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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
J Neurosci. Author manuscript; available in PMC Aug 17, 2009.
Published in final edited form as:
PMCID: PMC2727754
NIHMSID: NIHMS67120

Coordination of synaptic adhesion with dendritic spine remodeling by AF-6 and kalirin-7

Abstract

Remodeling of central excitatory synapses is crucial for synapse maturation, plasticity, and contributes to neurodevelopmental and psychiatric disorders. Remodeling of dendritic spines and the associated synapses, has been postulated to require the coordination of adhesion with spine morphology and stability; however, the molecular mechanisms that functionally link adhesion molecules with regulators of dendritic spine morphology are largely unknown. Here we report that spine size and N-cadherin content are tightly coordinated. In rat mature cortical pyramidal neurons, N-cadherin-dependent adhesion modulates the morphology of existing spines by recruiting the Rac1 guanine-nucleotide exchange factor kalirin-7 to synapses through the scaffolding protein AF-6/afadin. In pyramidal neurons, N-cadherin, AF-6, and kalirin-7 colocalize at synapses and participate in the same multiprotein complexes. N-cadherin clustering promotes the reciprocal interaction and recruitment of N-cadherin, AF-6, and kalirin-7, increasing the content of Rac1 and in spines and PAK phosphorylation. N-cadherin-dependent spine enlargement requires AF-6 and kalirin-7 function. Conversely, disruption of N-cadherin leads to thin, long spines, with reduced Rac1 contact, caused by uncoupling of N-cadherin, AF-6, and kalirin-7 from each other. By dynamically linking N-cadherin with a regulator of spine plasticity, this pathway allows synaptic adhesion molecules to rapidly coordinate spine remodeling associated with synapse maturation and plasticity. This study hence identifies a novel mechanism whereby cadherins, a major class of synaptic adhesion molecules, signal to the actin cytoskeleton to control the morphology of dendritic spines, and outlines a mechanism that underlies the coordination of synaptic adhesion with spine morphology.

Keywords: Rac1, GluR1, postsynaptic density, synaptic plasticity, cytoskeleton, synapse

Remodeling of existing dendritic spines plays crucial roles in synapse maturation and plasticity (Yuste and Bonhoeffer, 2001). Conversely, aberrant spine morphogenesis is associated with mental retardation (Fiala et al., 2002), psychiatric disorders including schizophrenia (Glantz and Lewis, 2001; Fiala et al., 2002), and addiction (Robinson and Kolb, 1999). Synaptic maturation and plasticity entail changes in multiple processes, including spine morphology, trans-synaptic adhesion, and glutamate receptor content, which have recently been postulated to be coordinately regulated (Luscher et al., 2000; Kasai et al., 2003). Accordingly, in vivo imaging studies revealed that in the mammalian cortex spine stability is well correlated with spine shape: thin spines are very dynamic, while large spines are stable (Trachtenberg et al., 2002). However the molecular mechanisms that accomplish the coordination of adhesion and morphology in spines are not known.

Changes in synaptic adhesion, which occur in parallel with spine remodeling, contribute to synapse maturation and plasticity (Tang et al., 1998; Bozdagi et al., 2000; Huntley et al., 2002). Cadherins are a major class of adhesion molecules (Wheelock and Johnson, 2003), which play crucial roles in nervous system development and physiology (Bamji, 2005). Cadherins and associated proteins control spine morphology and stability: reduced cadherin or α-N-catenin function cause thin and more motile spines, while α-N-catenin overexpression results in larger spine heads and increased spine number due to reduced spine turnover (Togashi et al., 2002; Abe et al., 2004). Cadherins also play important roles in synaptic plasticity: synaptic activity regulates N-cadherin clustering and α- and β-catenin abundance in spines (Bozdagi et al., 2000; Tanaka et al., 2000; Murase et al., 2002; Abe et al., 2004), while N-cadherin adhesion is important for LTP (Tang et al., 1998; Bozdagi et al., 2000) and memory (Schrick et al., 2007).

Cadherin clustering and signaling to the actin cytoskeleton are essential for adhesion. Signaling to the cytoplasm is accomplished by interactions of cadherins with cytoplasmic proteins including catenins, which in turn are thought to regulate Rho GTPases and subsequent actin rearrangements (Bamji, 2005). Rho GTPases are central regulators of actin dynamics and control spine morphology (Nakayama et al., 2000). Rac1 activation induces spine formation and enlargement; Rac1 inhibition produces thin and long spines (Tashiro and Yuste, 2004). However, the mechanisms whereby cadherins regulate GTPases are not known. We hypothesized that this may be accomplished through synaptic guanine-nucleotide exchange factors (GEFs), direct activators of Rho GTPases (Schmidt and Hall, 2002). Kalirin-7 is a neuron-specific Rac1-GEF concentrated in dendritic spines, where it activates Rac1 and regulates spine morphogenesis (Penzes et al., 2001; Penzes et al., 2003; Xie et al., 2007). The link between cadherins and kalirin-7 may be provided by the scaffolding protein AF-6/afadin, which interacted with kalirin-7 in a yeast two-hybrid screen (Penzes et al., 2001), but is enriched in cadherin adhesion junctions through interaction with α-catenin and nectin (Mandai et al., 1997; Pokutta et al., 2002). In neurons AF-6 is present in synapses (Buchert et al., 1999; Xie et al., 2005) and puncta adherentia (Nishioka et al., 2000), and controls spine morphogenesis in cortical pyramidal neurons (Xie et al., 2005).

To understand the mechanisms that allow synaptic adhesion molecules to control spine remodeling, which may also underlie the coordination of spine adhesion, structure, and stability, we investigated the roles of AF-6, kalirin-7, and Rac1 in N-cadherin-dependent spine remodeling.

Materials and methods

Reagents

The plasmid encoding N-cadherin was a gift from Dr. David R. Colman (Montreal Neurological Institute); myc-kalirin-7 and myc-L-AF-6 were described previously (Penzes et al., 2001; Xie et al., 2005). Myc-kal7-ΔGEF was generated by the deletion of the region between aa 1284–1484 in the myc-kalirin-7 plasmid; Rap-CA and AF-6-PDZ* was described in Xie et al., 2005. Antibodies: GFP, PSD-95, and GluR1-C-terminal polyclonal antibodies were generated in the laboratory of Dr. Richard L. Huganir, N-cadherin polyclonal (recognizing the C-terminus of N-cadherin, but also E and R cadherins) was a gift of Dr. David Colman (Montreal Neurological Institute), phospho-PAK antibody was a gift of Dr. Jonathan Chernoff (Fox Chase Cancer Center, Philadelphia). Kalirin antibodies were described in Penzes et al., 2001. The following antibodies were purchased: AF-6 polyclonal (Sigma), PSD-95 and Rac1 monoclonal (Upstate), N-cadherin monoclonal (recognizing the N-terminus) (Sigma), N-cadherin goat polyclonal (Santa Cruz), α-N-catenin monoclonal and myc monoclonal (University of Iowa Hybridoma Bank), GFP monoclonal (Chemicon), Rap1 polyclonal (Santa Cruz).

