Estradiol-17β Is Produced in Bovine Corpus Luteum1

Abstract The aim of this study was to investigate the expression of cytochrome P450 aromatase (aromatase) mRNA, its activity, and estradiol-17β (estradiol) secretion in bovine corpus luteum (CL) during the estrous cycle. Expression of aromatase mRNA was examined in CL at the early, mid, late, and regressed luteal stages by using a reverse transcription-polymerase chain reaction. Aromatase mRNA was detected in all luteal stages examined, although aromatase expression was significantly lower during the early and regressed luteal phases compared to the mid and late luteal phases. Moreover, cultured midluteal cells clearly converted exogenous [3H]androstenedione into estradiol, and an aromatase inhibitor significantly inhibited this conversion. To characterize the local release of estradiol within the CL during the estrous cycle, an in vitro microdialysis system (MDS) of CL was conducted. Estradiol in MDS perfusate was confirmed by a reverse-phase high-performance liquid chromatography in combination with enzyme immunoassays. Basal release of estradiol from microdialyzed CL did not change during the estrous cycle. Additionally, when freshly prepared midluteal cells were exposed to estradiol (10−14 to 10−9 M), estradiol stimulated prostaglandin (PG) F2α secretion (P < 0.05), although it did not affect progesterone and oxytocin secretion. The overall results indicate that estradiol is produced locally in bovine CL throughout the estrous cycle, and they suggest that estradiol plays a role in regulating PGF2α production in CL as an autocrine/paracrine factor.

[1]  R. Einspanier,et al.  Expression and localisation of vascular endothelial growth factor and basic fibroblast growth factor during the final growth of bovine ovarian follicles. , 2000, The Journal of endocrinology.

[2]  K. Okuda,et al.  Is Tumor Necrosis Factor α a Trigger for the Initiation of Endometrial Prostaglandin F2α Release at Luteolysis in Cattle?1 , 2000 .

[3]  K. Okuda,et al.  Sensitivity of bovine corpora lutea to prostaglandin F2alpha is dependent on progesterone, oxytocin, and prostaglandins. , 1999, Biology of reproduction.

[4]  A. Miyamoto,et al.  Local release of steroid hormones, prostaglandin E2, and endothelin-1 from bovine mature follicles In vitro: effects of luteinizing hormone, endothelin-1, and cytokines. , 1998, Biology of reproduction.

[5]  K. Okuda,et al.  Progesterone Stimulation by Prostaglandin F_ Involves the Protein Kinase C Pathway in Cultured Bovine Luteal Cells , 1998 .

[6]  K. Okuda,et al.  Up-regulation of oxytocin receptors in porcine endometrium by adenosine 3',5'-monophosphate. , 1997, Biology of reproduction.

[7]  W. Streich,et al.  [Sex steroid profiles and ovarian activities of the female panda Yan Yan in the Berlin Zoo]. , 1997, Berliner und Munchener tierarztliche Wochenschrift.

[8]  R. Einspanier,et al.  Detection of mRNA and immunoreactive proteins for acidic and basic fibroblast growth factor and expression of the fibroblast growth factor receptors in the bovine oviduct. , 1997, Journal of reproduction and fertility.

[9]  K. Okuda,et al.  Functional oxytocin receptors in bovine granulosa cells. , 1997, Biology of reproduction.

[10]  H. Shikama,et al.  Inhibitory effect of a novel non-steroidal aromatase inhibitor, YM511 on the proliferation of MCF-7 human breast cancer cell , 1996, The Journal of Steroid Biochemistry and Molecular Biology.

[11]  H. Kaneko,et al.  Changes in Plasma Concentrations of Immunoreactive Inhibin, Estradiol and FSH Associated with Follicular Waves during the Estrous Cycle of the Cow , 1995 .

[12]  D. Schams,et al.  Effects of Estradiol-17.BETA. on Oxytocin and Progesterone Release of the Bovine Corpus Luteum during the Estrous Cycle. , 1995 .

