- Research article
- Open Access
Impaired neurogenesis, learning and memory and low seizure threshold associated with loss of neural precursor cell survivin
- Vanessa Coremans1,
- Tariq Ahmed2,
- Detlef Balschun2,
- Rudi D'Hooge2,
- Astrid DeVriese1,
- Jonathan Cremer1,
- Flavia Antonucci3,
- Michaël Moons1,
- Veerle Baekelandt5,
- Veerle Reumers5,
- Harold Cremer6,
- Amelia Eisch7,
- Diane Lagace8,
- Tom Janssens1,
- Yuri Bozzi4, 9,
- Matteo Caleo4 and
- Edward M Conway1, 10Email author
© Coremans et al; licensee BioMed Central Ltd. 2010
Received: 24 July 2009
Accepted: 5 January 2010
Published: 5 January 2010
Survivin is a unique member of the inhibitor of apoptosis protein (IAP) family in that it exhibits antiapoptotic properties and also promotes the cell cycle and mediates mitosis as a chromosome passenger protein. Survivin is highly expressed in neural precursor cells in the brain, yet its function there has not been elucidated.
To examine the role of neural precursor cell survivin, we first showed that survivin is normally expressed in periventricular neurogenic regions in the embryo, becoming restricted postnatally to proliferating and migrating NPCs in the key neurogenic sites, the subventricular zone (SVZ) and the subgranular zone (SGZ). We then used a conditional gene inactivation strategy to delete the survivin gene prenatally in those neurogenic regions. Lack of embryonic NPC survivin results in viable, fertile mice (Survivin Camcre ) with reduced numbers of SVZ NPCs, absent rostral migratory stream, and olfactory bulb hypoplasia. The phenotype can be partially rescued, as intracerebroventricular gene delivery of survivin during embryonic development increases olfactory bulb neurogenesis, detected postnatally. Survivin Camcre brains have fewer cortical inhibitory interneurons, contributing to enhanced sensitivity to seizures, and profound deficits in memory and learning.
The findings highlight the critical role that survivin plays during neural development, deficiencies of which dramatically impact on postnatal neural function.
In the adult, two major, well-defined neurogenic regions persist . In the subventricular zone (SVZ), neural precursor cells (NPCs) that arise mostly from the embryonic lateral ganglionic eminence (LGE) , continuously proliferate, and then migrate tangentially along the rostral migratory stream (RMS) towards the olfactory bulb (OB) where they differentiate into granular and periglomerular inhibitory interneurons . In the subgranular zone (SGZ) of the hippocampus, newborn NPCs also migrate, but for shorter distances, into the granule cell layer, where they become excitatory granule cells . From these neurogenic sites, adult-generated neurons can migrate to regions of brain injury , and establish synaptic contacts and functional connections [6, 7]. Decreased neurogenesis induced by prenatal or postnatal stresses is implicated in the development of seizures and disorders in learning, memory and cognition [8, 9]. The possibility of preventing onset or progression of these neural diseases by therapeutically enhancing neurogenesis [10–15] is prompting efforts to delineate the mechanisms and regulatory factors underlying NPC survival, proliferation, differentiation, migration and function. Indeed, numerous neuro-regulatory transcription factors, growth factors and receptors have been identified and characterized (reviewed in [16–19]). However, in spite of advances, effective approaches to prevent and treat diseases of the central nervous system are lacking, underlining the urgent need to develop better models to elucidate the molecular mechanisms regulating integration of new neurons in the developing and adult brain. Survivin is a member of the inhibitor of apoptotis protein (IAP) family, that also promotes the cell cycle and is a chromosome passenger protein [20, 21]. During embryonic development, it is expressed by several tissues, but is particularly prominent in the nervous system . Inactivation of the survivin gene in neuroepithelial cells early in development  results in massive apoptosis throughout the central nervous system, with total destruction of the architecture of the brain and lethality. The severity of this phenotype precluded investigators from delineating the specific role of neural precursor cell survivin on postnatal neural function.
Therefore, to elucidate the properties of survivin in neural development and function, we inactivated the survivin gene in NPCs in the late-midterm murine embryo and evaluated the effects post-natally. By this approach, we generated a unique in vivo mouse model in which reduced neurogenesis is associated with epilepsy and profound deficits in learning and memory. Pilot rescue studies suggest that embryonic administration of survivin may enhance neurogenesis. The findings highlight the critical role that survivin plays during neural development, deficiencies of which dramatically impact on postnatal neural function.
