Nervous wreck (Nwk), a protein that is present at Type 1 glutamatergic synapses that contains an SH3 domain and an FCH motif, is a Drosophila homolog of the human srGAP3/MEGAP protein, which is associated with mental retardation. Confocal microscopy revealed that circles in Nwk reticulum enclosed T-shaped active zones (T-AZs) and partially colocalized with synaptic vesicle (SV) markers and both exocytosis and endocytosis components. Results from an electron microscopic (EM) analysis showed that Nwk proteins localized at synaptic edges and in SV pools. Both the synaptic areas and the number of SVs in the readily releasable (RRPs) and reserve (RPs) SV pools in nwk2 were significantly reduced. Synergistic, morphological phenotypes observed from eag1;;nwk2 neuromuscular junctions suggested that Nwk may regulate synaptic plasticity differently from activity-dependent Hebbian plasticity. Although the synaptic areas in eag1;;nwk2 boutons were not significantly different from those of nwk2, the number of SVs in the RRPs was similar to those of Canton-S. In addition, three-dimensional, high-voltage EM tomographic analysis demonstrated that significantly fewer enlarged SVs were present in nwk2 RRPs. Furthermore, Nwk formed protein complexes with Drosophila Synapsin and Synaptotagmin 1 (DSypt1). Taken together, these findings suggest that Nwk is able to maintain synaptic architecture and both SV size and distribution at T-AZs by interacting with Synapsin and DSypt1.
Normal development, maintenance and plasticity of neuronal circuits and synaptic architectures are critical for proper brain functions in humans and other animals.1, 2 Defects in one or more genes involved with neuronal wirings or with synapse formation, development, differentiation, plasticity or transmission have been identified as the causes of many neurological disorders, including mental retardations,3 Fragile X-syndrome,4 Rett syndrome,5 autism,6 Angelman syndrome7 and mild learning disability.8 The causative mutations may induce abnormal development of neuronal connections or synaptic architectures by perturbing one or more molecular or cellular mechanisms underlying homeostatic regulatory mechanisms, Hebbian plasticity or both.2, 8 Hebbian plasticity is the idea that strengthening or weakening synaptic efficacy in neuronal circuits is mainly determined by correlated presynaptic and postsynaptic activities.9 Increased neuronal excitabilities can strengthen neuronal circuits by increasing the sizes of synapses, and decreased neuronal activities can eliminate synaptic connections. Activity-dependent Hebbian plasticity may explain how long-term potentiation or depression is accomplished without extensive genetic instruction. Nevertheless, without a homeostatic regulatory mechanism keeping neuronal circuits from runaway excitation or quiescence, Hebbian plasticity may not be sufficient to explain how synaptic architectures and neuronal circuits in the brains maintain excitability within physiological limits during learning and development.9, 10, 11 Homeostatic regulatory mechanisms are considered to have important roles in maintaining some consistency in neuronal properties despite the changes induced by activity-dependent Hebbian plasticity by altering preneuronal and/or postneuronal properties, such as synaptic vesicle (SV) release probability, synapse sizes, neurotransmitter receptor localization or retrograde signaling.10, 12
