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Male behaviors require both testosterone and estrogen. Circulating testosterone activates the androgen receptor (AR) and is also converted into estrogen in the brain via aromatase. This conversion is the primary source of estrogen to the male brain. It is unclear whether testosterone and estrogen signaling interact to masculinize neural circuits. Using a genetic approach, we show extensive sexual dimorphism in the number and projections of aromatase expressing neurons. The masculinization of these cells is independent of AR but can be induced by either testosterone or estrogen, indicating a role for aromatase in sexual differentiation of these neurons. We provide evidence suggesting that aromatase is also important in activating male aggression and urine marking as these behaviors can be elicited by testosterone in males mutant for AR. Taken together with additional findings, our results suggest that aromatization of testosterone into estrogen is important for the development and activation of neural circuits that control male territorial behaviors.
All sexually reproducing species exhibit gender dimorphisms in behavior. Such sex differences can be observed in various displays, including in mating, aggression, territorial marking, and parental care. Behavioral dimorphisms can be observed in socially naive animals suggesting that sexual differentiation of the underlying neural circuits is tightly controlled by internal physiological regulators. In vertebrates, gonadal steroid hormones play a central role in the development and function of these neural circuits (Arnold et al., 2003; Goy and McEwen, 1980; Morris et al., 2004). Both testosterone and estrogen are required for male behaviors in many vertebrates, including mammals. It remains to be determined how these two hormonal pathways intersect to control dimorphic behaviors in males (Juntti et al., 2008).
Testosterone is required for male behaviors in most vertebrates, including mice and humans. Testosterone mediates its effects by activating AR and male mice mutant for this receptor do not display sexual behavior or aggression (Ohno et al., 1974). Testosterone is essential in newborn and adult male mice for the display of sex specific behaviors such as aggression (Finney and Erpino, 1976; Peters et al., 1972; Wallis and Luttge, 1975). This testicular hormone is thought to masculinize neural circuits in neonatal rodents, and to act upon these pathways in adult males to permit the display of dimorphic behaviors (Phoenix et al., 1959).
Estrogen is also essential for male behaviors. The requirement for estrogen to masculinize behavior seems counter-intuitive as this ovarian hormone is essentially undetectable in the male circulation. All estrogenic steroids are synthesized in vivo from testosterone or related androgens in a reaction catalyzed by aromatase. Aromatase expressing cells in the brain convert circulating testosterone into estrogen, and it is this local estrogen that is thought to control dimorphic behaviors in males (Figure 1A) (MacLusky and Naftolin, 1981; Naftolin and Ryan, 1975). Consistent with a requirement for estrogen in male behaviors, aromatase activity is essential for male behaviors. Mice mutant for aromatase exhibit a profound reduction in male sexual behavior and aggression (Honda et al., 1998; Toda et al., 2001). Similar to testosterone, estrogen is essential in neonates and adults for the display of dimorphic behaviors in males (Finney and Erpino, 1976; McCarthy, 2008; Scordalakes and Rissman, 2004; Toda et al., 2001; Wallis and Luttge, 1975). Estrogen mediates many of its effects by signaling through the estrogen receptors ERα and ERβ, which exhibit overlapping expression patterns, and regulate masculinization of the brain and behavior in a complex, redundant manner (Bodo et al., 2006; Ogawa et al., 1999; Ogawa et al., 2000; Ogawa et al., 2004; Perez et al., 2003; Rissman et al., 1997). The role of a third estrogen receptor, GPR30, in male behaviors is presently unknown (Revankar et al., 2005).
The dual requirement for testosterone and estrogen signaling in male behaviors suggests that these two pathways may interact genetically to control these dimorphic displays. One potential site of interaction is the control of aromatase expression. We have therefore sought to determine whether aromatase expression is regulated by testosterone or estrogen signaling. To visualize aromatase expression at cellular resolution, we have genetically modified the aromatase locus such that all cells expressing this enzyme co-express two reporters, nuclear targeted lacZ and placental alkaline phosphatase, thereby labeling the cell bodies and projections of aromatase positive neurons.
