Reelin immunoreactivity in neuritic varicosities in the human hippocampal formation of non-demented subjects and Alzheimer’s disease patients
© Notter and Knuesel; licensee BioMed Central Ltd. 2013
Received: 2 May 2013
Accepted: 10 June 2013
Published: 26 June 2013
Reelin and its downstream signaling members are important modulators of actin and microtubule cytoskeleton dynamics, a fundamental prerequisite for proper neurodevelopment and adult neuronal functions. Reductions in Reelin levels have been suggested to contribute to Alzheimer’s disease (AD) pathophysiology. We have previously reported an age-related reduction in Reelin levels and its accumulation in neuritic varicosities along the olfactory-limbic tracts, which correlated with cognitive impairments in aged mice. Here, we aimed to investigate whether a similar Reelin-associated neuropathology is observed in the aged human hippocampus and whether it correlated with dementia status.
Our immunohistochemical stainings revealed the presence of N- and C-terminus-containing Reelin fragments in corpora amylacea (CAm), aging-associated spherical deposits. The density of these deposits was increased in the molecular layer of the subiculum of AD compared to non-demented individuals. Despite the limitation of a small sample size, our evaluation of several neuronal and glial markers indicates that the presence of Reelin in CAm might be related to aging-associated impairments in neuronal transport leading to accumulation of organelles and protein metabolites in neuritic varicosities, as previously suggested by the findings and discussions in rodents and primates.
Our results indicate that aging- and disease-associated changes in Reelin levels and proteolytic processing might play a role in the formation of CAm by altering cytoskeletal dynamics. However, its presence may also be an indicator of a degenerative state of neuritic compartments.
KeywordsReelin Axonal and dendritic varicosities Hippocampal formation Aging Alzheimer’s disease
The increase in human life expectancy has entailed a pronounced rise in age-associated neurodegenerative diseases with the most prominent form being Alzheimer’s Disease (AD), affecting over 26 million people worldwide . Despite extensive research performed during the past, no efficient therapies for this progressive brain disease are currently available. Most of the scientific approaches were based on the “amyloid cascade hypothesis” that placed the β- and γ-secretase-generated amyloid-β peptides as causal factors of the pathophysiology [2, 3]. While this may hold true for the familial form of AD with its dominant mutations in either the amyloid precursor protein (APP, [4, 5]) or presenilin 1 and 2 (PSEN; [6, 7]) genes, the initiating trigger of the aging-associated, sporadic form of AD is still unknown. Based on recent experimental evidence demonstrating that multiple exposures to viral-like immune challenges are sufficient to induce AD-like neuropathology in aged wild-type mice , we were able to identify a crucial trigger and to reconstruct the temporal-spatial sequence of pathophysiological changes that characterize the earliest disease stages. The integration of experimental data of the last three decades enabled us to substantiate and expand our findings to propose a cellular mechanism of the neuropathological changes and its progression across interconnected brain areas that characterize sporadic AD [9, 10]. The new hypothesis highlights the detrimental effect of chronic inflammatory conditions on basic cellular functions in long-projection neurons of the olfactory-limbic system during aging. The selective vulnerability of these neurons includes inflammation-induced impairments in the Reelin-mediated signaling pathway across these fundamental neuronal networks . By binding to the apolipoprotein E receptor 2 (ApoER2) and the very low density lipoprotein receptor (VLDLR) [11, 12], the extracellular matrix protein Reelin regulates cytoskeletal dynamics essential for migrating neurons [13, 14], developing neurites [15, 16] and adult spines [17, 18]. The signaling pathway involves cytosolic cascades that ultimately inhibit the major tau kinases, Glycogen Synthase Kinase 3β (GSK3β) and Cyclin-Dependent Kinase 5 (CDK5) [19–21], as well as activates the LIM1 kinase and increases n-cofilin phosphorylation  to modulate both the microtubule and actin cytoskeleton, respectively. Engaging the same signaling pathway, Reelin also exerts a crucial role at adult synaptic sites by modulating NMDA receptor functions [23–27]. Recent experimental evidence further highlighted that Reelin maintains synaptic plasticity by competing with ApoE4 to prevent the latter from sequestering NMDA, AMPA, and ApoER2 receptors in intracellular compartments . In line with the well described aging-associated synaptic impairments, Reelin expression has been shown to decline in aging rodents, correlating with hippocampus-dependent learning and memory performance [28, 29]. Furthermore, Reelin accumulates within neuritic varicosities in both rodents and non-human primates [28, 30], possibly related to the aging associated decrease in Reelin signaling and its protective modulation of cytoskeleton dynamics . In agreement with these experimental data, recent genome wide association studies performed in elderly, non-demented individuals identified three single nucleotide polymorphisms (SNPs) in the Reelin gene that significantly correlated with increased Tau phosphorylation and concomitant appearance of neurofibrillary tangles (NFTs) . Moreover, immunohistochemical investigations involving human brains revealed significantly decreased levels of Reelin in patients with mild cognitive impairments (MCI) and AD compared to non-demented subjects [32, 33]. Further evidence of altered Reelin-mediated signaling in AD was provided by genetic  and biochemical studies [35, 36] suggesting that decreased Reelin production may contribute to the initiation and progression of AD by impairing synaptic functions, cytoskeleton stability and proper axonal transport. Interestingly, alterations in Reelin glycosylation, its proteolytic cleavage and degradation, as well as changes in its mRNA stability were shown to be changed in brain homogenates of AD patients [35, 36], further highlighting the importance of proper Reelin signaling during aging.
