Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice
© Uppal et al. 2015
Received: 7 January 2015
Accepted: 22 June 2015
Published: 30 June 2015
The genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act together to cause the behavioral phenotype associated with autism. One of the few single-locus causes of autism involves a mutation in the SH3 and multiple ankyrin repeat domains 3 (SHANK3) gene. Previous electrophysiological studies in mice with Shank3 mutations demonstrated impairment in synaptic long-term potentiation, suggesting a potential disruption at the synapse.
To understand how variants in SHANK3 would lead to such impairments and manifest in the brain of patients with autism, we assessed the presence of synaptic pathology in Shank3-deficient mice at 5 weeks and 3 months of age, focusing on the stratum radiatum of the CA1 field. This study analyzed both Shank3 heterozygous and homozygous mice using an electron microscopy approach to determine whether there is a morphological correlate to the synaptic functional impairment.
As both synaptic strength and plasticity are affected in Shank3-deficient mice, we hypothesized that there would be a reduction in synapse density, postsynaptic density length, and perforated synapse density. No differences were found in most parameters assessed. However, Shank3 heterozygotes had significantly higher numbers of perforated synapses at 5 weeks compared to 3 months of age and significantly higher numbers of perforated synapses compared to 5-week-old wildtype and Shank3 homozygous mice.
Although this finding represents preliminary evidence for ultrastructural alterations, it suggests that while major structural changes seem to be compensated for in Shank3-deficient mice, more subtle morphological alterations, affecting synaptic structure, may take place in an age-dependent manner.
KeywordsAutism Shank3 Electron microscopy CA1 Hippocampus Stratum radiatum Synapse
The behavioral symptoms that currently define autism have yet to be rooted in a cause, though it is generally understood that these symptoms originate from alterations in the brain. Many studies have validated this hypothesis, as regionally specific abnormalities including reduced neuronal size, decreased neuronal number, and cortical disorganization are present in individuals with autism (e.g., [1–6]). The abnormalities in neuronal architecture imply corresponding disruptions in communication among neurons, which likely manifest at the synapse. Of particular relevance is the growing number of synaptic function-related genes implicated in autism. The Src homology 3 and multiple ankyrin repeat domains 3 (SHANK3) gene, which encodes for the postsynaptic scaffolding protein SHANK3/ProSAP2, has been identified as one of the few genes which can by itself lead to autism when mutated. SHANK3 was identified as the cause of the neurobehavioral manifestations of the 22q13 deletion syndrome, or the Phelan-McDermid syndrome (PMS; ). Patients with PMS not only exhibit developmental, intellectual, and language delays as well as motor deficits but also frequently demonstrate autistic behaviors [8–11]. Although patients with 22q13 deletions have varying deletion sizes, SHANK3 is a gene that has been consistently implicated  and was later found to be exclusively affected through point mutations in some individuals with PMS [10, 13–15], leading to the conclusion that this gene is likely a strong candidate gene for autism as well. Upon further analysis, SHANK3 variants were identified in patients ascertained with autism [9, 11, 13, 16–18]. Given its crucial role in the etiology of PMS and autism, studying the impact of a loss of SHANK3 will allow for a detailed assessment of cellular and molecular mechanisms that underlie pathology.
SHANK3 belongs to a family of SHANK proteins, all of which have multiple domains for protein-protein interaction [19, 20]. Each of these domains interacts with specific proteins, in particular with cytoskeletal proteins, cell adhesion proteins, and ionotropic and metabotropic glutamate receptors [21–25], some of which are also implicated in autism (e.g., NLGN3, NLGN4, SHANK1, SHANK2). SHANK3 is strongly expressed at the postsynaptic density (PSD), as it is part of a molecular assembly (which includes PSD-95/GKAP/Shank/Homer) which comprises approximately 27 % of the total protein molecules in the PSD; Shank3 is estimated to comprise ~5 % of the total protein molecules in the PSD . To determine the effect of a loss of one copy of SHANK3, as observed in patients with PMS , Bozdagi and colleagues  created a mouse with a disruption in full-length Shank3, which is a form known to be specifically disrupted in patients with autism (e.g., ). Functionally, the authors demonstrated that Shank3 heterozygotes display significant impairments in long-term potentiation (LTP) maintenance when recording from the stratum radiatum in the CA1. Furthermore, they reported a significant decrease in α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor-mediated field potentials in the Shank3 heterozygotes as well as a reduction in the amount of glutamate receptor subunit 1 (GluA1), an AMPA receptor subunit. Subsequently, Yang and colleagues  corroborated the electrophysiologic impairments in Shank3 heterozygous mice and found impairments in both LTP induction and maintenance in Shank3 homozygous mice. While Shank3 protein is widely expressed throughout the brain, it is concentrated in the thalamus, cerebellum, and hippocampus . Because of the impairment in LTP seen in Shank3 heterozygous and homozygous mice, Shank3 expression in the hippocampus was particularly interesting to assess.
Given these findings and the crucial role of SHANK3 in the etiology of PMS and autism, this study examined ultrastructural alterations in the above Shank3 mouse model of autism. The primary morphological parameters assessed in the current study were synapse density, perforated synapse density, and PSD length in the Shank3-deficient mice, due to the likelihood these parameters would be affected by a loss of Shank3, given its role in the PSD and LTP (e.g., [27, 30]). Differences in PSD length would indicate a change in the ratio of plastic and stable spines, as PSD length is correlated with spine head size and type. We also assessed perforated synapses, which are distinguished by a discontinuous PSD despite being part of a single synapse. Perforated synapses have been implicated in many functions in the context of learning and memory, including maintenance of spatial learning ability, activity-dependent synaptic plasticity, and LTP induction [31–35]. The formation of a perforation in the synapse, which transiently occurs during LTP induction, is thought to enhance the efficacy of synaptic transmission due to the increase in PSD area and therefore increase in AMPA- and N-methyl-D-aspartic acid (NMDA)-receptor content [33, 34, 36]. Their formation, however, remains a subject of debate, with some postulating that non-perforated synapses become perforated, as a transient intermediary structure, to then form two separate synapses (for example, ), others postulating that perforated and non-perforated synapses are completely separate populations of synapses that develop in unique ways (for example, ), and others suggesting that perforations transiently develop in non-perforated synapses to briefly increase the efficacy of the synapse, which will later form back into its original non-perforated structure (for example, ). Despite the debate on perforated synapse origin and development, their role in increasing the efficacy of a synapse is generally agreed upon and is the reason we are assessing their presence in our mouse model. Changes in synapse functioning, as measured through morphological changes, would likely lead to alterations in normal neuronal functioning. Alterations in neuronal functioning, in turn, might be reflected in the behavioral changes that currently characterize individuals with disorders such as PMS and autism. There are very few studies that have assessed hippocampal differences in postmortem brains from this patient population and that have identified neuronal abnormalities that may affect synaptic functioning. Neuronal abnormalities in the hippocampus in patients with autism include reduction in neuron volume, dendritic branching, and nucleus volume [3, 6], although to our knowledge there are no studies that have quantified changes at the synaptic level in patients with autism. Unfortunately, as of yet, there have been no postmortem studies in individuals with PMS nor specifically on individuals with autism that have a disruption in SHANK3; however, we can presume that this region is likely also affected in these individuals, as they present with similar behavioral symptoms.
In the current study, synaptic measures were assessed at two time points: 5 weeks, corresponding to an early adolescence stage near sexual maturity when the relevant brain region is undergoing constant synaptic pruning, and 3 months, corresponding to a young adult that is socially mature and has a reduced rate of synaptic turnover. These ages were consistent with previous studies conducted on this mouse model [27, 28], which allowed for direct comparison of the synaptic measures in this study with electrophysiological and behavioral measures from earlier studies. Overall, this study aimed to clarify the effect of Shank3 deficiency on synapse morphology.
All procedures were compliant with the National Institute of Health Guidelines for the Care and Use of Experimental Animals and were approved by the Institutional Animal Care and Use Committee at the Icahn School of Medicine at Mount Sinai. Shank3 heterozygous and homozygous mice were generated using homologous recombination to delete the ankyrin repeat domain of Shank3. This constitutive knockout mouse model of Shank3 disruption has been previously characterized in detail [27, 28]. The study included 15 C57BL/6 male mice (5 weeks old: 5 Shank3 homozygous mice, 5 Shank3 heterozygous mice, and 5 wildtype mice) and 15 C57BL/6 male mice (3 months old: 5 Shank3 homozygous mice, 5 Shank3 heterozygous mice, and 5 wildtype mice). Mice were group-housed and were given standard mouse chow and water ad libitum.