Neuronal cultures

Dissociated cultures of primary cortical neurons were prepared from E17 Sprague-Dawley rat embryos, cultured in Neurobasal medium with B27 (InVitrogen) for 3–4 weeks (Xie et al., 2005), and transfected with plasmids (1–10 µg DNA) using Lipofectamine 2000 (InVitrogen). Mature neuron cultures (div 24~28) were used in all experiments unless otherwise indicated. Rats were used in accordance with ACUC institutional and national guidelines and regulations under approved protocols.

Quantitative Analysis of Spine Morphologies

Healthy pyramidal neurons were imaged with a confocal microscope (Zeiss LSM5 Pascal). Confocal images of single- and double-stained neurons were obtained with a Ziess LSM5 Pascal confocal microscope. To determine the lateral resolution of our confocal microscope, we imaged fluorescent microspheres (Duke Scientific) of known diameters, mounted in ProLong antifade solution, using the 63x oil-immersion objective (NA = 1.4). Quantification indicated that the lateral point spread function was smaller than 0.5 µm, and that areas equal to or larger than 0.21 µm2 were accurately measured. Therefore we did not include structures in our analysis that had an area of less than 0.25 µm2, as these structures are approaching the limit of our microscope’s resolution. It should also be noted that measurements of small spine features, such as thin spine necks, could be overestimated in our measurements. An anti-GFP antibody was used to circumvent potential unevenness of GFP diffusion in spines. Images of neurons were taken using the 63x oil-immersion objective as z-series of 3–8 images, averaged 4 times, taken at 0.37 µm intervals, 1024×1024 pixel resolution at a scan speed of 8 s per section. The acquisition parameters were kept the same for all scans. Two-dimensional maximum projection reconstructions of images, morphometric analysis and quantification were done using MetaMorph software (Universal Imaging). Synapses formed onto healthy neurons with pyramidal morphologies were imaged as described above. Cultures that were directly compared were stained simultaneously and imaged with the same acquisition parameters. For each condition, 5–6 neurons each from at least three separate experiments were used, and two dendrites from each neuron (approximately 75–100 µm per dendrite) were analyzed. Experiments were done blind to conditions and on sister cultures. To examine the morphologies of dendritic spines, individual spines on dendrites were manually traced, and the area, maximum length and head width of each spine was measured by MetaMorph. Student's unpaired t tests were used to determine the statistical significance of differences between two groups; one-way ANOVA were used to compare three or more groups, followed by Tukey-b post hoc for multiple comparisons. Statistical analyses were performed in Excel, SPSS, or GraphPad Prism.

Immunostaining and quantitative immunofluorescence

Changes in clustering were quantified using immunofluorescence on neurons fixed with 3.7% formaldehyde (for GFP-expressing neurons) or −20°C methanol (for synaptic proteins) and visualized with specific antibodies. Fixed neurons were permeabilized and blocked simultaneously in PBS containing 2% normal goat serum and 0.2% Triton-X-100 for 1 hr at room temperature. Primary antibodies were added in PBS containing 2% normal goat serum for 2 hr at room temperature or overnight at 4 °C, followed by 3 × 10 min washes in PBS. Secondary antibodies, anti-rabbit-FITC (Vector), anti-mouse-FITC (Vector), anti-rabbit-Rhodamine (Pierce), anti-mouse- Rhodamine (Pierce), anti-goat-Alexa 514 (InVitrogen), were incubated for 1 hr at room temperature in 2% normal goat serum in PBS. Further 3 washes (5 min each) were preformed before coverslips were mounted using ProLong antifade reagent (Invitrogen). Healthy neurons with pyramidal morphologies were imaged as described above. Cultures that were directly compared were stained simultaneously and imaged with the same acquisition parameters. For each condition, 5–6 neurons each from 3 separate experiments were analyzed. Experiments were done blind and on sister cultures. For fluorescence intensity measurements, the background corresponding to areas without cells were subtracted to generate a “background-subtracted” image. Images were then thresholded equally to include clusters with intensity at least two fold above the adjacent dendrite. To measure the intensity of clusters in spines or colocalized with another signal, regions around spines were generated based o GFP fluorescence or cluster immunofluorescence in one channel. These regions were then transferred into the target channel, and only fluorescence integrated intensities within the colocalizing regions were measured. To measure individual cluster immunofluorescence integrated intensities, total gray values of each cluster were measured automatically. For total integrated intensities/dendritic segment length regions were outlined along dendrites and total gray values of signals colocalized with a reference signal within these regions were measured and normalized to dendritic length.

N-cadherin activating and blocking treatments

To stimulate adhesion by engaging N-cadherins, we incubated neurons for 5 hr with recombinant Fc-N-cadherin (Fc-Ncad) protein chimera between the extracellular domain of N-cadherin (aa 1–724) and the Fc region of human IgG (R&D Systems) pre-clustered with anti-human Fc antibody (goat) (Lambert et al., 2000). To block N-cadherin-mediated adhesion, we incubated neurons for 5 hr with GC-4 interfering antibody (Sigma) which binds to the N-terminal extracellular domain of N-cadherin and disrupts N-cadherin mediated adhesion (Meyer et al., 1992).

Coimmunoprecipitation

For coimmunoprecipitation, hEK293 cells were harvested in RIPA buffer (in mM: 150 NaCl, 10 Tris-HCl, pH 7.2, 5 EDTA, 0.1% SDS, 1% Triton X-100, 1% Deoxycholate, plus inhibitors). Lysates were then sonicated, cleared by centrifugation at 14000 × g for 10 min, and pre-cleared with 30 µl Protein Sepharose A for 60 min at 4°C. Supernatants were incubated with 3–5 µl antibody for 2–4 hr; 60 µl of protein-A-Sepharose was added for 1 hr at 4°C, after which they were washed 3x with 1 ml RIPA. Coimmunoprecipitations from cortical pyramidal neurons were carried out essentially as described above. All samples were boiled for 5 min at 95°C after addition of Laemmli buffer and analyzed by SDS-PAGE and Western blotting.