Here, we investigated the localization and levels of Reelin in the postmortem human brain by selectively assessing its putative accumulation in neuritic varicosities in non-demented elderly and patients with AD by immunohistochemistry and unbiased stereological analyses. Complementary immunoblotting of corresponding CSF samples was performed to examine potential alterations in Reelin proteolytic processing.
Details of human postmortem brain tissue included in the analyses
Brain weight (g)
Renal insufficiency and decompensatio cordis
Squamous cell carcinoma of the left maxilla
Multi organ failure after a ruptured abdominal aneurysm
Pneumonia with dehydration
Organ failure due to dehydration
The following antibodies were used: mouse monoclonal anti-Reelin recognizing the N-terminus (clone G10, MAB 5364, Milipore 1:200 and clone 142, MAB 5366, Milipore 1:200); mouse monoclonal anti-Reelin antibodies (C-terminal subrepeats 8A and 8B, 1:200 each, kindly provided by Professor André Goffinet, University of Louvain Medical School, Brussels, Belgium); rabbit polyclonal anti-amyloid β (1-40/42), (AB5076; Millipore, 1:200); mouse monoclonal anti APP-A4, clone 22C11 (MAB348 Millipore, 1:500), mouse monoclonal anti-PHF Tau (clone AT100, MN1060; Thermo Scientific, 1:1000); polyclonal rabbit anti-Tau pS422 (44-764G, Invitrogen,1:1000); rabbit polyclonal anti-GFAP (Z0334, DAKO, 1:2500); mouse monoclonal anti-GFAP (MAB 360, Millipore, 1:10’000); rabbit polyclonal anti-Iba1 (019–19741, Wako Pure Chemical, 1:2000); polyclonal rabbit anti-MAP2(26*) (microtubule-associated protein 2) (AB5622, Chemicon, 1:2000); polyclonal rabbit anti-Synapsin-1 (A-6442, Molecular Probes, 1:1000); polyclonal rabbit anti-Synaptophysin (A010, DAKO, 1:500); rabbit polyclonal anti-α-Synuclein (ab52168, Abcam, 1:250); mouse monoclonal anti-CD 45 (M0701, 1:100, kindly provided by Prof. Karl Frei, Department of Neurosurgery, University Hospital Zürich, Switzerland).