We find extensive, previously uncharacterized sexual dimorphisms in both the number and projections of neurons expressing aromatase. The masculinization of these neural pathways is independent of AR but can be induced in neonatal females by testosterone or estrogen, indicating that aromatase plays an important role in the sexual differentiation of these neurons. Moreover, testosterone activates male typical fighting and urine marking independent of AR, demonstrating that the differentiation and function of the neural circuits underlying these behaviors are governed by testosterone, at least in part, after its conversion into estrogen. Finally, our results show that adult gonadal hormones of either sex can support male territorial marking and fighting provided estrogen has neonatally masculinized the underlying neural circuitry.
To define where testosterone may be converted into estrogen in the mouse brain, we sought to characterize the expression of aromatase at cellular resolution. We used homologous recombination in ES cells to insert an IRES-PLAP-IRES-nuclear LacZ reporter cassette into the 3′ UTR of the aromatase locus (Figure 1B). The use of IRES elements permits faithful expression of PLAP and nuclear β-galactosidase (βgal) in cells transcribing the targeted allele (Shah et al., 2004). This strategy maintains the expression and function of aromatase, thereby permitting the examination of neural pathways expressing this enzyme in otherwise wildtype (WT) animals. In sharp contrast to aromatase−/− animals, mice homozygous for the aromatase-IRES-PLAP-IRES-nuclear LacZ (aromatase-IPIN) allele are fertile and behaviorally similar to their WT littermates, and they have normal levels of serum testosterone and estrogen (Supplemental Text).
Analysis of βgal activity in the brain reveals small pools of cells that account for less than 0.5% of neurons in the brain (Figure 1C–F). We observe βgal labeled cells in discrete locations, including the posteromedial component of the bed nucleus of the stria terminalis (BNST), posterodorsal component of the medial amygdala (MeA), preoptic hypothalamus (POA), and lateral septum. The expression of βgal mirrors the distribution of aromatase mRNA as revealed by in situ hybridization (Figure S1) and RT-PCR (Harada and Yamada, 1992). The absence of sensitive, specific antibodies to aromatase precludes colocalization studies with βgal in single cells. While in situ hybridization (ISH) reveals low levels of aromatase mRNA with poor signal:noise, the activity of our reporters is robust and offers superior cellular resolution (Figure S2). In addition, labeling the brain for PLAP activity reveals the soma and projection fibers of neurons expressing aromatase (Figure S3).
A comparison of aromatase positive cells in adult male and female mice bearing the aromatase-IPIN allele reveals several previously undescribed sexual dimorphisms. We find sex differences in both the number and projection patterns of aromatase expressing neurons. We find more aromatase positive cells in the BNST and MeA in males compared to females (Figure 2A–D, P). These two regions have previously been shown to regulate sexual and aggressive behaviors (Albert and Walsh, 1984; Kondo et al., 1998; Liu et al., 1997). We also observe sexual dimorphism in cell number in the caudal hypothalamus, where we observe more aromatase expressing cells in females compared to males (Figure 2E, F, P). The presence of more aromatase positive neurons in the female caudal hypothalamus is surprising as there is little testosterone in the female circulation that could serve as a substrate for conversion to estrogen. In any case, most βgal positive cells (> 95%; n ≥ 3) in these dimorphic clusters express the pan-neuronal marker NeuN, indicating that they are neurons. A similar proportion of NeuN positive cells in the BNST and MeA expresses βgal in both sexes, indicating an absolute increase in the total number of neurons in these regions in males (Supplemental Text).
Labeling for PLAP activity also revealed sex differences in the fibers of aromatase expressing neurons. Consistent with the dimorphisms in cell number, PLAP labeling reveals a richer plexus of fibers in the BNST and MeA in males and in the caudal hypothalamus in females (Figure S3). We also observe previously undescribed dimorphic processes in the anterior hypothalamic region and the ventromedial hypothalamus (VMH), with PLAP labeled fibers occupying a larger volume in males compared to females (Figure 2G–J, P). In contrast to the poorly characterized anterior hypothalamic region, the VMH is known to regulate feeding and sexual behaviors (Musatov et al., 2006; Musatov et al., 2007). Within the limits of detection, the dimorphisms in PLAP activity are unlikely to reflect differences in aromatase expression levels as extended staining did not reveal additional fibers in the female brain. Both the anterior and ventromedial hypothalamic regions contain a few βgal positive cells in both sexes (Supplemental Text), indicating that the dimorphisms may reflect an increase in arborization of local neurons or projections from distant aromatase expressing neurons. There are more synapses on VMH neurons in males (Matsumoto and Arai, 1986), and our findings suggest that aromatase positive neurons may contribute to this dimorphic innervation. The pattern of PLAP labeled fibers surrounding the VMH resembles afferent input to this structure from the BNST, MeA, POA, and septum (Canteras et al., 1995; Choi et al., 2005; Dong and Swanson, 2004; Millhouse, 1973; Simerly and Swanson, 1988; Varoqueaux and Poulain, 1999). Each of these afferent regions expresses aromatase (Figures 1, S1), and may contribute to the dimorphic PLAP labeling in the VMH. Taken together, our studies using genetically encoded reporters reveal previously undescribed sex differences in aromatase expressing neural pathways.