Survivin is expressed in precursor cells in the neurogenic areas of the brain
In both the SVZ (Figure 2J-L) and the SGZ of the DG (Figure 2M-O), >95% of survivin expressing cells were positive for the proliferation marker PCNA, while at both sites, 25-50% of PCNA positive cells expressed survivin. Thus, survivin expressing cells represent a subpopulation of the mitotically active cells. Doublecortin (DCX), present in immature, migrating neuroblasts  also overlapped with survivin in the SVZ, the RMS and the SGZ. However, similar to PCNA, not all DCX positive cells expressed survivin, indicating that survivin is restricted to a subpopulation of cells in the SVZ-RMS (not shown). Mature neuronal marker NeuN  immunoreactivity did not overlap with survivin, consistent with the lack of survivin expression by mature neurons (Figure 2C-E).
Overall, survivin expression is restricted during fetal development to NPCs in neurogenic regions of the telencephalon, of which a fraction populates the major neurogenic regions of the postnatal brain, i.e. the SVZ and the SGZ. Within these neurogenic regions, a subpopulation of NPCs continues to express survivin, which is downregulated once the cells differentiate into neurons. In both the embryo or adult, survivin is not detected in neurons in the cortex, OB, or hippocampus.
In vivo Prenatal Survivin gene inactivation
To study the in vivo role of NPC survivin, we generated mice in which the survivin gene is inactivated in the neurogenic regions of the brain prenatally. Mice expressing cre recombinase driven by the CamKIIα promoter [30, 31] were bred with mice in which the entire survivin gene is flanked by loxP sites . The resultant CamKIIα-cre:survivin lox/lox (referred to as Survivin Camcre ) mice were born in the expected Mendelian distribution, i.e. there was no evidence of embryonic lethality.
We confirmed previous reports of cre recombinase activity in the CAMKIIα-cre embryos and mice [30, 31] by breeding the CAMKIIα-cre mice with the ROSA26 reporter mice, followed by immunohistochemical detection of GFP. Cre recombinase activity at E12.5 was detected prominently in the ventral telencephalon (ganglionic eminences), but less in the dorsal telencephalon, and not in the eye (Additional file 1: Supplemental Figure S1). Postnatally, it was restricted to postmitotic NeuN positive neurons in the hippocampus and cortex, with lower levels in the striatum, thalamus, hypothalamus and amygdala . Postnatal cre expression was absent in NPCs in the SVZ and SGZ (Additional file 1: Supplemental Figure S2). Thus, cross-breeding with the Survivin lox/lox mice resulted in deletion of both survivin alleles in the neurogenic regions in the prenatal period (ganglionic eminences and neocortex).
Neurogenesis defects in Survivin Camcre embryos
Altered postnatal neurogenesis in Survivin Camcre mice
The hypoplastic OB and absent RMS, in concert with reduced expression of NPC survivin in the Survivin Camcre mice might be caused by decreased NPC proliferation, increased cell death, and/or deficits in migration. Accumulation of cells in the anterior SVZ of the Survivin Camcre mice was not observed, mitigating against a predominant migration defect. NPC proliferation, assessed 1 hr after a single dose of BrdU, revealed a significant reduction in BrdU labeled cells in the SVZ of the Survivin Camcre mice (132 ± 16 cells versus 57 ± 8 cells for control and Survivin Camcre mice, respectively, n = 4-5 mice per group, p = 0.002) (Figure 4E, F, M). Furthermore, both BrdU and DCX labeled cells were almost completely absent in the RMS, in striking contrast to the controls (Figure 4E-H). Cell death in the SVZ of the Survivin Camcre mice was also significantly increased (Figure 4K, L, N), as quantified by the number of tunel+ cells in the anterior SVZ (1.5 + 0.21/100 nucleated cells versus 3.5 + 0.46 tunel+ cells/100 nucleated cells, for control and Survivin Camcre mice, respectively, n = 4-5 mice per group, p = 0.004) (Figure 4N). In the RMS and OB, there were some tunel+ cells identified in the brains of the control mice, but not in Survivin Camcre mice, the latter likely due to the lack of precursor cells in this region.
As noted above, survivin expression in the SGZ of the DG was not appreciably diminished after cre excision. There was also no alteration in the number of proliferating or immature neurons in the SGZ, as quantified by BrdU labeling (1010 + 88 versus 905 + 75 cells in controls and Survivin Camcre mice, respectively, n = 4-5 mice per group, p = 0.39) (Figure 4I, J, O) or DCX immunoreactivity (not shown). Nor could we detect changes in tunel+ staining (2.3 + 0.18 versus 1.6 + 0.63 tunel+ cells/section in controls and Survivin Camcre mice, respectively, n = 3-4 mice per group, p = 0.30) (Figure 4P).