Because the basic functional unit in the brain is a single synapse,13, 14 in order to understand the molecular and cellular mechanisms underlying synaptic plasticity and the molecular and cellular etiologies underlying neuronal disorders, identifying the molecular components localizes at synapses and investigating their roles in vivo are among the major foci in modern molecular neuro-genetics. The basic molecular components and neuronal signaling pathways in excitatory synapses in the human brains have been shown to be faithfully conserved at Type 1 glutamatergic synapses in Drosophila larval neuromuscular junctions (NMJs).15, 16, 17, 18 Therefore, the molecular and cellular mechanisms underlying synaptic plasticity have been intensively investigated in Type 1 glutamatergic synapses in Drosophila larval NMJs, the best-characterized synapses. A plethora of studies in Drosophila larval NMJs have shown that homeostatic regulatory mechanisms and Hebbian plasticity are present and actively participate in regulating the development, differentiation and plasticity of neuronal circuits and synapse architectures. Genetic alterations in neuronal activity have resulted in either increased or decreased synapse sizes in larval NMJs,19, 20, 21 accompanied by alterations in the localization and composition of synaptic molecular components that form postsynaptic or presynaptic terminal macromolecular complexes.22, 23 Synaptic macromolecular complexes harbor synaptic scaffolding proteins, cell adhesion molecules, ion channels, various protein kinases and neurotransmitter receptors.24 In addition, SVs are linked to active zones (including exocytosis and endocytosis machineries) by proteins regulating the trafficking of SVs from the reserve pool (RP) to readily releasable pool (RRP).25, 26 The in vivo functions of evolutionary conserved molecular components present at synapses were revealed by studies using available mutant alleles in Drosophila. Discs large (DLG), the Drosophila homolog of membrane-associated guanylated kinase (MAGUK) family proteins, are critical for the proper targeting and localization of Shaker type K+ channels,27 Ca2+/calmodulin-dependent kinase II28 and the Drosophila cell adhesion molecule, Fasciclin II (FasII),29 at synapses. Mutations in various K+ channels are resulted in increased sizes of synapses at larval NMJs, a typical example of Hebbian plasticity. In addition, hyperpolarization of muscle resting potentials via transgenic expression of inward rectifier K+ channel Kir2.1 induced increased presynaptic release of neurotransmitters to produce normal levels of depolarization, a typical example of homeostatic regulatory mechanisms.30 Furthermore, CaMKII and cAMP-dependent protein kinase have been shown to be involved with homeostatic regulatory mechanisms via regulating retrograde signaling that alters the physiological properties at the presynaptic terminals.
Nervous wreck (Nwk), a SRC homology 3 (SH3) domain and Fes/Cip4 homology-Bin/Amphiphysin/Rvs167 (F-Bar) domain containing protein present at Type 1 glutamatergic synapses in reticular structures, is a Drosophila homolog of human SLIT-ROBO Rho GTPase activating protein 3 (srGAP3)/mental disorder associated GTPase-acting protein (MEGAP), which has been linked to severe mental retardation.3 nwk was identified as a negative regulator of structural and functional synaptic plasticity.31 Key morphological phenotypes in NMJs in nwk loss-of-function mutants, such as increased numbers of synaptic bouton, were similar to those observed from mutations inducing increased neural activity, a classical example of Hebbian plasticity. However, the existence of other phenotypes, such as smaller synaptic boutons and synapses that were different from NMJs in hyperexcitability mutants suggested that nwk may not participate in canonical activity-dependent Hebbian plasticity. In this study, we provide genetic, anatomical and biochemical evidence supporting our hypothesis that ‘Nwk regulates synaptic plasticity by regulating synapse architecture and maintaining SV sizes and pools’.
Materials and methods
Flies were raised on standard Drosophila media at 25±1 °C with 60% relative humidity. Previously characterized Canton-S (CS), nervous wreck2 (nwk2), Df(3L)Rdl2,31 Fasciclin IIe76 (FasIIe76),29 ether a go-go1 (eag1) and UAS-neuronal-synaptobrevin-green fluorescence protein (n-Syb-GFP), UAS-Actin-GFP (Bloomington Drosophila Stock Center, Indiana University, Bloomington, IN, USA) were used in this study. eag1;;nwk2 and fasIIe76;;nwk2 double mutants were generated by recombining the first and third chromosomes.