We tested whether masculinization of aromatase positive neural pathways requires the activity of androgens such as testosterone signaling through AR. We crossed mice carrying the aromatase-IPIN allele to animals harboring the tfm allele, a loss-of-function allele of the X-linked AR (Charest et al., 1991). We find male typical differentiation of aromatase positive neurons in Tfm mutant males. The number of βgal positive neurons in the BNST, MeA, and caudal hypothalamus is similar between Tfm and WT males (Figure 3A–F, K). Staining for PLAP activity labels male typical projection patterns in the VMH and the anterior hypothalamic area of Tfm mutant males (Figure 3G–K). These findings demonstrate that masculinization of the number and projections of aromatase expressing neurons is largely independent of testosterone signaling through AR.
We next sought to determine the influence of estrogen in establishing the sexual dimorphisms in aromatase positive neurons. The complexity and redundancy within estrogen signaling pathways makes it difficult to test the relevance of individual ERs in establishing dimorphisms in aromatase expression. We therefore asked if estrogen is sufficient to masculinize aromatase expression in females. As estrogen influences sexual differentiation of neural pathways in the early neonatal period in male rodents (McCarthy, 2008), we treated female pups bearing the aromatase-IPIN allele with estrogen at P1 (postnatal day 1, the day of birth), P8, and P15. A cohort of control females was administered vehicle (NV) at these timepoints. The dosage and injection schedule were chosen as being the most effective at masculinizing aromatase positive neurons. We find that in females administered estrogen neonatally (NE), aromatase expressing neural pathways appear indistinguishable from those observed in WT males (Figure 4). These data demonstrate that neonatally administered estrogen can masculinize both the cell number and projection patterns of aromatase expressing neurons. Our results show that the masculinization of aromatase positive neurons is independent of AR (Figure 3) and can be induced in females by neonatal estrogen (Figure 4). In neonates, the ovaries are quiescent whereas the testes generate a surge in circulating testosterone immediately after birth (McCarthy, 2008). We therefore hypothesized that aromatization of testosterone into estrogen masculinizes aromatase positive neurons during this period. To test this hypothesis, we provided testosterone to neonatal females. We find that testosterone administration is equivalent to estrogen supplementation in masculinizing aromatase expressing neural pathways (Figure S6A), suggesting that testosterone induces male differentiation of these neurons after its conversion into estrogen in vivo.
We wished to uncover the mechanism whereby estrogen drives sexual differentiation of aromatase positive neurons. An equivalent number of cells expresses aromatase in both sexes in the BNST and MeA at P1, whereas there are more βgal positive cells in these regions in males compared to females at P14 (Figure 5A–E, and data not shown). Neurons in the BNST and MeA are born prenatally in rodents (al-Shamma and De Vries, 1996; Bayer, 1980), and we therefore asked if the sexual dimorphisms in these regions resulted from sex specific apoptosis. We labeled apoptotic nuclei in the neonatal BNST and MeA with the TUNEL assay. We find more TUNEL positive cells in the BNST in females compared to males at several timepoints from P1 -P10, a finding consistent with previous work (Gotsiridze et al., 2007). Moreover, we observe a similar increase in TUNEL positive cells in the MeA in females compared to males at these timepoints (Figure 5F–I). The most significant sex difference in cell death was observed at P4 in the MeA and P7 in the BNST, with a ~2 fold increase in apoptotic nuclei in females compared to males (Figure 5J). As the conditions for TUNEL preclude co-labeling for βgal, we immunolabeled sections through the BNST and MeA for βgal and effectors of apoptosis (using a cocktail of antibodies to activated Caspase-3, 9 and Apaf-1) in P7 mice bearing the aromatase-IPIN allele. In accord with results of the TUNEL assay, these effectors of apoptosis label significantly more cells in females compared to males in the BNST and MeA (≥2 fold in each region; n=3; p < 0.001). We find many apoptotic cells expressing βgal in both sexes, with significantly more double-labeled cells present in females compared to males (% apoptotic cells expressing βgal in BNST: females, 50 ± 1; males, 26 ± 2; n = 3; p < 0.001. % apoptotic cells expressing βgal in MeA: females, 54 ± 2; males, 35 ± 3; n = 3; p < 0.01).
