Automated 4D analysis of dendritic spine morphology: applications to stimulus-induced spine remodeling and pharmacological rescue in a disease model
© Swanger et al; licensee BioMed Central Ltd. 2011
Received: 29 August 2011
Accepted: 7 October 2011
Published: 7 October 2011
Uncovering the mechanisms that regulate dendritic spine morphology has been limited, in part, by the lack of efficient and unbiased methods for analyzing spines. Here, we describe an automated 3D spine morphometry method and its application to spine remodeling in live neurons and spine abnormalities in a disease model. We anticipate that this approach will advance studies of synapse structure and function in brain development, plasticity, and disease.
Dendritic spines are dynamic, actin-rich protrusions that form the postsynaptic compartment at most glutamatergic synapses . Synapse strength is closely correlated with dendritic spine morphology, and synaptic activity regulates spine number and shape during brain development, behavioral learning, and aging [2–4]. In addition, abnormal spine morphology is prevalent in neurological diseases such as intellectual disabilities, autism spectrum disorders, schizophrenia, mood disorders, and Alzheimer's disease [5–7]. Although many details regarding the spine structure-synapse function relationship remain unclear, it is evident that spine morphology can impact excitatory neurotransmission and is an important aspect of neuronal development, plasticity, and disease [6, 8–10].
The lack of automated methods for quantifying spine number and geometry has hindered analysis of the mechanisms linking spine structure to synapse function . Cultured neurons are the primary model system for studying the basic mechanisms regulating neuronal structure and function as these mechanistic studies require complex designs and large sample sizes in order to produce meaningful results. While several recent reports have described automated algorithms for analyzing neuron morphology in vivo[12–18], few independent studies have validated these methods [19, 20] and there are no established methods for automated 3D spine analysis in cultured neurons. Son et al. developed an automated spine analysis algorithm using 2D images of cultured neurons, but 2D analyses do not consider a significant amount of information including all protrusions extending into the z-plane . The majority of spine morphology studies have relied on manual measurements, which are time consuming, often biased by experimenter error and fatigue, and have limited reproducibility .
Here, we present, validate, and apply an automated 3D approach using the commercially available software program Filament Tracer (Imaris, Bitplane, Inc.). Filament Tracer has been used for automated spine detection in vivo, but geometric measurements were limited to spine head width [22, 23]. Also, we have used Filament Tracer to facilitate spine density calculations in cultured neurons, but this analysis required manual validation and extensive editing of false-positive spines . Now, our improved approach generates an accurate 3D reconstruction without any manual validation. Moreover, our approach can be applied to either fixed or live neurons as well as images acquired using either widefield fluorescence or confocal microscopy.
To demonstrate the applicability of our approach, we analyzed changes in spine morphology following acute brain-derived neurotrophic factor (BDNF) application in live hippocampal neurons. We verified our method by showing that acute BDNF treatment increased spine head volume, as was previously published . Furthermore, we demonstrated that BDNF application induced rapid alterations in spine neck and length geometry and resulted in an overall maturation of the dendritic spine population within 60 minutes. We also applied our method to the study of aberrant spine morphology in a mouse model of fragile X syndrome (FXS), an inherited intellectual disability . We not only accurately detected the established spine abnormalities in cultured neurons from this mouse model, but we also demonstrated that these abnormalities were rescued by inhibiting phosphoinositide-3 kinase activity, a potential therapeutic strategy for FXS . These findings demonstrate that our approach is an efficient and accurate method for investigating dendritic spine development and plasticity as well as neurological disease mechanisms and therapies.
