Astrocyte-secreted thrombospondin-1 modulates synapse and spine defects in the fragile X mouse model
© The Author(s). 2016
Received: 16 May 2016
Accepted: 15 July 2016
Published: 2 August 2016
Astrocytes are key participants in various aspects of brain development and function, many of which are executed via secreted proteins. Defects in astrocyte signaling are implicated in neurodevelopmental disorders characterized by abnormal neural circuitry such as Fragile X syndrome (FXS). In animal models of FXS, the loss in expression of the Fragile X mental retardation 1 protein (FMRP) from astrocytes is associated with delayed dendrite maturation and improper synapse formation; however, the effect of astrocyte-derived factors on the development of neurons is not known. Thrombospondin-1 (TSP-1) is an important astrocyte-secreted protein that is involved in the regulation of spine development and synaptogenesis. In this study, we found that cultured astrocytes isolated from an Fmr1 knockout (Fmr1 KO) mouse model of FXS displayed a significant decrease in TSP-1 protein expression compared to the wildtype (WT) astrocytes. Correspondingly, Fmr1 KO hippocampal neurons exhibited morphological deficits in dendritic spines and alterations in excitatory synapse formation following long-term culture. All spine and synaptic abnormalities were prevented in the presence of either astrocyte-conditioned media or a feeder layer derived from FMRP-expressing astrocytes, or following the application of exogenous TSP-1. Importantly, this work demonstrates the integral role of astrocyte-secreted signals in the establishment of neuronal communication and identifies soluble TSP-1 as a potential therapeutic target for Fragile X syndrome.
KeywordsFragile X syndrome Autism Astrocytes Secreted factor Thrombospondin-1 Synapses Dendritic spines
Fragile X syndrome (FXS) is the most common form of intellectual disability and is a leading cause of autism spectrum disorders , affecting about 1/4000 males and 1/8000 females. The causative mutation for the majority of cases is a trinucleotide CGG expansion in the promoter region of the fragile X mental retardation 1 gene (FMR1), which induces transcriptional gene silencing and the loss of the fragile X mental retardation 1 protein (FMRP). FMRP is an RNA-binding protein that is highly involved in binding and regulating the translation, transport and stability of a subset of mRNAs to synapses [2, 3]. Fundamental research on the Fmr1 knockout (KO) mouse has provided promising insights into the cellular and molecular underpinnings of the condition. A well-described characteristic feature of FXS is the presence of “immature” dendritic spines [4, 5]. These dendritic spine abnormalities in Fmr1 KO mice are most pronounced during development, but also persist into adulthood . As spines are thought to be the site of functional changes that mediate memory storage, an immature or otherwise aberrant morphology could represent the critical effect of the FXS mutation that underlies learning impairments.
The appropriate formation of neural connections is vastly dependent on reciprocal neuronal and glial interactions. Until recently, the majority of research into the function of FMRP, and the consequences of its absence, has largely been focused on neurons. However, it is now known that FMRP is also expressed in cells of the glial lineage [7, 8]. The expression of FMRP is typically highest in astrocytes within the first week of birth and subsequently declines to low or undetectable levels . Based on these findings, work in our laboratory investigated the role of astrocytes in the development of the abnormal neurobiology of FXS. Using an astrocyte-neuron co-culture system, hippocampal neurons showed developmental delays in dendritic growth patterns and also in the expression of excitatory synapses when interfaced with astrocytes lacking FMRP [9, 10], suggesting that dysfunction in non-neuronal cells may be a contributing factor into the pathogenesis of FXS.
