Estrogen receptor-beta mRNA expression in rat ovary: down-regulation by gonadotropins.

We have examined the expression and regulation of the two estrogen receptor (ER alpha and ER beta) genes in the rat ovary, using Northern blotting, RT-PCR, and in situ hybridization histochemistry. Northern blotting results show that the ovary expresses both ER alpha and ER beta genes as single (approximately 6.5-kb) and multiple (ranging from approximately 1.0-kb to approximately 10.0-kb) transcripts, respectively. ER alpha mRNA is expressed at a level lower than ER beta mRNA in immature rat ovaries. This relationship appears unchanged between sexually mature adult rats and immature rats. In sexually mature adult rats undergoing endogenous hormonal changes, whole ovarian content of ER beta mRNA, as determined by RT-PCR, remained more or less constant with the exception of the evening of proestrus when ER beta mRNA levels were decreased. Examination of ER beta mRNA expression at the cellular level, by in situ hybridization, showed that ER beta mRNA is expressed preferentially in granulosa cells of small, growing, and preovulatory follicles, although weak expression of ER beta mRNA was observed in a subset of corpora lutea, and that the decrease in ER beta mRNA during proestrous evening is attributable, at least in part, to down-regulation of ER beta mRNA in the preovulatory follicles. This type of expression and regulation was not typical for ER alpha mRNA in the ovary. Although whole ovarian content of ER alpha mRNA was clearly detected by RT-PCR, no apparent modulation of ER alpha mRNA levels was observed during the estrous cycle. Examination of ER alpha mRNA expression at the cellular level, by in situ hybridization, showed that ER alpha mRNA is expressed at a low level throughout the ovary with no particular cellular localization. To further examine the potential role of the preovulatory pituitary gonadotropins in regulating ER beta mRNA expression in the ovary, we used immature rats treated with gonadotropins. In rats undergoing exogenous hormonal challenges, whole ovarian content of ER beta mRNA, as determined by RT-PCR, remained more or less unchanged after an injection of PMSG. In contrast, a subsequent injection of human CG (hCG) resulted in a substantial decrease in whole ovarian content of ER beta mRNA. In situ hybridization for ER beta mRNA shows that small, growing, and preovulatory follicles express ER beta mRNA in the granulosa cells. The preovulatory follicles contain ER beta mRNA at a level lower than that observed for small and growing follicles. In addition, there is an abrupt decrease in ER beta mRNA expression in the preovulatory follicles after hCG injection. The inhibitory effect of hCG on ER beta mRNA expression was also observed in cultured granulosa cells. Moreover, agents stimulating LH/CG receptor-associated intracellular signaling pathways (forskolin and a phorbol ester) readily mimicked the effect of hCG in down-regulating ER beta mRNA in cultured granulosa cells. Taken together, our results demonstrate that 1) the ovary expresses both ER alpha and ER beta genes, although ER beta is the predominant form of estrogen receptor in the ovary, 2) ER beta mRNA is localized predominantly to the granulosa cells of small, growing, and preovulatory follicles, and 3) the preovulatory LH surge down-regulates ER beta mRNA. These results clearly implicate the physiological importance of ER beta in female reproductive functions.

[1]  J. Gustafsson,et al.  Cloning of a novel receptor expressed in rat prostate and ovary. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[2]  K. Sarge,et al.  Cis-regulatory elements conferring cyclic 3',5'-adenosine monophosphate responsiveness of the progesterone receptor gene in transfected rat granulosa cells. , 1995, Endocrinology.

[3]  K. Korach,et al.  Analysis of transcription and estrogen insensitivity in the female mouse after targeted disruption of the estrogen receptor gene. , 1995, Molecular endocrinology.

[4]  K. Korach Insights from the study of animals lacking functional estrogen receptor. , 1994, Science.

[5]  D. McDonnell,et al.  The A and B isoforms of the human progesterone receptor operate through distinct signaling pathways within target cells , 1994, Molecular and cellular biology.

[6]  H. Sasano,et al.  Immunohistochemical distribution of progesterone, androgen and oestrogen receptors in the human ovary during the menstrual cycle: relationship to expression of steroidogenic enzymes. , 1994, Human reproduction.

[7]  R. Stouffer,et al.  Progesterone receptor, but not estradiol receptor, messenger ribonucleic acid is expressed in luteinizing granulosa cells and the corpus luteum in rhesus monkeys. , 1994, Endocrinology.

[8]  K. Mayo,et al.  Regulation of the progesterone receptor gene by gonadotropins and cyclic adenosine 3',5'-monophosphate in rat granulosa cells. , 1994, Endocrinology.

[9]  B. Lunenfeld,et al.  Follicular development and its control. , 1993, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

[10]  K. Korach,et al.  Alteration of reproductive function but not prenatal sexual development after insertional disruption of the mouse estrogen receptor gene. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[11]  J. Gorski,et al.  Estrogen receptor and progesterone receptor genes are expressed differentially in mouse embryos during preimplantation development. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[12]  K. Horwitz,et al.  Antagonist-occupied human progesterone B-receptors activate transcription without binding to progesterone response elements and are dominantly inhibited by A-receptors. , 1993, Molecular endocrinology.

[13]  B. O’Malley,et al.  Human progesterone receptor A form is a cell- and promoter-specific repressor of human progesterone receptor B function. , 1993, Molecular endocrinology.

[14]  B. Katzenellenbogen,et al.  Regulation of progesterone receptor gene expression and growth in the rat uterus: modulation of estrogen actions by progesterone and sex steroid hormone antagonists. , 1993, Endocrinology.

[15]  Y. Wan,et al.  Detection of estrogen receptor messenger ribonucleic acid in human oocytes and cumulus-oocyte complexes using reverse transcriptase-polymerase chain reaction. , 1993, Fertility and Sterility.

