Alpha 2-macroglobulin expression in the mesometrial decidua and its regulation by decidual luteotropin and prolactin.

During decidualization, cells of the endometrium grow and differentiate giving rise to two different decidual tissues located in either the antimesometrial or mesometrial site of the uterus in the rat. These tissues have different functions in pregnancy. The antimesometrial decidua is an endocrine gland that secretes hormones, whereas the mesometrial decidua appears to play an important role in limiting trophoblast invasion. Since the decidual tissue of the rat produces alpha 2-macroglobulin (alpha 2MG), we examined whether this potent protease inhibitor is specifically expressed by the mesometrial tissue, the site of trophoblast invasion, and whether the alph 2MG gene is regulated by decidual luteotropin (DLt), the PRL-like hormone secreted by the neighboring antimesometrial cells. To determine the secretory proteins of the rat decidua, antimesometrial and mesometrial tissues were dissected out from pseudopregnant rats and cultured with [35S]methionine. The major protein secreted by the antimesometrial cell was the 29-kilodalton decidual luteotropin, whereas a 180-kilodalton protein was predominantly secreted by the mesometrial tissue. Immunoprecipitation studies of 35S-radiolabeled proteins revealed that this high mol wt protein is alpha 2MG and that it is secreted exclusively by the cells forming the mesometrial tissue. To examine whether the alpha 2MG gene was also expressed specifically in the mesometrial decidua, total RNA was isolated from both mesometrial and antimesometrial tissues of day 9-12 pseudopregnant rats and hybridized with alpha 2MG cDNA. Northern blot analysis revealed a 5.4-kilobase message, which was abundantly expressed in the mesometrial decidua. Little, if any, alpha 2MG mRNA was detected in antimesometrial decidua. The ontogeny of the message in the decidua correlated well with the development of the mesometrial tissue. To examine whether alpha 2MG expression is regulated by DLt and/or PRL, a highly specific polyclonal antibody to DLt was generated and decidual tissues were cultured in the presence or absence of DLt antibodies with or without PRL. Neutralization of DLt caused a marked decrease in alpha 2MG mRNA levels. This down-regulation was totally reversed by the addition of PRL and was not affected by alpha 2MG antibodies. In summary, the results of this investigation revealed a compartmentalized gene expression, synthesis and secretion of alpha 2MG in the decidua. The secretion of this protease inhibitor, specifically by the mesometrial tissue which is the site of trophoblast invasion, may be the reason for the minimal amount of tissue damage that occurs during placentation.(ABSTRACT TRUNCATED AT 400 WORDS)

Isolation, characterization, and culture of cell subpopulations forming the pregnant rat corpus luteum.

The aim of this investigation was to isolate, characterize, and culture the small and large luteal cell subpopulations forming the corpus luteum of the pregnant rat. Since the large luteal cells are extremely fragile and do not survive standard cell dispersion, a method which allows the survival and the long-term culture in serum-free media of small and large cells was developed. The two luteal cell populations differed not only by their size but also by their morphology in culture. The small luteal cells (12-20 mu in diameter) are characterized by a large oval nucleus, contain few lipid droplets and have a stellate shape. In contrast, the large luteal cells have a smaller spherical nucleus, high lipid content, and do not flatten out completely in culture, most probably due to the abundance of lipid droplets. Both luteal cell types express 3 beta HSD and the cytochrome P450 enzymes involved in steroidogenesis. However, it is the lipid filled large luteal cells that secrete the most progesterone, androgen, and estradiol; express greater amounts of P450scc and P450AROM; and possess more PRL and LH receptors. Despite the greater expression of LH receptor in the large luteal cells, small and large luteal cells responded to LH with equal increase in steroidogenic output. In serum free culture, luteal cells produced progesterone for up to 20 days; however, an exogenous source of cholesterol was a prerequisite for maximal progesterone secretion. The pattern of progesterone secretion by cultures of small and large luteal cells differed remarkably from that of mixed cell population. When nonsteroidogenic corpus luteum cells were cocultured with the large luteal cells, a severalfold increase in progesterone secretion was observed. This stimulation occurred even when cells were cocultured in the absence of exogenous source of cholesterol. In summary, a successful method was developed to disperse, isolate, and independently culture the two luteal cell populations forming the rat corpus lutem. The results indicate that the marked difference in the steroidogenic capacity of these two cell populations is due, in large part, to the difference in their size rather than to their origin in the follicle. In addition, the results have revealed an important effect of the nonsteroidogenic cells forming the corpus luteum on luteal cell steroidogenesis.