Subcellular fractionation and detergent extractions

Rat forebrain homogenates were fractionated by centrifugation to yield soluble (S2) and particulate (P2) synaptosomal fractions using standard techniques (Penzes et al., 2000). P2 fraction was then extracted with 1% Triton X-100 (TX), 1% SDS (SDS), 1% deoxycholate (Doc), or 1% RIPA, for 30 min on ice, followed by centrifugation. Supernatant (S) and pellet (P) fractions were analyzed by SDS-PAGE and Western blotting.

Statistics

All data represent means ± SEM. Student's unpaired t-test was used to determine the statistical significance of the differences between two groups. One-way ANOVA followed by post-hoc Tukey’s multiple comparison test was used to determine the statistical significance of the differences among multiple groups (GraphPad Prism). Differences were deemed significant when p < 0.05.

Results

N-cadherin-mediated adhesion controls spine morphology and GluR1 content

Recent studies reported that interfering with N-cadherin, β-catenin, p120 catenin, and α-N-catenin functions affected spine morphology in hippocampal neurons (Murase et al., 2002; Togashi et al., 2002; Abe et al., 2004; Elia et al., 2006) providing support for the hypothesis that synaptic adhesion and spine size are coordinated (Kasai et al., 2003). Indeed, we observed a close correlation between dendritic spine sizes and N-cadherin contents in mature (div 28) cortical pyramidal neurons (Fig. 1a, b), further establishing a relationship between adhesion and spine morphology. N-cadherin was concentrated in clusters along dendrites where it colocalized with PSD-95, indicating enrichment in excitatory synapses (Fig. S1a), and thus is well-positioned to control adhesion-dependent spine remodeling in these neurons. To determine whether N-cadherin-mediated adhesion affected spine size, we activated or inhibited N-cadherin adhesion in pyramidal neurons (Fig. 1c, d). To mimic enhanced adhesion, we incubated mature (div 28) cortical pyramidal neurons with recombinant Fc-N-cadherin pre-clustered with an anti-Fc antibody (Lambert et al., 2000) to engange N-cadherins. To disrupt N-cadherin adhesion, we incubated neurons with GC-4 interfering antibody, which binds to the N-terminal extracellular domain (Meyer et al., 1992). Treatment with pre-clustered Fc-N-cadherin (clust FcNcad) resulted in the enlargement of existing spines (areas, control 0.88 ± 0.02, clust FcNcad 1.69 ± 0.05 µm2) and substantial increase of N-cadherin immunofluorescence inside spines (N-cadherin integrated intensities, control 1.93 ± 0.22, clust FcNcad 8.33 ± 1.39, arbitrary unit), without affecting spine length and linear densities; while GC-4 (interf Ab) resulted in longer spines (length, control 1.20 ± 0.04, interf Ab 2.42 ± 0.05 µm) and slightly elevated linear spine density (Fig. 1d; control 5.40 ± 0.43, interf Ab 7.40 ± 0.67 spines/10 µm). While interference did not cause an apparent reduction in average spine area, analysis of the spine length/breadth ratios revealed that this was due to the simultaneous elongation of spines, which occluded the changes in areas (as reflected by higher length/breadth ratios) (Fig. 1e–f). In summary, N-cadherin activation caused enlargement of existing spines, while interference with N-cadherin dimerization caused remodeling of spines into thin, long shapes (Fig. 1f). IgG alone, unclustered Fc-Ncadherin (not shown), or clustered ephrinB1 (Fig. S2a, b) had no detectable effect. As expected, clustered Fc-N-cadherin induced formation of large N-cadherin clusters localized in spines (Fig. 1c, right, arrows), while GC-4 resulted in N-cadherin clusters in the dendritic shaft (arrowheads) (although no significant reduction in spine heads), indicating that endogenous N-cadherin was affected by these reagents (Fig. 1d). The N-cadherin-mediated spine enlargement observed in this study is independent of the ephrinB-EphB receptor pathway identified previously, in that ephrinB-induced spine morphogenesis was only seen in young hippocampal but not in mature cortical neurons (Penzes et al., 2003). We confirmed these results by treating mature cortical neurons with clustered ephrinB: no change in spine size, length or density was observed (Fig. S2a, b). Furthermore, treatment with clust FcNcad in neurons expressing a kinase-dead mutant of the EphB receptor still produced spine enlargements concurrent to those in treated untransfected cells (Fig. S2a, b).

Figure 1
Activation and inhibition of N-cadherin adhesion result in spine remodeling

Spine size and AMPA receptor content are thought to be tightly coordinated in that larger spines, as those induced by N-cadherin activation, have more AMPA receptors, resulting in stronger and more stable synapses (Kasai et al., 2003). Recent studies reported that N-cadherin interacts with AMPA receptors (Dunah et al., 2005; Nuriya and Huganir, 2006), suggesting that cadherin-mediated adhesion may regulate spine AMPA receptors. We tested this hypothesis by stimulating or blocking N-cadherin adhesion and examining the content of GluR1 subunit of AMPA receptors in spines (Fig. 1g. h). N-cadherin engagement resulted in more GluR1 in clusters, while N-cadherin inactivation resulted in less GluR1 in clusters (integrated intensities/cluster: control 10.0 ± 1.0, clust FcNcad 17.3 ± 2.9, interf Ab 7.0 ± 0.4 a.u.). These experiments indicate that synaptic adhesion strength actively controls spine morphology and AMPA receptor content, consistent with the requirement for N-cadherin adhesion in LTP (Tang et al., 1998; Bozdagi et al., 2000).