As neonatally administered estrogen is sufficient to masculinize aromatase positive neurons in the female BNST and MeA, we asked whether such supplementation promoted the survival of cells fated to die in these regions. Neonatal estrogen treatment promotes cell survival such that the number of TUNEL positive nuclei in the BNST and MeA is indistinguishable between NE females and WT males (Figure 5J). Such cell survival promoting effects of estrogen are reminiscent of the known neuroprotective effects of this hormone (Arai et al., 1996). Is estrogen synthesis essential for cell survival in the BNST and MeA? To address this issue, we analyzed cell death in male mice null for aromatase (Honda et al., 1998). In these males, the number of apoptotic figures is comparable to that observed in WT females, and significantly different from WT males (Figure 5J). In summary, we observe more cell death in the BNST and MeA in females than in males, with an increase in the survival of aromatase expressing cells in males compared to females. Further, administration of estrogen to female pups reduces cell death whereas abrogation of estrogen synthesis increases apoptosis in males, demonstrating that estrogen is necessary and sufficient to promote cell survival in the BNST and MeA.
We tested adult NE females bearing the aromatase-IPIN allele to determine whether sex specific behaviors were also masculinized. Males reliably mate with females at high frequency whereas females exhibit male pattern sexual behavior at a low frequency towards females (Baum et al., 1974; Jyotika et al., 2007; Spors and Sobel, 2007). NE and NV females were individually housed as adults and presented with a WT female in estrus. Some resident females, regardless of hormone treatment, mated with the intruder, showing no apparent differences in mounting or pelvic thrusts, which are indicative of intromission (penetration) in males. In sharp contrast to resident males, both NE and NV females mated with intruders in fewer assays, consistent with the notion that neonatal estrogen does not alter the low frequency of male sexual behavior in females (Figure 6C) (Burns-Cusato et al., 2004; Vale et al., 1973).
We next examined NE females for male territorial behaviors. Individually housed male but not female residents attack male intruders (resident intruder aggression test) (Miczek et al., 2001). In striking contrast to NV females who never displayed aggression, we find that, like males, most NE female residents attack a male intruder (Figure 6A; Movies S1, S2). Similar to male residents, NE females initiated bouts of biting, chasing, wrestling, and tumbling. The aggression displayed by NE animals is not a response to mating attempts by the male: in most assays (73%; n = 11 assays) the fighting preceded any mating attempt, and most individual attacks (93%; n = 90 events) were not preceded by sexual behavior. As part of territorial defense, resident male mice mark their territory by scattering many urine drops across the cage floor, whereas females pool their urine at the cage perimeter (Desjardins et al., 1973; Kimura and Hagiwara, 1985). NE females deposit urine in a pattern resembling that of males (Figure 6D–G). Unlike NV females who pool urine, NE mice scatter significantly more urine drops, with a large fraction of such drops deposited away from the perimeter. Because neonatal testosterone exposure mimicked neonatal estrogen exposure in masculinizing aromatase-expressing circuits, we wished to test if neonatal testosterone would also mimic the effects of neonatal estrogen on territorial behaviors. Our data show that neonatal testosterone and estrogen are equivalent in eliciting male territorial behaviors in females (Figure S6B-D). Taken together, these results suggest that neonatal testosterone masculinizes territorial marking and aggression, at least in part, after its aromatization into estrogen in vivo.
