Interactions with the young down-regulate adult olfactory neurogenesis and enhance the maturation of olfactory neuroblasts in sheep mothers

New neurons are continuously added in the dentate gyrus (DG) and the olfactory bulb of mammalian brain. While numerous environmental factors controlling survival of newborn neurons have been extensively studied, regulation by social interactions is less documented. We addressed this question by investigating the influence of parturition and interactions with the young on neurogenesis in sheep mothers. Using Bromodeoxyuridine, a marker of cell division, in combination with markers of neuronal maturation, the percentage of neuroblasts and new mature neurons in the olfactory bulb and the DG was compared between groups of parturient ewes which could interact or not with their lamb, and virgins. In addition, a morphological analysis was performed by measuring the dendritic arbor of neuroblasts in both structures. We showed that the postpartum period was associated with a decrease in olfactory and hippocampal adult neurogenesis. In the olfactory bulb, the suppressive effect on neuroblasts was dependent on interactions with the young whereas in the DG the decrease in new mature neurons was associated with parturition. In addition, dendritic length and number of nodes of neuroblasts were significantly enhanced by interactions with the lamb in the olfactory bulb but not in the DG. Because interactions with the young involved learning of the olfactory signature of the lamb, we hypothesize that this learning is associated with a down-regulation in olfactory neurogenesis and an enhancement of olfactory neuroblast maturation. Our assumption is that fewer new neurons decrease cell competition in the olfactory bulb and enhance maturation of those new neurons selected to participate in the learning of the young odor.


INTRODUCTION
In most mammals, newborn neurons are continuously provided in two main structures of the brain throughout life, the dentate gyrus (DG) of the hippocampus and the olfactory bulb (Ming and Song, 2005;Curtis et al., 2007;Brus et al., 2013). In the DG, stem cells reside in the subgranular zone (SGZ) and give rise to neuroblasts which become new granule neurons in the overlying granule cell layer (GCL; Ming and Song, 2005). In the olfactory system, neural stem cells function as primary precursors in the subventricular zone (SVZ) located on the wall of the lateral ventricles. These cells produce transient amplifying cells which rapidly divide to produce neuroblasts. The neuroblasts migrate toward the olfactory bulb along the rostral migratory stream. After reaching the olfactory bulb, the new cells migrate radially and mature into granular interneurons for the majority of them (Rochefort and Lledo, 2005).
In rodents, a growing body of literature aiming to block neurogenesis by using various methodologies shows the role of hippocampal neurogenesis in some forms of hippocampusdependent learning tasks despite some inconsistent results (Deng et al., 2010;Arruda-Carvalho et al., 2011;Gu et al., 2012). Similarly, olfactory neurogenesis is involved in the memory processing of olfactory cues (Lazarini and Lledo, 2011). Blocking neurogenesis impaired olfactory perceptual learning (Moreno et al., 2009), short-term and long-term memory (Breton-Provencher et al., 2009;Lazarini et al., 2009;Sultan et al., 2010). In addition it has been recently demonstrated that immediate activation of newborn olfactory neurons, by using an optogenetic approach, enhances discrimination learning and memory when the task is difficult (Alonso et al., 2012). A common role in pattern separation has been proposed for newborn hippocampal and olfactory neurons and adult neurogenesis could constitute an Frontiers in Human Neuroscience www.frontiersin.org February 2014 | Volume 8 | Article 53 | 1 adaptive mechanism to optimally encode contextual or olfactory information (for review, see Sahay et al., 2011). While the implication of adult neurogenesis has been demonstrated in spatial and olfactory learning, a better understanding of the role of adult born neurons in an ethological context has begun to emerge. Social environment can modify hippocampal neurogenesis. Decrease in cell proliferation induced by social isolation rearing could be reversed by subsequent group rearing (Lu et al., 2003). Exposure to chronic social stress dramatically decreases cell proliferation in the DG of rats, mice and tree shrews (Gould et al., 1997;Czeh et al., 2002;Mitra et al., 2006). In a socio-sexual context, exposure to the male urine compounds that are involved in mate recognition increased the survival of granule cells in the accessory olfactory bulb, the main olfactory bulb (MOB), and the DG of female mice (Mak et al., 2007;Oboti et al., 2011). Moreover, suppression of neurogenesis by an anti-mitotic agent prevented mate recognition (Oboti et al., 2011) and the display of preference for dominant male in female mice (Mak et al., 2007). Another approach to assess the role of adult neurogenesis consists in evaluating whether newly-generated neurons might functionally integrate the olfactory network which process olfactory information. In male hamsters, double immunohistochemistry labeling for Fos, a marker of cell activation, and neuronal nuclei (NeuN), a marker of post-mitotic neurons, shows that olfactory bulb cells born in adulthood are activated by socio-sexual stimuli such as estrous female or aggressive male (Huang and Bittman, 2002).