In summary, striking survivin-dependent defects in neurogenesis are evident postnatally in the RMS and OB of Survivin Camcre mice, due to a combination of increased SVZ NPC apoptosis and diminished cellular proliferation. Despite the fetal abnormalities, and in striking contrast to the RMS-OB, there were no obvious structural defects or alterations in hippocampal neurogenesis in the Survivin Camcre mice that had no appreciable reduction in survivin expression within the hippocampus.
Embryonic survivin administration increases neurogenesis
In pilot studies, we assessed whether prenatal administration of survivin to increase expression in NPCs could promote neurogenesis. E12.5 control Survivin lox/lox and Survivin Camcre embryos received an intracerebroventricular injection in utero with the lentiviral vector pCHMWS-eGFP-T2A-SRV140 (survivin vector) or pCHMWS-eGFP-T2A-Fluc (control vector). At P21, immunohistochemical analysis of the control Survivin lox/lox mice that received the survivin vector revealed an increased number of embryonic precursor cell-derived cells in the OB as compared with the control vector (Additional file 1: Supplemental Figures S3A, B). With Survivin Camcre embryos, the survivin vector did not apparently reverse the OB hypoplasia when examined at P21, but there were notably more embryonic precursor cell-derived cells in the OB of 3 out of 3 Survivin Camcre mice that received the survivin vector, as compared with the 2 Survivin Camcre mice that received the control vector (Additional file 1: Supplemental Figures S3C, D). Overall, these preliminary findings suggest that enhanced expression of NPC survivin may increase neurogenesis.
Survivin Camcre mice have a thinner cortex with fewer GABAergic interneurons and a lower seizure threshold
Neuropeptide Y (NPY) is a multifunctional peptide that is expressed in GABAergic interneurons, regulates pre-synaptic excitatory transmission in the DG, and has anti-epileptic properties . Hilar NPY interneuron degeneration, ectopic expression of NPY in mossy fibers, and axonal sprouting are common features of limbic hyperexcitability . Due to the increased seizure activity in the Survivin Camcre mice, we examined NPY expression under both basal conditions (saline treatment) and following induction of seizures (KA 20 mg/kg i.p.). The number of hilar NPY+ interneurons was not different between saline-treated control and Survivin Camcre mice (490 ± 17 versus 398 ± 53 cells/mm2, for control and Survivin Camcre mice, respectively; n = 4-5 mice per group, p = 0.11). However, two weeks after 20 mg/kg KA treatment, there were significantly fewer NPY+ cells in the hilus of the Survivin Camcre mice (446 ± 22 versus 306 ± 65 cells/mm2 for control and Survivin Camcre mice, respectively; n = 6-9 mice per group, p = 0.032). Moreover, ectopic NPY expression in mossy fibers was readily detected in 3 out of 4 saline-treated Survivin Camcre mice but not in any of the corresponding controls (n = 5) (Figure 6C, D). This effect became more prominent after KA (5/6 Survivin Camcre mice as compared to 0/9 controls). In 2 of these Survivin Camcre mice, we furthermore observed ectopic NPY immunoreactivity in the supragranular layer, likely reflecting sprouting of mossy fibers (not shown).
Since seizure activity modulates hippocampal neurogenesis, we also evaluated the seizure-induced neurogenic response of the control and Survivin Camcre mice. The volumes of the GCL and the hilus were not different between control and Survivin Camcre mice (see above), and KA had no effect on that relationship (data not shown). To assess cell proliferation, BrdU was injected 3 days after KA or saline injection, and mice were sacrificed 1 day later. After saline injection, the total number of SGZ BrdU+ cells was not different in control and Survivin Camcre mice (648 ± 58 cells versus 705 ± 99 cells in controls and Survivin Camcre mice, respectively, n = 4 mice per group, p = 0.64) (Figure 6E). Compared to saline treated controls, KA treated mice exhibited an increase in the number of BrdU+ cells in the SGZ after KA injection. However, the neurogenic response was significantly dampened in the Survivin Camcre KA treated mice compared to control KA treated mice (3578 ± 392 cells versus 1955 ± 233 cells for controls and Survivin Camcre mice, respectively, n = 5 mice per group, p < 0.001) (Figure 6E). Numbers of BrdU+ cells remained reduced 2 weeks following KA in the Survivin Camcre mice as compared to controls (data not shown). Thus, despite the higher seizure scores following KA in the Survivin Camcre mice, there was less seizure-induced neurogenesis in the Survivin Camcre versus the control mice.