We next asked whether NE females are sexually receptive to males. The standard test of female mating involves surgical removal of the ovaries (ovariectomy) followed by estrogen and progesterone injections to induce estrus on the day of testing (Beach, 1976). Accordingly, we hormonally primed ovariectomized females treated neonatally with estrogen (NEAOP) or vehicle (NVAOP), and presented them to male residents. Male mice vigorously mount females, but only receptive females permit such mounts to proceed to intromission. Thus, one measure of female receptivity is the ratio of intromissions to the total number of mounts (receptivity index). There was a large reduction in the receptivity index and the duration of intromissions in NEAOP females compared to NVAOP controls (Figure 6I, J), consistent with the notion that neonatal estrogen defeminizes sexual receptivity (Whalen and Nadler, 1963). Unlike NVAOP mice, NEAOP females actively rejected mounts, often attacking and chasing the male (Figure 6I). This reduction in sexual behavior does not reflect a lack of interest from males as these residents attempted to mate with NEAOP or NVAOP females in most assays (Figure 6H). Moreover, the low receptivity index of NEAOP females resulted from an absolute increase in the number of mounts (Figure 6J), demonstrating the males’ interest in mating with these mice. Thus, neonatal estrogen treatment appears to permanently defeminize sexual receptivity, even under estrus-inducing hormonal conditions.
Gonadal hormones are required to activate the display of sex specific behaviors such as aggression in adults (Beeman, 1947; Goy and McEwen, 1980; Morris et al., 2004). However, we observe male type fighting and urine marking in NE females in the absence of adult supplements of sex steroids. We hypothesized that male type fighting and urine marking may be activated by ovarian hormones. We directly tested this by ovariectomizing a cohort of adult NE animals: such females did not fight (0/5 females attacked males) or scatter urine (5/5 females pooled urine), demonstrating that the masculinized brain in NE animals utilizes ovarian hormones to activate these male behaviors. In summary, NE females exhibit a dissociation of sex typical behaviors: they do not mate like females or males but they display masculinized patterns of aggression and urine marking in the presence of ovarian hormones.
There are significant quantitative differences in fighting and urine marking between NE females and WT males (Figure 6B, G). We hypothesized that such differences reflect the low levels of circulating testosterone in NE mice. Testosterone titers are equivalent between NE and NV females, and > 10 fold lower than male titers. By contrast, all three groups of animals have similar, low baseline levels of estrogen, with periodic elevations of estrogen in the females that presumably accompany estrus (Supplemental Text). We masculinized circulating testosterone levels by providing this hormone to adult, ovariectomized females that were treated neonatally with estrogen (NEAOT) or vehicle (NVAOT) (Serum testosterone: males, 5.8 ± 1.4 nM; NEAOT females, 8.6 ± 3 nM; NVAOT females, 9.1 ± 4.3 nM; n = 4; p > 0.42). In resident intruder aggression tests, we find that NEAOT but not NVAOT females attack male intruders (Figure 7A; Movies S3, S4). Moreover, the pattern, frequency, and duration of attacks were similar between NEAOT and male residents (Figure 7B). The number and pattern of urine marks were also indistinguishable between NEAOT females and males (Figure 7C). These findings demonstrate that neonatal estrogen exposure masculinizes the response to testosterone in adults, and that male typical levels of testosterone augment the degree of male territorial displays without substantially altering the nature of these behaviors.
These data show that adult testosterone administration is sufficient to activate male territorial behaviors in NE females, consistent with a functional role for aromatase expressing neural pathways in these mice. It is possible, however, that neonatal estrogen treatment masculinizes AR positive pathways in the brain, which in turn respond to adult testosterone and activate male territorial displays. We therefore examined the behavioral response of adult AR mutant (Tfm) males to testosterone administration. At birth, AR mutants have normal titers of testosterone (Sato et al., 2004), thereby leading to the development of a male pattern of aromatase expressing neurons following local conversion into estrogen (Figure 3). However, these mutants subsequently develop testicular atrophy, resulting in extremely low levels of circulating testosterone in adult life (Sato et al., 2004). As adults, these mutants do not attack intruders and they pool urine at the cage perimeter (Ohno et al., 1974) (Scott Juntti and NMS, unpublished observations). We find that provision of testosterone to adult Tfm males (TfmAT) significantly increases the number of urine marks compared to mutants administered vehicle (TfmAV) (Figure 7F). The number of urine spots was lower compared to WT males, indicating that a male typical frequency of urine marking may require additional contributions from AR signaling. While TfmAT males deposited more urine spots in the cage center compared to TfmAV controls, this trend did not reach statistical significance, suggesting AR signaling is essential for this component of territorial marking. In contrast to this complex control of male urine marking, we find that TfmAT mice attack intruders in the resident intruder assay similar to WT residents. Indeed, all TfmAT males attacked the intruder in most assays, whereas none of the TfmAV residents initiated attacks (Figure 7D). Moreover, both the frequency and duration of the attacks were similar between WT and TfmAT males (Figure 7E). Taken together, these results provide evidence that testosterone elicits many components of male territorial behaviors in adult animals independent of AR.