Protein secretion by mesometrial and antimesometrial rat decidual tissue: evidence for differential gene expression.

Our recent finding that decidual luteotropin, a PRL-like hormone secreted by the rat decidua, is found primarily in the antimesometrial cells suggests strongly that the synthesis of this hormone may well be an important function of the antimesometrial tissue. The objective of this investigation was, therefore, 1) to determine whether antimesometrial tissue expresses mRNA for and actively secretes a protein(s) with PRL-like activity, and 2) to examine the pattern of protein production by the antimesometrial and mesometrial zones throughout decidual development. RNA obtained from decidual tissue of day 8 pseudopregnant rats was translated in a cell-free system. The translated products were subjected to PRL receptor affinity chromatography in the presence or absence of ovine PRL to assess binding specificity. The eluted 35S-labeled proteins were analyzed by both sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting. A major 28K protein bound specifically to and was eluted from PRL receptor-enriched luteal membranes. This protein also cross-reacted with antibodies to human PRL. To determine where the mRNA for this 28K protein is expressed and whether this protein represents a prohormone, RNA isolated from both antimesometrial and mesometrial tissue was translated in the presence or absence of microsomal membranes. The 28K protein was synthesized specifically by RNA isolated from the antimesometrial zone. No apparent change in the relative mol wt of the 28K protein was observed when translation was performed in the presence of microsomal membranes. To determine whether this protein is a secreted product and to investigate the pattern of protein secretion by the mesometrial and antimesometrial decidua, tissue explants obtained from both zones between days 9-13 of pseudopregnancy were cultured in the presence of [35S]methionine. Antimesometrial tissue secreted one major 28K protein which was capable of binding to PRL receptors on luteal membranes and was immunoprecipitated by antibodies to human PRL, whereas the mesometrial tissue primarily secreted an approximately 180K protein. The overall pattern of protein synthesis and release not only differed between the mesometrial and antimesometrial tissues but also differed with each day of pseudopregnancy. The secretion of several proteins decreased with advancing gestational age, while the secretion of other proteins began abruptly after day 11, coincident with regression of the antimesometrial tissue. In summary, results of this investigation have established that rat decidual tissue synthesizes and selectively secretes proteins, and the specificity and rate of production of these distinct

Effects of estradiol on calcium-specific protein phosphorylation in the rat corpus luteum.

Estradiol regulates progesterone synthesis by the corpus luteum of several species. The molecular mechanism(s) of the action of estradiol is unknown, but appears to be independent of exogenous gonadotropins and tissue cAMP. A role for Ca2+ in steroidogenesis has been implicated, and we demonstrate here that estradiol alters Ca-specific protein phosphorylation in rat luteal cells. Corpora lutea obtained from rats hypophysectomized and hysterectomized on day 12 of pregnancy and subsequently treated for 3 days with vehicle or estradiol were assayed in vitro for Ca-specific phosphorylation. Estradiol elevated the content of a number of cytosolic proteins (mol wt X 10(-3), 58, 82, 100, 166, and 183); however, phosphorylation of the 100K protein alone appeared to be specifically enhanced by estradiol. In the presence of Ca2+, phosphorylation of the luteal 100K protein increased 2.33 +/- 0.2-fold in estradiol-treated vs. 1.42 +/- 0.2-fold in vehicle-treated rats (n = 6; P less than 0.05). Phosphorylation of 100K was inhibited by trifluoperazine and stimulated by calmodulin (CaM). Phosphopeptide maps revealed that the 100K luteal protein is identical to the cytosolic CaM-protein kinase III substrate, termed 100K, present in a number of tissues. Estradiol increased both 100K content and CaM-kinase III activity in luteal cells. Immunochemical analysis using antibodies prepared against pancreatic 100K revealed that estradiol treatment increased by at least 5 to 7-fold the luteal content of 100K. In addition, luteal cytosol of estradiol-treated rats enhanced phosphorylation of purified pancreatic 100K 3-fold, whereas that of vehicle-treated rats caused a 1.8-fold stimulation. The effects of estradiol on cytosolic proteins appear to be specific for 100K, since it does not after the activities of CaM-kinases I and II or cAMP-PK. In summary, results of this investigation demonstrate for the first time that estradiol increases the content of several proteins in the corpus luteum; estradiol enhances specifically the Ca-CaM-dependent phosphorylation of a 100K cytosolic protein; and the CaM-kinase III-100K substrate system is hormonally regulated.

Decidual luteotropin secretion and action: its role in pregnancy maintenance in the rat.

Studies of rat decidual luteotropin production and action have revealed that decidual mRNA directs the synthesis of a 28,000 MW protein in a cell-free system which binds to prolactin receptors in luteal cells and appears to represent a prohormone for decidual luteotropin. Hybridization studies indicate that although rat decidual and prolactin-like placental hormones bind to prolactin receptors, they possess little homology to other members of the prolactin family. In addition, results of this investigation have revealed a possible physiological relationship between the mesometrial and the antimesometrial cells of the decidual tissue. The large antimesometrial cells produce decidual luteotropin in which secretion and/or synthesis is inhibited by the neighboring mesometrial cells. Since mesometrial cells possess binding sites for decidual luteotropin, it is possible that decidual luteotropin acts on the mesometrial cell to affect the formation of its own inhibitor. Mesometrial cells are rich in glycogen, whose synthesis is stimulated by prolactin-like hormones in other tissues. Therefore, decidual luteotropin may also act on these cells to enhance glycogen formation. In summary, decidual luteotropin appears to have at least two sites of action--the luteal cell, where it can substitute for prolactin in maintaining progesterone production, and the mesometrial cell, where its role remains to be investigated.

Ontogeny of prolactin receptors in rat decidual tissue: binding by a locally produced prolactin-like hormone.

The objectives of this investigation were to determine whether decidual tissue possesses specific binding sites for prolactin, and to examine whether the locally produced prolactin-like hormone binds to these receptors. Characterization of the binding of prolactin to decidual tissue from rats at day 9 of pseudopregnancy revealed specific, high-affinity sites. Binding approached saturation with increasing concentrations of either the ligand or the protein. Cytosolic extracts of day-9 decidual tissue, containing various amounts of decidual luteotrophin which possesses several of the physiological and biochemical characteristics of prolactin, displaced the binding of 125I-labelled prolactin to decidual membranes in a linear fashion. Prolactin-binding sites were detectable 72 h after induction of decidualization and 48 h after the appearance of decidual luteotrophin in the decidua. Prolactin receptor concentrations increased significantly between days 8 and 9, reached a plateau between days 9 and 12 and declined abruptly on days 14 and 15, accompanied by a similar decline in decidual luteotrophin concentration in the tissue. Thus rat decidual tissue possesses specific receptors for prolactin to which decidual luteotrophin locally produced can bind, thereby suggesting an auto/paracrine role for this substance.

Evidence for the secretion of decidual luteotropin: a prolactin-like hormone produced by rat decidual cells.

Rat decidual tissue contains a PRL-like hormone named decidual luteotropin. We have recently revealed some of its physiological and biochemical characteristics. However, because rat decidual tissue contains specific binding sites for PRL, it was important to demonstrate that the hormone found in the tissue is not locally stored and structurally transformed PRL but a hormone actively synthesized by the rat decidual tissue. Decidual explants or decidual cells obtained from day 9 pseudopregnant rats were incubated for different times under either static conditions or continuously perifused with medium at a rate of 1 ml/h. Levels of decidual luteotropin were measured by a specific radioreceptor assay using luteal membranes as source of receptors and [125I]iodo-ovine(o)PRL as a tracer. In the static incubation, no proof of hormone production was obtained; levels of decidual luteotropin in medium and tissue or cells at the end of the incubation were similar to levels found in either cells or tissue before incubation. In sharp contrast, decidual cells perifused with media secreted large amounts of hormone. This may suggest that an inhibitor of decidual luteotropin production was being removed from the culture by the perifusion. For the first 4 h of perifusion, no hormone was produced. However by the fifth hour, cells began to actively release decidual luteotropin. Secretion of the hormone increased with time and reached maximal values between 7-15 h of perifusion. During the 15 h of perifusion, decidual cells released approximately 1000 times more decidual luteotropin than the amount they originally contained. A dose-response increase in hormone secretion was obtained with increased concentrations of decidual cells. The net amount of decidual luteotropin released into the medium over an 18-h period was approximately 6.5 micrograms/30 X 10(6) cells, 3.5 micrograms/10 X 10(6) cells, and 0.5 micrograms/2 X 10(6) cells. A similar profile of decidual luteotropin release was obtained when decidual explants were perifused. However, in contrast to decidual cells which secreted no hormone for the first 4 h of culture, decidual explants immediately began to release decidual luteotropin in the medium. The secretion of decidual luteotropin in vitro was inhibited 75% by the protein synthesis inhibitor, cycloheximide. In summary, results of this investigation demonstrate for the first time that rat decidual cells secrete in vitro a PRL-like hormone, decidual luteotropin.

Identification and partial characterization of a prolactin-like hormone produced by rat decidual tissue.

Previous studies have strongly, but indirectly, suggested that rat decidual tissue produces a prolactin-like hormone, decidual luteotropin, which markedly affects luteal cell function. However, it was also found that extracts of decidual tissue do not cross-react with antisera to either rat or ovine prolactin (PRL). The purpose of this study was to determine whether the decidual tissue contains a substance that binds to PRL receptors in rat luteal membranes and, if so, to identify, quantitate, and characterize this molecule with the use of an ovarian radioreceptor assay. Decidual tissue was induced in day 5 pseudopregnant rats by scratching the antimesometrial wall of the uterus; it was collected on day 9 and homogenized and extracted. Decidual tissue extracts bound specifically to ovarian PRL receptors. Graded dilutions of the extracts yielded curves that were parallel to the ovine PRL standard, indicating that decidual luteotropin competes for the same receptor sites on rat luteal membranes. To determine the levels of decidual luteotropin throughout pseudopregnancy, decidual tissue was obtained on each day between days 6-12. The PRL-like activity was detectable in decidual tissue as early as day 6, reached a maximum on day 9, and declined thereafter. The elution profile obtained from gel filtration of a day 9 decidual tissue extract displayed a major component of decidual luteotropin eluting at a Ve/Vo ratio of approximately equal to 2.0. Column chromatography indicated that decidual luteotropin corresponds to a protein with a molecular weight of 23,500. The hormone was heat labile, digestible by trypsin, and appears to contain disulfide linkages. In summary, this study reports the identification, quantitation, and partial characterization of a PRL-like hormone produced by the decidual tissue of the rat.

Relationship between luteinizing hormone and decidual luteotropin in the maintenance of luteal steroidogenesis.

Between Days 6-11 of pregnancy or pseudopregnancy, the decidual tissue of the rat produces a prolactin-like hormone, decidual luteotropin, which can sustain luteal progesterone production when prolactin is suppressed. However, this effect is dependent upon the presence of the pituitary. The present investigation was undertaken to determine whether decidual luteotropin and luteinizing hormone (LH) act together to sustain luteal steroidogenesis and if so, to find out whether the need for LH is due to the inability of the decidual tissue to produce LH-like material and/or whether LH affects decidual luteotropin production. Pseudopregnant rats with or without decidual tissue were hypophysectomized on Day 8 and treated with either 1.5 IU human chorionic gonadotropin (hCG)/day or with vehicle. Within 24 h, serum progesterone dropped in both vehicle-treated groups and decidual luteotropin levels declined by 80% in the decidual tissue. Human CG administration had no effect on progesterone production in the control group. Yet in rats with decidual tissue, hCG stimulated progesterone production for at least 48 h and maintained the decidual tissue content of decidual luteotropin. Progesterone, but not hCG treatment, maintained decidual luteotropin concentrations in ovariectomized rats. To compare the luteotropic activity of the decidual tissue with that of the placenta, pregnant or pseudopregnant rats with decidual tissue were hypophysectomized on Day 8 and treated with 1.5 IU hCG. Control groups had decidual tissue or placentas removed and were similarly treated. Human CG stimulated progesterone production only in rats with placental or decidual tissue.(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of castration on 24-hour periodicity of hypothalamo-pituitary gonadotropic function.

Groups of 6 castrated or sham-castrated (controls) adult male rats were decapitated 7 days after the operation at 4 h intervals within a 24 h period. Serum LH, FSH and PRL were measured by radioimmunoassay and GnRH activity in medial basal hypothalamus was estimated by bioassay using donor pituitaries from normal adult rats. Finally, the responsiveness of pooled pituitaries from each experimental group to 5 ng synthetic GnRH was tested in vitro immunoreactive LH in medium being used as the end point. It was found that the castration of male rats results in the abolition of 24 h periodicity of hypothalamic GnRH content. Furthermore, a shift in the occurrence of peak levels (acrophase) and about 100 percent increase of the pituitary sensitivity to GnRH was observed. The castration also resulted in a shift in the acrophase of serum gonadotropins levels. In conclusion, the presented data suggest that the gonadal secretion possibly maintains the circadian periodicity of hypothalamo-pituitary gonadotropic function.

Role of adrenals on the 24-hour periodicity in hypothalamo-pituitary axis in male rat.

Studies were carried out to investigate the influence of adrenalectomy on the 24 hour periodicity in the hypothalamo-pituitary axis in adult male rat. Adrenal gland ablation resulted in the shift in the occurrence of peak content of hypothalamic LHRH and attenuation in the responsiveness of the pituitary to synthetic LHRH. Following adrenalectomy, the circadian serum LH peak was attenuated and serum FSH showed a 24 hour periodicity. In conclusion, the results suggest the possible role of adrenal gland in the maintenance of 24 hour periodicity of hormones in the hypothalamo-hypophyseal axis in male rat.

Enhancement of serum FSH levels after pinealectomy.

The effect of pinealectomy on the circadian periodicity in serum gonadotropins was investigated in adult male rats. Pinealectomy resulted in an elevation of the serum FSH concentration 7 days after the operation. A 4-fold increase in serum FSH over 24 h with no concommitant increase in serum LH following pinealectomy suggests that the control of FSH secretion could be mediated via the pineal gland.

The role of adrenal and pineal glands on the hypothalamo-pituitary axis in adult male rats.

Although there have been reports on the effects of adrenal and pineal gland secretions on the hypothalamus and the pituitary, the maintenance of rhythmicity by these glands has not been reported so far. The present data deals with the alterations in the periodicity of hypothalamo-pituitary axis after the surgical removal of either adrenal, gonad or pineal in adult male rats. The data indicated an alteration in the 24 hour pattern of hypothalamic content of LHRH after adrenalectomy, castration or pinealectomy. In adrenalectomy group, the in vitro responsiveness of pituitary decreased at 0600 h and 100 h as compared to the intact rats, resulting in a low amplitude of LH circadian rhythm. The pituitaries of pinealectomized rats showed increased sensitivity at 1000 h and 1800 h which resulted in two peak LH concentration at those time intervals. Further, pinealectomized rats showed a selective five fold increase over 24 hr in serum FSH concentration as compared to intact rats suggesting dissociation in the release of FSH and LH.

Effect of an indigenous drug (Speman) on accessory reproductive functions of mice.

PIP: The effects of an indigenous drug preparation, Speman (Himalaya Drug Company), on the accessory reproductive organs were studied in castrated adult mice and immature intact mice. Oral administration of Speman to castrated adults markedly increased the weights of the seminal vesicles and ventral prostate, as well as the level of fructose and maltase activity. These increases were dose-dependent and highly significant (p less than .001). The results indicate that Speman possesses both androgenic and anaboliclike activities.^ieng

Effect of administration of a single dose of testosterone oenanthate on constituents of human seminal plasma and serum gonadotropins.

Testosterone oenanthate was administered intramuscularly in six infertile men with oligozoospermia and its effects on serum gonadotropins and some constituents in the seminal plasma were studied. One week after injection the mean serum FSH level was decreased to about 50%. Serum LH levels did not change. The mean ornithine decarboxylase activity in human semen was increased by 100% after the testosterone administration. The androgen dependent nature of ODC, fructose and sialic acid have been demonstrated.

PIP: The effect of a single im injection of testosterone enanthate (TE) on serum gonadotropins and constituents of seminal plasma was studied in 6 oligospermic men. Within 1 week of injection, mean serum follicle stimulating hormone (FSH) levels were reduced by 50%, while luteinizing hormone (LH) levels were unaltered. Treatment increased the mean ornithine decarboxylase activity in seminal plasma by 100%. The citric acid content and maltase activity of seminal plasma were not markedly altered. Fructose concentrations were significantly (p less than .05) higher during the 3rd and 4th weeks after injection, while sialic acid concentrations were significantly (p less than .05) elevated during the 2nd week. The results indicate that ornithine decarboxylase activity in seminal plasma may be a useful indicator for evaluating the secretory function of the accessory sex glands.