During development and in the mature brain, astrocytes are known to provide signals that guide synapse formation and neurite development [11–14]. Astrocytes can regulate the stability, dynamics and maturation of dendritic spines through the release of secreted factors [15, 16]. In particular, astrocyte-derived thrombospondins (TSPs) are large extracellular matrix proteins (450 kDa) that have been identified as major contributors to astrocyte-regulated excitatory synapse formation . The TSP family consists of two subfamilies, A and B, according to their organization and domain structure [18, 19]; A includes the trimeric TSP-1 and TSP-2, while B includes the pentameric TSP-3, TSP-4 and TSP-5 [20, 21]. Recently, the THBS1 gene, which encodes the TSP-1 protein, has been identified as an autism risk gene . In the central nervous system (CNS), TSP-1 is mostly enriched in glia and predominantly expressed by developing astrocytes during early postnatal development in the rodent cortex , which correlates with the onset of synaptogenesis. TSP-1 regulates excitatory synaptogenesis through the gabapentin receptor α2δ-1 [24, 25], and neuroligin-1 in hippocampal neurons . Double TSP-1 and −2 knockout mice show a reduced number of excitatory synapses in the cortex  and display dendritic spine irregularities . Given that FMRP and TSP-1 are both expressed in immature astrocytes and have been associated with the timely development of synapses, there is reason to believe that the early regulation of synaptogenesis could be influenced by TSP-1.
Previously, our group has demonstrated that astrocytes modulate neuronal development in FXS; however, it is unknown whether the effects can be attributed to direct physical astrocyte-neuron interactions and/or to the release of extrinsic synaptic cues derived from astrocytes that are responsible for guiding development. Here, we determined the role of astrocyte-secreted TSP-1 on neuronal maturation and synaptic development in FXS. To explore the consequences of altered astrocyte signaling during development, we optimized an indirect (non-contact) astrocyte-neuron co-culture method with either astrocyte-conditioned medium or an astrocyte feeder layer to promote neuronal attachment and survival. Using this experimental paradigm, our results showed abnormal spine maturation and synapse development in normal hippocampal neurons grown with conditioned media and a feeder layer from FXS astrocytes. We also found that TSP-1 levels were markedly reduced in FXS cultured astrocytes and conditioned media. Further, the addition of TSP-1 to FXS cultures prevented synaptic and spine alterations. These findings provide insight into the significance of astrocyte-derived cues during early developmental periods in the brain that underlie the proper establishment of neural circuitry.
The FMRP mouse colony was established from breeding pairs of FVB.129P2(B6)-Fmr1tm1Cgr mice. The wildtype (WT) and Fmr1 knockout (KO) mice were maintained as individual strains and genotyped regularly. Both male and female mice were used in the experiments. The mice used for these experiments were housed and bred at the McMaster University Central Animal Facility. All experiments complied with the guidelines set out by the Canadian Council on Animal Care and were approved by the McMaster Animal Research Ethics Board.
Hippocampal neuron isolation
Hippocampal neurons were obtained from embryonic day E15–17 (day of sperm plug counted as E1) WT and Fmr1 KO animals. Hippocampal tissue was isolated from at least six embryonic pups, digested with 2.5 % trypsin, and triturated through a fire-polished glass Pasteur pipette. The neurons were subsequently plated on poly-L-lysine (1 mg/ml, Sigma) and laminin (0.1 mg/ml, Invitrogen) coated glass coverslips in 24-multiwell plates immediately after dissociation at a density of 20 000 cells per well in Neural Growth Medium consisting of Neurobasal (NB) (Invitrogen) enriched with 0.5 mM GlutaMAX (Invitrogen), and 2 % B-27 Supplement (Invitrogen). Neurons remained in culture for 17 days in vitro (DIV) to allow for the development and maturation of dendritic spines. Immunocytochemical studies subsequently ensued to identify alterations in spine density, morphology and length, and the formation of excitatory synapses.
Primary cortical astrocyte cultures
Cortical astrocytes were prepared from four WT or Fmr1 KO postnatal day 0 to day 2 (P0–P2) pups, as detailed previously by our laboratory . Briefly, whole brains were extracted and cortical tissue was dissected and incubated with 2.5 % trypsin (Invitrogen) and 15 mg/mL DNase (Roche) at 37 °C. Following successive mechanical trituration using a serological pipette, the cells were passed through a 70 μm cell strainer (Fisher Scientific), dissociated into a single-cell suspension, and re-suspended in 10 % Glial Media (GM) comprised of Minimum Essential Medium (MEM) (Invitrogen), 0.6 % glucose and 10 % horse serum (Invitrogen). The astrocytes were seeded in a T75 flask and maintained in culture for 7–12 days in a humidified 5 % CO2, 95 % O2 incubator at 37 °C. Partial medium changes were performed every 2–3 days. Cultures consisted of at least 95 % astrocytes as determined by glial fibrillary acidic protein (GFAP) immunocytochemistry.