We have used genetic reporters to visualize aromatase expressing neural pathways. Our reporters reveal aromatase expression at cellular resolution in discrete pools in regions previously shown to express aromatase (Roselli et al., 1998; Wagner and Morrell, 1996). This small set of aromatase positive neurons is therefore likely to influence the diverse neural circuits that utilize estrogen signaling to control male behaviors. The sensitive nature of the reporters reveals previously unreported sex differences in the number and projections of aromatase positive neurons. Even within regions such as the BNST, only a subset of cells expresses aromatase, suggesting functional specialization within these large dimorphic neuronal pools (Hines et al., 1992; Morris et al., 2008; Shah et al., 2004). Indeed, most aromatase positive cells in the BNST (98% ± 0.5; n = 3) express AR, whereas only a subset of AR positive neurons co-labels with aromatase (35% ± 2; n = 3). The reciprocal connectivity between the aromatase expressing regions we have identified suggests the interesting possibility that aromatase positive neurons may form an interconnected network that regulates sexually dimorphic behaviors.
Aromatase expressing neurons are largely restricted to neural pathways implicated in sexual and aggressive behaviors. Our results show that aromatization of testosterone into estrogen plays an important role in activating male territorial behaviors. However, the behavioral relevance of the dimorphisms we observe in aromatase positive neurons remains to be determined. These neurons may serve as a dimorphic neuroendocrine source of estrogen or they may directly participate in the circuits that control male behaviors. It is unlikely that such dimorphisms are required solely to provide a dimorphic source of local estrogen as NE females exhibit male territorial displays in response to circulating ovarian hormones. Consistent with the notion that these cells may function within neural circuits that mediate dimorphic behaviors, many aromatase positive neurons also express ERα in the BNST and MeA (Figure S4 and data not shown). It will be important, in future studies, to understand the functional significance of the sex differences in cell number and connectivity that we have identified in this study.
We find that neonatal estrogen exposure masculinizes aromatase expressing neurons and territorial behaviors in females. These results seem counter-intuitive as one would expect that estrogen produced by the neonatal ovaries should induce male typical differentiation in all WT females. In fact, the ovaries are quiescent in neonates (McCarthy, 2008). By contrast, males experience a neonatal surge in circulating testosterone, leading to a corresponding increase in estrogen in the brain via local aromatization (Amateau et al., 2004). Our provision of estrogen to female pups therefore exposes their brains to this hormone during a period when only males would experience a local rise in estrogen. Such plasticity of the female brain to the masculinizing effects of estrogen is transient as adult females do not have a male pattern of aromatase expression despite the spikes in estrogen within the ~4 day estrous cycle. Indeed, we find that estrogen administration to adult WT females does not masculinize aromatase positive neurons and behavior (Figure S5 and data not shown). In order to determine whether testosterone exposure could masculinize aromatase positive neural pathways and territorial behavior, we provided testosterone to neonatal females. We find that this manipulation masculinizes aromatase expressing neurons and territorial behaviors to levels similar to those observed in NE females (Figures 4, S6). This finding suggests that the masculinizing effects of neonatal estrogen treatment are unlikely to be a gain-of-function of estrogen signaling, but rather reflect, at least in part, the physiological conversion of testosterone into estrogen by aromatase. Such locally derived estrogen may also influence the differentiation of other, aromatase negative, neuronal pools, which may play an important role in the subsequent display of sex typical behaviors.
Our results do not exclude the possibility that androgen and estrogen signaling masculinize aromatase expressing neurons in a redundant manner. Previous work in rats indicates that testosterone signaling can upregulate aromatase activity (Roselli et al., 1987). These biochemical studies are not incompatible with our data as the expression of βgal and PLAP report cell number and fiber projections of neurons expressing aromatase and not aromatase activity. Nevertheless, we find that restoring circulating testosterone titers to WT male levels in AR mutants is sufficient to elicit male typical aggression and some components of urine marking. Taken together, our results demonstrate that estrogen synthesis in neonatal and adult life is sufficient to masculinize aromatase expressing neurons and territorial behaviors independent of AR.