A link between adult neurogenesis and parenting has not been clearly established yet (Lévy et al., 2011). Some studies indicate a regulation of neurogenesis by parturition and the onset of motherhood. In all of rodent species studied so far parturition and the early postpartum period are accompanied by a significant decrease in cell proliferation in the hippocampus. In primiparous mother rats, this was reported at postpartum day 1, 2 and 8 (Darnaudery et al., 2007;Leuner et al., 2007;Pawluski and Galea, 2007) although no effect was observed later, at postpartum day 28 and after weaning (Leuner et al., 2007). Parturition and early postpartum period do not stimulate cell proliferation in the SVZ of mice but an increase is observed at 7 days postpartum (Shingo et al., 2003). Surprisingly, whether cell survival in the DG or in the MOB is altered during parturition and early postpartum period at the onset of maternal behavior is not known in rodents. Rather, cell survival in the DG of rats was assessed either at postpartum day 14 (Darnaudery et al., 2007) or 21 (Pawluski and Galea, 2007) and both studies report a significant decrease when compared to virgins. A few studies have investigated the importance of stimuli provided by neonatal pups but outside the context of parturition. Nulliparous rats exposed to pups show increased cell proliferation in the DG when compared to nulliparous females regardless of their parental response (Pawluski and Galea, 2007). Likewise, virgin female prairie voles exposed to pups exhibit increased hippocampal cell proliferation (Ruscio et al., 2008).
Although an increase in cell survival in the DG was reported in virgin females 21 days after pup-exposure (Pawluski and Galea, 2007), the influence on survival of the newborn neurons either in the DG or in the MOB at the time of pup-exposure is not known. The consequences of neurogenesis ablation on the onset of maternal behavior have been investigated in mice. Irradiation of the SVZ induces minor disturbances of maternal behavior (Feierstein et al., 2010b). However, infusion of an anti-mitotic agent which transiently impairs both hippocampal and olfactory neurogenesis has been shown to affect maternal behavior but only when animals are tested in an anxiogenic environment (Larsen and Grattan, 2010), whereas genetic manipulations inducing profound and long-term alterations of neurogenesis impair nursing behavior in the home cage (Sakamoto et al., 2011).
In sheep, a down-regulation of cell proliferation has been observed in mothers in contact with their lambs for 2 days both in the DG and the SVZ (Brus et al., 2010). However there has been no report examining a change in survival of newly-born neurons in the DG or the MOB that could occur during the early postpartum period. In addition, no study has disentangled the influence of parturition and the first interactions with the young on cell survival and this could improve our understanding of the contribution of neurogenesis to maternal behavior. In this context, maternal behavior in sheep constitutes an interesting model in which endocrine changes occurring at parturition and olfaction play a central role (Lévy et al., 1995;Lévy and Keller, 2008). In addition, not only infantile odors become very potent stimuli allowing the development of maternal care but they also provide a basis for individual recognition of the offspring. Ewes develop discriminative maternal care, called maternal selectivity, favoring their own young at suckling while rejecting any alien young. This recognition is based on the learning of olfactory characteristics of the lamb and takes place within the first hours after parturition (Lévy et al., 2004;Lévy and Keller, 2009). Some of the learning mechanisms reside in extensive neurochemical changes occurring in the MOB at parturition (Lévy et al., 1993;Lévy and Keller, 2009). In addition to these neurochemical changes, olfactory neurogenesis could provide another mechanism through which olfaction can contribute to the onset of maternal behavior and associated learning.