Preparation of astrocyte-conditioned medium (ACM)
After 4–5 days in culture and achieving 50–65 % confluency, the monolayers of astrocytes were subjected to a Neuronal Growth Media (NGM) switch. The cultures were washed extensively with Neurobasal (Invitrogen) and the media was replaced with NB/B-27 culture medium to generate the ACM. In preparation for conditioning, ACM was harvested for 4 days and collected. The media was filtered using a 0.22 μm syringe filter for the removal of cellular debris and concentrated ten times by filtration through a 10 kDa molecular weight cut-off (MWCO) centrifuge concentrator (Satorius Stedim). ACM was stored at −80 °C and used at a final concentration of 5×. Notably, this procedure closely follows that of Christopherson et al.  used for the isolation of thrombospondins. The ACM was spun at 5000 rpm for 5 min to remove cell debris prior to protein quantification or plating with the neurons.
Astrocyte feeder layer
To evaluate astrocyte non-contact mediated influences on morphological parameters, ThinCert™ cell culture inserts from Greiner Bio-One were utilized and placed in 24-multiwell plates to facilitate the growth of the cortical astrocytes. These culture inserts consist of a 0.4 μm porous, PET membrane support that forms a two-compartment system. In this set-up, cultures were co-cultivated with neurons and astrocytes in physically separated compartments to facilitate paracrine-signaling interactions involving diffusible astrocyte-secreted factors. For preparation of the astrocyte feeder layers (AFL), confluent astrocyte monolayer cultures were trypsinized with 0.05 % Trypsin-EDTA to lift adherent cells and subsequently passaged. The dissociated cells (9000 cells) were seeded into the cell culture inserts (positioned above the bottom of the well) and maintained in 10 % GM for 3 days. Media was switched to Neural Growth Media (NGM) at least one day before plating neurons. Subsequently, hippocampal neurons supplemented with NGM were plated below the cell culture inserts on the coverslips. NGM was replenished every 3–4 days.
DiI neuronal labeling
Dendritic spines were identified using the well-characterized fluorescent marker DiI (1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate), as described by Cheng et al. . In brief, the neurons were fixed with 2 % paraformaldehyde and stained with lipophilic DiI (Invitrogen). For the staining, 2–3 DiI crystals were applied to each coverslip. A small amount of Dulbecco’s Phosphate Buffered Saline (DPBS, Invitrogen) was dispensed to the edge of the wells to prevent dehydration of the cells. The neurons were stained for 10 min on an orbital shaker and copiously washed with DPBS to remove all crystals. The cells were incubated in DPBS overnight at room temperature. The following day, the coverslips were rinsed with dH2O, air-dried and mounted to slides with Prolong Gold Anti-fade (with DAPI) fluorescent mounting medium (Invitrogen). The cells were visualized 72 h from the initial staining to allow for the complete migration of the dye into the dendritic spines.
Visual imaging of dendritic spines was acquired using a Zeiss 510 confocal laser-scanning microscope (LSM 510). All images were taken using a 63×/1.2 water immersion lens. A 543 nm Hene-1 Rhodamine laser was utilized to visualize the fluorescence emitted by DiI with the filter channel 3 BP560–615 nm. To view the specimen with reflected fluorescent light, the reflector turret was programmed to position F set 15 in correlation to the Rhodamine laser, and the single-track configuration was chosen. We used 1024 × 1024 pixels for image size and set the scan speed at a setting of 6. Scan direction and line averaging were also adjusted to a setting of 6. The pinhole diameter was configured to 1 Airy unit (124 μm). Series stacks were collected from the bottom to the top covering all dendrites and protrusions, with an optical slice thickness of 0.5 to 1 μm. The resulting images (4–6) were then reconstructed according to z-stack projections of the maximum intensity.