[16]  M. Kawashima,et al.  Comparison of follicular estrogen receptors in rat, hamster, and pig. , 1993, Biology of reproduction.

[17]  R. Billiar,et al.  Evidence for the presence of the estrogen receptor in the ovary of the baboon (Papio anubis). , 1992, The Journal of clinical endocrinology and metabolism.

[18]  A. Ree,et al.  Down-regulation of messenger ribonucleic acid (mRNA) for the estrogen receptor (ER) by phorbol ester requires ongoing RNA synthesis but not protein synthesis. Is hormonal control of ER mRNA degradation mediated by an RNA molecule? , 1992, Endocrinology.

[19]  K. Mayo,et al.  Cellular localization and hormonal regulation of follicle-stimulating hormone and luteinizing hormone receptor messenger RNAs in the rat ovary. , 1991, Molecular endocrinology.

[20]  S. Nakanishi,et al.  Luteinizing hormone induces progesterone receptor gene expression in cultured porcine granulosa cells. , 1991, Endocrinology.

[21]  K. Mayo,et al.  Transient expression of progesterone receptor messenger RNA in ovarian granulosa cells after the preovulatory luteinizing hormone surge. , 1991, Molecular endocrinology.

[22]  S. Batra,et al.  Molecular cloning and sequence analysis of the human ribosomal protein S16. , 1991, The Journal of biological chemistry.

[23]  B. Katzenellenbogen,et al.  Multihormonal regulation of the progesterone receptor in MCF-7 human breast cancer cells: interrelationships among insulin/insulin-like growth factor-I, serum, and estrogen. , 1990, Endocrinology.

[24]  P. Chambon,et al.  The cloned human oestrogen receptor contains a mutation which alters its hormone binding properties. , 1989, The EMBO journal.

[25]  B. Katzenellenbogen,et al.  Regulation of estrogen receptor messenger ribonucleic acid and protein levels in human breast cancer cell lines by sex steroid hormones, their antagonists, and growth factors. , 1989, Molecular endocrinology.

[26]  K. M. Gianola,et al.  A highly conserved mouse gene with a propensity to form pseudogenes in mammals , 1988, Molecular and cellular biology.

[27]  K. Struhl,et al.  Current Protocols in Molecular Biology (New York: Greene Publishing Associates and Wiley-Interscience). Host-Range Shuttle System for Gene Insertion into the Chromosomes of Gram-negative Bacteria. , 1988 .

[28]  S. Koike,et al.  Molecular cloning and characterization of rat estrogen receptor cDNA. , 1987, Nucleic acids research.

[29]  M. Walters Steroid hormone receptors and the nucleus. , 1985, Endocrine reviews.

[30]  D. Magoffin,et al.  The ovarian androgen producing cells: a review of structure/function relationships. , 1985, Endocrine reviews.

[31]  E. Adashi,et al.  Hormonal regulation of the differentiation of cultured ovarian granulosa cells. , 1984, Endocrine reviews.

[32]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[33]  A. Hsueh,et al.  Estrogen augmentation of gonadotropin-stimulated progestin biosynthesis in cultured rat granulosa cells. , 1983, Endocrinology.

[34]  G. Erickson Primary cultures of ovarian cells in serum-free medium as models of hormone-dependent differentiation , 1983, Molecular and Cellular Endocrinology.

[35]  P. Leung,et al.  Further evidence in support of a short-loop feedback action of estrogen on ovarian androgen production. , 1980, Life sciences.

[36]  B. Katzenellenbogen Dynamics of steroid hormone receptor action. , 1980, Annual review of physiology.

[37]  J. Richards,et al.  Maturation of ovarian follicles: actions and interactions of pituitary and ovarian hormones on follicular cell differentiation. , 1980, Physiological reviews.

[38]  J. Darnell,et al.  Production of mRNA in chinese hamster cells: Relationship of the rate of synthesis to the cytoplasmic concentration of nine specific mRNA sequences , 1979, Cell.

[39]  J. Richards,et al.  Adenosine 3',5'-monophosphate, luteinizing hormone receptor, and progesterone during granulosa cell differentiation: effects of estradiol and follicle-stimulating hormone. , 1979, Endocrinology.

[40]  H. P. Zassenhaus,et al.  Estradiol-17β receptors in the immature rat ovary , 1977, Steroids.

[41]  A. R. Midgley,et al.  Ovarian follicular development in the rat: hormone receptor regulation by estradiol, follicle stimulating hormone and luteinizing hormone. , 1976, Endocrinology.

[42]  J. Richards,et al.  Estradiol receptor content in rat granulosa cells during follicular development: modification by estradiol and gonadotropins. , 1975, Endocrinology.

[43]  E. Baulieu,et al.  Steroid hormone receptors. , 1975, Vitamins and hormones.

[44]  J. Richards Estradiol binding to rat corpora lutea during pregnancy. , 1974, Endocrinology.

[45]  R. Goldenberg,et al.  Estrogen and follicle stimulation hormone interactions on follicle growth in rats. , 1972, Endocrinology.

[46]  F. Merk,et al.  An intercellular response to estrogen by granulosa cells in the rat ovary; an electron microscope study. , 1972, Endocrinology.

[47]  S. Saiduddin 3H-Estradiol Uptake by the Rat Ovary 1 , 1971, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[48]  W. Stumpf Nuclear concentration of 3H-estradiol in target tissues. Dry-mount autoradiography of vagina, oviduct, ovary, testis, mammary tumor, liver and adrenal. , 1969, Endocrinology.

[49]  M. Feresten THE CORPUS LUTEUM OF PREGNANCY IN RELATION TO THE ANTERIOR PITUITARY GLAND , 1935 .