The aim of the present study was to evaluate the influence of parturition and learning of the lamb odor on the survival of newborn neurons. Bromodeoxyuridine (BrdU), a marker of cell division, was used in combination with two markers of neuronal maturation (doublecortin (DCX), an early maturation marker and NeuN), to compare both hippocampal and olfactory neurogenesis between virgins and parturient ewes which could interact or not with their lamb. In addition, because learning accelerates the maturation of the dendritic trees of newborn neurons in the DG (Tronel et al., 2010;Lemaire et al., 2012), and motherhood is accompanied by changes in the morphology of newborn neurons in the MOB (Kopel et al., 2012), we assessed the influence of lamb olfactory learning on this maturation by measuring the dendritic length and the number of nodes of new neuroblasts. access to water and were fed with lucerne, maize, straw and a supplement of vitamins and minerals. Animal care and experimental treatments complied with the guidelines of the French Ministry of Agriculture for animal experimentation and European regulations on animal experimentation (86/609/EEC) and were performed in accordance with the local animal regulation (authorization No. 006352 of the French Ministry of Agriculture in accordance with EEC directive). Ewes were sacrificed by a licensed butcher in an official slaughterhouse (authorization No. A37801 E37-175-2 agreement UEPAO). All efforts were made to minimize the number of animals (5-6 animals per group).

BROMODEOXYURIDINE INJECTIONS AND TISSUE PREPARATION
Four months before sacrifice, ewes were housed in an individual pen (2 × 1 m) and received four intravenous injections of BrdU, (1 injection/day, 20 mg/Kg in 0.9% saline; Sigma-Aldrich, France), a thymidine analogue incorporated into the DNA during the S-phase of the mitotic division. Doses of BrdU and timing between injections and sacrifice were based on a previous study reporting that maturation of adult-born cells both is much longer in sheep than that of rodents and that the highest proportion of new mature neurons is found at 4 months after BrdU injections (Brus et al., 2013).

GROUPS
Three groups of ewes were constituted (Figure 1). In parturient groups, mating was synchronized by the use of vaginal sponges containing 45 mg of fluorogestone acetate for 14 days followed by an intra-muscular injection of pregnant-mare-stimulating gonadotropins to induce ovulation. Just after parturition, mothers were either left 48 h with their lambs in their individual pen in the same barn ("With Lamb" group, n = 5), or were separated from them for 48 h ("No Lamb" group, n = 6). After being separated from their lamb immediately after birth, ewes of the "No Lamb" group were placed in a different barn to avoid any contact with lambs and ewes were housed together in a large pen to avoid stress induced by separation from the young. All the ewes had never given birth before the study. Lambing occurred within a period of gestation of 149 ± 4 days. Against all expectations, at birth the lambs displayed low vigor preventing them from feeding normally, probably due to BrdU injections in early pregnancy. Thus, in the "With lamb" group, adoptions have been performed with newborn lambs provided by the flock of the research center. It has been well established in previous studies that adoption, when performed at birth, are without any consequences on the quality of the mother-young relationship in comparison to normal mother-young lambing (Keverne et al., 1983;Kendrick et al., 1991;Lévy et al., 2010). In this group, maternal behavior was observed for 10 min at 0, 6 and 24 h after parturition to completely ensure that maternal care was normally provided to lambs. At 2 days postpartum just before sacrifice, selectivity was tested by presenting an alien lamb to the mother and rejection and acceptance behaviors were recorded for 3 min. The alien lamb was then taken away and the ewe was observed FIGURE 1 | Time table and protocol design. All ewes received four intravenous injections of BrdU (20 mg/kg, 1 injection/day) 4 months before sacrifice. In the two parturient groups ("With Lamb" and "No Lamb"), BrdU injections were performed 1 month after fecundation. In the "With Lamb" group (n = 5), ewes could interact with her lamb and maternal behavior was observed at 0, 6 and 24 h after parturition for 10 min each and selectivity test was performed at 2 days postpartum just before sacrifice. In the "No Lamb" group (n = 6), lambs were removed just after delivery. Virgin group (n = 6) is composed of nulliparous ewes. with her own lamb for an additional 3 min (Keller et al., , 2005. These tests indicated that all the ewes of the "With Lamb" group were maternal and selective. The "Virgin" group (n = 6) was composed of nulliparous anoestrus ewes of similar age than the two parturient groups and housed together.