Dendritic spine analysis
ImageJ software (RSB, NIH) was used for viewing the confocal images and for spine quantification. In order to increase the magnification for a better view of the spines without loss of image quality, the resolution of the stack image was increased by a factor of 5 in the X and Y directions with the plug-in Transform J Scale . The length of a spine was obtained by drawing a line from its emerging point on the dendrite to the tip of its head. Approximately, 25 neurons were selected at random per condition across three coverslips from two batches of cultures per group were used for quantitative analysis. Secondary dendritic branches were selected for analysis. Density, morphology and length of spines were scored in dendritic segments 10 μm in length. Morphologically, two populations of spines were identified: (1) ‘mature’ stubby/mushroom-like spines, which are small, rounded spines with or without a short neck and (2) ‘immature’ filopodium-like spines, which are typically longer, thin and lack a head. Two to three independent experiments were performed. For each independent culture, 40–50 dendritic segments (10 μm in length) were selected and evaluated for spine analysis.
Following 17 DIV, hippocampal neurons were fixed with ice-cold (−20 °C) acetone for 20 min and processed for immunocytochemistry. Cells were washed three times in PBS and permeabilized with 0.1 % Triton X-100, respectively. Non-specific binding was blocked with 1 % bovine serum albumin (BSA) with the appropriate normal animal serum for 30 min at room temperature (RT). Primary antibodies were applied to the coverslips and incubated overnight at 4 °C. The second day, following washes with PBS, secondary antibodies were incubated with the cells for 3 h at RT. Lastly, the coverslips were mounted on to slides with Prolong Gold Anti-fade fluorescent mounting medium (Invitrogen) containing DAPI to stain for nuclei. The following antibodies, diluted in PBS, were used: monoclonal synaptophysin (clone SVP-38; 1:250; Sigma-Aldrich), mouse monoclonal postsynaptic density 95 (PSD-95) (clone 6G6-1C9; 1:200; Millipore Bioscience Research Reagents), donkey anti-mouse AlexaFluor 594 (1:1500, Life Technologies), and goat anti-rabbit FITC (1:100, Jackson ImmunoResearch).
Primary cortical astrocytes were also processed in a similar manner to visualize the localization of TSP-1 at 7 DIV. The following antibodies were used to label the astrocytes: mouse monoclonal thrombospondin-1 (A6.1; 1:100; ThermoFisher Scientific), polyclonal rabbit anti-GFAP (1:500, Dako), donkey anti-mouse AlexaFluor 594 (1:1500, Life Technologies), and goat anti-rabbit FITC (1:100, Jackson ImmunoResearch).
Synaptic puncta analysis
Images were acquired using a Zeiss AxioImager.M2 at 40× magnification configured with the ApoTome.2 and Zeiss Zen Blue image acquisition software. Synapses were identified by the co-localization of the pre-(synaptophysin) and post-synaptic (PSD-95) puncta, using a custom written plug-in for ImageJ. After selecting a 50 μm segment along the dendrite, the image was processed using the above plug-in. Briefly, low frequency background from each channel (red and green) of the image was removed with the rolling ball background subtraction algorithm. Then, the puncta in each single-channel was ‘masked’ by thresholding the image so that only puncta remained above threshold. Puncta were then identified in each channel by the “Puncta Analyzer” plug-in for Image J. Co-localization of the puncta in each channel was identified when the distance between the centers of the two puncta was less than the radius of the larger puncta. The number of co-localized puncta was then recorded as synapses. Two to three independent experiments were performed. Approximately 20–25 neurons from at least two coverslips were analyzed per condition/group. For each independent culture, 45–50 (50 μm long) segments along the dendrites were evaluated for synaptic protein co-localization. Multiple dendritic segments were sampled within a given neuron. The PSD95/synaptophysin-immunoreactive puncta along the dendrites in each photomicrograph were counted manually and normalized by dendrite length. The photography and analysis of immunoreactivity were conducted in an investigator-blinded manner.
