUGs), were examined from 16 days fetal (gestation = 19-20 days) to 10 days postnatal. All fetal reproductive organs strongly expressed mesenchymal ER. Stromal cells of these organs remained ER+ at later times. However, smooth muscle cells in organs such as the ductus deferens, BUG, prostate, and caudal epididymis were only weakly ER+ or ER- after their differentiation from mesenchyme, although fibroblasts interspersed within the smooth muscle remained strongly ER+. Efferent ductules were the first site of epithelial ER expression in the developing male tract; this organ expressed epithelial ER on day 16 of gestation and subsequently. Wolffian ducts and urogenital sinus did not contain epithelial ER on day 16 of gestation. Epididymis began expressing epithelial ER soon after its differentiation, on day 19 of gestation. A clear gradient of ER expression was noted in the regions of the developing epididymis, with the efferent ducts and the initial segment of the epididymis containing 3-fold more silver grains per epithelial cell than more distal regions of the epididymis. Epithelium of the seminal vesicle and coagulating gland was initially ER-, but became weakly ER+ at day 6 postnatal and later. The epithelium of all other organs (ductus deferens, prostate, and BUGs) never expressed ER at any time.
Similar articles
-
Androgen receptor expression in developing male reproductive organs.Endocrinology. 1991 Jun;128(6):2867-73. doi: 10.1210/endo-128-6-2867. Endocrinology. 1991. PMID: 2036966
-
Age-, cell- and region-specific immunoexpression of estrogen receptor alpha (but not estrogen receptor beta) during postnatal development of the epididymis and vas deferens of the rat and disruption of this pattern by neonatal treatment with diethylstilbestrol.Endocrinology. 2001 Feb;142(2):874-86. doi: 10.1210/endo.142.2.7978. Endocrinology. 2001. PMID: 11159861
-
Localization of androgen and estrogen receptors in adult male mouse reproductive tract.J Androl. 2002 Nov-Dec;23(6):870-81. J Androl. 2002. PMID: 12399534
-
Estrogen and its receptors in efferent ductules and epididymis.J Androl. 2011 Nov-Dec;32(6):600-13. doi: 10.2164/jandrol.110.012872. Epub 2011 Mar 25. J Androl. 2011. PMID: 21441425 Review.
-
Estrogens and epididymal function.Reprod Fertil Dev. 2001;13(4):273-83. doi: 10.1071/rd00100. Reprod Fertil Dev. 2001. PMID: 11800166 Review.
Cited by
-
Sperm, a source of estrogen.Environ Health Perspect. 1995 Oct;103 Suppl 7(Suppl 7):59-62. doi: 10.1289/ehp.95103s759. Environ Health Perspect. 1995. PMID: 8593876 Free PMC article. Review.
-
Estrogen in the male: a historical perspective.Biol Reprod. 2018 Jul 1;99(1):27-44. doi: 10.1093/biolre/ioy043. Biol Reprod. 2018. PMID: 29438493 Free PMC article. Review.
-
The antiestrogen ICI 182,780 decreases the expression of estrogen receptor-alpha but has no effect on estrogen receptor-beta and androgen receptor in rat efferent ductules.Reprod Biol Endocrinol. 2003 Oct 10;1:75. doi: 10.1186/1477-7827-1-75. Reprod Biol Endocrinol. 2003. PMID: 14613549 Free PMC article.
-
Ex3αERKO male infertility phenotype recapitulates the αERKO male phenotype.J Endocrinol. 2010 Dec;207(3):281-8. doi: 10.1677/JOE-10-0290. Epub 2010 Sep 10. J Endocrinol. 2010. PMID: 20833731 Free PMC article.
-
Estrogen, efferent ductules, and the epididymis.Biol Reprod. 2011 Feb;84(2):207-17. doi: 10.1095/biolreprod.110.087353. Epub 2010 Oct 6. Biol Reprod. 2011. PMID: 20926801 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources