Estradiol and Bisphenol A Stimulate Androgen Receptor and Estrogen Receptor Gene Expression in Fetal Mouse Prostate Mesenchyme Cells

Background Hormonal alterations during development have lifelong effects on the prostate gland. Endogenous estrogens, including 17β-estradiol (E2), and synthetic estrogenic endocrine disruptors, such as bisphenol A (BPA), have similar effects on prostate development. Increasing exposure to estrogens within the low-dose, physiologic range results in permanent increases in the size and androgen responsiveness of the prostate, whereas exposure within the high-dose, pharmacologic range has the opposite effects. Objectives We tested the hypothesis that the low-dose effects of estrogens on the developing prostate are associated with increased expression of androgen receptor (Ar) and estrogen receptor 1 (α) (Esr1) genes in mesenchyme cells. Methods Ar and Esr1 mRNA levels were quantified in primary cultures of fetal mouse prostate mesenchyme cells treated with E2 and BPA. Discussion Ar and Esr1 mRNA expression increased in response to E2, with thresholds of 0.001 and 0.037 nM, respectively; and in response to BPA, with a threshold of 1 nM for both mRNAs. We did not observe the expected inhibition of Ar mRNA expression by pharmacologic levels of E2 relative to unexposed cells. Conclusions The observed induction of gene expression occurred at concentrations within the range of free E2 previously shown to permanently increase prostate size, thus supporting the involvement of direct effects of estrogens on gene expression in prostate mesenchyme. The effects of BPA occurred within the range of concentrations currently measured in human serum, demonstrating the vulnerability of developing tissues to xenoestrogens.

During fetal life, alterations in normal prostate gland development can produce permanent changes that persist throughout adulthood and may increase the risk of disease in later life (Ho et al. 2006;Risbridger et al. 2005). The prostate differentiates from the cranial region of the urogenital sinus (UGS) (Marker et al. 2003). In humans, the first epithelial buds are observed in the lateral region of the UGS during the tenth week of gestation in a pattern that shows a remarkable similarity to that of bud development in mice and rats during the early phase of gland genesis (Timms et al. 1994). Prostate ductal budding begins on gestation day (GD) 17 in mice (2 days before birth) (Timms et al. 1994). Prostate development is dependent on 5α-dihydrotestosterone (DHT) production from testosterone within the UGS mesenchyme (Marker et al. 2003). Androgen receptor expression in prostatic mesenchyme is required for directing growth and branching morphogenesis of epithelial buds, presumably by induction of paracrine factors secreted by mesenchyme (Cunha and Donjacour 1987;Kokontis and Liao 1999). During development, prostatic epithelial cells exhibit little androgen binding, and androgen receptor protein expression in epithelium is not required for differentiation (Cunha and Donjacour 1987;Prins and Birch 1995;Timms et al. 1999). Therefore, fetal mouse UGS mesenchyme cells provide an informative model of endocrine control of prostate development.
There is now considerable evidence that estrogens modulate the activity of androgens in regulating prostate development. The UGS mesenchyme in mice and rats responds to estrogens via estrogen receptor 1 (α), whereas in the human prostate estrogen receptor 2 (β) may mediate most responses to estrogens during development (Adams et al. 2002;Prins et al. 1998). Prostatic growth and androgen receptor ligand-binding activity are permanently decreased in response to high, pharmacologic doses of both natural and xenobiotic estrogens during development (Prins and Birch 1995;Rajfer and Coffey 1978;vom Saal et al. 1997). In contrast, increases in prenatal estrogen levels within the physiologic range (the normal range for endogenous estradiol) stimulate prostate development, leading to permanently increased prostate size and androgen receptor ligand-binding activity (Gupta 2000;Timms et al. 1999;vom Saal et al. 1997).
Estrogenic endocrine disruptors have the potential to alter prostate development in a manner similar to that of endogenous estradiol. In this study, we chose to examine bisphenol A (BPA), the monomer used to make polycarbonate plastic and as an additive in many other plastic products. BPA is produced in excess of 6 billion pounds per year, and the potential for human exposure is great due to leaching from plastic and plasticlined metal food and beverage containers, as well as from dental sealants (Takao et al. 2002;Welshons et al. 2006).
We have proposed that one mechanism by which fetal estrogen exposure stimulates prostate development is by increasing prostatic androgen receptor gene [Ar; GenBank accession no. X53779 (Benson et al. 2007)] expression, thereby increasing the androgen responsiveness of the developing prostate, leading to enhanced gland genesis and growth vom Saal et al. 1997). In the present study we sought to determine whether the endogenous hormone 17β-estradiol (E 2 ), within its physiologic range, and the manmade estrogenic endocrine disruptor BPA, within the range measured in human serum (Schönfelder et al. 2002), directly influence Ar and estrogen receptor 1 (α) (Esr1; GenBank accession no. NM_007956.2) gene expression at the transcriptional level in fetal mouse UGS mesenchyme.

Materials and Methods
Animals, housing, mating, and organ collection. CD-1 mice were purchased from Charles River Laboratories (Wilmington, MA) and bred at the University of Missouri in a facility accredited by the Association for Assessment and Accreditation of Laboratory Animal Care. Animals were housed on corncob bedding in standard polypropylene cages. They received water purified by ion exchange and carbon filtration from glass bottles. Pregnant and lactating females were fed Purina 5008 chow (Purina Mills, St. Louis, MO). After being weaned, animals were fed Purina 5001 chow (Ralston Purina). Rooms were maintained at 25 ± 2°C under a 12 hr:12 hr light:dark cycle. Animals were treated humanely and with regard for alleviation of suffering. Animal procedures were approved by the University of Missouri Animal Care and Use Committee and conformed to the NIH Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources 1996).
Tissue collection, primary cell culture, and dosing. Timed-pregnant females were killed on GD17 (mating = GD0) by CO 2 asphyxiation, and fetuses were removed from the uterine horns. The bladder and UGS were removed from male fetuses as previously described (Timms et al. 1999;vom Saal et al. 1997). The prostatic region of the UGS was removed from the bladder at the bladder neck, and mesenchymal cells were isolated as described by Gupta (1999). Briefly, UGS tissue was disrupted by digestion with 3 mg collagenase type I/mL (Sigma Chemical Co., St. Louis, MO) for 30-50 min at 37°C in a shaking water bath followed by manual pipetting. Clumps of epithelium were allowed to settle out, and suspended mesenchymal cells were collected and cultured in complete medium [RPMI-1640 without phenol red (Gibco, Grand Island, NY) supplemented with 2 mM L-glutamine, 100 U penicillin G sodium/mL, 100 mg streptomycin sulfate/mL, and 0.25 mg fungizone/mL] with 10% (vol/vol) fetal bovine serum (FBS; U.S. Bio-Technologies, Parkerford, PA). Cells were grown to 95% confluence and then passaged by digestion with 0.05% trypsin in 0.53 mM EDTA (Gibco) for 5 min at room temperature. Cell viability was assayed with alamarBlue (BioSource International, Camarillo, CA) according to the manufacturer's instructions.
We characterized the cell-type composition of the UGS cell primary cultures by immunofluorescent staining of cytokeratins with mouse anti-pan-cytokeratin clone PCK-26 fluorescein isothiocyanate conjugate (Sigma), and co-staining of the mesenchymal cell marker vimentin with goat anti-vimentin (Sigma) and rabbit anti-goat Cy3 conjugate (Sigma) (Prins et al. 1991).
During experimental treatments with E 2 , BPA, tamoxifen, and raloxifene, FBS was charcoal-stripped to remove all hormones, and cells were maintained in a constant background of 690 pM DHT (200 pg/mL). Cells were treated with DHT rather than testosterone to control for potential treatment effects on the intracellular concentration of this high-affinity ligand for the androgen receptor, which is formed from testosterone in UGS mesenchyme cells in vivo, and also to avoid the intracellular metabolism of testosterone to E 2 by aromatase; DHT is not a substrate for aromatase (Kokontis and Liao 1999). First passage cells were seeded onto 24-well plates at 7 × 10 4 cells/well in estrogen-free complete medium with 5% (vol/vol) charcoal-stripped FBS, 5% (vol/vol) charcoalstripped horse serum (Sigma), 690 pM DHT (Steraloids, Wilton, NH), and ITS supplement (insulin-transferrin-selenium; Cambrex, Walkersville, MD) for final concentrations of 10 µg insulin/mL, 10 µg transferrin/mL, and 10 ng selenium/mL. Cells were maintained in this estrogen-free medium for 3 days, with one medium change, before the start of treatments. E 2 , BPA, and tamoxifen were obtained from Sigma. Raloxifene (LY 156,758) was obtained from Eli Lilly (Indianapolis, IN). During treatments with E 2 and BPA, cells were grown for 4 days, and the medium was changed every day, except where noted. The concentration of E 2 in culture medium during treatments was measured by radioimmunoassay as previously described by vom Saal et al. (1990).
Real time RT-PCR measurement of gene expression. Total RNA was isolated with the RNAqueous kit (Ambion, Austin, TX) according to the manufacturer's instructions. Total RNA was quantified by absorbance at 260 nm. Expression of specific mRNAs were measured by one-step real-time reverse transcriptionpolymerase chain reaction (RT-PCR) as described by Bustin (2000), with the TaqMan EZ RT-PCR kit (PE Applied Biosystems, Foster City, CA) on the ABI PRISM 7700 Sequence Detection System (PE Applied Biosystems). The concentrations of Mn 2+ , probe, and primers were optimized for each primer/probe set. Primer/probe sets for Ar, vimentin (Vim; GenBank accession no. NM_011701.3), and acidic ribosomal phosphoprotein P0 (Arbp; GenBank accession no. NM_007475.2) were designed using Primer Express software (PE Applied Biosystems) and are shown in Table 1. Primers were designed to span exon boundaries in order to prevent amplification of genomic DNA. Primers were synthesized by Invitrogen (Carlsbad, CA), and probes were synthesized by PE Applied Biosystems. The primer/probe set for Esr1 was TaqMan Gene Expression Assay ID Mm00433149_m1 (PE Applied Biosystems), which spans Esr1 exons 3-4.
The relative concentrations of specific mRNAs in each sample were normalized to total RNA per well, as described by Bustin (2000) and Latil et al. (2001). Normalization to total RNA allowed for comparisons between independent experiments. In parallel experiments, total DNA per well was measured by fluorescence of Hoechst 33258 (Sigma), as described by Labarca and Paigen (1980). From these data, the average RNA/DNA ratio was calculated for each treatment; we used these values to convert the mRNA/total RNA measurements to mRNA/DNA to assess the effect of E 2 and BPA on gene expression per cell.
Statistical analyses. Treatments were replicated in three wells per experiment and at least two, and in most cases more (up to 10), replicate experiments. Outliers were detected with Grubbs' test (Grubbs 1969) and removed. Treatment effects were evaluated on untransformed data for RNA, and on reciprocals for DNA and gene expression, with the analysis of variance (ANOVA) general linear model procedure using SAS software (SAS Institute Inc., Cary, NC). We made planned comparisons of means for each treatment relative to controls using the least-squares means test only if the overall ANOVA showed significant treatment effects. To avoid inflation of error rates, we did not use multiple comparisons among all treatments. The criterion for statistical significance was p < 0.05.

Characterization of UGS cells and nominal E 2 concentration in primary culture.
Consistent with previous reports (Gupta 1999), immunofluorescent staining for the mesenchymal cell marker vimentin revealed no epithelial cells in first passage cells treated for 5 days with 0.1 nM E 2 or with no E 2 (data not shown). The UGS primary cell cultures that we examined were thus homogenous populations of mesenchyme cells that retained mesenchymal differentiation markers throughout the incubation period.
After the initial administration of E 2 in culture medium, the E 2 concentration slowly In the experiments we conducted, test chemicals were added to medium every 24 hr. Thus, at the midpoint of the dose-response curve tested, the actual E 2 concentration in the culture medium was approximately 60% of the initial concentration at the time we collected the cells for analysis of mRNA. Measurement of DNA and RNA content and induction of gene expression confirmed that bioactive amounts of E 2 were thus present at nominal concentrations < 0.001 nM (Figures 1 and 2). E 2 induces growth of UGS mesenchyme cells. E 2 treatment induced a small increase in cell growth and proliferation as indicated by DNA and RNA content at doses of 0.01-10,000 nM ( Figure 1A, 1B). At 100,000 nM E 2 , inhibition of cell growth and proliferation was observed ( Figure 1A, 1B). Cell viability was not affected at any E 2 dose tested (data not shown). Subsequent experiments used a dose range of 0.0001-10,000 nM in order to avoid the cell growth-inhibiting effects of very high doses of E 2 . Relative total RNA was induced to a greater degree than DNA ( Figure 1A, 1B). The housekeeping genes Vim, a component of the cytoskeleton in mesenchyme cells, and Arbp, a component of the ribosome, were examined to determine whether either could be used as a reference gene. However, both of these genes increased expression in response to E 2 , consistent with a general induction of cell growth ( Figure 1C, 1D). Vimentin and acidic ribosomal phosphoprotein P0 exhibited differently shaped dose-response curves, suggesting differences in their mechanisms of transcriptional regulation by E 2 . Because neither housekeeping gene was an appropriate control gene, expression of specific mRNAs was normalized to DNA. E 2 induces the steroid receptor mRNAs Ar and Esr1. Ar mRNA expression was induced by E 2 up to just over 2-fold above control levels ( Figure 2A). The observed threshold of induction, 0.001 nM, is slightly higher than the measured free serum E 2 concentration of 0.00077 nM or 0.21 pg/mL in male mouse fetuses on GD18 (vom Saal et al. 1997). The increase in Ar mRNA with E 2 dose was monotonic up to 100 nM E 2 . At doses of ≥ 1,000 nM E 2 , Ar mRNA levels declined relative to the maximum observed induction at 100 nM E 2 . Inhibition of cell growth was only evident at 100,000 nM E 2 .
The induction of Ar mRNA by a physiologically relevant level of E 2 , 0.037 nM (10 pg/mL), was significantly inhibited by antiestrogen treatment (Figure 3A). The antiestrogen raloxifene (100 nM) had similar effects to 100 nM tamoxifen (raloxifene data not shown). The inhibition of the Ar response to E 2 by tamoxifen was overcome by addition of a pharmacologic dose of 100 nM E 2 , demonstrating that the inhibition by tamoxifen observed at 0.037 nM E 2 is not due Richter et al. 904 VOLUME 115 | NUMBER 6 | June 2007 • Environmental Health Perspectives to cytotoxicity or other nonspecific effects ( Figure 3A). Esr1 mRNA expression was induced by E 2 by approximately 3-fold over the control, with a threshold at 0.037 nM ( Figure 3B) and a peak at 10-100 nM E 2 ( Figure 2B). The induction of Esr1 mRNA by 0.037 nM E 2 was not significantly inhibited by antiestrogen treatment ( Figure 3B).
BPA acts as an estrogen agonist in UGS mesenchyme cells. The effects of BPA on cell growth as indicated by DNA and RNA content ( Figure 4) were much less pronounced than the effects of E 2 (Figure 1). The doseresponse curve for RNA was biphasic, with significant reductions in RNA content, but not DNA, at very low concentrations of BPA (Figure 4). Ar and Esr1 mRNA expression were induced by BPA treatment (Figure 5). The dose-response curves for BPA were shifted to the right by approximately 1,000-fold for Ar and approximately 30-fold for Esr1, relative to E 2 (based on the significant stimulation of Esr1 in response to 0.037 nM E 2 ; Figure 3B). As indicated in Figure 5A and 5B, a significant increase in both Ar and Esr1 transcription occurred at BPA concentrations within the range typically reported in human blood and tissues, including fetal blood (Schönfelder et al. 2002;Welshons et al. 2006). The induction of both Ar and Esr1 mRNAs by a physiologically relevant low dose of BPA (10 nM) was inhibited by a 100-nM dose of tamoxifen. For both genes, the inhibition by tamoxifen was overcome by a high dose of BPA (1,000 nM) ( Figure 6).

Discussion
The aims of the present study were to investigate whether there were direct effects on Ar and Esr1 gene activity that could be related to the previously observed stimulatory effect on prostate development caused by prenatal exposure to serum concentrations of bioactive E 2 in fetal mice and the concentration of bioactive BPA currently measured in human fetal serum. We found that both the natural estrogen E 2 and the synthetic estrogenic endocrine disruptor BPA stimulated increases in prostate Ar and Esr1 mRNAs. The stimulation occurred at physiologically relevant part-per-trillion doses of E 2 , and at parts-perbillion doses of BPA, which are within the range found in human fetal blood (reviewed by Welshons et al. 2006).
Exposure of male mouse and rat fetuses to slightly elevated estrogen levels results in permanent prostate enlargement and elevated androgen receptor levels in adulthood (Timms et al. 1999;vom Saal et al. 1997). Some confusion concerning effects of estrogen on the prostate has been created by studies in which only very high, pharmacologic (supraphysiologic) doses of estrogen were tested. Effects of pharmacologic doses of estrogenic chemicals on prostate development are not predictive of effects at physiologic doses. The dramatic effects of physiologic doses of estrogens have been revealed in studies in which pregnant mice were administered low doses of E 2 , the drugs diethylstilbestrol (DES) and ethinylestradiol, BPA, or the estrogenic insecticide methoxychlor, resulting in a permanent increase in prostate size in male offspring (Gupta 2000;Nagel et al. 1997;Thayer et al. 2001;vom Saal et al. 1997;Welshons et al. 1999). As the dose of E 2 or DES was increased into the pharmacologic range, the stimulating effect observed at low doses disappeared and inhibition of prostate development occurred (Gupta 2000;Timms et al. 2005;vom Saal et al. 1997). Thus, the inhibitory effects of pharmacologic doses of estrogens on the developing prostate are opposite to effects of physiologic doses of the same estrogenic chemicals.
Available data on short-term effects of developmental estrogen exposures are consistent with the long-term effects observed in adulthood. For example, a high, pharmacologic dose of estradiol benzoate given to neonatal rats induced down-regulation of androgen receptor protein expression as early as postnatal day (PND) 6 (Prins and Birch 1995). In contrast, low, physiologically relevant doses of estrogenic chemicals (DES and BPA) fed to pregnant mice induced up-regulation of prostatic androgen receptor ligand binding activity in male offspring as early as PND3; this observation was replicated in organ culture of fetal mouse prostate treated with 0.1 pg/mL DES or 50 pg/mL BPA (Gupta 2000). The increase in prostate size in *Values significantly different from the control (p < 0.05). **Significant differences between the same E 2 treatment with and without Tam (p < 0.05).
Our findings support the hypothesis that prenatal exposure to elevated estrogen levels permanently increases prostate size and androgen responsiveness at least in part by inducing Ar mRNA expression. Importantly, the effects on Ar mRNA expression occurred with a threshold at 0.001 nM E 2 (0.28 pg/mL), consistent with concentrations previously shown to alter prostate development in vivo. Specifically, the total serum E 2 concentration in male mouse fetuses on GD18 is approximately 0.35 nM (94 pg/mL), and the free (unconjugated and unbound to plasma proteins) serum concentration of E 2 is 0.00077 nM (0.21 pg/mL), or 0.2% of total serum E 2 , similar to findings in rats (Montano et al. 1995). An increase in free serum E 2 in male mouse fetuses (due to maternal administration of E 2 via Silastic capsule) to 0.0012 nM (0.31 pg/mL) significantly increased prostate size and the number of prostatic androgen receptors in adulthood . Our results show that at these same physiologic doses, E 2 acts directly on fetal UGS mesenchyme cells to increase Ar mRNA expression. This response was inhibited by the antiestrogens raloxifene (data not shown) and tamoxifen (Figure 3), suggesting that the induction of Ar mRNA by E 2 is mediated through the classical genomic estrogen receptor pathway.
The differences in the shapes of the doseresponse curves for Ar and Esr1 suggest that the receptors are regulated by distinct mechanisms. Distinct dose-response relationships were also noted for vimentin, acidic ribosomal protein P0, total RNA content, and DNA content. These findings are consistent with data from microarray studies demonstrating considerable diversity in doseresponse relationships of different estrogenresponsive genes; in particular, as one moves across the dose-response curve, entirely different sets of genes are activated or inhibited (Coser et al. 2003;Shioda et al. 2006). Induction of Ar and Esr1 also displayed different responses to inhibition by antiestrogens, in that Esr1 induction was not significantly inhibited by antiestrogen cotreatment ( Figure 3). The threshold for effects on Esr1 expression was between 0.01 nM (2.3 ng/mL) and 0.037 nM (8.4 ng/mL) E 2 ( Figures 2B and 3B). This is above the normal range of free E 2 in serum in male mouse fetuses. However, serum estradiol may underestimate estrogen levels in prostate tissue because cells in the developing prostate express aromatase, which metabolizes testosterone to E 2 (Ellem and Risbridger 2006;Risbridger et al. 2003), and because estrogen receptor agonists, including xenoestrogens, exhibit additive effects in combination (Rajapakse et al. 2002). The induction of Esr1 expression by E 2 suggests that estrogen exposure may create a positive feedback loop in the UGS, such that exposure to estrogens increases sensitivity to future or continuing exposure.
Although the observed effects of physiologic concentrations of E 2 on Ar mRNA expression are consistent with established in vivo effects, our pharmacologic dose range (e.g., 100 nM) in vitro observations are not consistent with established in vivo effects (Gupta 2000;Prins and Birch 1995;vom Saal et al. 1997), which predicted a decline in Ar mRNA expression relative to control levels at this high dose of E 2 (Figure 2A). The in vivo regulation of androgen receptors by pharmacologic doses of estrogens may thus involve systemic and posttranscriptional effects that are not observable in terms of Ar mRNA levels in isolated mesenchyme cells. The involvement of posttranscriptional mechanisms is supported by the observation that developmental exposure to pharmacologic doses of estrogens permanently up-regulates androgen receptor degradation by the proteasome (Woodham et al. 2003).