Measurements of TSP-1 expression and release
TSP-1 levels were determined in astrocyte cultures and astrocyte-conditioned medium (ACM). Confluent astrocyte cultures were incubated with 0.05 % Trypsin-EDTA for 5 min at 37 °C. Once cells were fully lifted, media with serum was added to stop the digestion. The cells were centrifuged at 250 g for 5 min, washed with ice-cold PBS, and lysed with cell lysis buffer containing 50 mM Tris–HCl, 150 mM NaCl, 1 % Triton-X and 5 mM EDTA with protease inhibitors (Roche). The lysates were collected in Eppendorf tubes, centrifuged at 12000 rpm in an Eppendorf microcentrifuge for 20 min at 4 °C, and the supernatants were used to determine the intracellular concentration of TSP-1. Aliquots of ACM from the same cultures were also processed to determine secreted, extracellular levels of TSP-1. TSP-1 protein measurements were determined using the Mouse Thrombospondin-1 ELISA kit (Biotang, Inc) following the vendor’s instructions. Sample protein content normalization was based on total protein concentration, which was determined for each sample by Bradford assay.
To assess the neuromodulatory effect of exogenous TSP-1 on spine development, hippocampal neuronal cultures derived from Fmr1 KO mice were treated with human recombinant TSP-1 (R&D System) to stimulate spine formation. Recombinant TSP-1 was added to the neuronal media one day after plating, and replenished every 3 days for 17 days. A dose concentration of 250 ng/ml was used to restore TSP-1 levels . Control cultures were incubated with heat-inactivated TSP-1 (TSP1-HI, 100 °C for 5 min), or gabapentin (GBP; 32 μM)  to inhibit astrocyte induced spine and synapse formation.
Statistics were performed using GraphPad Prism 5.0. Differences were detected using a Student’s t-test or one-way analysis of variance (ANOVA). Following one-way ANOVA, post hoc differences were resolved using the Bonferroni correction. A p-value of <0.05 was considered significant. All values are expressed as mean ± SEM; n = number of neurons (unless otherwise specified); N = number of experiments.
Fmr1 knockout neurons display dendritic spine and synaptic abnormalities relative to their wildtype counterparts
Consistent with findings from the literature, we found a clear difference in dendritic spine length between WT and Fmr1 KO hippocampal neurons. Fmr1 KO neurons displayed remarkably longer spines (~1.5 fold increase) relative to their WT counterparts at 17 DIV (Fig. 1b and c, p < 0.01). The structural profiles of the spines also differed considerably between the WT and Fmr1 KO hippocampal neurons. Fmr1 KO neurons displayed a higher density of immature thin/filopodia-like spines (Fig. 1d, p < 0.05), and a striking decrease in the number of mature stubby subtypes compared to WT hippocampal neurons (Fig. 1e, p < 0.05). The increased prevalence of elongated spines, characteristic of immature synapses, suggests that dendritic development is delayed in the Fmr1 KO neurons. Notably, a slight decrease in the overall spine density was observed in the Fmr1 KO neurons; however, the differences were not statistically significant (p > 0.05, Additional file 1: Figure S1).
WT hippocampal neurons exhibit morphological spine and synaptic deficits and when grown with an Fmr1 KO astrocyte feeder layer
Next, we sought to ascertain the ability of ACM or astrocyte-feeding layers to induce the development of synapses in neurons (Fig. 3f). WT neurons grown in the presence of an Fmr1 KO feeder layer displayed significantly reduced co-localization relative to WT neurons cultured alone (p < 0.05) or with a WT AFL (p < 0.001). These results demonstrate that synaptic protein clustering is impaired when WT neurons are grown with a feeder layer derived from Fmr1 KO astrocytes.
Spine and synaptic protein abnormalities are prevented in Fmr1 KO neurons by WT astrocyte conditioned media or a WT feeder layer
Next, given that soluble factors derived from FMRP-deficient astrocytes affect excitatory synapse formation, we investigated whether normal astrocytes could prevent the alterations observed in Fmr1 KO neurons. Consistent with previous studies showing that ACM induces synapse formation , we found that the addition of WT ACM to Fmr1 KO neurons significantly increased the number of synaptophysin/PSD95 co-localized puncta per 50 μm length of dendrite (Fig. 4e, p < 0.05). Our results also showed that a greater number of synaptic contacts were formed in Fmr1 KO neurons supplemented with a WT feeder layer (p < 0.01). Together, these results demonstrate that synaptic protein clustering in Fmr1 KO neurons can be restored to normal levels in the presence of FMRP-expressing astrocytes and further suggest a role for secreted factors in regulating synaptic development.