Results and discussion
Automated detection and 3D measurement of dendritic spines
To generate the 3D reconstructions for spine analysis, we selected a dendritic region that was 40 - 60 μm in length and void of dendritic branch points and crossing neurites. A point within the dendrite and at the edge of the selected region was assigned as the dendrite starting point, and the following parameters were set: minimum dendrite end diameter (0.75 μm; empirically determined to be the minimum dendritic width enabling accurate tracing), minimum spine end diame ter (0.215 μm; 2 times the pixel width), and maximum spine len gth (5 μm) . The dendritic segment was then traced and volume rendered using automatic thresholds without any additional manual input or editing. On occasion the algorithm inappropriately assigned dendritic protrusions as dendrites instead of spines, so we applied a mathematical filter that selected all dendritic protrusions ≤ 5 μm in length and assigned them as spines. To validate the automated spine detection, spine density was calculated within the same dendritic regions using manual and automated analyses (Figure 1b). The automated measures accurately predicted the manual spine counts as determined by linear regression analysis (Figure 1c) . The mean spine density (spines per 10 μm) did not significantly differ between the manual (4.36 ± 0.46) and automated (4.47 ± 0.41) analyses (Student's t-test, P = 0.836), but there was a consistent trend toward higher spine density using the automated method. The coefficient of variation was lower for the automated results (0.9) as compared to the manual measurements (0.11), suggesting that automated spine detection was slightly more reproducible than manual detection.
Statistical comparison of geometric spine measurements
Estimated population statistics based on published electron microscopy studies
Statistical comparison of spine shape classification
Automated tracking of dendritic spines in live neurons
Dendritic spine density and morphology are dynamically regulated by many extracellular cues and neurotransmitters. For example, many more dendritic protrusions are formed during development than remain into adulthood, indicating that spine formation and morphogenesis are highly regulated processes; yet, the mechanisms determining which spines become stabilized remain unclear. In the adult brain, stimulus induced potentiation of the postsynaptic response can convert spines with small heads to large spines, whereas large spines can shrink in response to long-term depression of the postsynaptic response [40, 41]. However, the detailed mechanisms governing these differential responses remain poorly understood. Therefore, time-lapse imaging in living neurons is an essential tool for studying stimulus-induced synapse development and plasticity.
Acute BDNF treatment induces synapse maturation through spine remodeling
In support of the above assertion, the observed increases in head and neck width and the decrease in protrusion length are associated with increased signaling between the dendritic spine and shaft, which promotes greater signal integration within the neuron [33–35]. Furthermore, we observed an increased proportion of mushroom-shaped spines, which have many GluA receptors and large PSDs; whereas, BDNF decreased the proportion of thin protrusions, which often lack surface GluA receptors and have less defined PSDs . Importantly, our results agree with previous studies showing that acute BDNF enhances postsynaptic glutamate receptor function, increases excitatory postsynaptic currents, and increases intracellular calcium concentration in hippocampal neurons . Thus, our observations provide extensive morphological evidence supporting a role for BDNF in the acute regulation of synapse structure.
To quantitatively analyze remodeling, we calculated the percentages of each protrusion type (stubby, mushroom, or thin) that maintained classification, remodeled into another protrusion type, or were pruned over 60 min. All newly formed spines were excluded from this analysis. Under control conditions, similar proportions of thin protrusions and stubby spines were either remodeled into mushroom spines (28.9% and 27.3%, respectively) or pruned (26.3% and 18.2%, respectively), whereas 78.6% of mushroom spines maintained their shape and only 7.1% were pruned (Figure 4a). Acute BDNF treatment increased the remodeling of both thin and stubby protrusions into mushroom spines (40.5% and 42.9%, respectively) as well as the percentage of mushroom spines (26.7%) and thin protrusions (40.5%) that were pruned. However, BDNF slightly decreased the percentage of stubby spines that were pruned (14.3%). Interestingly, thin- and mushroom-shaped protrusions rarely morphed into stubby spines, and stubby spines were never observed to remodel into thin protrusions. These observations suggest that stubby and thin protrusions have similar propensities for remodeling into mushroom spines, but they likely do so through distinct mechanisms.