AF-6 colocalizes and interacts with N-cadherin in neurons

The interaction of N-cadherin’s cytoplasmic tail with cytoplasmic proteins, including α-N-catenin, β-catenin, and p120-catenin, are important for N-cadherin-dependent spine morphogenesis (Murase et al., 2002; Togashi et al., 2002; Abe et al., 2004; Elia et al., 2006). However the detailed mechanism whereby N-cadherin controls spine remodeling is not known. Because the protein AF-6 is a component of the cadherin-based adhesion complexes in epithelial cells (Pokutta et al., 2002) and controls spine remodeling in cultured neurons (Xie et al., 2005), we reasoned that it may also control adhesion-dependent spine remodeling. Therefore, we examined the colocalization and interaction of AF-6 with components of the N-cadherin complexes in cultured pyramidal neurons and rat forebrain. Consistent with previous reports (Nishioka et al., 2000; Mizoguchi et al., 2002), we found that in young neurons (div 7) AF-6 was enriched in contact sites between neurites, where it partially colocalized with N-cadherin (Fig. S1b). In developing neurons (div 14), AF-6 and N-cadherin partially colocalized in clusters along dendrites, suggesting a role for this interaction in synapse maturation (Fig. S1c). In mature (div 24–28) neurons, AF-6 colocalized with N-cadherin at the somatic plasma membrane, in clusters along dendrites, and in spines (Fig. 2a). Similarly, AF-6 partially colocalized with α-N-catenin, its direct interacting partner in the N-cadherin complex (arrows, Fig. 2b). As revealed by colocalization with PSD-95, a large fraction of AF-6 clusters in dendrites were at excitatory synapses (Fig. S1d, e). Taken together, these data support a role for AF-6 in N-cadherin-dependent adhesion events in neurons at different stages of development. While a large fraction of AF-6 is present in spines, AF-6 is also associated with adhesion complexes at other sites, such as soma and dendritic shafts, where it may participate in adhesion events with specific functions. To confirm in vivo the interaction between AF-6 and N-cadherin-associated protein complexes, we performed coimmunoprecipitation from rat forebrain homogenates. An AF-6 antibody specifically co-precipitated N-cadherin, and an N-cadherin antibody specifically co-precipitated AF-6 (Fig. 2c), suggesting that AF-6 and N-cadherin participate in the same protein complexes. Together with their colocalization, this indicates that AF-6 interacts with components of the N-cadherin-based adhesion complexes in neurons.

Figure 2
Activation and inhibition of N-cadherin adhesion result in AF-6 redistribution that underlies spine remodeling

AF-6 is regulated by N-cadherin-mediated adhesion and is required for cadherin-dependent spine enlargement

If AF-6 was a functional component of adhesion complexes, activation of N-cadherins would likely affect its subcellular localization. Our results revealed that N-cadherin activation induced the formation of larger clusters of endogenous AF-6 along dendrites (Fig. 2d, arrowheads) and in spines (Fig. 2e, arrowheads). Furthermore, AF-6 recruitment to N-cadherin clusters is greatly enhanced by N-cadherin activation (Fig. 2f), as evidenced by an increase in N-cadherin-colocalized AF-6 cluster immunofluorescence (integrated inetsity/cluster: control 4.14 ± 0.39, clust FcNcad 120.90 ± 5.70, interf Ab 2.62 ± 0.17; a.u.). Similar changes were found when total integrated intensity of colocalized AF-6 clusters along a segment of dendrite were measured and normalized to dendritic length (control 3.64 ± 0.43, clust FcNcad 60.41 ± 5.27, interf Ab 1.59 ± 0.08; a.u.). Disruption of N-cadherin adhesion did not affect AF-6 clusters.

We have previously shown that AF-6 controls spine morphogenesis, and overexpression of AF-6 induced formation of spines with diverse morphologies, including spines with large heads (arrowheads) as well as thin/long spines (arrows; Fig. S1f), while deletion of AF-6 N-terminal Rap-association domains also resulted in large spines (Xie et al., 2005). Conversely, a mutation in the PDZ domain of AF-6 (AF-6-PDZ*) eliminated the ability of AF-6 to induce larger spines. This suggests that AF-6 plays a role in spine enlargement caused by N-cadherin activation. To test this, we incubated neurons expressing GFP and AF-6-PDZ* with clustered Fc-N-cadherin (Fig. 2g, h). AF-6-PDZ* abolished spine enlargement induced by clustered Fc-N-cadherin (spine areas: control 0.89 ± 0.04, clust FcNcad 1.37 ± 0.05, clust FcNcad+AF-6-PDZ* 0.98 ± 0.06; µm2), supporting the requirement for AF-6 in N-cadherin adhesion-induced spine enlargement. Spine length and density were not affected by AF-6-PDZ* expression (not shown). The effects on spine morphology were not caused by altered surface expression of N-cadherin, since in neurons expressing AF-6-PDZ*, surface N-cadherin clusters were equally accessible to “decoration” by clustered Fc-Ncadherin as in non-transfected control neurons (Fig. S1g). These experiments indicate that N-cadherin-dependent recruitment of AF-6 molecules to synapses is crucial for adhesion-dependent spine enlargement, and that interactions mediated by the PDZ domain of AF-6 play a key role in these processes.

AF-6 interacts with the Rac1-GEF kalirin-7 in neurons

Previously we demonstrated that AF-6 controls spine morphology; however, the he downstream mechanisms by which AF-6 regulates spine morphogenesis remain unknown. Two splice variants of AF-6 are expressed in the brain: the long form (205 kDa) (L-AF-6) contains a C-terminal filamentous actin-binding domain that is not present in the short form (190 kDa) (s-AF-6). The presence of an F-actin binding domain in L-AF-6 suggested that AF-6 may directly crosslink actin filaments, implying L-AF-6 would control actin rearrangements differently to s-AF-6 due to the presence of this domain. Contrary to this prediction, we found that AF-6 did not affect F-actin distribution, demonstrated by the lack of F-actin redistribution in COS7 cells transfected with either L- or s-AF-6 (Fig. 3a). Both AF-6 forms contain a PDZ domain. The inactivation of its PDZ domain reduced its ability to induce spine morphogenesis (Xie et al., 2005) (Fig. 2g–h), suggesting that proteins interacting with this domain are important. To further dissect the downstream signaling mechanisms by which AF-6 regulates adhesion-dependent spine morphogenesis, we focused on proteins interacting with its PDZ domain. Using a yeast two-hybrid screen, AF-6 was found to interact with the C-terminus of kalirin-7, a brain-specific Rac1-GEF and a regulator of spine morphogenesis (Xie et al., 2007). Therefore we reasoned that kalirin-7 may mediate the actions of AF-6 on spines. To confirm that these two proteins interacted in vivo, we performed coimmunoprecipitations from rat forebrain homogenates. Antibodies specific to AF-6 and kalirin co-precipitated each other respectively (Fig. 3b). The importance of the PDZ-mediated interaction between AF-6 and kalirin-7 was further confirmed by coimmunoprecipitation from transfected hEK293 cells (Fig. 3c): while AF-6 with an intact PDZ domain interacted with kalirin-7, AF-6-PDZ*, which blocked adhesion-dependent spine morphogenesis, did not interact with kalirin-7. Furthermore, AF-6 and kalirin-7 colocalize in numerous dendritic spines (Fig. 3e, arrows).