Survivin Camcre mice exhibit learning and memory defects
Adult Survivin Camcre mice exhibited several defects that may contribute to disorders in behavior and cognition, including reduced SVZ-RMS-OB neurogenesis [38, 39], OB hypoplasia , diminution of cortical GABAergic neurons, and seizures. We therefore evaluated the effects of depleting NPCs of survivin by subjecting the Survivin Camcre and matched controls to a range of behavioral studies.
There was no difference in body weight between the Survivin Camcre and control mice at the start of behavioral testing (21.6 ± 0.6 gm versus 20.1 ± 0.6 gm for the Survivin Camcre and controls, respectively, p = 0.081), and the Survivin Camcre mice had normal visual and auditory skills, grip strength, rotarod performance, pain response and cage activity (Additional file 1: Supplemental Figures S4, S5; Additional file 2: Supplemental Methods and Results).
The Survivin Camcre mice exhibited a significant impairment in passive avoidance learning. During the initial training trial, there was no difference in step-through latencies (12.5 ± 4.5 versus 13.9 ± 1.8 sec, Survivin Camcre and control mice respectively, p = 0.783). However, during testing, the Survivin Camcre mice demonstrated significantly shorter latency to enter the dark compartment than the controls (235 ± 27 versus 71 ± 24 sec for control and Survivin Camcre mice, n = 12, p < 0.001) (Additional file 1: Supplemental Figure S6), consistent with poor associative memory of aversive stimuli.
We examined auditory and contextual fear memory using an auditory cue as the conditioned stimulus (CS), and a foot shock as an aversive stimulus. Freezing times in baseline, pre-US, post-US, and pre-CS trials were not different between the groups (Figure 7B). However, Survivin Camcre mice exhibited significantly less freezing response in the context and auditory cue (CS) trials compared to control mice (context: 25.7 ± 5.5 versus 68.2 ± 4.5; auditory: 34.3 ± 9.0 and 84.4 ± 7.8, respectively for Survivin Camcre and control mice, n = 12 mice per group, p < 0.001) (Figure 7B).
In the first probe trial performed after 5 days of training, the control mice already had a preference for the target quadrant compared to adjacent 1 (p = 0.002) and opposite (p = 0.02) quadrants, whereas the Survivin Camcre mice had no preference at all (p = 0.46) (Figure 8C). In the second probe trial after 10 days of training, the control mice continued to show a strong preference for the target quadrant compared to all other quadrants (p < 0.001), whereas the Survivin Camcre mice equally favoured the target and adjacent 2 quadrants (p = 0.60) versus the other 2 quadrants (p < 0.05) (Figure 8D, E). Since the Morris water maze test is a stress that might alter neural cell proliferation, we also quantified the number of Ki67+ cells in the dentate gyrus of the Survivin Camcre mice (n = 4) and the corresponding littermate controls (n = 4) after the probe trials. There was no significant difference in the number of Ki67+ cells between the two groups (534 + 49 cells versus 480 + 28 cells in controls versus Survivin Camcre mice, respectively, p = 0.378).
Overall, the Survivin Camcre mice exhibited exploratory behavioral abnormalities, with global deficits in various forms of learning and memory.
In this report, we show that survivin is prominently expressed in the neurogenic regions of the embryonic mouse brain, and that its expression by a subpopulation of NPCs is maintained postnatally in the two key sites of adult neurogenesis - the SVZ and the SGZ. Lack of expression of survivin in the NPCs during embryonic development, was associated with profound SVZ-RMS-OB postnatal defects in neurogenesis and loss of interneurons, manifest by major deficits in learning and memory, and heightened sensitivity to seizures. Prenatal administration of survivin in the brain enhanced neurogenesis in the SVZ-RMS-olfactory system. Our findings position survivin as a central player in regulating neurogenesis during embryonic development, alterations of which impact on postnatal brain function.
The embryonic forebrain, the telencephalon, consists of two parts. The dorsal aspect is the origin of glutamatergic excitatory neurons of the cerebral cortex and hippocampus . The ventral part, comprising the ganglionic eminences, gives rise to the basal ganglia. The LGE provides neurons for the striatum , interneurons of the olfactory bulb (OB) , and most adult SVZ NPCs . The MGE is the source of most neocortical  and hippocampal interneurons , as well as striatal interneurons. At E12.5, survivin is widely expressed in the neurogenic region of the ventral and dorsal telencephalon. Since cre recombinase expression in the CamKIIα-cre mice is low in the dorsal telencephalon, generation of principal glutamatergic neurons was largely unaffected in the adult, and the overall integrity of the hippocampus and cortex was maintained, albeit the latter was thinner. In contrast, the number of cortical GABAergic neurons, which arise primarily in the ganglionic eminences and comprise 25-30% of cortical neurons, was significantly reduced in the Survivin Camcre mice. This reduction may have been further contributed to by the paucity of SVZ NPCs, recently shown to be a continuous postnatal source of GABAergic interneurons in the cortex .