Wandering-stage third-instar larvae were dissected in ice-cold Ca2+ free saline (128 mM NaCl, 2 mM KCl, 4 mM MgCl2, 35.5 mM sucrose, 5 mM HEPES, 1 mM EGTA, pH 7.2; Sigma-Aldrich, St Louis, MO, USA) and fixed with 4% paraformaldehyde in 0.1 M phosphate buffer (PB, pH 7.2) for 1 h at room temperature.32 Goat anti-horseradish peroxidase (HRP)-fluorescein isothiocyanate,33 rabbit anti-Nwk,31 mouse monoclonal antibody (Mab)-Bruchpilot (Brp, Developmental Studies Hybridoma Bank (DSHB), University of Iowa, Iowa City, IA, USA), Mab-Fasciclin II (FasII, DSHB), Mab-Synapsin (DSHB), Mab-Drosophila cysteine string protein (Dcsp; DSHB), rabbit-anti- Like-clathrin adaptor protein 180 (Lap),34 Mab-Futsch (DSHB), Mab-Neuroglian (DSHB), Mab-Highwire (Hiw, DSHB), Mab-Drosophila glutamate receptor IIA (DGluRIIA, DSHB), Mab-Discs larges 1 (DLG1, DSHB), Mab-Drosophila synaptotagmin 1 (DSypt1, DSHB), rabbit anti-DAP16035 and rabbit anti-Drosophila P-21 activated kinase (Dpak) were used. Donkey anti-mouse Alexa-488 and anti-rabbit-Alexa 568 (ThermoFisher Scientific, Waltham, MA, USA) were used as secondary antibodies. The numbers of synaptic boutons on muscles 6 and 7 in the abdominal segment 2 were counted under epifluorescence microscopy. The lengths of synaptic branches and sizes of synaptic boutons were measured using measure functions in NIH Image J (Bethesda, MD, USA).36 A Zeiss LSM700 confocal microscope (Zeiss, Oberkorchen, Germany) was used to acquire images of samples. Images were processed with the Zen (Zeiss) and Adobe Photoshop (Adobe, San Jose, CA, USA) software.
The relative intensities of anti-FasII immunoreactivity were calculated from single-slice confocal images of synaptic boutons on muscles 6 and 7 in the abdominal segment 2 processed with the anti-FasII antibody 1D4 under similar conditions. Briefly, the longitudinal axis of the synaptic boutons were decided and lines at an angle of approximately 0°, 90°, 180° and 270° from that axis were traced from the center of the synaptic bouton to the outer limit occupied by FasII immunoreactivity. Then the maximum intensity along lines (on a linear scale of 0–255) was determined using the Plot Profile function of Scion Image analysis program (version 1.62). To quantify FasII immunoreactivity at synaptic boutons, 57 synaptic boutons in eag1, 83 in CS, 70 in nwk2, 79 in nwk2/Df or 60 in eag1;;nwk2 from 4 independent NMJs processed simultaneously were used for quantification. One-way analysis of variance with Tukey’s post hoc test was performed using Excel (Microsoft, Redmond, WA, USA) to analyze the data.
Third-instar wandering-tage control and mutant larvae were dissected in ice-cold Ca2+-free saline and then fixed with 0.005% glutaraldehyde and 4% paraformaldehyde in 0.1 M PB for 1 h. Body wall muscle preparations were marked and processed in the same well. After washing three times with 0.1 M PB with 0.2% Triton-X 100 (PBT), samples were incubated with rabbit anti-Nwk antibodies (diluted 1:2,000) overnight at 4 °C. After being blocked with 4% bovine serum albumin and 4% normal goat serum in 0.1 M PB, tissues were incubated with anti-rabbit-IgG conjugated to 1 nm gold (1:200 diluted; Nanoprobes.com, Yaphank, NY, USA). After washing three times with PBT, silver enhancement of nano-gold particles was performed according to the manufacturer’s recommendation (Nanoprobes) for 10 min. After washing with H2O for 5 min, samples were incubated with gold enhancement solution for 5 min. Gold enhancement was used to prevent silver deposits from etching. Silver- and gold-enhanced tissues were fixed with 1% glutaraldehyde and 4% paraformaldehyde in 0.1 M PB overnight. Tissues were washed three times with dH2O, fixed with 1% OsO4 in 0.1 M PB for 1 h and then dehydrated in serial EtOH and 100% Propylene-oxide (Ted Pella Inc., Redding, CA, USA). Tissues were embedded with Spurr’s resin (Ted Pella Inc.) and polymerized at 60 °C overnight. The membrane-coated one-slot grids were used to collect serial thin sections (100 nm) and observed under a Jeol 1011 (Jeol Inc., Tokyo, Japan). Only Type 1b synaptic boutons on muscle 6 and 7 in the abdominal segment 2 were used for examination.