Figure 3
AF-6 interacts with kalirin-7 in neurons

The requirement of a PDZ-mediated interaction for AF-6-dependent spine morphogenesis suggested that AF-6 may recruit kalirin-7 to specific sites on the plasma membrane in dendrites and thereby control spine remodeling. Indeed, in transfected hEK293 cells, while kalirin-7 alone was diffusely distributed in the cytoplasm and AF-6 alone was partially associated with the plasma membrane (arrows), AF-6 recruited kalirin-7 to the plasma membrane (arrowheads; Fig. 3d). Since activation of N-cadherin adhesion modulated the clustering of AF-6 in dendrites, this may have also modulated the localization of kalirin-7. Thus, we examined the N-cadherin adhesion-dependent recruitment of endogenous kalirin-7 to AF-6 puncta in dendrites (Fig. 3e, f). N-cadherin engagement increased kalirin-7 recruitment to AF-6 puncta: colocalized kalirin-7 cluster integrated intensity (control 3.15 ± 0.52, clust FcNcad 6.41 ± 1.24, interf Ab 2.95 ± 0.39; a.u.); total integrated intensity of colocalized kalirin-7 clusters on a segment of dendrite normalized to dendritic length (control 51.7 ± 7.03, clust FcNcad 99.6 ± 20.4, interf Ab 44.9 ± 5.78; a.u.).

AF-6 recruits kalirin-7 to spines

Anchoring by the AF-6 PDZ domain may be a mechanism to recruit kalirin-7 to adhesion sites on the dendritic and synaptic plasma membrane. To test this hypothesis, we expressed kalirin-7 with or without AF-6 or AF-6-PDZ* in cortical neurons and examined kalirin-7 clusters. Coexpression of AF-6 increased the integrated intensity of kalirin-7 puncta, while coexpression with AF-6-PDZ* resulted in reduced integrated intensity of kalirin-7 clusters (Fig. 4a, b; kal7 alone 12.37 ± 1.0, kal7+AF-6 19.6 ± 1.6, kal7+AF-6-PDZ* 9.8 ± 0.5, kal7 cluster intensities).

Figure 4
AF-6 PDZ domain mediates interaction with kalirin-7 in neurons

To test whether an intact PDZ domain of AF-6 was required for N-cadherin-dependent kalirin-7 recruitment, we examined the clustering of endogenous kalirin-7 in presence or absence of overexpressed AF-6-PDZ* (Fig. 4c, d). In dendrites of neurons expressing AF-6-PDZ* (Fig. 4c (#)), N-cadherin engagement failed to induce kalirin-7 clustering; while in dendrites of neurons not expressing AF-6-PDZ* (Fig. 4c (##)), kalirin-7 was clustered upon N-cadherin engagement (kalirin-7 cluster integrated intensity: control 2.25 ± 0.22, clust FcNcad 11.81 ± 1.43, AF-6-PDZ* + clust FcNcad 3.17 ± 0.29; total kalirin-7 integrated intensity on a segment of dendrite normalized to dendritic length: control 4.64 ± 1.07, clust FcNcad 194.80 ± 48.33, interf Ab 17.55 ± 6.98; a.u.). These data indicate that AF-6 may regulate spine morphogenesis by recruiting kalirin-7 to synapses through a PDZ domain-dependent interaction.

Since kalirin-7 also interacted with PSD-95 (Penzes et al., 2001) we compared the relative strength of the association of AF-6 vs. PSD-95 vs. kalirin-7 with cytoskeletal and post-synaptic density (PSD) elements, as an indirect measure of the mobility of a certain kalirin-7 pool, specifically associated with one or the other scaffolding protein (Fig. 4e). One possibility is that different scaffolding proteins that bind kalirin-7 may have different degrees of mobility within the post-synaptic density (PSD), therefore leading to more stable vs. more dynamic pools of kalirin in spines. While both AF-6 and PSD-95 co-fractionate with kalirin-7 in the crude synaptosomal fraction, the strength of the association of AF-6 vs. PSD-95 with cytoskeletal and PSD is different. AF-6 can be solubilized with a weaker detergent (Triton-X100, deoxycholate, RIPA buffer), along with a fraction of kalirin-7, indicating a more mobile pool of protein. These results suggest that a larger fraction of kalirin-7 is loosely associated with PSD, possibly through interaction with proteins like AF-6, indicating a higher mobility within spine. On the contrary, PSD-95 along with another fraction of kalirin-7 can only be solubilized by strong detergents (SDS) but is left in the pellet by (deoxycholate, RIPA buffer), indicating a pool of kalirin-7 stably associated with PSD, likely by interaction with PSD-95.

Kalirin-7 interacts with N-cadherin-containing adhesion complexes in neurons

Rho GTPase activation is thought to play a key role in N-cadherin-dependent spine remodeling (Bamji, 2005; Elia et al., 2006). In particular, Rac1 activation induces spine enlargement similar to N-cadherin activation (Nakayama et al., 2000), while its inhibition causes remodeling into thin and long morphologies (Tashiro and Yuste, 2004). AF-6, by linking the N-cadherin complex with the Rac1-GEF kalirin-7, may provide adhesion complexes the ability to rapidly control Rac1-dependent spine remodeling. We reasoned that a signaling pathway that includes N-cadherin/AF-6/kalirin-7 may control adhesion-dependent spine remodeling. We first examined the colocalization of kalirin-7 with components of the N-cadherin adhesion complexes in dendrites. Indeed, kalirin-7 colocalized with α-N-catenin (Fig. 5a–b) and N-cadherin (Fig. 5c) in clusters on dendrites and in many spines (arrows). Since AF-6 interacts with both kalirin-7 and N-cadherin-associated proteins, a subset of AF-6 molecules may interact with both kalirin-7 and components of the N-cadherin complex. To test this possibility in a cellular system, hEK293 cells were transfected with all three proteins simultaneously (Fig. 5d); N-cadherin, AF-6, and kalirin-7 were observed to partially colocalized at the plasma membrane (Fig. 5d).

Figure 5
Kalirin-7 colocalizes and interacts with N-cadherin adhesion complexes

Together, these experiments suggested that in neurons, kalirin-7 participates in N-cadherin containing multiprotein complexes through interaction with AF-6. In addition, since AF-6 clustering is modulated by N-cadherin adhesion, the reciprocal interaction between kalirin-7, AF-6, and N-cadherin in such multiprotein complexes may also be modulated by N-cadherin adhesion. To test this, we stimulated or inhibited N-cadherin in neurons and examined the interactions between kalirin-7, AF-6, and N-cadherin through coimmunoprecipitation (Fig. 5e). All three proteins were found to interact with one another, demonstrating the existence of protein complexes that contain all three proteins: N-cadherin, AF-6 and kalirin-7. In addition, N-cadherin engagement enhanced the reciprocal interaction of N-cadherin, AF-6, and kalirin-7, while N-cadherin interference reduced the extent of coimmunoprecipitation between these proteins. These results demonstrate that N-cadherin adhesion modulates the extent of interaction between N-cadherin, AF-6, and kalirin-7 in neurons. We further confirmed the interaction of kalirin-7 with N-cadherin in vivo and compared it with its interaction with the synaptic scaffolding protein PSD-95. While coimmunoprecipitation from rat forebrain homogenate confirmed that kalirin-7 interacted with N-cadherin (Fig. 5f), as expected the interaction between kalirin-7 with PSD-95 was comparatively stronger. This suggests that the kalirin-7/N-cadherin interaction is indirect and potentially mediated by AF-6.