Sections were deparaffinized in xylol (3 times for 3 minutes), rehydrated in decreasing ethanol concentrations (twice 100%, 96%, 70% and twice dH2O for 3 minutes each) and washed in 50 mM Tris-saline, pH 7.4 (1×Tris). The following antigen retrieval techniques were applied: two 5-minute citrate buffer microwave irradiations at 800 W (to visualize Reelin-producing cells with anti-Reelin 142 antibody, see Additional file 1: Figure S1), 10-minute citrate buffer microwave irradiation at 80°C, either followed by a 10-minute pepsin treatment  or not, and a 5-minute 95% formic acid treatment (to visualize Aβ plaques). Furthermore, a 10-minute 3% H2O2/methanol treatment was used to block endogenous peroxidase reactivity. Sections were then incubated for 30 min in blocking solution (1×Tris containing 5% normal horse serum, 5% normal goat serum, 4% of BSA), transferred to the primary antibody solution (diluted in 1×Tris, containing 2.5% normal horse serum, 2.5% normal goat serum, 2% BSA) for overnight incubation at 4°C. Sections were washed in 1×Tris and incubated for 30 minutes with biotinylated secondary antibodies (1:200 in same solution as used for primary antibodies). After 3 washes in 1×Tris, sections were processed for the DAB immunoperoxidase using the Avidin-Peroxidase-Complex (ABC, Vectastain Elite kit) staining techniques as described previously [40–42]. To visualize cell nuclei and corpora amylacea (CAm), sections were counterstained with Harry's Hematoxylin (HHS-128, Sigma-Aldrich; very weak staining of CAm) or Ehrlich’s Hematoxylin (100 ml dH2O, 100 ml 96% ethanol, 100 ml glycerol, 10 ml glacial acetic acid, 2 g hematoxylin, 3 g kalialaun, 0.4 g sodium jodate; strongly reacts with CAm , kindly provided by Charlotte Burger, University of Zurich, Institute for Anatomy). In brief, sections were incubated for 2 minutes in the Hematoxylin solution, rinsed in tap water, differentiated in acetic alcohol and blued in running tap water for 10 minutes, dehydrated and coverslipped with Eukitt (Erne Chemie). Toloidinblue staining was performed according to standard protocols.
The protocol was identical to the described immunoperoxidase staining with the following changes: All washing steps and antibody dilutions were done in phosphate-buffered saline (PBS) at pH 7.4. Sections were blocked for 1 hour and incubated for 45 min with the secondary antibodies (coupled to either Alexa Fluor488 or Cy3 (dilution 1:1000 and 1:500, respectively; Molecular Probes, Invitrogen). To reduce lipofuscin-associated auto-fluorescence in aged cells, sections were incubated in 0.1% Sudan Black (Carl Roth GmbH) dissolved in 70% methanol for 2 minutes, briefly washed with PBS and air-dried . Sections were then coverslipped with Dako-DAPI solution (Dako) or ProLong Gold Antifade reagent (Invitrogen) to visualize cell nuclei.
Microscopy and image acquisition
Immunoperoxidase-stained sections were scanned and visualized with an automated upright slide-scanning microscope (Zeiss) in brightfield mode and the Pannoramic Viewer 220.127.116.11 (3D Histotech Ltd), respectively. High magnification images were acquired with a brightfield light microscope (Axioscop 2, Zeiss) connected to a digital camera (AxioCam, Zeiss) and captured with AxioVision software (Version 4.5., Zeiss), or with a confocal microscope (LSM 710, Zeiss) and processed with Imaris 7.1.1 software (Bitplane Inc.) and Adobe Photoshop CS5 (Adobe) software.
Quantitative and statistical analyses
Western blot analysis
Protein concentrations of the CSF samples were measured using NanoDrop (Table 1). Equal volumes of CSF were analyzed. The sample preparation was performed as previously described . Western blotting was done as described  with the following adaptations: 3–8% Tris-Acetate Midi Gels were used (NuPAGE Novex Tris-Acetate Midi Gel). The electrophoresis was performed using the Xcell4 SureLock Midi-Cell system (Cat.No. WR0100, Invitrogen). Proteins were blotted onto PVDF membranes using the Novex Semi-Dry Blotter (Cat.No. SD1000, Invitrogen). Films were scanned and analyzed using ImageJ Launcher software; intensities of bands were measured (area under the curve, AUC) and quantified. Reelin immunoreactivity was statistically compared between ND and AD subjects using the non-parametrical Mann–Whitney U test using StatView software. Statistical significance was set at p<0.05. Scanned films were processed with Adobe Photoshop CS5 for visual display (Adobe software).