BRAIN PERFUSION AND IMMUNOHISTOCHEMISTRY
Two days after lambing, ewes were anesthetized with thiopental and decapitated by a licensed butcher in an official slaughterhouse. Brains were immediately perfused via carotid arteries with 2 L of 1% sodium nitrite in phosphate buffer saline, followed by 4 L of ice-cold 4% paraformaldehyde solution in 0.1M phosphate buffer (pH 7.4). The brain was dissected out, cut into blocks and post-fixed in the same fixative for 48 h. The tissues were then stored in 30% sucrose for 2 days until sectioned. Frontal sections were cut at a thickness of 30 µm using microtome or cryostat and stored at −20 • C in cryoprotectant.
Because in a previous study we observed cell proliferation within the MOB (Brus et al., 2010), we evaluated the influence of parturition and interactions with the young on cell proliferation in this olfactory structure as well as in the DG. To this end, single-immunolabeling was performed against the Ki67 marker, an endogenous marker of cell division which is expressed at all the phases of the cellular cycle (Kee et al., 2007). Sections were treated with TBSTA-BSA for 1 h and were incubated overnight in primary antibody rabbit anti-Ki67 (1:500, Abcam ab15580-25, Cambridge, UK) in TBSTA-BSA at room temperature. The following day, sections were rinsed four times in TBS and were incubated in secondary antibody sheep anti-rabbit (1:400, produced by the INRA center of Nouzilly) in TBS-BSA 0.1% during 3 h at 4 • C. After four rinses in TBS 0.1%, sections were incubated with rabbit peroxydase anti peroxydase (PAP, 1:80000, Dako Z0113, Trappes, France) overnight at 4 • C. The last day, after two rinses in TBS and two rinses in Tris-HCl (0.05M, pH 7.6) sections were reacted for peroxydase detection in a solution of 3,3 -Diaminobenzidine tetrahydrochloride (DAB, 0.15 mg/mL; Sigma) containing 0.001% H 2 O 2 and 0.018% nickel ammonium sulfate for 7 min.

QUANTIFICATION
The number of BrdU+ (10 sections/animal, 800 µm between sections) and Ki67+ cells (6 sections/animal, 950 µm between sections) was assessed by counting peroxydase/DAB-stained frontal sections of the MOB and the DG through different levels along the rostrocaudal axis, using a light microscope (Axioskope 2, Zeiss, Germany) on a magnification of x20 and cell count analysis software (computerized image analysis Mercator, Explora Nova, La Rochelle, France). The counter was blind to the experimental group. Areas of the MOB (granular and periventricular layers) and the DG (GCL and SGZ) were measured with this system through an x2.5 objective (MOB) and an x10 objective (DG). Cell densities were then calculated by dividing the numbers of BrdU+ or Ki67+ cells by the layer area. The Ki67+ cell density corresponds to the mean of cell density measured in the granular and the periventricular layers for the MOB and in the GCL and the SGZ for the DG. Densities of BrdU+ cells and proportions of new neurons and neuroblasts were counted only in the target structures of newly-born cells integration, the granular layer of the MOB and the GCL of the DG.