[13]  J. Ireland,et al.  Selection, dominance and atresia of follicles during the oestrous cycle of heifers. , 1994, Journal of reproduction and fertility.

[14]  D. Schams,et al.  Acute actions of prostaglandin F2 alpha, E2, and I2 in microdialyzed bovine corpus luteum in vitro. , 1993, Biology of Reproduction.

[15]  A. Voss,et al.  Levels of messenger ribonucleic acid for cytochrome P450 17 alpha-hydroxylase and P450 aromatase in preovulatory bovine follicles decrease after the luteinizing hormone surge. , 1993, Endocrinology.

[16]  D. Schams,et al.  Evidence for oxytocin receptors in cultured bovine luteal cells. , 1992, Biology of reproduction.

[17]  J. Kitawaki,et al.  Contribution of aromatase to the deoxyribonucleic acid synthesis of MCF-7 human breast cancer cells and its suppression by aromatase inhibitors , 1992, The Journal of Steroid Biochemistry and Molecular Biology.

[18]  W. Rath,et al.  Paracrine actions of oxytocin, prostaglandin F2 alpha, and estradiol within the human corpus luteum. , 1992, The Journal of clinical endocrinology and metabolism.

[19]  H. Jarry,et al.  Determination of secretion rates of estradiol, progesterone, oxytocin, and angiotensin II from tertiary follicles and freshly formed corpora lutea in freely moving sows. , 1991, Endocrinology.

[20]  E. Gregoraszczuk The interaction of testosterone and gonadotropins in stimulating estradiol and progesterone secretion by cultures of corpus luteum cells isolated from pigs in early and midluteal phase. , 1991, Endocrinologia japonica.

[21]  D. Schams,et al.  Oxytocin stimulates progesterone release from microdialyzed bovine corpus luteum in vitro. , 1991, Biology of reproduction.

[22]  H. Jarry,et al.  Effects of oxytocin on in vitro steroid release of midstage small and large porcine luteal cells. , 1990, Endocrinology.

[23]  H. Sauerwein,et al.  Immunoaffinity chromatography and a biotin-streptavidin amplified enzymeimmunoassay for sensitive and specific estimation of estradiol-17 beta. , 1990, Journal of steroid biochemistry.

[24]  M. Marchello,et al.  Prostaglandin F2α, oxytocin and progesterone secretion by bovine luteal cells at several stages of luteal development: Effects of oxytocin, luteinizing hormone, prostaglandin F2α and estradiol-17β☆ , 1989 .

[25]  K. Okuda,et al.  A study of the central cavity in the bovine corpus luteum , 1988, Veterinary Record.

[26]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[27]  H. V. van Tol,et al.  Steroid and pituitary hormone concentrations in the fluid of preovulatory bovine follicles relative to the peak of LH in the peripheral blood. , 1983, Journal of reproduction and fertility.

[28]  S. Dieleman,et al.  Changes in oestradiol, progesterone and testosterone concentrations in follicular fluid and in the micromorphology of preovulatory bovine follicles relative to the peak of luteinizing hormone. , 1983, The Journal of endocrinology.

[29]  T. Beck,et al.  Estradiol control of serum luteinizing hormone concentrations in the bovine. , 1977, Journal of animal science.

[30]  P. Keyes,et al.  Synthesis of 17beta-estradiol by isolated ovarian tissues of the pregnant rat: aromatization in the corpus luteum. , 1976, Endocrinology.

[31]  R. Shearman,et al.  Radioimmunoassay of progesterone, 17-hydroxyprogesterone, estradiol-17β and prostaglandin F in human corpus luteum , 1975, Steroids.

[32]  W. Hansel,et al.  Estrogen cytosol binding proteins in bovine endometrium and corpus luteum. , 1974, Biology of reproduction.

[33]  G. Telegdy,et al.  Steroid formation in the bovine corpus luteum. , 1965, Steroids.