Reelin immunoreactivity in the human hippocampal formation
To analyze the localization and levels of Reelin in the human hippocampal formation we performed an immunoperoxidase staining using Reelin antibodies recognizing the N- (G10 and 142) and C-terminal domains of Reelin (R12/14), to identify putative enrichments in proteolytic fragments of Reelin. Paraffin-embedded sections of ND and AD (n = 8, Table 1) were employed. We detected spherical Reelin-positive structures varying in their size from approximately 60 up to 250 μm2 predominantly located in fiber-rich structures (Figure 1 and Additional file 1: Figure S1) in both groups of subjects. They were most abundant in the fornix, enriched in myelinated axons of afferent and efferent projection neurons. A high density of these immunoreactive deposits was also evident in the neuropil of layer I of the pre-/parasubiculum and subiculum. Fewer deposits were detected in layer I of the entorhinal cortex (EC) and the stratum lacunosum moleculare (SLM) of the hippocampus (see Figure 1A for overview). In some cases, Reelin deposits were located in the hilus and rarely also in the pyramidal layer of CA3 and CA1. The immunoreactive signals were specific for Reelin, since control stainings with isotypic IgGs (mouse anti-human CD45) or the omission of primary antibodies did not yield any specific labeling (Figure 1D-E). The control staining using the well-characterized anti-CD45 antibody also indicated that the Reelin-immunoreactivity was not linked to putative invading lymphocytes. Based on their distinct morphology and enrichment in fiber-rich structures, however, we reasoned that they might be related to corpora amylacea (Cam), the age-related spherical bodies suggested to contain a collection of neuronal breakdown products including aggregated proteins and abnormal glycogen bodies [48, 49]. Indeed, hematoxylin (according to Ehrlich) and toloidinblue counterstaining identified the Reelin-positive structures as CAm. While all antigen retrieval techniques applied here diminished the Hematoxylin or Toloidinblue stainings, the immunoreactive anti-Reelin signal associated with CAm was never affected (see Methods and Additional file 2: Figure S2).
Reelin-positive deposits in AD versus non-demented subjects
Reelin levels in the human cerebral spinal fluid (CSF)
Levels of AD-relevant proteins in Reelin-positive CAm
Here we describe for the first time the presence of the extracellular matrix protein Reelin within spherical depositions in the human hippocampal formation. Our immunohistochemical stainings revealed the presence of considerable amounts of N- and C-terminus-containing Reelin fragments in these deposits. Stereological analyses indicated that their density in the hippocampal formation is largely independent of the dementia status; however, it revealed a trend towards higher levels in patients with AD and a putative link to alterations in Reelin proteolytic processing. Based on hematoxylin and toluidinblue labeling and their distinct morphology, it is highly conceivable that Reelin and its fragments constitute a major component of CAm, a prominent structure of the aging human brain whose origin and biological significance in the CNS is poorly understood. In the following, we summarize the current status of the CAm literature and discuss the presence and putative role of Reelin in their formation in the human hippocampal formation.
Aging-associated CAm in the human hippocampal formation
Despite the numerous studies, the role of CAm during aging and neurological diseases has remained obscure. They are commonly seen in the glial feltwork of subpial, subependymal, and perivascular regions, but can also be detected in fiber-rich areas in the CNS, most prominently within the hippocampal formation . The major components of CAm are glucose polymers, presumably linked to aging associated glucose metabolism defects, peptides and proteins (approximately 4%), many of which have been linked to cellular stress responses [56–58]. Several studies indicated that they evolve from neurons, astrocytes or oligodendrocytes due to the presence of cell-specific proteins [48, 49, 59, 60]. However, it is currently unclear whether their glial association is the result of phagocytosis of remnants of degenerated neurons/neurites and vascular metabolites [49, 61] or an indicator of glia pathophysiology/degeneration . In line with these data, neurological and neurodegenerative diseases such as temporal lobe epilepsy, multiple sclerosis, and AD are characterized by elevated levels CAm [61, 63], and these spherical bodies were shown to correlate with neuronal loss associated with hippocampal sclerosis . The frequent detection of CAm within axons and terminal neurites in the aging ocular system , as well as the prominent accumulation of axonal proteins including Tau [56, 65], APP , and α-Synuclein , indicate that they may form in response to cellular stress and/or aging-related impairments in cytoskeletal stability and axonal transport that ultimately lead to axonal swellings, a mechanism recently proposed for amyloid plaque formation in AD .
Reelin accumulates in two types of CAm – link to its expression pattern?