Among the total spine population, thin protrusions had the highest incidence of remodeling, and mushroom spines showed the lowest incidence of remodeling (Figure 4b). Following BDNF treatment, stubby spines had the lowest incidence of remodeling (see sample movie in Additional File 2), suggesting that stubby spines may not be simply a transitional structure, but that they might have an important end function as a stable structure under certain conditions. The BDNF-induced increases in the proportion and stability of stubby spines, reported in Figure 3, are difficult to interpret, because the role of stubby spines in neuronal function remains controversial. Stubby spines do not maintain or recruit GluA receptors as efficiently as mushroom spines, nor do they form synapses as often [47–50]. On the other hand, stubby spines might have enhanced coupling to the dendritic shaft as compared to the other spine types . Also, stubby spine incidence is increased during learning in vivo, and it has been theorized that they are transitional structures that will be enlarged/stabilized or have undergone shrinkage due to synaptic weakening [2, 6, 41, 46, 52, 53]. Our data suggest that it is unlikely for an increase in stubby spines to result from the weakening of mushroom spines or the retraction of thin protrusions, but it is possible that the increase in stubby spines is linked to the increase in total protrusion number following BDNF stimulation. Future studies in systems having a higher overall incidence of stubby spines, perhaps neurons in an earlier developmental stage, will be important for advancing our understanding stubby spine formation, remodeling, and function.
These results also have implications regarding spine formation. Several mechanisms have been proposed for how stable, mushroom-shaped spines are formed, including growth of mushroom spines from the dendritic shaft, morphogenesis of a filopodia into a mushroom spine, and retraction of filopodia into the dendritic shaft resulting in a shaft or stubby spine synapse followed by growth of a mushroom spine at the same location [47, 54–56]. Our data clearly support the formation of mushroom spines de novo and through morphogenesis of an existing filopodia (Figure 4) as has been previously observed in vitro and in vivo[53, 55–63]. However, our data suggest that mushroom spine formation via filopodia retraction into a stubby spine followed by re-growth is not a common occurrence, at least in this model system, as we rarely observed morphogenesis of a filopodia into a stubby spine. Whether filopodia were retracted fully into the shaft and re-emerged as mushroom spines at the same locus was not evaluated in the current study, but this analysis is possible using our automated method and can be investigated in future studies.
To investigate whether any geometric parameters were associated with BDNF-induced remodeling, the initial (t = 0) mean head width, neck width, and protrusion length were compared among stable, remodeled, and pruned mushroom spines or stable, remodeled, and pruned thin protrusions (Figure 4g,h). Large neck width was the best predictor of mushroom spine stability, whereas head width was not significantly different between stable and remodeled mushroom spines (Figure 4g). Mushroom spine pruning was associated with reduced head and neck width and increased length compared to the other two groups (Figure 4g). For thin protrusions, a high ratio of head width to neck width was the best indicator of stability (see Figure 4d and the sample movie in Additional File 3). Interestingly, these data are consistent with functional studies reporting that large neck width is associated with greater synaptic strength  and synaptic potentiation of thin protrusions is promoted by maintaining high concentrations of signaling molecules within the head, which might be due to a high ratio of head width to neck width [46, 64].
An interesting observation was that BDNF decreased the percentage of mushroom spines that remained as mushroom spines from 79% to 53% (Figure 4e). Moreover, 26% of mushroom spines were pruned following BDNF. Both observations imply BDNF-induced turnover of mushroom spines, suggesting that the overall net gain in spine maturation (increased density and spine width, reduced length) (Figure 3) involves extensive remodeling. This process may involve pruning of mushroom spines that passed certain thresholds approaching immature phenotypes (e.g. low head or neck width, or increased length), which are apparently replaced by more mature mushroom spines developed from other less mature populations (thin, stubby).
In the future, it will be important to study the different mechanisms underlying specific types of spine formation and remodeling, such as the distinctions between stubby and thin protrusion remodeling into mushroom spines. Furthermore, there is still much debate regarding the functional significance of different spine morphologies in brain development, plasticity, and disease. One necessary step towards understanding the structure-function relationship of dendritic spines is generating reproducible and interpretable spine morphology data. The accuracy and speed of our method makes it well-suited for studies of this type, and we anticipate that our approach will facilitate studies on spine structure and its relation to synapse function.
