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Vertebrate reproductive science and technology
RESEARCH ARTICLE

Expression of androgen receptor and 3β-hydroxysteroid dehydrogenase in corpora lutea during pregnancy in the rat

M. Szołtys A B , M. Słomczyńska A , J. Galas A , M. Duda A and A. Sakiewicz A
+ Author Affiliations
- Author Affiliations

A Laboratory of Endocrinology and Tissue Culture, Institute of Zoology, Jagiellonian University, Kraków, Poland.

B Corresponding author. Email: msol@zuk.iz.uj.edu.pl

Reproduction, Fertility and Development 19(2) 356-365 https://doi.org/10.1071/RD06095
Submitted: 21 August 2006  Accepted: 23 October 2006   Published: 29 January 2007

Abstract

Immunoexpression of androgen receptor (AR) and 3β-hydroxysteroid dehydrogenase (3β-HSD) was investigated in three generations of corpora lutea (CLs), found in the ovaries of rats on Days 1, 2, 5, 9, 14 and 20 of pregnancy. The youngest generation of CLs functioned during the whole pregnancy, whereas the older and the oldest generations underwent earlier regression. The newly formed CLs exhibited weak cytoplasmic 3β-HSD expression. During subsequent days, a gradual increase in 3β-HSD immunolabelling was observed, followed by a decrease on Day 20. In the older and the oldest CLs, surviving luteal cells demonstrated strong, although in the oldest CLs mostly perinuclear, 3β-HSD immunoreaction. The newly formed CLs showed weak nuclear AR immunolabelling, which became stronger during the following days. On Day 20, luteal cells demonstrated a weaker nuclear immunoreaction. The older and oldest generations of CLs exhibited weaker and almost negative AR immunolabelling, respectively. Of special interest was the richly vascularised apical region of young CLs. Here luteal cells with more intensive 3β-HSD staining predominated, whereas cytoplasmic AR immunoreaction was accompanied by positive or negative nuclear AR immunoexpression. The present studies showed differences in AR and 3β-HSD distribution within various generations of CLs and within particular regions of the same young CL.


Acknowledgements

Research on the expression of AR was supported by the State Committee for Scientific Research as a Solicited Project PBZ-KBN-084/PO6/2002 from 2002 to 2005, and studies concerning the expression of 3β-HSD were supported by DS/BiNoZ/IZ/770/2007.


References

Amsterdam, A. , Keren-Tal, I. , and Aharoni, D. (1996). Cross-talk between cAMP and p53-generated signals in induction of differentiation and apoptosis in steroidogenic granulosa cells. Steroids 61, 252–256.
Crossref | GoogleScholarGoogle Scholar | PubMed | Gibori G. (1993). The corpus luteum of pregnancy. In ‘The Ovary’. (Eds E. Y. Adashi and P. C. K. Lueng.) pp. 261–317. (Raven Press: New York.)

Goyeneche, A. A. , Calvo, V. , Gibori, G. , and Telleria, C. M. (2002). Androstenedione interferes with luteal regression by inhibiting apoptosis and stimulating progesterone production. Biol. Reprod. 66, 1540–1547.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Heinlein, C. , and Chang, C. H. (2002). The roles in of androgen receptors and androgen-binding proteins in non-genomic androgen action. Mol. Endocrinol. 16, 2181–2187.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Hild-Petito, S. , West, N. B. , Brenner, R. M. , and Stouffer, R. L. (1991). Localization of androgen receptor in the follicle and corpus luteum of the primate ovary during the menstrual cycle. Biol. Reprod. 44, 561–568.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Hillier, S. G. , Tetsuka, M. , and Fraser, H. M. (1997). Location and developmental regulation of androgen receptor in primate ovary. Hum. Reprod. 12, 107–111.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Hoyer, P. E. , and Andersen, H. (1977). Histochemistry of 3β-hydroxysteroid dehydrogenase in rat ovary. Histochemistry 51, 167–193.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Marcal, J. M. , Chew, N. J. , Salomon, D. S. , and Sherman, M. I. (1975). Δ5, 3β-hydroxysteroid dehydrogenase activities in rat trophoblast and ovary during pregnancy. Endocrinology 96, 1270–1279.
PubMed |

Morishige, W. K. , Pepe, G. J. , and Rothchild, I. (1973). Serum luteinizing hormone, prolactin and progesterone levels during pregnancy in the rat. Endocrinology 92, 1527–1530.
PubMed |

Nelson, S. E. , McLean, M. P. , Jayatilak, P. G. , and Gibori, G. (1992). Isolation, characterization, and culture of cell subpopulations forming the pregnant rat corpus luteum. Endocrinology 130, 954–966.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Noworyta, B. , and Szołtys, M. (1975). Dynamics of Δ5-3β-hydroxysteroid dehydrogenase activity in rat follicular granulosa cells during proestrus. Bull. Acad. Anim. Bioch. Biophs. 23, 65–69.