Perfusion and tissue processing
Prior to perfusion, mice were anesthetized with 15 % chloral hydrate. The mice were perfused with 1 % cold paraformaldehyde (pH 7.2–7.4) in phosphate buffer saline (PBS) for 1.5 min. This was followed by a solution of 4 % paraformaldehyde in 0.1 M PBS and 0.125 % glutaraldehyde for 10.5 min at 5 ml/min. The brain was then removed from the skull and postfixed in a 4 % paraformaldehyde/0.125 % glutaraldehyde solution overnight at 4 °C. The brain was washed in phosphate buffer (PB), cut into 250-μm-thick sections using a vibratome, and stored in PB overnight. The sections were cryoprotected the next day in a graded glycerol/PB solution. After remaining in a 30 % glycerol solution overnight, the CA1 was manually microdissected into blocks (four per animal) that underwent cryosubstitution and low-temperature embedding as described in .
Once the polymerization was complete, the hardened capsules were removed from the cryosubstitution system and stored at room temperature. Block faces were trimmed to include the stratum pyramidale, stratum radiatum, stratum lacunosum-moleculare, and white matter. At least eight consecutive ultrathin sections were cut at 90 nm with a diamond knife (Diatome, Bienne, Switzerland) on an ultramicrotome (Reichert-Jung) and mounted onto a Formvar-supported slot grid (Electron Microscopy Sciences).
Serial section imaging was carried out at 75 kV on a Hitachi H-7000 transmission electron microscope (Hitachi High Technologies America) with an AMT Advantage CCD camera (Advanced Microscopy Techniques). Eight sets of five serial sections of distinct regions in the stratum radiatum of the CA1 were imaged at ×15,000. Electron micrographs were adjusted for brightness, contrast, and sharpness using Adobe Photoshop (Photoshop CS4, version 11.0.2) prior to being analyzed. All morphological analysis was carried out in Adobe Photoshop.
We compared two ages and three genotypes of mice. Both the 5-week and 3-month group had an n = 5 per genotype, with a total of 15 mice each. Comparisons of potential genotypic variations within one age group were determined using one-way analysis of variance (ANOVA). To reduce type I error while comparing several means, a Tukey post hoc test was used to calculate whether there were significant differences between pairs of genotypes. Calculations were performed with GraphPad Prism (version 5). To determine whether there was an interaction between age and genotype on the parameters assessed, we used two-way ANOVA to assess for significant differences and corrected for multiple comparisons using the Tukey post hoc test. Calculations were performed with SPSS (version 20). A p value of 0.05 was used as the criterion for statistical significance.
The Shank family of postsynaptic scaffolding proteins consists of three members (Shank1, Shank2, and Shank3; [21, 22]). Shank1 and Shank3 mRNA transcripts are strongly expressed in the pyramidal and molecular layers of the hippocampus, indicating dendritic localization, whereas Shank2 mRNA transcripts are restricted to cell bodies [29, 42]. Shank2 protein localizes at the PSD early (prior to PSD-95 and NR1; ) and is thought to act as an initial “organizer” of the PSD; Shank3 is recruited next, interacting with Homer1b to create a complex on which postsynaptic proteins, such as GKAP, can bind ; lastly, Shank1 enters after the PSD-95/GKAP complex is in place to stabilize synapses and may have a role in activity-induced regulation of spine head size [22, 44, 45].
With the loss of a major synaptic scaffolding protein, we expected to find significant morphologic changes in the Shank3-deficient mice. However, Shank3 heterozygous and homozygous mice exhibited no difference in spine head size, PSD length, and PSD area when compared to wildtype mice. This result suggests that the absence of Shank3 may be compensated for or may lead to deficits that are only observed early in development. Two obvious candidates for this compensation are Shank1 and Shank2. Shank2 is more similar to Shank3 in its recruitment to the synapse and its protein structure, making it a more likely candidate for compensation . In fact, Shank3 was thought to compensate for Shank2 in Shank2-deficient mice, while Shank2 was thought to compensate for Shank3 in another form of Shank3 variant homozygous mice, as indicated by the upregulation of Shank3 at the synapse in Shank2 homozygous mice and vice versa .