To determine the percentage of BrdU+/NeuN+ cells and BrdU+/DCX+ cells in the MOB and in the DG, approximately 100 cells per ewe were observed for the three groups (around 500-600 cells per group). Each BrdU+ cell was analyzed in its entire z-axis, with 0.5 µm step intervals, through an x40 oil immersion objective, using a confocal laser-scanning microscope (LSM700, Zeiss, Germany) equipped of excitation wavelengths 488 and 555. Cells rotated in orthogonal planes to verify double labeling with NeuN or DCX. For each selected cell that showed colocalization of BrdU with NeuN or DCX, an image was collected with the software Zen (Carl Zeiss, Germany). All images shown correspond to one focal plane (0.5 µm) and were imported into Gimp Pack Mode 2.6 software to adjust brightness and contrasts.
To determine the development of the newborn neuroblasts in the different groups, the number of nodes and the length of the dendritic arbor were measured in 16-18 BrdU+/DCX+ cells per ewe in the GCL of the MOB and of the DG. Each BrdU+/DCX+ cell was analyzed with confocal laser scanning microscope (LSM 700, Zeiss, Germany), in its entire Z-axis with 0.5 µm step interval, using x63 oil immersion objective to measure the length between the cell body to the end of the longest process. Total length of the dendritic tree was obtained by summing the length of all processes of each BrdU+/DCX+ cell. The number of nodes was obtained by counting the number of occurrences of branch points in the dendritic arbor. Interestingly, these newborn cells seemed to be at an early stage of maturation as most of them displayed only one process. Thus, the population of BrdU+/DCX+ was separated in two categories depending on the number of nodes and the percentage of cells with no nodes (one process, less mature) or with one or more nodes (two or more processes, more mature) was calculated (Figures 4B-E). Ambiguous cases were further analyzed using a semiautomatic neuron tracing system Imaris (Bitplane, USA).

STATISTICAL ANALYSIS
As densities of BrdU+ and Ki67+ cells, proportions of BrdU+/NeuN+ and BrdU+/DCX+ cells, and dendritic lengths of BrdU+/DCX+ cells were not normally distributed, the data were analyzed with nonparametric tests (Siegel, 1956). Intergroup comparisons were analyzed using two-tailed Kruskal-Wallis and Mann-Whitney tests. As the percentage of BrdU+/DCX+ cells which displayed one or more nodes was normally distributed, the data were analyzed with a one-way analysis of variance (ANOVA), and significance was probed by the Newman-Keuls test. Statistical analyses were performed using the statistical package SPSS 10 (Chicago, IL, USA) and the level of statistical significance was set at p ≤ 0.05. All data were represented as median and interquartile ranges except the number of nodes which were represented as mean ± SEM. Because we found that cell proliferation is down-regulated in postpartum ewes (Brus et al., 2010), we predicted that density of Ki67+ cells will be lower in parturient groups and therefore we used one-tailed Kruskal-Wallis and Mann-Whitney tests for this variable.

SURVIVAL OF NEUROBLASTS AND NEW MATURE NEURONS IN THE MAIN OLFACTORY BULB (MOB) AND THE DENTATE GYRUS (DG)
In the granular layer of the MOB and in the GCL of the DG, the densities of BrdU+ cells did not significantly differ between groups (MOB: H = 2.27, p = 0.3; DG: H = 4.48, p = 0.1; Figures 2A, B). The proportion of newborn neurons was measured in each group by using a double immunofluorescent labeling for BrdU and NeuN, a marker of post-mitotic neurons, and DCX, a marker of neuroblasts (Figures 3E-H). In the granular layer of the MOB, only the proportion of BrdU+/DCX+ cells significantly differed between groups (H = 8.27, p = 0.02; Figure 3A). This proportion was significantly lower in the "With Lamb" group compared to the "Virgin" or the "No Lamb" groups ("With Lamb" vs. "Virgin" or "No Lamb" groups: U = 2.47, p = 0.01; Figure 3A). The proportion of new post-mitotic neurons (BrdU/NeuN+ cells) did not differ between groups (H = 1.23, p = 0.5; Figure 3B).