Orly, J. (1989). Orchestrated expression of steroidogenic side-chain cleavage cytochrome P-450 during follicular development in the rat ovary. J. Reprod. Fertil. Suppl. 37, 155–162.
PubMed |

Pelletier, G. , Li, S. , Luu-The, V. , Tremblay, Y. , Belanger, A. , and Labrie, F. (2001). Immunoelectron microscopic localization of three key steroidogenic enzymes (cytochrome P450scc, 3β-hydroxysteroid dehydrogenase and cytochrome P450c17) in rat adrenal cortex and gonads. J. Endocrinol. 171, 373–383.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Rider, V. , McRae, A. , Heap, R. B. , and Feinstein, A. (1985). Passive immunization against progesterone inhibits endometrial sensitization in pseudopregnant mice and has antifertility effects in pregnant mice which are reversible by steroid treatment. J. Endocrinol. 104, 153–158.
PubMed |

Słomczyńska, M. , and Tabarowski, Z. (2001). Localization of androgen receptor and cytochrome P450 aromatase in the follicle and corpus luteum of the porcine ovary. Anim. Reprod. Sci. 65, 127–134.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Stocco, C. O. , Chedrese, J. , and Deis, R. P. (2001). Luteal expression of cytochrome P450 side-chain cleavage, steroidogenic acute regulatory protein, 3β-hydroxysteroid dehydrogenase, and 20α-hydroxysteroid dehydrogenase genes in late pregnant rats: effect of luteinizing hormone. Biol. Reprod. 65, 1114–1119.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Szołtys, M. (1976). Progestagen dynamics in preovulatory follicles of rats. J. Reprod. Fertil. 48, 397–398.
PubMed |

Szołtys, M. , and Jabłonka, A. (1989). Hormonal function of rat ovarian tissue during pregnancy.  Trends in Vertebrate Morphology 35, 103–105.


Szołtys, M. , and Słomczyńska, M. (2000). Changes in distribution of androgen receptor during maturation of rat ovarian follicle. Exp. Clin. Endocrinol. Diabetes 108, 228–234.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Takiguchi, S. , Sugino, N. , Kashida, S. , Yamagata, Y. , Nakamura, Y. , and Kato, H. (2000). Rescue of the corpus luteum and an increase in luteal superoxide dismutase expression induced by placental luteotropins in the rat: action of testosterone without conversion to estrogen. Biol. Reprod. 62, 398–403.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Taya, K. , and Greenwald, G. S. (1981). In vivo and in vitro ovarian steroidogenesis in the pregnant rat. Biol. Reprod. 25, 683–691.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Teerds, K. J. , and Dorrington, J. H. (1993). Immunohistochemical localization of 3β-hydroxysteroid dehydrogenase in the rat ovary during follicular development and atresia. Biol. Reprod. 49, 989–996.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Telleria, C. M. , Stocco, C. O. , and Deis, P. (1995a). Luteolytic action of RU486: modulation of luteal 3β-hydroxysteroid dehydrogenase and 20α-hydroxysteroid dehydrogenase activities in late pregnant rats.  J. Steroid. Mol. Biol. 52, 567–573.
Crossref | GoogleScholarGoogle Scholar |

Telleria, C. M. , Stocco, C. O. , Stati, A. O. , Rastrilla, A. M. , Carrizo, D. G. , Aguado, L. I. , and Deis, R. P. (1995b). Dual regulation of luteal progesterone production by androstenedione during spontaneous and RU486-induced luteolysis in pregnant rat. J. Steroid. Mol. Biol. 55, 385–393.
Crossref | GoogleScholarGoogle Scholar |

Telleria, C. M. , Zhong, L. , Deb, S. , Srivastava, R. K. , Park, K. S. , Sugino, N. , Park-Sarge, O. K. , and Gibori, G. (1998). Differential expression of estrogen receptors alpha and beta in the rat corpus luteum of pregnancy: regulation by prolactin and placental lactogens. Endocrinology 139, 2432–2442.
Crossref | GoogleScholarGoogle Scholar | PubMed |

Tetsuka, M. , Whitelaw, P. F. , Bremner, W. J. , Millar, M. R. , Smyth, C. D. , and Hillier, S. G. (1995). Developmental regulation of androgen receptor in rat ovary. J. Endocrinol. 145, 535–543.
PubMed |

Thordarson, G. , Galosy, S. , Gundmundsson, G. O. , Newcomer, B. , Sridaran, R. , and Talamantes, F. (1997). Interaction of mouse placental lactogens and androgens in regulating progesterone release in cultured mouse luteal cells. Endocrinology 138, 3236–3241.
Crossref | GoogleScholarGoogle Scholar | PubMed |