Intriguingly, many of the areas enriched in CAm overlap with the localization of Reelin. This relates to the well characterized cell types in the murine brain that are part of the entorhino-hippocampal, lateral olfactory and retino-collicular tract as well as the parallel fiber system of the cerebellum [67–71]. Furthermore, in vitro studies reported the expression of Reelin in progenitor cells of oligodendrocytes as well as mature oligodendrocytes , highlighting the possibility that the Reelin immunoreactivity associated with CAm in fiber-rich areas like the fornix may stem from its production and secretion by progenitors of oligodendrocytes and oligodendrocytes . Studies in primates identified additional areas with Reelin-positive cells showing a wider distribution of Reelin throughout cortical areas than in any other species, indicating that Reelin influences most cerebral circuits in higher mammals . Findings in macaque monkeys showed strong Reelin immunoreactive soma of Cajal-Retzius cells located in layer I, pyramidal neurons in EC layer II, and interneurons of the subicular complex molecular layer (subiculum, pre/parasubiculum), areas which harbor considerable amounts of Reelin-positive CAm. It is conceivable that these cells, shown to degenerate during preclinical stages of AD [74–76] are a major source of Reelin that is detected within CAm. In line with the findings that Reelin is transported along axons and secreted to act on postsynaptic cells [69–71], the deposits located in the SLM, the projection zone of the layer II pyramidal cells, are most likely distal axonal accumulations of Reelin. It is conceivable that aging-associated impairments of axonal stability and hence axonal transport increase the likelihood of accumulations of transported proteins and organelles. This may aggravate during phases of cellular stress that is frequently accompanied by increased levels in damaged and misfolded proteins, which show a much higher propensity to aggregate (for recent review, see ). It is therefore plausible, that the decrease in Reelin levels during aging [28, 32, 33] with its concomitant in- and decrease in Tau [12, 52] and n-cofilin phosphorylation , respectively, may reduce axonal and dendritic cytoskeletal stabilities and strongly impair transport from and to synaptic sites. In agreement with this hypothesis, our data showed that highly abundant and cellular stress-induced/associated axonal proteins such as APP and α-Synuclein co-accumulate with Reelin in CAm. Our findings that the formic acid pretreatment (used to detect Aβ peptides in amyloid plaques) abolished the anti-Aβ1–40/42 immunoreactivity in CAm indicates that soluble APP and/or APP fragments, rather than Aβ peptide aggregates, accumulate in CAm, which is in line with previous reports . The presence of MAP2 in CAm may be indicative of dendritic varicosities or related to missorting of this dendritic cytoskeletal protein into axonal compartments. In support of a putative protein mistargeting, we did not find evidence of phosphorylated Tau species in Reelin-positive CAm, a result that is also in agreement with previous studies [56, 65]. This phenomenon may also be linked to potential dephosphorylation of Tau in the putative acidic  and/or protein cross-linking and polymerization environment , a potential scenario that would also explain the lack of Synapsin-1 and Synaptophysin immunoreactivity in CAm. It is further conceivable that the change in glucose metabolism – potentially linked to aging-related alterations in glial support – promote the formation of abnormal polysaccharide chains that further block axonal transport. The presence of Reelin in the filled type of CAm could be indicative of such an axonal pathophysiology as previously suggested by the findings and discussions in rodents and primates [9, 30, 77]. However, the detection of Reelin in the hollow type shows that the core of CAm can be formed independently of Reelin and could indicate that this rare type of spheroid might be linked to the accumulation of Reelin in astrocytic endfeet . This is in agreement with the findings shown here and by others that GFAP-positive astrocytes are associated with but not found in the core of CAm . This hypothesis is also in line with our previous findings, demonstrating with 3D-electron microscopy that Reelin-positive varicosities can be extruded from neurites and detected in astrocytic endfeet, potentially related to phagocytosis . The lack of CAm-associated microglia activation reported here is also indicative that these spherical bodies are inert, despite the presence of putative toxic peptides, proteins and cellular metabolites . The distinct association of Reelin at the boarder of CAm – particularly prominent in the hollow type - may be linked to its extracellular secretion and accumulation around CAm that precludes a microglia response. Altogether, this may explain why CAm – despite their close association with aging-associated neurodegenerative processes linked to impairments in glucose metabolism, protein synthesis, transport and degradation – have no major effects on the physiology of neighboring neurons. It would be highly relevant to assess the levels of Reelin associated with CAm localized outside the hippocampal formation (i.e. hypothalamic nuclei), which have been reported to display pronounced cytoskeletal alterations during the course of aging and AD .