N-cadherin adhesion modulates Rac1 and PAK signaling in dendrites

Since N-cadherin activation modulates AF-6 clustering in addition to the interaction between N-cadherin, AF6, and kalirin-7, it may also modulate the localization of kalirin-7 in dendrites. Indeed, N-cadherin engagement enhanced kalirin-7 recruitment to N-cadherin clusters (Fig. 6a, b), indicated by increased integrated intensities of colocalized kalirin-7 clusters (Fig. 6a, arrows) (control 1.55 ± 0.11, clust FcNcad 9.08 ± 1.46, interf Ab 1.55 ± 0.20; a.u.); similar changes were found in the total colocalized kalirin-7 integrated intensity on a segment of dendrite normalized to dendritic length (control 18.49 ± 1.72, clust FcNcad 114.40 ± 16.93, interf Ab 21.12 ± 2.67; a.u.). We also compared the intensities of exogenous kalirin-7 clusters (Fig. 6c). In control neurons overexpressed kalirin-7 was concentrated in small puncta along the dendrites. Co-expression with N-cadherin resulted in clusters containing more kalirin-7, without affecting the number of clusters, suggesting that overexpressed N-cadherin recruited more kalirin-7 to preexisting clusters (kalirin-7 cluster integrated intensities: kal7 alone 12.37 ± 0.10, kal7+Ncad 18.96 ± 0.14 a.u.; p < 0.001).

Figure 6
N-cadherin adhesion modulates kalirin-7 and Rac1 localization in dendrites and spines

Since N-cadherin activation or inhibition modulates the interaction between N-cadherin, AF6, and kalirin-7, it may also modulate the amount of Rac1 in spines. To test this, we measured the intensity of Rac1 immunofluorescence contained within dendritic spines (Fig. 6d–f). Rac1 intensity was normalized to spine sizes to eliminate the passive effect of changes in Rac1 levels caused by altered spine size (control 9.37 ± 0.85 clust FcNcad 14.18 ± 1.22, interf Ab 2.76 ± 0.45; a.u.). In control neurons (Fig. 6 d, e left panel), small puncta of Rac1 immunoreactivity were detectable in dendrites and in spines (arrows); N-cadherin activation increased significantly the size of Rac1 puncta in spines (Fig. 6 d, e center). On the contrary, interference with N-cadherin resulted in reduced Rac1 content in spines (Fig. 6 d, e right panel) and remodeling of spines into of thin, long shapes, consistent with the reported effects of reduced Rac1 activity on spine morphology: inhibition of Rac1 caused spine thinning and elongation (Tashiro and Yuste, 2004).

A major substrate of Rac1 is p21-activated kinase (PAK). Binding of Rac1 causes activation and autophosphorylation of PAK, hence PAK phosphorylation can be used as a readout of Rac1 activation. We have also shown that kalirin-7-induced spine morphogenesis is dependent on Rac1-mediated PAK activation (Xie et al., 2007). Therefore, to test whether N-cadherin engagement activated the Rac1-PAK pathway, and whether this was dependent on kalirin-7 GEF activity, we examined the phosphorylation of endogenous PAK (P-PAK) in neurons (Fig. 7a–c). N-cadherin engagement caused an increase in P-PAK immunoreactivity compared to untreated control neurons, indicating N-cadherin-dependent PAK phosphorylation. Expression of myc-kalirin-7-ΔGEF, a kalirin-7 truncation mutant lacking the GEF domain but containing an intact C-terminus, reduced N-cadherin-dependent PAK phosphorylation (control 3.24 ± 0.51, clust FcNcad 12.55 ± 1.85, kal7-ΔGEF + clust FcNcad 5.71 ± 1.20; a.u.); this reduction was not seen in dendrites of neighboring non-transfected neurons (Fig. 7a–c).

Figure 7
Kalirin-7 GEF activity is required for N-cadherin-dependent PAK phosphorylation

N-cadherin-dependent spine enlargement requires kalirin

Because kalirin-7 promotes spine enlargement, overexpression of kalirin-7 may prevent the remodeling of spines into thinner and longer shapes induced by interference with N-cadherin adhesion. We tested this hypothesis by treating neurons expressing GFP together with or without myc-kalirin-7 with the interfering antibody GC4, and comparing spine morphologies (Fig. 8a–c). Overexpression of kalirin-7 prevented the formation of long and thin spines induced by interference with N-cadherin adhesion (spine length: interf Ab vs. control, p < 0.05; kal7+interf Ab vs. control, no difference; spine area: kal7+interf Ab vs. control, p < 0.05), demonstrating that kalirin-7 functions downstream of N-cadherin in this pathway (spine length: control 1.77 ± 0.11, interf Ab 2.47 ± 0.27, kal7 + interf Ab 2.02 ± 0.15 µm; spine area: control 0.64 ± 0.06, interf Ab 0.90 ± 0.11, kal7 + interf Ab 1.05 ± 0.15 µm2; spine linear density: control 5.09 ± 0.36, interf Ab 7.40 ± 0.67, kal7 + interf Ab 5.73 ± 0.38 per 10 µm).

Figure 8
N-cadherin-dependent spine enlargement requires kalirin

As kalirin has been shown to be crucial for spine morphogenesis induced by extracellular signals (Penzes et al., 2003; Xie et al., 2007), we tested whether it was required for N-cadherin-dependent spine enlargement. Using a kalirin-7-specific RNAi, previously characterized in detail (Xie et al., 2007), we knocked down kalirin expression in neurons. While knockdown for 3 days does not cause significant effects on spines (Xie et al., 2007), it prevented N-cadherin-induced spine enlargement (Fig. 8d). This blocking of N-cadherin-induced spine enlargement was reversed in rescue experiments where an RNAi-insensitive mutant of kalirin-7 was overexpressed (Fig. 8d; spine area: control 0.68 ± 0.06, clust FcNcad 1.17 ± 0.14, clust FcNcad + kal7 RNAi 0.71 ± 0.04, clust FcNcad + kal7 RNAi + kal7 rescue 1.08 ± 0.07 µm2), demonstrating that these effects were indeed due to kalirin-7 and not some offsite target of the characterized RNAi construct. To test whether kalirin’s GEF domain was also required for N-cadherin-dependent spine enlargement, neurons expressing GFP and myc-kal7-ΔGEF were treated with clustered Fc-N-cadherin or left untreated (Fig. 8e). Quantification of spine lengths and areas revealed that kal7-ΔGEF prevented spine enlargement induced by N-cadherin activation (spine area: control 0.65 ± 0.03, clust FcNcad 0.68 ± 0.04, p = 0.47; spine length: control 1.92 ± 0.07, clust FcNcad 1.81 ± 0.07, p = 0.25), without affecting spine linear densities (spine linear density: control 7.52 ± 0.74, clust FcNcad 7.54 ± 0.81, p = 0.98). Overexpression of kal7-ΔGEF did not affect the availability of N-cadherin on the dendritic surface, as shown by decorating transfected and non-transfected neurons with Fc-N-cadherin (Fig. S1h).