In Shank3 heterozygotes, there is still one functional copy of Shank3, and therefore, a proportional amount of Shank3 protein is present at the synapse . A reduced amount of Shank3 could affect multiple associated proteins [20, 22, 43, 44, 47] and may result in changes in protein composition at the synapse, which may explain functional impairment in Shank3 heterozygous and homozygous mice [27, 28, 48]. While the Shank family does have highly conserved protein-protein interaction domains, they are not redundant; each Shank protein can have specific mechanisms and proteins it targets . Thus, while replacing one Shank protein with another might prevent the synapse from disassembling, it does not guarantee appropriate functioning. This is well illustrated through the mild behavioral abnormalities in these mice, consistently showing impairments in juvenile reciprocal interactions, novel object recognition, and rotarod performance [27, 28]. The mice also showed some evidence for excess self-grooming, reduced ultrasonic vocalizations, and impaired reversal of water maze learning.
The fact that synapse density was not changed despite the marked LTP deficit may reflect that a portion of the synapses in Shank3 variant mice may be “silent synapses” that have NMDA but not AMPA receptors, rendering the synapse non-functional . Silent synapses are present in wildtype mice as well, forming during LTP induction and often undergoing remodeling to become functional during LTP maintenance [50, 51]. It is possible that to compensate for the increase in silent synapses in Shank3-deficient mice at baseline, some silent synapses undergo remodeling to form perforated synapses, which are thought to have a higher efficacy of synaptic transmission [52, 53]. The presence of increased silent synapses is corroborated by reduced basal synaptic transmission in both Shank3 heterozygous and homozygous mice [27, 28] and reflects a reduction in AMPA receptors, as they are constitutively active even during basal conditions . In fact, a decrease in GluA1-immunoreactive puncta in CA1 was previously reported in Shank3 heterozygous mice, indicating a decrease in AMPA receptors . This is substantiated by the significant impairment in the maintenance phase of LTP, which is AMPA receptor-dependent .
While there are no directly correlated studies on synaptic morphology measures in individuals with autism or PMS in the hippocampus, there are several studies that imply alterations at the synaptic level. Neuropathology studies have revealed abnormalities in neuronal numbers [1–6], and imaging studies have revealed a variable degree of altered connectivity localized to specific areas (e.g., [56, 57]). Additionally, work at the protein level has shown abnormalities in receptors in the hippocampus, which may reflect changes at the synapse as well [58, 59]. In accordance with these studies, it will be crucial to use electron microscopy to assess whether there are changes in the synapse at the protein level. Future studies will also expand the age range in these mice, particularly at a younger age as autism is a neurodevelopmental disorder; additionally, expanding the number of mice per group will allow for stronger conclusions regarding the synaptic alterations in these mice.
This study examined whether synaptic pathology was present in Shank3 heterozygous and Shank3 homozygous mice at 5 weeks and 3 months of age. Shank3 heterozygous mice (5-weeks-old) had a statistically significantly higher density of perforated synapses and no change in other measured parameters (synapse density, PSD length, PSD area, and spine head size); 3-month-old mice had no changes across groups for any measured parameter. It is remarkable that there are so few detectable behavioral and neuropathologic changes in these Shank3 variant mice despite the loss of this dominant scaffolding protein. These results highlight the importance of seeking even more subtle alterations, in the form of changes in specific protein levels, at the synapses of these mice. Understanding the subtle effects of this single-locus cause of autism will provide a framework for similar explorations in other genetic causes associated with the disorder, which will allow us to determine whether alterations in these disparate genes lead to similar effects at the most basic functional level, namely, the synapse.
α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid
analysis of variance
glutamate receptor subunit 1
phosphate buffer with saline
SH3 and multiple ankyrin repeat domains 3
The authors greatly appreciate the expertise and guidance of Dr. Yuko Hara in electron microscopy techniques and data interpretation. They would also like to thank Dr. Lilijana Minwalla for expert technical assistance and Dr. James Schmeidler for advice on statistical analyses.
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