Western blot analysis
Ten wandering-stage third-instar larvae were dissected in ice-cold Ca2+ free saline and homogenized in ice-cold radio-immuno-precipitation assay (RIPA) buffer (150 mM NaCl, 1% IGEPAL CA-630, 0.5% Na-oxycholate, 0.1% sodium dodecyl sulfate (SDS), 50 mM Tris, pH 8.0; Sigma-Aldrich) with protease inhibitors (Halt protease inhibitor cocktail, ThermoFisher Scientific, Rockford, IL, USA). After being centrifuged at 14 000 g for 20 min at 4 °C to remove cellular debris, the amount of protein in each supernatant was determined using the BCA Protein Assay Kit (ThermoFisher Scientific, Waltham, MA, USA). A total of 20.0 μg of protein from each sample was separated on a 10% tris-glycine polyacrylamide SDS gel and then transferred to a nitrocellulose membrane (GE Healthcare Bio-Sciences AB, Uppsala, Sweden). The membranes were probed with rabbit anti-Nwk antibodies. Mouse anti-α-tubulin antibody was used as a loading control.
Twenty wandering-stage third-instar larvae were dissected in ice-cold Ca2+ free saline and homogenized in ice-cold RIPA buffer with protease inhibitors (Halt protease inhibitor cocktail, ThermoFisher Scientific, Rockford, IL, USA). Supernatants were collected by spinning down at 14 000 g for 15 min at 4 °C. Protein A+G agarose beads (SantaCruz Biotech., San Jose, CA, USA) were blocked with RIPA buffer with 1% bovine serum albumin for 2 h with rolling at 4 °C. After being washed three times with RIPA buffer, protein A+G agarose beads were mixed with the supernatants, which contained 20 μl of Mab-Synapsin and were rocked overnight at 4 °C. Protein A+G agarose beads were harvested by centrifugation at 14 000 g for 10 min at 4 °C, washing three times with RIPA buffer and then boiling with 1 × SDS sample buffer. Proteins were separated by 10% SDS-polyacrylamide gel electrophoresis and immediately transferred onto nitrocellulose membranes. Membranes were probed with rabbit anti-Nwk, Mab-DSypt1 and Mab-Synapsin.
Transmission electron microscopy
The protocols for transmission EM and morphometric analysis of synaptic boutons have been previously published.33 For this experiment, serial thin sections (100 nm) were collected from only Type 1b glutamatergic synaptic boutons on muscle 6 and 7 (abdominal segment 2). The thickness of thin sections was confirmed by examining wrinkles of thin sections at 15 000 × with a Jeol 1011 (Jeol Inc.).
Three-dimensional tomography of synapses with high-voltage electron microscope
Thick sections (1 μm) were collected from CS and nwk2 mutant synaptic boutons. Then 20 nm colloidal gold was applied on the surface of thick sections to create a list of fiducial points and used as a standard for determining sizes of SVs and T-shaped active zones (T-AZs). The specimens were tilted from−60° to+60° and imaged at 1° steps (121 images per view) using a high-voltage electron microscope (HVEM; Jeol) operated at 1 MV. Tilted images were aligned using the IMOD software37 to visualize three-dimensional (3D) structures of synapses and active zones. The presynaptic and postsynaptic membranes, SVs and T-AZs were visualized. The sizes and distances of SVs from active zones were analyzed. One-way T-tests were performed by Excel (Microsoft) for statistical analyses.
Nwk reticulum localizes at the peri-synaptic area and SVs
The precise localization patterns of Nwk at Type I glutamatergic boutons in Drosophila larval NMJs were examined by performing anti-Nwk immunocytochemistry. The specificity of anti-Nwk in immunocytochemistry was confirmed by using nwk2 null mutants (Supplementary Figure 1). Nwk signals were observed mainly at the presynaptic terminals of Type I boutons and did not overlap with DLG signals in wild-type CS NMJs (Supplementary Figure 1). DLG has been shown to be present mainly at the postsynaptic terminals of Type I boutons that have elaborated and convoluted membrane structures, named subsynaptic reticulum (SSR).28, 29 However, the outer boundaries of Nwk immuno-reactivity overlapped with anti-HRP signals, indicating neuronal membrane structures (Supplementary Figure 1)38 and suggesting that Nwk is distributed within the presynaptic terminals of Type I boutons at the confocal microscopic level. No detectable Nwk signals were observed from NMJs or muscles of nwk2 animals (Supplementary Figure 1C2), even though anti-DLG and anti-HRP signals appeared to be normal in nwk2 NMJs (Supplementary Figure 1C1).