Collectively, these data suggest that in pyramidal neuronal dendrites, kalirin-7 colocalizes and interacts with N-cadherin-containing adhesion complexes. N-cadherin-mediated adhesion events recruit kalirin-7 and Rac1 to these synaptic adhesion sites, resulting in increased PAK phosphorylation. Furthermore, these results demonstrate crucial role for kalirin-7 in cadherin-dependent spine morphogenesis.

Active Rap interferes with N-cadherin-dependent spine enlargement

AF-6 contains two Ras/Rap-association domains (RA) that preferentially bind activated Rap (Boettner et al., 2003). Interestingly, while overexpression of AF-6 induced formation of both thin spines and spines with large heads, deletion of the RA domains from AF-6, consistently induced spine head enlargement (Xie et al., 2005). This suggested that the RA domains of AF-6 may prevent or reduce the ability of AF-6 to induce spine enlargement. We have previously shown that expression of constitutively active Rap1 (Rap1-CA) results in the localization of AF-6 at the dendritic plasma membrane and in the formation of thin and long spines. Contrary to this, expression of RapGAP, which inactivates Rap, resulted in AF-6 relocalization from the dendritic plasma membrane to the dendritic cytosol and in enlarged spines (Xie et al., 2005). Therefore, we hypothesized that the binding of active Rap to AF-6 may interfere with its ability to mediate N-cadherin-induced spine enlargement. Indeed, expression of Rap1-CA blocked spine head enlargement induced by N-cadherin activation (Fig. S3a–b), and resulted in thin spines (area: clust FcNcad 1.69 ± 0.05, clust FcNcad+Rap1-CA 1.18 ± 0.04; p < 0.01; length: clust FcNcad 1.41 ± 0.05, clust FcNcad+Rap1-CA 2.40 ± 0.03; p < 0.001). These spines were statistically undistinguishable from those caused by the expression of Rap-CA alone, but were longer and had larger areas than untreated controls (area: Rap1-CA 1.25 ± 0.08, control 0.88 ± 0.02; p < 0.01; length: Rap1-CA 2.5 ± 0.03, control 1.24 ± 0.04; p < 0.001); spine density was not affected by Rap1-CA. Expression of Rap1-CA did not reduce the amount of N-cadherin expressed on neuronal surface, as shown by unaffected binding of clustered N-cadherin to neurons (Fig. S1i). These experiments, together with our previous studies, demonstrate that active Rap interferes with AF-6 in mediating N-cadherin-induced spine enlargement.

Discussion

Dendritic spine remodeling is an important element of synapse maturation and plasticity. Previous studies have shown that increased N-cadherin adhesion or increased expression of N-cadherin and associated proteins induce spine enlargement (Togashi et al., 2002; Murase et al., 2002; Abe et al, 2004). These concurrent processes lead to increased synapse stability (Abe et al., 2004), and higher AMPA receptor content (Liao et al., 1999). Large spine are also more stable (Trachtenberg et al., 2002). Activity-dependent potentiation is also associated with simultaneous spine enlargement (Yuste and Bonhoeffer, 2001; Kasai et al., 2003) as well as recruitment and clustering of N-cadherin and associated proteins (Bozdagi et al., 2000; Murase et al., 2002). Conversely, disruption of N-cadherin or associated proteins caused formation of thin long spines and spine destabilization (Togashi et al., 2002; Murase et al., 2002; Abe et al, 2004). In all of these cases, synaptic adhesion, spine morphology, stability, and synaptic AMPA receptor content are coordinated (Kasai et al., 2003). However, the molecular mechanisms that coordinately regulate spine morphology and synaptic adhesion are not well understood. This coordination may be achieved by adhesion-dependent control of spine morphology, but little is known about the mechanisms whereby synaptic adhesion molecules such as N-cadherin modulate spine morphology.

While N-cadherin adhesion has been shown to modulate the morphology of existing spines (Togashi et al., 2002; Abe et al., 2004), the mechanism underlying this process was not known. Our studies identify a novel mechanism that coordinates synaptic adhesion and spine morphology, accomplished by N-cadherin signaling to the Rac1-GEF kalirin-7, mediated by the scaffold protein AF-6, supporting the following model (Fig. 9). Increased trans-synaptic N-cadherin clustering at spine heads, occurring during synapse maturation, stabilization, and potentiation, associated with increased adhesion, leads to the recruitment of AF-6 and kalirin-7 to adhesion sites in spines. Enrichment of kalirin-7 at in these spines enhances local activation of Rac1, causing enlargement of spines and increased stability of existing synaptic connections. Conversely, reduced N-cadherin-mediated adhesion, which occurs in less mature synapses, when synapses are dynamic and undergo extensive motility and remodeling (Lendvai et al., 2000), during synapse elimination (Mataga et al., 2004), experience-dependent plasticity of cortical circuits (Trachtenberg et al., 2002), or in LTD (Zhou et al., 2004), results in the dissociation of AF-6 and kalirin-7 from adhesion complexes, preventing the signal flow from N-cadherin to kalirin-7. This causes decreased Rac1 activation and content in spines, leading to formation of thin, long spines, which are less stable. Because N-cadherin-dependent adhesion is regulated during excitatory synapse development and in synaptic plasticity, this mechanism may underlie spiny synapse maturation and activity-dependent structural plasticity, and thus may contribute to experience-dependent plasticity and learning.

