Differential expression of oestrogen receptor α and β proteins in the testes and male reproductive system of human and non-human primates

被引:170
作者
Saunders, PTK [1 ]
Sharpe, RM [1 ]
Williams, K [1 ]
Macpherson, S [1 ]
Urquart, H [1 ]
Irvine, DS [1 ]
Millar, MR [1 ]
机构
[1] MRC, Human Reprod Sci Unit, Edinburgh EH3 9ET, Midlothian, Scotland
关键词
efferent ductules; epididymis; oestrogen receptor; testis; vas deferens;
D O I
10.1093/molehr/7.3.227
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The role(s) oestrogens play in male adult reproductive function remains uncertain. We have used antibodies specific for oestrogen receptor-alpha (ER alpha) and -beta (ERP) to investigate their distribution within the male, In testes from adult human, macaque and marmoset, ER beta protein was detected in Sertoli cells, Leydig cells and peritubular myoid cells. In germ cells, the intensity of immunostaining for ER beta was variable between species, Immunoexpression in preleptotene, leptotene and zygotene spermatocytes was low/absent in all species, Elongated spermatids were consistently immunonegative. No ER alpha immunoexpression was detected in testes, ER beta was detected in epithelial and stromal cell nuclei throughout the male reproductive system [efferent ductules (ED), epididymis, vas deferens, seminal vesicles] and in the bladder, ER alpha was detected in non-ciliated epithelial cells in the ED, but rarely in epithelial and basal cells within the epididymis, Epithelial cells from seminal vesicles and bladder were immunonegative for ER alpha, Expression of ER alpha in stromal cells was rare in the ED, epididymis and bladder but more frequent in seminal vesicles. Expression of ER alpha, and long and short forms of ER beta, was confirmed by Western blotting. The widespread expression of ER beta suggests that it is the primary target for modulation of tissue function via oestrogenic ligands in the male reproductive system.
引用
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页码:227 / 236
页数:10
相关论文
共 55 条
[1]  
Aceitero J, 1998, ANAT REC, V252, P17
[2]   Comparative effects of neonatal exposure of male rats to potent and weak (environmental) estrogens on spermatogenesis at puberty and the relationship to adult testis size and fertility: Evidence for stimulatory effects of low estrogen levels [J].
Atanassova, N ;
McKinnell, C ;
Turner, KJ ;
Walker, M ;
Fisher, JS ;
Morley, M ;
Millar, MR ;
Groome, NP ;
Sharpe, RM .
ENDOCRINOLOGY, 2000, 141 (10) :3898-3907
[3]   Permanent effects of neonatal estrogen exposure in rats on reproductive hormone levels, sertoli cell number, and the efficiency of spermatogenesis in adulthood [J].
Atanassova, N ;
McKinnell, C ;
Walker, M ;
Turner, KJ ;
Fisher, JS ;
Morley, M ;
Millar, MR ;
Groome, NP ;
Sharpe, RM .
ENDOCRINOLOGY, 1999, 140 (11) :5364-5373
[4]   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
[5]   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
[6]   Estrogen receptors alpha and beta form heterodimers on DNA [J].
Cowley, SM ;
Hoare, S ;
Mosselman, S ;
Parker, MG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (32) :19858-19862
[7]  
Dupont S, 2000, DEVELOPMENT, V127, P4277
[8]   Estrogenic induction of spermatogenesis in the hypogonadal mouse [J].
Ebling, FJP ;
Brooks, AN ;
Cronin, AS ;
Ford, H ;
Kerr, JB .
ENDOCRINOLOGY, 2000, 141 (08) :2861-2869
[9]   Targeted disruption of the estrogen receptor gene in male mice causes alteration of spermatogenesis and infertility [J].
Eddy, EM ;
Washburn, TF ;
Bunch, DO ;
Goulding, EH ;
Gladen, BC ;
Lubahn, DB ;
Korach, KS .
ENDOCRINOLOGY, 1996, 137 (11) :4796-4805
[10]   Human estrogen receptor β-gene structure, chromosomal localization, and expression pattern [J].
Enmark, E ;
Pelto-Huikko, M ;
Grandien, K ;
Lagercrantz, S ;
Lagercrantz, J ;
Fried, G ;
Nordenskjöld, M ;
Gustafsson, JÅ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (12) :4258-4265