In addition to advancing morphological studies, the described technique has the potential to facilitate studies evaluating the synaptic localization of specific molecules. The fluorescence intensity of multiple channels can be automatically quantified within each dendritic spine; thus, one could evaluate whether a particular fluorescently tagged or stained molecule is differentially localized between spine types or shows altered localization following a pharmacological, molecular, or genetic manipulation. Therefore, the combination our optimized spine analysis method with automated quantification of spine fluorescence creates a powerful and efficient technique for simultaneously studying spine morphology and the molecules regulating synapse structure and function.
Inhibiting PI3 kinase activity rescues dendritic spine defects in neurons from Fmr1 KO mice
The importance of dendritic spine morphology is emphasized by the fact that spine abnormalities are associated with varied neurological diseases such as intellectual disabilities, neurodegenerative diseases, and psychiatric disorders . Cultured neurons are a valuable model system for studying the mechanisms underlying brain diseases; as such, it is critical that spine analysis methods effectively detect aberrant spine phenotypes in disease models and identify treatments that ameliorate disease phenotypes. Here, we used our approach to study spine morphology in neurons from Fmr1 knockout mice, a mouse model of fragile X syndrome (FXS).
Next, we investigated whether treating hippocampal neurons with a phosphoinositide-3-kinase (PI3K) inhibitor affected spine morphology. Previously, we discovered that inhibiting PI3K activity is a potential therapeutic strategy for FXS. We showed that the loss of FMRP leads to excess PI3K activity and treatment with a PI3K inhibitor, LY294002, rescues several neuronal phenotypes in Fmr1 knockout mice, including aberrant synaptic protein synthesis, GluA receptor internalization, and dendritic spine density . Here, using our automated approach, we reproduced our previous findings by demonstrating that LY294002 treatment (10 μM for 72 hrs) reduced spine density in hippocampal neurons from Fmr1 knockout mice to wild type levels (Figure 5b). Furthermore, our analysis revealed that LY294002 treatment significantly increased spine head width, decreased spine length, and increased spine volume in neurons from Fmr1 KO mice (Figure 5c-e). Additionally, LY294002 significantly increased mushroom-shaped spines and decreased thin spines in FMRP-deficient neurons such that all spine proportions were similar to those of wild type neurons (Figure 5f). These data indicate that inhibiting PI3K activity not only rescues increased spine density in a mouse model of FXS, but also restores aberrant spine shape to the wild type morphology. These findings are an important advance of our previous findings and further support the pharmacological inhibition of PI3K as a potential FXS treatment strategy . More broadly, these data demonstrate that our automated approach can be used to study dendritic spine abnormalities and potential pharmacotherapeutics in neurological disorders.
Although spine defects are apparent in many brain diseases, a vital unanswered question is whether altered spine morphology contributes to disease onset and progression or is secondary to disordered neuronal activity [5, 73]. Of note, cortical neurons in a mouse model of Alzheimer's disease exhibit reduced spine density, a phenotype evident in patients with Alzheimer's disease, but these neurons do not show overt electrophysiological impairments; whereas, other mouse models of Alzheimer's disease show both structural and functional phenotypes in cortical neurons . In addition, it is possible to alter synaptic efficacy without inducing long-term changes in spine morphology, and altering spine morphology through manipulating the neuronal cytoskeleton is not always sufficient to alter synapse function . These data highlight the complexity inherent in the spine structure-synapse function relationship and emphasize the importance of developing powerful techniques for studying the mechanisms regulating spine morphology in brain development, plasticity, and disease.