Figure 9
Model of the role of N-cadherin and associated proteins, AF-6, and kalirin-7 in the dynamic coordination of synaptic adhesion and spine morphology

A key role has been hypothesized for Rho GTPase activation in cadherin-dependent actin cytoskeletal rearrangements and spine remodeling (Bamji, 2005). However, until recently the mechanisms whereby N-cadherin controls Rho GTPase activation in spines has not been clear. A recent study has shown that p120-catenin controls the formation of new spines, reflected in spine and synapse density, through activation of Rac1 and inactivation of RhoA (Elia et al., 2006). On the contrary, our results indicate that the N-cadherin/AF-6/kalirin-7 pathway may provide adhesion complexes the ability to rapidly control Rac1-dependent remodeling of existing spines. The two pathways may to function in tandem to control spine formation and density vs. remodeling of existing spines. Kalirin-7, which is an enzyme, may provide an amplification step to this pathway: recruitment of one molecule of kalirin-7 may result in activation of many molecules of Rac1, leading to extensive and sustained changes in actin dynamics and spine morphology. In addition, direct participation of N-cadherin in multiprotein complexes with molecules that rapidly control actin dynamics, such as Rho-GEFs, offers adhesion events the ability to rapidly regulate spine morphology. This mechanism may underlie rapid activity-dependent coordinated changes in adhesion and spine structure during plasticity.

In several previous studies we have shown that kalirin-7 is regulated by tyrosine or threonine phosphorylation (Penzes et al., 2003; Xie et al., 2007). On the other hand, in this study we identify a novel mode of regulation of kalirin-7, mediated by its adhesion-dependent recruitment to synapses through its interaction with AF-6. Kalirin-7 targeting to spines depends on its C-terminus (Penzes et al., 2001); however, the relative importance of proteins such as AF-6 or PSD-95 which interact with the kalirin-7 C-tail is not clear. The ability of AF-6 to bind kalirin-7 even in presence of PSD-95 in the brain, as shown by coimmunoprecipitation experiments, suggests that AF-6 links some kalirin-7 molecules to adhesion complexes even in the presence of PSD-95. AF-6 and PSD-95 may link kalirin-7 to two separate sets of upstream regulatory proteins, such as cadherin and EphB receptors, or NMDA receptors, respectively. Weaker association of AF-6 with the synaptic cytoskeleton relative to PSD-95 suggests that the AF-6/kalirin-7 complexes may be more dynamic, while the PSD-95/kalirin-7 complexes may be stably associated with the PSD.

Although AF-6 has been known to interact directly with α-catenin and nectins in adhesion junctions of epithelial cells (Pokutta et al., 2002; Honda et al., 2006), its role in synaptic adhesion was uncharacterized. In this study we identified a mechanism linking synaptic adhesion with the remodeling of existing spines, and we show for the first time that AF-6 plays an important role in these processes. Our results place AF-6 in association with N-cadherin adhesion complexes in forebrain neuron synapses in culture and in vivo, demonstrate a role for N-cadherin in concentrating AF-6 in spines, and support a functional role for AF-6 in adhesion-dependent spine remodeling. Because AF-6 is rapidly recruited to spines upon N-cadherin activation and because of its role in spine remodeling and its interactions with kalirin-7, it may provide adhesion complexes the ability to dynamically regulate the actin cytoskeleton, allowing synaptic adhesion events to rapidly control spine remodeling.

Previous studies have reported that in different brain regions and at different stages of development AF-6 is localized to different sites (Buchert et al., 1999; Nishioka et al., 2000; Mizoguchi et al., 2002; Honda et al., 2006). Our data show that AF-6 is enriched in most excitatory synapses in cultured neurons and PSD fractions of brain (Xie et al., 2005) and in spines of cortical pyramidal neurons. AF-6 also interacts with nectins, another class of Ca2+-independent adhesion molecules, raising the possibility that nectins may be upstream or downstream of AF-6 in regulating spine morphology. In cultured neurons, disruption of nectin-1-mediated adhesion resulted in a decrease in size and an increase in number of presynaptic puncta (Mizoguchi et al., 2002). Nectins have also been shown to mediate a specific interaction between axons and dendrites (Togashi et al., 2002). However, these results were not confirmed in nectin knockout mice (Honda et al., 2006), suggesting that nectins play a minor role in controlling excitatory synapse morphology in cortical pyramidal neurons. On the other hand, nectins play a more important role in the formation and maintenance of hippocampal puncta adherentia between mossy fiber synapses and CA3 dendrites (Nishioka et al., 2000; Honda et al., 2006).

In this study we show that active Rap1 prevents N-cadherin-induced spine enlargement. This novel role for Rap1 is likely mediated by AF-6, for several reasons. AF-6 promotes the formation of spines with large heads, similar to that induced by N-cadherin adhesion, while, blocking N-cadherin adhesion results in formation of thin and elongated spines, similar to those caused by overexpression of activated Rap1 (Xie et al., 2005), suggesting that active Rap1 may interfere with the ability of N-cadherin to induce spine enlargement. Moreover, deletion of the N-terminal portion of AF-6, containing Rap-association domains, induced spine enlargement, suggesting that binding of active Rap1 to the Rap/Ras association (RA) domains of AF-6 was required for spine elongation. Indeed, we showed here that activated Rap1 blocked spine head enlargement caused by N-cadherin activation. Rap1 may interfere with N-cadherin/AF-6 downstream signaling in one of several possible ways. Binding of Rap1-GTP to AF-6 may affect its conformation and prevent it from interacting with N-cadherin-associated proteins. In addition, since active Rap1 recruits AF-6 to the plasma membrane through direct interaction between the two proteins, Rap1 may compete with the interaction of AF-6 with N-cadherin/α-N-catenin. Alternatively, Rap1 may sequester AF-6 away from adhesion junctions, preventing its interaction with N-cadherin/α-N-catenin or kalirin-7. Future studies are needed to investigate how the Rap1 and N-cadherin mediated upstream pathways interact to control AF-6 localization and function in neurons, as some studies suggested involvement of Rap1 in adhesion.

In summary, this study identifies a novel mechanism whereby N-cadherin, a major synaptic adhesion molecule, signals to the actin cytoskeleton to control the morphology of dendritic spines, and outlines a mechanism that may underlie the coordination of synaptic adhesion with spine morphology during synapse maturation and plasticity.

Supplementary Material

Fig 1

Fig 2

Fig 3

legends

Acknowledgements

We thank Dr. Anjen Chenn (Northwestern University) for critically reading the manuscript and Dr. Anis Contractor (Northwestern University) for advice. We thank Ms. Kelly Jones for carefully editing the manuscript. This work was supported by the National Institutes of Health (NIH), National Alliance for Autism Research (NAAR), and the National Alliance for Research on Schizophrenia and Depression (NARSAD) (to P.P.); National Institutes of Health (NIH) and Howard Hughes Medical Institute (HHMI) (to R.L.H.).

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