Imbalances in inhibitory and excitatory circuits due to decreases in numbers of interneurons, are well known to be associated with seizures in humans and experimental animal models [46, 47]. This was clearly evident in the Survivin Camcre mice which, even under naïve conditions, displayed spontaneous, generalized tonic-clonic motor seizures, a phenotype that was more dramatically revealed following challenge with KA. Indeed, Survivin Camcre mice showed a rapid and consistent generalization of seizures at KA doses that normally result in focal hippocampal epileptic activity . Thus, a defect in the cortical inhibitory system may explain the higher susceptibility to generalized convulsions in the Survivin Camcre mice.
Our studies demonstrate that the loss of a subpopulation of NPCs in the SVZ of neonatal and adult Survivin Camcre mice, with resultant near-absence of the RMS and OB, was due to a combination of increased apoptosis and decreased cellular proliferation of NPCs in the corresponding embryonic neurogenic region (ganglionic eminences). Indeed, this is in line with the fact that survivin is a pro-survival molecule with the capacity to inhibit apoptosis and to promote the cell cycle and mitosis (reviewed in ). Somewhat surprisingly, in spite of profound disturbances in neurogenesis in the SVZ, we did not detect baseline changes in neurogenesis in the SGZ of the DG in the Survivin Camcre mice, or significant loss of survivin expressing DG NPCs. Although this may be due to cre recombinase inefficiency, the finding may also be due to the embryonic origin of SGZ NPCs being different from the SVZ NPCs, which still remains to be clarified . There is however, a defect in SGZ neurogenesis in the Survivin Camcre mice that is only evident under stress conditions. This may mean that the baseline source(s) of SGZ NPCs is different from that recruited during stress, an hypothesis that requires testing. In the Survivin Camcre mice, the neurogenic response was significantly impaired as compared to the controls after KA-induced seizures. Alterations in GABA signaling in the Survivin Camcre mice may be implicated , but other factors that are important in maintaining the function of the neurogenic niche in the hippocampus could also contribute to the dampened response . Further study to identify those that are relevant is ongoing.
Although the integrity of the hippocampus was apparently maintained under baseline conditions, upon testing, the Survivin Camcre mice exhibited striking defects in memory and cognition, that are consistent with hippocampal dysfunction. In fact, the behavioral abnormalities were associated with a significant impairment of long-term potentiation (LTP) in the CA1 region of the hippocampus (not shown), a finding that frequently is associated with poor memory, and often with increased epileptic activity. As with the seizure disorder, a loss of cortical inhibitory interneurons likely contributed to the behavioral abnormalities and cognitive defects in the Survivin Camcre mice. We also cannot exclude a contribution of suboptimal neurogenic responses to the behavioral phenotype, as neurogenic defects in both the SGZ and SVZ have been implicated in memory, cognition, mood, and hippocampal-dependent learning . Moreover, olfactory bulbectomy in rodents impairs neurogenesis in both the SGZ and the SVZ, disrupts normal hippocampal LTP, and causes significant deficits in learning and memory. Thus, the OB, which sends projections to the hippocampus , also plays a role in normal behavior and cognition [12, 13, 40]. Indeed, since the Survivin Camcre mice have major defects in neurogenesis, as well as notable hypoplasia of the OB, all of which are associated with epileptic activity and major alterations in behavior, it is reasonable to consider that the effective lack of an OB exacerbates the loss of SVZ and possibly SGZ NPCs, which in turn, contributes to the behavioral abnormalities and enhanced seizure activity.
We have established that prenatal expression of survivin in neurogenic regions of the developing brain plays a key role in learning and memory and in determining seizure susceptibility. Prenatal stresses are recognized to suppress postnatal neurogenesis that in turn, induces behavioral abnormalities in the neonate and adult [8, 9]. While the underlying molecular mechanisms have not been delineated, it is reasonable to consider that alterations in embryonic NPC survivin expression might contribute to those phenotypic changes. Pilot data indicate that prenatal administration of survivin can enhance neurogenesis in the olfactory system. We do not yet know whether the resultant new neurons differentiate or integrate, or whether the SGZ is also affected. Nonetheless, the findings are promising, supporting the critical nature of this molecule, and its potential as a therapeutic target. Our mouse model provides the opportunity to elucidate the relevance of survivin-expressing NPC subpopulations in vivo in response to a range of environmental stresses, and genetic or epigenetic factors.