We have developed an automated 3D approach for dendritic spine analysis using neurons expressing fluorescently labeled Lifeact. This versatile method can be applied to images of either fixed or live cultured neurons that were collected using widefield fluorescence or confocal microscopy. The increased speed and accuracy of our automated spine analysis, as compared to manual spine assessments, is critical for uncovering the complicated mechanisms underlying normal and aberrant dendritic spine formation and remodeling. Using our automated approach, we showed that acute BDNF treatment leads to rapid spine remodeling consistent with enhanced synaptic efficacy. We also found that inhibiting PI3 kinase activity rescues aberrant spine shape in neurons from a mouse model of FXS. We predict that this method will significantly advance studies of glutamatergic synapse structure and function in neuronal health and disease.
Neuron culture, transfection, and drug treatments
Hippocampal neurons were isolated from embryos at E18 (rat) or E17 (mouse) and cultured at high-density as previously described with minor modifications . Rat hippocampal neurons were cultured in Neurobasal medium (Invitrogen) supplemented with NS21 . Neurons were either plated on 15 mm glass coverslips and co-cultured with glia, or plated on 35 mm MatTek glass bottom dishes in glia-conditioned media that was exchanged every 2 days with new glia-conditioned media.
Fixed neuron experiments: 16-17 DIV neurons were transfected with plasmids encoding Lifeact-ruby (a generous gift from Dr. Roland Wedlich-Soldner, Max Planck Institute, Martinsried, Germany), Lifeact-GFP, GFP, or membrane-tagged GFP using NeuroMag (OZBiosciences). DiI labeling was performed on 16 DIV neurons by incubating the coverslips covered with a small volume of neuronal culture media containing Vybrant DiI solution (Invitrogen) for 25 min at 37°C. For LY294002 experiments, 15 DIV neurons were treated with 10 μM LY294002 or an equivalent volume of DMSO for 72 hrs total; the culture media was exchanged with conditioned media containing freshly prepared drug (or vehicle) after 24 and 48 hrs.
Live neuron experiments: 11 DIV rat hippocampal neurons were transfected with a plasmid encoding Lifeact-ruby using Lipofectamine 2000 and used for imaging 24 hrs later. Thirty minutes prior to imaging, neurons were equilibrated to glia-conditioned imaging media (phenol red-free Neurobasal media supplemented with HEPES, sodium pyruvate, NS21, and Glutamax). For BDNF experiments: One hour prior to imaging, neurons were starved in glia-conditioned imaging media without NS21, and immediately prior to time lapse imaging neurons were treated with BDNF (100 ng/ml; Peprotech) or vehicle (H2O).
Widefield fluorescence: Twenty-four hours after transfection, hippocampal neurons were fixed with 4% paraformaldehyde in 1x phosphate-buffered saline (PBS), washed 3 times with 1x PBS, and the coverslips were mounted on microscope slides with propyl gallate-containing polyvinyl alcohol. Neurons were imaged on a Nikon Eclipse Ti microscope with a Nikon Intensilight and Photometrics Coolsnap HQ2 camera. GFP was imaged using a 480/40 excitation filter, a 535/50 emission filter, and a 505 dichroic (Nikon), and ruby and DiI were imaged using a 545/30 excitation filter, a 620/60 emission filter, and a 570 dichroic. Images were acquired using a 60X oil-immersion objective (Nikon Plan Apo, N.A. 1.40). Z-series images were acquired at 0.15 μm increments through the entire visible dendrite.
Confocal laser scanning: Time lapse imaging was performed on a Nikon A1R confocal encased in a plexiglass humidified chamber maintained at 37°C and 5% CO2 using a 60X oil immersion objective (Nikon Plan Apo, N.A. 1.40). Images of Lifeact-ruby were collected using a 561 nm laser for excitation and a 650 emission filter. Z-series were acquired at 0.15 μm increments, and a Nikon Perfect Focus system was enabled for the duration of the experiment.