Intracellular and extracellular TSP-1 expression levels are decreased in Fmr1 KO astrocytes
Addition of TSP-1 corrects abnormal dendritic spine development and excitatory synapse formation in Fmr1 KO neurons
To elucidate the neuromodulary effects of TSP-1 on excitatory synapse formation, Fmr1 KO neurons were treated with a dose of 250 ng/ml of rTSP-1. At 17 DIV, an increase in the co-localization of pre-and post-synaptic puncta was observed when Fmr1 KO neurons were treated with rTSP-1 (Fig. 6f and g; p < 0.001). Therefore, these results support the concept that rTSP-1 can increase the number of both presynaptic and postsynaptic protein clusters, contributing to the recovery of the alterations in excitatory synapses in Fmr1 KO neurons.
Dendritic spine abnormalities have long been recognized as structural correlates of learning impairments in FXS and various forms of ASDs [44, 45]. However, the origin and mechanisms involved in spine dysgenesis are not well understood. In contrast to the expression of FMRP in neurons, relatively little is known about the function of FMRP in glial cells during CNS development. In these particular experiments, we investigated the role of astrocytes in the development of the abnormal dendritic spine morphology and synaptic aberrations seen in FXS. Primary hippocampal neurons were grown in a non-contact co-culture set-up with astrocytes for 17 DIV, allowing for the continuous exchange of molecules between both cell types via the shared defined medium. In this setting, we focused on the contribution of secreted CNS matricellular molecules to neuronal development and synapse formation using an Fmr1 knockout (KO) Fragile X mouse model. Here, we show that: i) Fmr1 KO astrocytes display deficits in TSP-1 levels; ii) An altered expression of astrocyte-secreted factors plays a significant role in dendritic spine dysgenesis and excitatory synapse formation; iii) Exogenous TSP-1 reverts Fmr1 KO astrocyte-mediated spine and synaptic alterations to normal levels.
Role of astrocytes in fragile X neurobiology
Astrocytes are important regulators of neuronal growth and maturation, and are key players in the abnormal neurobiology of a number of developmental disorders, including FXS [27, 46, 47]. In cultured hippocampal neurons, astrocytes have been shown to be a critical component for appropriate dendritic spine morphology and the ability of neurons to form synapses [48–51]. Several studies have recently linked the absence of FMRP in astrocytes to abnormal neuronal structure and function in FXS. Our previous work showed that the loss of FMRP in astrocytes causes abnormal dendritic morphology, including aberrant dendritic branching and dysfunctional synapse development [9, 10]. It has also been shown that the selective loss of FMRP from astrocytes (but not neurons) leads to the reduced expression of the glutamate transporter GLT-1 (EAAT2) and subsequent reduced glutamate uptake by these cells . In this study, we confirmed that synapse formation between neurons is driven by factors released from astrocytes, and astrocytes devoid of FMRP affect proper spine development. More importantly, factors derived from normal astrocytes protect the loss of synapse formation, decrease the density of immature spines, and promote mature spine formation in Fmr1 KO neurons.
Under normal conditions, the release of soluble factors from astrocytes guide neurite growth, synapse formation and maturation [34, 53]. In FXS, dendritic contacts fail to mature and the result is aberrant neural connectivity. We hypothesized this was due to a deficit in astrocyte-derived factors since Fmr1 KO astrocytes grown with WT neurons lacking direct contact contributed to the abnormal spine morphology, evidenced by a greater number of longer, thinner spines. In support of this, a recent study by Yang et al.  showed that elevated levels of neurotrophin-3 in Fmr1 KO astrocytes partially altered dendritic growth in neurons. Therefore, we aimed to identify potential additional astrocyte-derived soluble factors that contribute to the spine development and maturation impairment in FXS. Our study revealed that Fmr1 KO astrocytes show a notable deficit in the expression of soluble factor TSP-1, resulting in dendritic spine dysgenesis in Fmr1 KO neuronal cultures that can be corrected with the exogenous addition of TSP-1.