Transgenic mice and genotyping
Mice that express Cre recombinase driven by the promoter of the gene for calmodulin-dependent protein kinase IIα (CamKIIα) [30, 31] (gift of Dr. G. Schütz, Heidelberg, Germany) were bred with mice in which the survivin gene is flanked by loxP sites . The resulting offspring that were heterozygous for Cre and homozygous for floxed survivin (Survivin lox/lox ) (hereafter referred to as Survivin Camcre mice) were compared to littermate control mice which did not express Cre and were Survivin lox/lox . Survivin lox/lox embryos and adults were not different from Survivin lox/wt , Survivin wt/wt or CamKIIα-cre:survivin lox/wt mice. Mice were maintained on a C57B/6:Swiss:129svj 75:12.5:12.5 background. Genotyping of tail DNA was performed by PCR as previously reported [30, 32]. Mice were group-housed in standard mouse cages in a room with a 12 h light-dark cycle and ad libitum access to food and water and all animal experiments were approved by the ethics committee of the University of Leuven.
BrdU labeling and quantification
Adult mice and pregnant females were injected intraperitoneally (ip) with 5-bromo-2-deoxyuridine (BrdU, Sigma Aldrich, Bornem, Belgium) at a concentration of 50 mg per kg body weight. For the analysis of the embryos, 1 hour after injection of BrdU, pregnant females were killed by cervical dislocation, after which the embryos were harvested, placed in ice-cold PBS, and then fixed in 4% paraformaldehyde (Para) for cutting 20 μm cryo sections using a microtome/cryostat (HM550, Microm, Walldorf, Germany). For analysis of adults, mice were anesthetized with sodium pentobarbital at 1 hour (unless stated otherwise) after BrdU and perfused transcardially with 0.9% NaCl, followed by fixation with 4% paraformaldehyde. Brains were dissected and post-fixed overnight at 4°C and 40 μm tissue sections were prepared using a vibrating microtome (HM650V, Microm, Walldorf, Germany).
The number of BrdU+ cells in the adult dentate gyrus (DG) was quantified using a modified version of the optical fractionator method  with Stereo Investigator software (MicroBrightField, Colchester, VT, USA). Cells were counted with a 40× objective on every sixth section through the entire rostrocaudal extension of one half of the DG, restricted to the subgranular zone (SGZ) . The number of BrdU+ cells in the SVZ of one lateral ventricle was counted with a 40× objective on 1 coronal section (bregma level + 0.14 mm) per animal.
Immunostaining protocols were optimized for the different tissue preparations and antibodies. In general, tissue sections were treated with 1% H202 in PBS/methanol for 15 min, incubated in 5% serum for 30 min, and incubated overnight at 4°C in following primary antibodies: rabbit anti-neuropeptide Y (NPY) antibody (1:5000, Bachem, UK); mouse anti-NeuN (1:500, Chemicon, Hofheim, Germany); mouse anti-PCNA (1:1000, Chemicon, Hofheim, Germany); rabbit anti-DCX (1:500, Cell Signaling, MA, USA); rat anti-BrdU (1:500, Immunologicals Direct, Oxford, UK); chicken anti-GFP (1:3000, Aves, Oregon, USA); and rabbit anti-Cre recombinase (1:3000, gift from Dr. Schütz, Heidelberg, Germany); rabbit anti-Ki67 (1:1000 Monosan, Uden, The Netherlands). After washes, the corresponding biotinylated secondary antibody was added for 1 hour and the signal was amplified using the Vectastain Elite ABC kit (Vector Laboratories, CA, USA). Peroxidase activity was detected with 3,3'-diaminobenzidine (DAB peroxidase substrate tablet set, Sigma Aldrich, Bornem, Belgium). For fluorescent staining, Alexa-conjugated secondary antibodies (Molecular Probes, Leiden, The Netherlands) were used. BrdU staining was performed as reported previously .
In situ hybridization
Digoxygenin (DIG)-labeled RNA probes for Dlx1 , Dlx5 , Ngn2 (gift from Dr. A. Simeone), GAD65 , GAD67AE  and vGLUT1 (Allen Institute for Brain Science) were generated using the DIG RNA Labeling Kit (Roche Diagnostics, Basel, Switzerland), according to the manufacturer's instructions. GAD65 and GAD67AE probes were mixed to detect the total number of GABAergic interneurons. For survivin riboprobes, full-length murine survivin cDNA was cloned into the pcDNA3 plasmid vector (Invitrogen, CA, USA) , and linearized for generation of antisense and sense probes using Sp6 RNA polymerase or T7 polymerase, respectively. In situ hybridization and combined immunohistochemistry protocols were adapted from those reported [33, 62] and completed on 20 μm cryostat or 40 μm vibratome sections.