The behavior of BPA in this system is consistent with the established activity of BPA as an estrogen receptor agonist (reviewed by vom Saal and Hughes 2005;vom Saal and Welshons 2006;Welshons et al. 2006), which was first reported in 1936 (Dodds and Lawson). The weak effects of BPA on cell growth, measured as DNA and RNA content, Richter et al. 906 VOLUME 115 | NUMBER 6 | June 2007 • Environmental Health Perspectives are consistent with previous reports that the relative potency of BPA is greater in stimulating estrogen receptor-dependent gene transcription than in stimulating growth of uterine tissue (Nagel et al. 2001). There are several interesting differences between the dose-response curves of Ar and Esr1 in response to BPA compared with E 2 . Based on the thresholds of induction of gene expression, BPA is approximately 1,000-fold less potent than E 2 for induction of Ar, but only about 30-fold less potent than E 2 for induction of Esr1 (based on a threshold of Esr1 induction of 0.037 nM E 2 ; Figure 3B). In addition, the shape of the dose-response curve for Esr1 differs between E 2 and BPA; induction of Esr1 by BPA was inhibited by tamoxifen, whereas induction of Esr1 by E 2 was not significantly inhibited by tamoxifen. These differences between E 2 and BPA, which are seen in the Esr1 dose-response curves but not the Ar dose-response curves, underline the probability that distinct mechanisms are at work in the induction of Ar and Esr1 by estrogens. Of great importance, the doses of BPA required for induction of both Ar and Esr1 are within the range of typical levels of BPA measured in human serum, which range from approximately 1 to 10 nM ( Figure 5) (Schönfelder et al. 2002;Welshons et al. 2006). Because our experiments measured the response to BPA in the absence of other estrogens, they are likely to underestimate the induction of Ar and Esr1 expression in response to the additive mixture of endogenous estrogens, BPA, and other xenoestrogens to which humans are continuously exposed in our modern world (Colborn et al. 1993). The consequences of developmental induction of Ar and Esr1 for the adult phenotype of the prostate have not been directly examined, but exposure during fetal life to very low doses of BPA (2-50 µg/kg/day) permanently increases prostate size in mice (Gupta 2000;Nagel et al. 1997). Neonatal exposure to a 10 µg/kg/day dose of BPA results in precancerous lesions (prostate interepithelial neoplasia) in adult male rats, associated with epigenetic changes (Ho et al. 2006). The report of Ho et al. (2006) is consistent with the finding that estrogenic chemicals stimulate an abnormal rate of proliferation in basal epithelial cells in the primary ducts of the mouse fetal prostate . Basal cells are progenitor cells proposed to be involved in prostate cancer (Kirschenbaum et al. 2006). We are currently examining whether the permanent increase in prostate AR receptor protein in mice exposed during fetal life to low doses of estrogenic chemicals is caused by a permanent increase in expression of the Ar gene, and whether this is associated with a change in DNA methylation at the Ar gene.

Conclusions
Ar mRNA in mesenchyme cells isolated from fetal mouse prostate is up-regulated by E 2 within its physiologic range, and by BPA within the range detected in human fetal serum. Induction of Ar mRNA by E 2 or BPA was inhibited by antiestrogen co-treatment. Therefore, the low-dose effects of estrogens on prostatic Ar regulation are estrogen receptor-dependent, act at the transcriptional level, are mediated through local effects on UGS mesenchyme cells, and can be modeled in a primary cell culture system. In contrast, down-regulation of androgen receptor protein in response to high doses of estrogens in vivo likely includes systemic and post-transcriptional mechanisms. Esr1 mRNA is also upregulated by E 2 and BPA in a dose-dependent manner, suggesting the possibility of positive feedback in estrogen effects on the prostate. The induction of Esr1 by E 2 is not significantly inhibited by antiestrogen treatment, suggesting the involvement of non-estrogen receptor-mediated mechanisms.
Taken together, these results are consistent with the hypothesis that prenatal exposure to elevated estrogen or xenoestrogen levels within the physiologic range results in an increase in androgen receptor and estrogen receptor 1 (α) number in the developing prostate mesenchyme, which increases androgen and estrogen responsiveness and growth. The estrogen receptor-dependent induction of Ar by BPA confirms that this mechanism is not unique to E 2 and underscores the vulnerability of the developing reproductive system to the additive effects of exogenous estrogenic endocrine disruptors.