The dimorphic projections in the anterior hypothalamus and VMH could arise from sex specific neurite outgrowth or retraction. However, both regions contain aromatase expressing neurons in the postnatal period, making it difficult to distinguish the sexually dimorphic fibers from the processes of local neurons. The small number of aromatase expressing cells in the caudal hypothalamus makes it difficult to elucidate the mechanism underlying the sex difference in this region. Increased survival of aromatase positive cells in the neonatal male BNST and MeA likely accounts for the dimorphism in cell number in these regions. Moreover, estrogen is necessary and sufficient to promote such cell survival in vivo. Most aromatase expressing cells in the neonatal BNST and MeA also express ERα (Figure S4). Both regions also express ERβ (Figure S4), suggesting that estrogen may mediate cell survival of aromatase positive cells by signaling through one or more classes of receptors in a cell autonomous manner. Irrespective of the mechanism underlying cell survival, our study demonstrates that estrogen ultimately acts on the very cells that synthesize this hormone to promote their sexual differentiation in a positive feedback manner.
Several research groups have recently provided insight into the molecular mechanisms underlying sex specific behaviors in fruitflies (Manoli et al., 2005; Stockinger et al., 2005; Vrontou et al., 2006). These studies show that the repertoire of sexually dimorphic displays in Drosophila appears to be regulated in an unitary manner by Fruitless, a putative transcription factor. In contrast to flies, and similar to humans (Byne, 2006; Hines, 2006), we find that dimorphic behaviors can be dissociated in mice: neonatal estrogen exposure masculinizes territorial but not sexual behaviors. The male typical fighting displayed by females treated neonatally with estrogen is unlikely to result from altered gender discrimination as these mice direct their aggression, like WT males, exclusively towards male intruders. What controls male sexual behavior? Previous work has demonstrated that testosterone supplementation to adult female mice is sufficient to elicit male mating behavior (Edwards and Burge, 1971). Consistent with these studies, we find that the majority of NEAOT and NVAOT residents exhibit male sexual behavior towards estrus intruders (5/5 NEAOT and 4/5 NVAOT females mated with estrous mice; p = 0.29, Chi-squared test). Such mating attempts were displayed in ≥ 70% of assays by both cohorts of females, a frequency that is comparable to WT males. These findings further underscore the notion that the neural circuits that mediate sexual and territorial behaviors are regulated by distinct hormonal and temporal mechanisms.
Previous work has demonstrated that females treated neonatally with estrogen fight with males in resident intruder assays (Simon et al., 1984). Such studies coupled neonatal and adult hormonal interventions, making it difficult to understand the long term behavioral consequences of neonatal estrogen exposure. We find that females treated solely with neonatal estrogen display masculinized patterns of fighting and urine marking in the presence of sex hormones produced by the ovaries. Administration of testosterone to these females to mimic normal male circulating titers of this hormone increases these behavioral displays to approximate the levels observed in males. These results indicate that the adult hormonal profile produced by the testes may not be instructive for male territorial behaviors: hormones produced by the adult gonads of either sex support male patterns of fighting and territorial marking provided that neonatal estrogen has masculinized the underlying neural circuits.
Marking behavior defines a range within which the animal will defend resources and advertise its social and reproductive status (Ralls, 1971). Sex differences in territorial marking appear to be innate and mice display dimorphic urine marking patterns even in social isolation (Desjardins et al., 1973; Kimura and Hagiwara, 1985), providing an objective assessment of what appears to be an internal representation of sexual differentiation of the brain. Females treated neonatally with estrogen fight and mark territory like males, demonstrating masculinization of social and solitary sex typical behaviors.
Circulating testosterone and locally derived estrogen in the brain are critical for the expression of male behaviors. It has been difficult to determine the individual contributions of these two hormones to masculinization of the brain and behavior. Our gene targeting strategy has allowed us to identify at cellular resolution the small population of aromatase expressing neurons that can synthesize estrogen from testosterone. Testosterone appears to serve, at least in part, as a pro-hormone for estrogen for the male typical differentiation of aromatase positive neurons and for masculinization of territorial behaviors. The genetic marking of this discrete set of aromatase expressing neural pathways should ultimately permit us to functionally link them with distinct sex specific behavioral outcomes.
The IRES-PLAP-IRES-nLacZ reporter was inserted into the 3′ UTR of the aromatase locus using previously described strategies (Supplemental Methods) (Shah et al., 2004). All experiments involving animals were in accordance with IACUC protocols at UCSF.