Contrary to the MOB, only the proportion of BrdU+/NeuN+ cells significantly differed between groups in the GCL of the DG (H = 11.07, p = 0.004; Figure 3D). The proportion of new mature neurons was significantly lower in the two parturient groups

FIGURE 2 | Effects of parturition and/or interactions with the young on cell survival. Number of BrdU+ cells per millimeter 2 (median and interquartile ranges) in the granular layer of the MOB (A) and in the DG (B).
There is no significant difference between groups for both regions.

DENDRITIC LENGTHS OF NEWBORN NEURONS IN THE MAIN OLFACTORY BULB (MOB) AND THE DENTATE GYRUS (DG)
To assess the influence of interactions with the young on the development of the dendritic arbor of new neurons, we measured dendritic lengths and number of nodes of BrdU+/DCX+ cells in the granular layer of the MOB and in the GCL of the DG (Figure 4).
In the MOB, dendritic lengths and number of nodes significantly differed between groups (dendritic length: H = 6.01, p = 0.049; nodes: F = 6.58, p = 0.01). The highest dendritic lengths were found in the "With Lamb" group and significantly differed from the "No Lamb" (U = 3, p = 0.03; Figure 4A) and showed a tendency to differ from the "Virgin" group due to an animal showing an extreme value (U = 5, p = 0.08; Figure 4A). The percentage of BrdU+/DCX+ cells possessing nodes was significantly greater in the "With Lamb" group than in the "Virgin" or "No Lamb" groups ("With Lamb" vs. "Virgin" groups: p = 0.04; "With Lamb" vs. "No Lamb" groups: p = 0.007; Figure 4B). By contrast in the DG, no difference in dendritic lengths and in the number of nodes were found between groups (dendritic length: H = 1.35, p = 0.5; nodes; F = 1.04, p = 0.38; Figures 4D, E). Finally, the diameter of BrdU+/DCX+ cell bodies did not differ between groups in both structures (MOB; F = 2.33, p = 0.13; DG: F = 1.56, p = 0.24).

CELL PROLIFERATION IN THE MAIN OLFACTORY BULB (MOB) AND THE DENTATE GYRUS (DG)
To evaluate the influence of parturition and interactions with the young on cell proliferation, a single immunolabeling was performed against the Ki67 protein, an endogen marker of cell division, in the MOB and the DG (Figure 5). In both the MOB and the DG, the density of Ki67+ cells significantly differed between groups (MOB: H = 6.13, p = 0.025, Figure 5A; DG: H = 7.59, p = 0.01, Figure 5B). For both structures, in the two parturient groups, the density of Ki67+ cells in the MOB was significantly lower compared to the "Virgin" group (MOB: "With Lamb" vs. "Virgin" groups: U = 2, p = 0.01; "No Lamb" vs. "Virgin" groups: U = 7, p = 0.04; DG "With Lamb" and the "Virgin" groups: U = 1, p = 0.01; "No Lamb" group vs. "Virgin" groups: U = 8, p = 0.05).

DISCUSSION
Two main results have been obtained in this study. First, interactions with the young and associated learning, but not parturition, reduce the survival of neuroblasts in the MOB, whereas in the DG, parturition induces a decrease in the number of new neurons. These results suggest that learning of the olfactory signature of the lamb, which occurred during the first mother/young interactions, is specifically associated with a down-regulation in olfactory neurogenesis. Secondly, a positive effect on the development of the dendritic length of new neuroblasts has been specifically observed in the MOB of mothers interacting with their lamb suggesting that olfactory learning accelerates the maturation of adult-born neurons in the MOB but not in the DG.