Measurement of granular cell layer (GCL) volume and hilar volume
Coronal sections through the DG were stained with cresyl violet. Pictures were taken at 4× magnification, and the area of the GCL and the hilus was determined off line using Metamorph software (Molecular Devices, Sunnyvale, CA). Volumes were calculated and expressed in mm3.
Quantification of apoptosis (tunel+ cells)
Detection of cellular apoptosis in 10 μm coronal paraffin sections, prepared using a HM360 microtome (Microm, Walldorf, Germany), was accomplished using the ApopTag Peroxidase In Situ Apoptosis Detection Kit (Chemicon, Hofheim, Germany). The number of tunel+ cells was counted with a 40× objective. The anterior subventricular zone (SVZa) was analyzed at level bregma +0.98 mm and the data are presented as the number of tunel+ cells per 100 nucleated cells. The subgranular zone (SGZ) was analyzed at bregma levels -1.34/-1.70/-2.46/-2.80 mm and the data are presented as the number of tunel+ cells per section.
Quantification of inhibitory and excitatory neurons
Numbers of neurons and interneurons were quantified hemilaterally on coronal vibratome sections at 4 bregma levels (-1.34/-1.70/-2.46/-2.8 mm). GAD65/67+ cells were counted with a 10× objective in the hilus plus the granule cell layer, and in the parieto/temporal cortex, in a 1.4 mm wide band from the white matter to the pial surface. vGLUT1+ cells in the parieto/temporal cortex were counted with a 20× objective in a 0.7 mm wide band. NPY+ cells in the hilus were counted with a 20× objective on every sixth section (40 μm thick). Results are presented as the number of cells per mm2.
Quantification of Ki67 positive cells
Ki67 positive cells in the SGZ were counted hemilaterally with a 40× objective on every third 40 μm section between bregma levels -1.34 and -2.8 mm. The number of counted cells was multiplied by 3 to obtain the total number of Ki67 positive cells.
Intracerebroventricular (ICV) injection of lentiviral vector in embryos
Lentiviral vectors were prepared, encoding enhanced green fluorescent protein (eGFP) and survivin separated by a T2A sequence starting from pCHMWS-eGFP-T2A-Fluc (gift from Dr. V. Baekelandt, KULeuven). The Fluc fragment was removed from pCHMWS-eGFP-T2A-Fluc using Bam HI and Mlu I and replaced by the cDNA encoding full-length murine survivin. Survivin expression from this vector was confirmed by Western blot analysis of lysates from transfected COS cells. Human immunodeficiency virus type 1 (HIV-1)-derived lentiviral vectors were produced by a standard protocol. The viral vector was mixed with Fast Green dye (0.005% final concentration, Sigma-Aldrich, Bornem, Belgium), which allowed visualization of the distribution of the viral vector in the cerebral ventricles after injection. Pregnant mice (stage E12.5) were anesthetized with 50 mg/ml ketamine, 2% xylazine in saline and placed supine on a heating pad. A 2-cm midline incision was made through the skin and the abdominal wall. The uterine horn was drawn out through the hole onto gauze, and with the uterus transilluminated, a 35 gauge needle (beveled NanoFil needle, World Precision Instruments, FL, USA) was inserted into the ventricle, and 1 μl viral vector solution was injected at a speed of 406 nanoliters per second using a Mycro4® MicroSyringe Pump Controller (World Precision Instruments, FL, USA).
Seizures in adult male mice were evoked by ip administration of kainic acid (KA) (Sigma, MO, USA). KA was dissolved in saline and injected at 20 or 30 mg/kg body weight. Saline-injected animals were used as controls. Seizure severity was quantified by an observer blind to the mouse genotype using the following scale [48, 63]: stage 0, normal behavior; stage 1, immobility; stage 2, forelimb and/or tail extension, rigid posture; stage 3, repetitive movements, head bobbing; stage 4, rearing and falling; stage 5, continuous rearing and falling; stage 6, severe whole-body convulsions; and stage 7, death. For each animal, seizure severity was scored every 10 min over a period of 2 hours after KA administration. The maximum score reached by each animal over the entire observation period was used to calculate the maximum seizure score for each treatment group. Seizure severity over the 2 hour observation period was calculated for each mouse as the area under the seizure score versus time curve (AUC), and the average AUC was calculated for each treatment group.