Thromobspondin-1 contributes to astrocyte-regulated synapse formation
TSPs have been previously identified as important CNS synaptogenic molecules. TSP-1 and −2 are transynaptic organizers, highly expressed by immature astrocytes, which strongly promote structural synapse formation . In particular, they act as permissive switches that time CNS synaptogenesis and enable neuronal molecules to assemble into synapses within a specific window of CNS development. This narrow developmental window typically coincides with the initiation of nascent synaptic contacts between dendrites and axons. Therefore, TSP-1 and −2 serve a transient function and are not required for maintenance of synapses in the adult. Both in vitro and in vivo studies have demonstrated the capacity of TSPs to increase synapse number, promote the localization of synaptic molecules, and refine the pre- and postsynaptic alignment [17, 56]. Furthermore, TSP1/2-deficient mice display a significant decrease in the frequency of excitatory synapses . TSPs have also been shown to regulate presynaptic function by limiting presynaptic release at glutamatergic synapses, serving as a protective mechanism against excitotoxicity . Recently, two transmembrane molecules were uncovered in mediating TSP-induced synaptogenesis. Firstly, neuroligin 1 interacts with TSP-1 and mediates the acceleration of synaptogenesis in young hippocampal neurons . Secondly, α2δ-1, a subunit of the L-type Ca2+ channel complex (LTCC), was also identified as the postsynaptic receptor of TSP in excitatory CNS neurons . Interaction between TSP and α2δ–1 sequentially recruits synaptic scaffolding molecules and initiates synapse formation . Several other known receptors for TSP include the CD47 integrin- associated protein (CD47/IAP), a variety of integrins, and the low-density lipoprotein receptor-related protein LRP1; however, the role of each of these interacting proteins have not been elucidated.
Deficits in TSP-1 affect synapse and dendritic spine development
Our findings revealed a decrease in TSP-1 protein expression in cellular lysates and in astrocyte-conditioned media from Fmr1 KO astrocytes, which suggests that the lack of TSP-1 derived from FMRP-deficient astrocytes interferes with proper spine development and synapse formation in FXS. Likewise, deficits in TSP-1 expression in astrocytes has also been implicated in Down Syndrome (DS) from human brain tissue samples and DS cultured astrocytes . In a study by Jayakumar et al. , a shortage of astroglial-derived TSP-1 contributed to synaptic dysfunction in hepatic encephalopathy, which was linked to a decrease in the neuronal expression of synaptophysin, synaptostagmin, and PSD-95, all of which are critically involved in maintaining the integrity of glutamatergic synapses. In line with these findings, we observed that a decrease in TSP-1 expression resulted in the reduced co-localization of pre- and post-synaptic synaptophysin and PSD-95 in Fmr1 KO neurons.
Spine morphology is linked to synapse function and mushroom-shaped spines are considered to represent the most mature and stable spine morphology [59, 60]. Several categories of spines have been identified based on their shape and size, including thin, stubby, cup, and mushroom-shaped. Recent studies suggest that excitatory synapses are a component of mushroom-shaped dendritic spines . Thus, the increase in mushroom-shaped spines in response to TSP-1 treatment is consistent with our findings that TSP-1 stimulates the formation of excitatory synapses. In our study, we also found that spine length, a measure of synaptic immaturity, was increased in Fmr1 KO mice, suggesting a delay in the development of spines. The prevalence of thin, elongated dendritic spine morphology in Fmr1 KO mice is reminiscent of that observed during early synaptogenesis  in the developing brain, as well as the morphology seen following sensory deprivation [63, 64]. The increase in immature-appearing spines could be due to augmented spine turnover , which fails to decrease in the early postnatal weeks in FXS . Alternatively, the abundance of immature-looking spines in the Fmr1 KO mice could be caused by a failure of a subset of spines to mature.