In the MOB, while the number of BrdU+ cells was similar between parturient groups and the "Virgin" group, the population of neuroblasts was decreased by interactions with the young. This reduction is probably not a consequence of a decrease in new cell production during gestation since a positive, rather than a negative, influence of pregnancy on cell proliferation has been described in the SVZ of rodents (Shingo et al., 2003;Furuta and Bridges, 2005;Larsen and Grattan, 2010). In addition, parturient ewes separated from their lambs did not show any change of cell survival in comparison to virgins indicating that parturition could not account for this down-regulation. However, the suppressive effect of interactions with the lamb for 2 days on the survival of neuroblasts could be a consequence of various behaviors involved in maternal care. For instance licking the newborn lamb depends on olfactory attraction to amniotic fluids . However since licking behavior occurs at parturition and only last for 2 h it is unlikely involved in the decrease in neuroblasts population observed after 2 days of mother-young contact. Somatosensory stimulation associated with suckling could also account for this suppressive effect. However there is so far no evidence in the literature that suckling can have a direct effect on olfactory neurogenesis. In this respect, it would be of interest to assess olfactory neurogenesis in mothers whose udders are covered to prevent lambs from suckling. In rodents, restriction of suckling and tactile stimulation in lactating mothers in the presence of pups modulate neurochemical activity of the MOB, suggesting the importance of olfactory interactions with the young (Munaro, 1990). In sheep, during the early postpartum period various neurochemical and electrophysiological changes in the functional circuitry of the MOB underlie the formation of olfactory memory for lamb (Sanchez-Andrade et al., 2005;Lévy and Keller, 2008). Learning of the lamb odor could also be accompanied by changes in olfactory neurogenesis. Numerous studies report that bulbar neurogenesis varies following olfactory learning and that these changes could affect or not mature new neurons (see review : Feierstein et al., 2010a). However, whether these changes concern neuroblasts is not known. Here we show that neuroblasts but not more mature neurons are sensitive to social interactions. The decrease in the number of BrdU+/DCX+ cells cannot be explained by an enhancement of neuronal maturation since we did not observe an increase in BrdU+/NeuN+ cells in ewes interacting with their lambs. This decrease rather suggests that neuroblasts die during the 2 days of lamb exposure. Studies of adult-born neurons showed that olfactory learning has a complex effect on neuronal turnover, increasing or decreasing the survival of newborn olfactory cells as a function of their age (Mandairon et al., 2006;Mouret et al., 2008). Further studies using different timing of BrdU injections are needed to examine whether newborn cells of different age and maturation could have been differently affected. Together with a reduced number of neuroblasts, a decrease in cell proliferation in the MOB is observed in both groups of parturient ewes in comparison to virgins, as previously shown (Brus et al., 2010). The functional significance of this reduced proliferation and maturation processes in the MOB remains unknown. It may accentuate a survival-promoting effect by eliminating newborn neurons that are not functional and would favor the maturation and integration of new neurons which participate in learning by reducing cell competition. Computational studies support this hypothesis by showing that the rate of cell proliferation and cell survival contribute to the stability of the neural activity in the network (Lehmann et al., 2005;Butz et al., 2006). This assumption is supported by our results showing that dendritic maturation of neuroblasts is only enhanced in mothers interacting with their lamb in the MOB.