Behavioral tests were initiated when the mice were 3-4 months of age, n = 12-25 per group. Neuromotor, exploration, and learning tests were performed in the following sequence: cage activity, grip strength, rotarod, open field, elevated plus maze, Morris water maze, passive avoidance. Contextual fear conditioning was performed on a separate group of mice. Animals were tested during the light phase of the light-dark cycle. All studies were performed by observers who were blinded to the genotype of the mice.
Open field exploratory activity was assessed in a 50 cm × 50 cm arena using EthoVision video tracking and software (Noldus, Wageningen, The Netherlands). Mice were individually placed in a specific corner of the open field, and were allowed a 1 min adaptation period. The path was recorded for 10 min to measure dwells and entries in different parts of the field. Measures included total path length, percentage path length in the center circle (diameter 30 cm), entries into the four corner squares, entries into the center, time spent in the center versus periphery, latency of first center approach, and frequency of rearing.
The elevated plus maze [64, 65], to evaluate anxiety-like behavior, had two open arms (21 cm × 5 cm) and two closed arms of the same size, with high side walls, and was raised 30 cm above the table. Each mouse was placed in the central square of the maze, facing one of the closed arms. After 1 min, exploratory behavior was recorded automatically during a 10 min period using five infrared beams, connected to an activity logger. For each mouse, the number of arm entries, percentage of open arm entries, and percentage time spent in the open arms was assessed.
Passive avoidance (aversive) learning  was tested in a two-compartment step-through box. Animals were adapted to the dark for 30 min, and then placed into a small illuminated compartment. After 5 s, a sliding door leading to the large dark compartment was opened. Upon entry, the door was closed and the animal received an electric foot shock (0.3 mA, 1s). Twenty-four hours later, the animals were placed again in the light compartment and the latency to enter the dark compartment was measured up to 300 s, to evaluate memory of the foot shock.
Contextual and auditory-cued fear conditioning [67, 68] was tested in a Plexiglas chamber with a grid floor through which a foot shock could be administered. Mice were trained and tested on 3 consecutive days: On the day 1, the mice were individually placed in the testing chamber and allowed to adapt for 5 min. On the day 2, the animals were allowed to explore the testing chamber for 2 min, after which an auditory cue (conditioned stimulus, CS) was presented for 28 s, followed by a foot shock (0.3 mA, 2 s; unconditioned stimulus, US). The time (%) spent freezing during the first 2 min and 28 s is the pre-US score. The mice were then allowed to explore again for 1 min, and the auditory cue and shock were again presented, followed by another 2 min exploration (post-US score). On day 3 (24 hours after training), mice were returned to the same context in which training occurred, and freezing behavior was recorded for 5 min (context test). Ninety min later, freezing was recorded in a novel environment (the grid floor was hidden and a scent of peppermint was added) for 3 min without the auditory cue stimulus (pre-CS test). Finally, the auditory cue was turned on, and the time spent freezing was recorded over the following 3 min (cue CS test).
Spatial learning and memory were examined in a Morris water maze [69, 70], which consisted of a circular tank (32.5 cm high × 150 cm diameter), filled with water (up to 16 cm deep), maintained at 26°C, and made opaque with nontoxic white paint. A circular platform (15 cm high × 15 cm diameter) remained hidden 1 cm below the water surface at a fixed position. The room housing the tank had a permanent display of distal extra-maze cues. The swim paths of the mice were recorded using computerized EthoVision video tracking equipment. During training (acquisition phase), the mice were given four swim trials daily with an inter-trial interval of 15 min. The mice were placed in the pool facing the wall at one of four starting positions. If the animal did not find the platform after 120 s, it was guided there by the experimenter. Mice were allowed to rest 15 s on the platform before being removed from the pool. Latency to reach the platform, path length, and average swim speed were recorded. After five training days, there were two days of rest, followed by another five days of training and two days of rest. Probe trials were performed on days 8 and 15. During probe trials, the platform was removed and each animal was monitored once for 100 s, recording the percentage time in each quadrant. Over all the trials, one Survivin Camcre mouse floated with a speed of < 5 cm/s, and this mouse was therefore excluded from the study.
Data are presented as the mean ± SEM. Data were analyzed with a two tailed t-test, Mann-Whitney Rank Sum Test, one way ANOVA, or two way repeated measures ANOVA. All statistical tests were performed at a significance level of 0.05.
This work was supported in part by the Fonds voor Wetenschappelijk Onderzoek (FWO), Belgium. YB was supported by grants from Parents Against Childhood Epilepsy (PACE, Inc.), NY, USA, and the Italian National Research Council (CNR - "Ricerche Spontanee a Tema Libero" - RSTL Program).
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