Reelin levels and deposits in AD compared to ND individuals
Previous reports indicated that several neurological and neurodegenerative conditions are accompanied by an increase in CAm, potentially linked to higher levels of cellular stress. However, quantitative data are largely missing. Here, we intended to assess the density of Reelin-positive CAm with an unbiased stereological approach involving five distinct areas of the hippocampal formation, complemented with immunoblot analyses to measure the Reelin levels in CSF samples of the same ND and AD individuals. Our stereological analysis revealed that the total amount of Reelin-positive CAm – independent of the type of deposit - was found to be increased in the subicular complex of AD compared to ND individuals. However, due to the small cohort and the high between subject-variability, only the density in the subiculum molecular layer yielded a significant group effect. Despite the limitation due to the small sample size, our data indicate the increase in CAm density may reflect the aggravation the aging-related impairments in cellular functions that result in increased intracellular accumulation of missorted, misfolded or poorly degraded proteins which is known to be increased in AD . It is very likely that putative differences in other areas measured were covered by an aging effect, as there is a clear age-dependent increase in the number of CAm . Currently, it is unknown how these histopathological changes relate to the level of Reelin protein and its proteolytic products in the CSF. While our assessment of full-length Reelin and its proteolytic fragments in the CSF revealed no statistical differences between groups, a correlation analyses highlighted a significant relationship between the levels of the 60kDa fragment and the overall CAm density in the susubiculum and pre/parasubiculum in ND subjects but not AD patients. While a higher sample size is absolutely required to substantiate this finding, the preliminary data indicate that the accumulation of Reelin in CAm might be related to its proteolytic degradation, a phenomenon that appears to be altered in AD versus ND subjects. It will also be highly relevant to assess Reelin levels in CSF and brain tissue homogenates in younger cohorts of ND subjects, as well as MCI and early stages of AD, which is expected to show larger differences to age-matched ND individuals. Differences in the age range of the subjects included in previous studies may have also accounted for the conflicting results regarding the levels of Reelin and its fragments in the CSF published earlier [36, 50, 51]. It would be therefore highly relevant to investigate the levels of Reelin and all its proteolytic fragments (including the 60 kDa product) and its putative enrichment in neuritic varicosities in a substantially larger cohort of human subjects across aging and AD.
Altogether, our results indicate that aging- and disease-associated changes in Reelin levels and proteolytic processing might play a role in the formation of CAm by altering cytoskeletal dynamics. Its presence may also be an indicator of a degenerative state of neuritic compartments. However, this remains to be experimentally determined using preclinical models of aging and AD.
We detected the Reelin-positive deposits using various antibodies raised against different Reelin epitopes (Additional file 1: Figure S1A-C). Reelin deposits were stained with all antibodies used, independently of the antigen retrieval technique. To visualize CAm with hematoxylin or toloidinblue, antigen retrieval was omitted in order to maintain the coloration. Figure 1E illustrates the high morphological variations in Reelin/CAm deposits. Besides the prominent staining of Reelin within deposits, we also detected intracellular Reelin immunoreactivity in pyramidal cells of the cornu ammonis, particularly in CA3 and to lesser extent CA1 pyramidal cells, using N-terminal but not C-terminal targeting antibodies (Additional file 1: Figure S1F), in line with a previous report . These immunoreactive signals were, however, only seen using an antigen retrieval approach involving microwave irradiation in citrate buffer followed by pepsin pretreatment (see Methods). Chromatin filters and high magnification microscopy revealed Reelin to be present within cytosolic vesicles (insert, Additional file 1: Figure S1F). To visualize Reelin-expressing cells, which were sparse in our cohort of aged non-demented individuals and shown to further decrease in AD patients [32, 79], repeated microwave irradiation in citrate buffer had to be applied (Additional file 1: Figure S1C, insert).
This study was supported by the Swiss National Science Foundation grant number 310030–132629, Center for Neuroscience Zurich (ZNZ), University of Zurich Candoc Forschungskredit, and Rahn & Bodmer, Private Banking, Zurich. We thank the Netherland Brain Bank and Professor Manuela Neumann, University of Tubingen, for providing the post-mortem human tissue and CSF samples, as well as Dr Lutz Slomianka and Ms Charlotte Burger and Iris Miescher, Institute of Anatomie, University of Zurich, for their expert stereology and experimental support, respectively. We are also very grateful to Professor Karl Frei, University Hospital Zurich and Professor André Goffinet, Catholic University of Louvain, for providing the anti-CD45 and anti-Reelin antibodies, respectively, as well as Professor Jean-Marc Fritschy, Dr Dimitrije Krstic and Sandra Pfister, Institute of Pharmacology and Toxicology, for their advice and inputs to this project.
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