We injected steroid hormones into all females within a litter to test the effects of these steroids on neuronal differentiation and behavior. We injected pups subcutaneously with 5 μg of 17β-estradiol benzoate (EB) (Sigma) or 100 μg of testosterone propionate (Sigma) dissolved in 50 μL of sterile sesame oil (Sigma) at P1, P8, and P15. Control females in other litters were injected with 50 μL vehicle at the same timepoints.
To generate NEAOT and NVAOT mice, we ovariectomized adult NE or NV females and allowed them to recover for three weeks. We injected 100 μg of testosterone propionate (TP) dissolved in 50 μL sesame oil subcutaneously on alternate days in these animals. Such animals were used for behavioral testing ≥ 3 weeks after initiating TP injections. The same injection regimen was used to generate TfmAT and TfmAV males. Hormone titers were assayed with kits from Cayman Chemicals (estradiol) and DRG International (testosterone).
Sexually naive, group housed, age matched mice were used in all histological studies. PLAP or βgal activity was visualized in 80 μm (adult) or 12 μm (neonate) thick brain sections obtained from mice homozygous for the aromatase-IPIN allele. Immunolabeling was performed on 65 μm (adult) or 20 μm (neonate) thick brain sections obtained from mice heterozygous for the aromatase-IPIN allele. We used previously described protocols to process these sections for histochemistry or immunolabeling (Shah et al., 2004). Message for aromatase, ERα and ERβ was localized by ISH as described in the Supplemental Methods. Sections of 16 μm thickness were processed for TUNEL according to the manufacturer’s instructions (Chemicon). In these studies, we processed in parallel at least one animal of each sex or experimental manipulation (WT and Tfm males; NE and NV females; NT and NV females) bearing the aromatase-IPIN allele and one control animal with an unmodified aromatase allele. Quantitation of cell numbers and fiber innervation was performed using unbiased stereology and other approaches (Supplemental Methods). All histological analysis was performed by an investigator blind to sex, age, genotype, and hormone treatment.
We used 10 – 24 week old singly housed mice in behavioral tests, which were done ≥ 1 hour after lights were switched off. Mice were first tested for male sexual behavior in their home cage in a 30 minute assay with an estrous female. The residents were subsequently tested for territorial marking. Mice were allowed to explore a fresh cage lined with Whatman filter paper for one hour, and then returned to their homecage. The marking pattern was visualized with UV transillumination. Residents were subsequently tested for aggression directed towards a WT intruder male for 15 minutes. NE and NV females were then ovariectomized and tested for female sexual behavior after estrus induction in the homecage of a sexually experienced male for 30 minutes. Each animal was tested twice for sexual behavior and aggression, allowing us to analyze the total fraction of assays in which these behaviors were observed. We always exposed the experimental animals to mice they had previously not encountered, and individual assays were separated by ≥ 2–3 days. A separate cohort of NE and NV females was used to generate NEAOT and NVAOT mice. All tests were scored by an experimenter blind to the sex, genotype, and hormone treatment of mice, using a software package we developed in Matlab.
We used the Chi-squared test to determine whether the proportion of experimental animals exhibiting a particular behavior was significantly different from control subjects. All other experimental comparisons were analyzed using both parametric (Student’s t test) and non-parametric (Kolmogorov-Smirnov, ks-test) tests of significance. All statistically significant results presented in the text (p < 0.05) using the Student’s t test were also determined to be statistically significant with the ks-test.
We thank C. Barberini for software programming; C. Cheung for technical assistance with ISH; D. Lubahn for providing us with aromatase–/+ animals; V. Mandiyan, L. Crothers, and C. Carey for technical assistance; P. Ohara for assistance with stereology; and R. Axel, T. Clandinin, H. Ingraham, D. Julius, S. Lomvardas, and Shah lab members for critical discussions and comments on the manuscript. This work was supported by Genentech Graduate Fellowships (MVW, JKC); National Science Foundation Graduate Research Fellowship (EJF); Achievement Rewards for College Scientists Scholarship (JKC); National Institutes of Health Institutional Training Grant (JT); National Institutes of Health (R01), Career Awards in the Biomedical Sciences, UCSF Program for Breakthrough Biomedical Research, Edward Mallinckrodt, Jr. Foundation, and McKnight Foundation for Neuroscience (NMS).
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