Interestingly, significant differences in overall spine density between the WT and Fmr1 KO neurons were not observed. Similar studies in Fmr1 KO mice have also found normal hippocampal spine densities  and individual spines with longer lengths . In contrast, others have reported decreased spine density in the Fmr1 KO mice compared to WT littermates [67, 68] and spines of normal length . However, the discrepancies are likely attributed to the use of different staining and quantification methods of spines, and the choice of tissue source (cultured hippocampal neurons versus in vivo or ex vivo brain tissue). As we observed for hippocampal neurons, Braun et al.  also reported a lower abundance of excitatory synapses in Fmr1 KO hippocampal neurons relative to WT at 2 weeks in culture. The failure of excitatory synapse maturation has also been noted in cortical neurons of Fmr1 KO mice [69–71], as well as in Fmr1 KO cerebellar granule cells .
Severe learning deficits have been associated with synaptic dysfunction in FXS and intellectual disabilities [73–75]. Here, we showed that deficits in the formation of dendritic spines in Fmr1 KO neurons could be normalized with conditioned media or a feeder layer derived from normal astrocytes. Similarly, we demonstrated that the addition of exogenous TSP-1 to neuronal cultures markedly promoted the formation of mature (mushroom-shaped) dendritic spines and restored the number of synaptic protein clusters in Fmr1 KO neurons comparable to the level that of WT neurons at 17 DIV. Notably, the application of ACM + TSP-1 has been shown to increase synaptic puncta to the same extent as either ACM or TSP-1 alone, indicating that TSP-1 alone is sufficient to recover synapse formation . Mechanistically, TSP-1 may exert its restoring role in Fmr1 KO neurons by specifically counteracting the loss in FMRP on the dendritic spines that are immature as a result of FMRP loss. Therefore, these findings identify TSP-1 as a critical astrocyte-secreted factor that modulates spine morphology and provide evidence that astrocytes are important contributors to synaptogenesis within the developing CNS. As such, defects in the secretion of astrocyte-derived TSP-1 during a crucial window of development likely contribute to the abnormal neurobiology seen in FXS. The potential therapeutic role of TSP molecules in excitatory synaptogenesis and their relevance to learning and memory in FXS will be an exciting avenue of future investigation.
Correspondingly, these findings highlight the important role of FMRP in astrocytes during the early postnatal weeks of synaptic development in FXS. However, the full extent of the cellular and molecular interactions that govern non-contact-mediated synaptogenic signaling between astrocytes and neurons is not clear. For instance, WT neurons cultured with an astrocyte feeder layer derived from Fmr1 KO mice exhibit fewer mature spines than WT neurons cultured alone. These results suggest that Fmr1 KO astrocytes may potentially release inhibitory substances that prevent normal spine development. Given that profound changes in both excitatory and inhibitory neurotransmission have been reported in FXS , the mechanisms involving a lack of factor and/or the exertion of inhibitory effects warrant further investigation. Therefore, studies exploring the contributions of additional factors may provide greater insight into the underlying mechanisms of FXS.
ACM, astrocyte-conditioned media; AFL, astrocyte feeder layer; CNS, central nervous system; DIV, days in vitro; Fmr1, fragile x mental retardation gene 1; FMRP, fragile x mental retardation protein; FXS, fragile X syndrome; GBP, gabapentin; HI, heat-inactivated; KO, knockout; PSD-95, postsynaptic density 95; rTSP-1, recombinant thrombospondin-1; SYN, synaptophysin; TSP-1, thrombospondin-1; WT, wildtype
We genuinely thank Dr. Angela Scott for her editorial work on this manuscript.
This work was supported by the Natural Sciences and Engineering Research Council of Canada (NSERC), Fragile X Research Foundation of Canada, and the Brain Canada/Azrieli Neurodevelopmental Research Program. The funding bodies contributed the financial resources for the collection and analysis of data in the manuscript.
Availability of data and material
All experimental data is presented in the paper and additional supporting file.
CC participated in the design of the study, carried out the in vitro studies, performed the TSP-1 measurements and immunocytochemistry, conducted the spine/synapse counts and analysis, and drafted the manuscript. SL assisted in the immunocytochemistry and cell counts. LD conceived the study, participated in the design of the study and helped to draft the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the McMaster Animal Research Ethics Board (Animal Utilization Protocol #: 13-12-49). Consent to participate: Not applicable.
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