Two main non-exclusive mechanisms could be considered to account for this accelerated maturation. Firstly, nursing and suckling could influence the morphology of new neurons as several studies report an effect of lactation on dendritic arbor in the mother brain. For instance, enhanced spine density has been reported in the hippocampus of lactating rats (Kinsley et al., 2006). Similarly lactating females have longer basal dendritic length compared to diestrous females in the medial preoptic area, a key region for maternal behavior (Keyser-Marcus et al., 2001). However, a negative effect has been reported on oxytocin neurons having less dendritic branches and a fewer total dendritic length in lactating rats compared to virgin rats Stern and Armstrong, 1998). Secondly and more interestingly, learning the familiar lamb odor could induce this increased maturation as a positive influence of olfactory stimulation. The effect of odor learning on dendritic trees of newborn neurons has already been reported. Sensory deprivation drastically decreases Frontiers in Human Neuroscience www.frontiersin.org February 2014 | Volume 8 | Article 53 | 8 the number, the dendritic length and the spine density of newborn granule cells in the MOB (Rochefort and Lledo, 2005) and odor enrichment induces structural synaptic plasticity of adult-born granule neurons (Livneh and Mizrahi, 2011). Since evidence of an influence of learning but not of suckling on the maturation of new adult neurons has been reported in the literature, we hypothesized that learning of the olfactory signature of the lamb is involved in this maturation process. Further studies need to be done to establish whether suckling and/or learning of the lamb odor are responsible for this increased maturation of neuroblasts and whether this could also affect new mature neurons.
In the DG, while no change in the number of BrdU+ cells was found between groups, survival of new mature neurons was reduced by parturition itself, since parturient ewes isolated from their lamb showed a decrease in BrdU+/NeuN+ cells in comparison to virgins. The effect of pregnancy on the decrease in cell production is unlikely since no changes in hippocampal neurogenesis have been reported either during early or late pregnancy in rodents (see review: Lévy et al., 2011). However we cannot exclude a species dependent regulation of neurogenesis during pregnancy. These effects could also be due to the stress induced by removal of the lamb. This is however unlikely since we observed a similar decrease in the survival of mature neurons in mothers staying with their lambs. The inhibition of neurogenesis could be the consequence of hormonal changes, mainly steroids and glucocorticoids occurring at parturition. Oestradiol induced a decrease in survival of newborn neurons (Barker and Galea, 2008) and applications of corticosterone suppress cell survival in the DG of the hippocampus Herbert, 2004, 2006). Interestingly, oestradiol and corticosterone were found to affect neurogenesis and some interactions exist between both hormones. For example, adrenal steroids mediate the suppression of cell proliferation induced by oestradiol in ovariectomized females (Ormerod and Galea, 2001). The interplay between estradiol and cortisol at parturition may also mediate levels of cell survival in the DG and further studies are needed to better determine this complex influence on neurogenesis. In addition, our results suggest a hormonal influence depending on cell type since no change in the proportion of neuroblasts was found between groups in the DG. Recent studies report that high corticosterone differently affects population of new cells according to their maturity stage (Gonzalez-Perez et al., 2011;Lussier et al., 2013). Different effects on different cell lineages may represent adaptative actions of glucocorticoids, which provide a compensatory mechanism to protect some types of cells from death in the hippocampus. Such a mechanism would prevent from a dysfunction of the hippocampus during the postpartum period and would allow a better spatial memory in lactating females (Kinsley et al., 1999).
In conclusion, this study supports the hypothesis that the maternal brain undergoes neuronal changes, such as adult neurogenesis, which could constitute an adaptive response to motherhood by favoring learning ability. More specifically, interactions with the young are associated with a down-regulation in olfactory neurogenesis and an enhancement of neuroblast maturation. Our hypothesis is that fewer new neurons decrease cell competition in the olfactory bulb and enhance maturation of those new neurons selected to participate in the learning of the lamb odor. Further experiments will aim at understanding how these adult born neurons could be integrated to the neural network involved in maternal behavior.

AUTHOR CONTRIBUTIONS
Maïna Brus, Maryse Meurisse, Matthieu Keller and Frédéric Lévy designed and performed research, analyzed data and wrote the paper.