Images were deconvolved in AutoQuant X (MediaCybernetics) using the blind algorithm, which employs an iteratively refined theoretical PSF. No further processing was performed prior to image analysis. For preparation of figures, maximum intensity Z-projections were created in Imaris (Figures 1 and 5) or average intensity Z-projections were created using ImageJ (Figures 2 and 4). For visualization, brightness and contrast levels were adjusted using ImageJ.
Automated image analysis
In Imaris Surpass mode, a new filament was created using the Autopath mode and a region of interest (ROI) was selected. To select an ROI, we identified a dendritic region 40 - 60 μm length that was distal to a dendritic branch point and void of crossing neurites or any additional dendritic branch points. A minimum dendrite end diameter of 0.75 μm was entered and a single dendrite starting point was assigned at the edge of the ROI. For time-lapse image series, a single dendrite starting point was assigned at each timepoint by using the AutoDepth mode. Automatic thresholds were used for assigning dendrite end points and dendrite surface rendering. To trace spines, the maximum spine length and minimum spine end diameter were set at 5 μm and 0.215 μm, respectively, for fixed neuron experiments and 15 μm and 0.3 μm, respectively, for live imaging experiments. Automatic thresholds were used for generating spine seed points and surface rendering. After generating the trace, a filter was applied to ensure all dendritic protrusions ≤ 5 μm (or 15 μm) were assigned as spines; to do so, we created a filter that selected all dendritic segments with "Branch level" = 2 and "length" ≤ 5 (or 15) and the selected segments were assigned as spines by choosing "Assign as spine" under the Edit tab. All of the geometric parameters and filters were set, or loaded from a previously analyzed image, at the start of the analysis session after which the software maintained these values. For each subsequent image processed, an ROI was selected, a dendrite starting point was assigned, and then the trace was built by clicking "Finish". To apply the filter, the Filter tab was opened (which automatically selected the appropriate segments), then by clicking on the Edit tab followed by "Assign as spine" the final 3D trace was generated. Filament statistics were exported into Excel (Microsoft), where they were compiled and graphed.
Manual image analysis
Manual analyses were performed in Imaris Surpass mode using the same dendritic ROIs as above. The dendrite length was measured using Measurement Points and each spine was marked using Spots (Imaris). Using Measurement Points, head width was measured at the maximum width of the spine tip, neck width was measured at the minimum point along the spine length, and spine length was measured from the dendrite shaft to the spine tip. Each ROI was processed in duplicate and the values were averaged.
These logic statements return a value of 1 if true and 0 if false. The total number of spines in each class was tallied by summing the results of the logic statements. For live imaging experiments, a maximum length of 15 μm was used instead of 5 μm.
Unless otherwise noted, statistics were completed using PASW Statistics 18 (SPSS, Inc). All datasets were analyzed for equal variance using Levene's test and normality using the Kolmogorov Smirnov test. Normally distributed datasets were compared using either Student's t-test or an ANOVA followed by post-hoc tests as noted in figure legends. Non-normal datasets were compared using the Mann-Whitney U test or Kruskal Wallis test. Cumulative distributions were compared using the Kolmogorov-Smirnov test. Alpha was set at 0.05 for all comparisons. Power analysis was performed using G*Power 3.1.2 (University of Kiel, Germany) with β = 0.8 and α = 0.05, and effect size and standard deviation were determined using pilot experiment results. The experimenter was blind to treatment and genotype during all image analysis.
The authors would like to thank Dr. Alexa Mattheyses for technical assistance and critically reading the manuscript and Andrew Swanson for technical assistance and helpful discussions. SAS was supported by predoctoral fellowships from the NIH (F31NS063668, T32GM0860512 and T32NS007480) and the Epilepsy Foundation and Lennox & Lombroso Trust Fund. CG was supported by a Basic Science Grant from NFXF. This work was supported by NIH MH085617 and NARSAD Investigator Award to GJB, the Emory/Baylor Fragile X Center (P30HD024064) and the Neuronal Imaging Core of the Emory Neuroscience NINDS Core Facility (P30NS055077).
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