The localization patterns of Nwk at synapses in Type 1b boutons in CS were further revealed by serial double-labeling confocal microscopy employing antibodies targeting Nwk and other synaptic or cytoskeletal components (Figure 1). Nwk signals, indicated in red in Figure 1, were distributed at the presynaptic terminals in reticular structures that were formed of several interlinked circles and termed Nwk reticulum. Nwk reticulum at the presynaptic terminal was observed from the surface (Figure 1b) through the center of synaptic boutons (Figures 1a and c–n). Narrow passages clear of Nwk signals are present in the middle of boutons indicated by gray arrow heads (Figure 1a and c–e). A single-slice confocal image taken from the midline of a bouton double-labeled for anti-Nwk and the T-AZ marker, Mab-Brp,39, 40 indicated that Nwk circles were present at the peri-active zones (Figure 1a). Double-labeling with a postsynaptic density maker (Mab-DGluRIIA)17 showed that Nwk circles directly faced the edges of postsynaptic densities. There was a hole at the center of DGluRIIA signals corresponding to T-AZs (Supplementary Figure 2A) indicated by a white arrow (Figure 1b). When another postsynaptic density marker, anti-Drosophila p-21 activated protein kinase (Dpak, red), was used for double-labeling with Mab-Brp (green), T-AZs were localized at the center of postsynaptic density (Supplementary Figure 2C). FasII, a Drosophila homolog of cell adhesion molecule has been shown to be localized on both the presynaptic and postsynaptic membranes in Type I glutamatergic NMJs.22, 29 Anti-Nwk and Mab-FasII double-labeling experiments showed that Nwk reticulum and FasII signals are not overlapped (Figure 1c). FasII signals were observed surrounding circles in the Nwk reticulum but were not present on the inner sides of Nwk circles. In addition, FasII was present at the narrow passages in the middle of synaptic boutons that were clear of Nwk signals pointed by gray arrow heads. In addition, FasII signals did not colocalize with Mab-Brp signals (Supplementary Figure 2B). These distribution patterns suggested that Nwk circles are closer to T-AZs than FasII signals at the presynaptic membranes and may regulate synapse stability. Double-labeling with a postsynaptic terminal maker (anti-DLG) showed that the Nwk reticulum was restricted to within the presynaptic terminals of Type Ib boutons (Figure 1d).
Distribution patterns of Nwk reticulum at the presynaptic terminals were further analyzed by using SV markers, such as Mab-Synapsin (Figure 1e), anti-DSypt1 (Figure 1f) or Mab-Dcsp (Figure 1g); molecular components of exocytosis compartments, such as n-syb-GFP (Figure 1h), and endocytosis markers, such as anti-LAP180 (Figure 1i) and anti-Dap 160 (Figure 1j). Nwk reticulum was partially colocalized with SV markers (Figures 1e–g), n-syb-GFP signals (Figure 1h) and LAP-180 signals (Figure 1i), as indicated by the yellow colors clearly visible in the merged images. Interestingly, anti-Dap160 and anti-Nwk signals partially colocalized at Type Ib boutons (Figure 1j). Previous studies in dap160 loss-of-function mutant showed that Nwk localizations at boutons was impaired, even though Dap160 localization at nwk2 boutons was not clearly perturbed.41
To understand how Nwk reticulum is linked to the cytoskeleton in the presynaptic terminals, the microtubule marker Mab-Futsch (Figures 1k and l) and Actin-GFP (Figure 1m) were used to reveal cytoskeleton networks in the boutons. Presynaptic Futsch–microtubule structures traversed the synaptic boutons that were not undergoing division or sprouting (Figure 1k). However, synaptic boutons undergoing division or sprouting were usually present at the end of synaptic branches and did not have Futsch–microtubule cytoskeleton loops. Instead, Futsch–microtubule signals were diffuse and present at the center of Nwk circles, indicating that the destabilization of Futsch–microtubule loop structures is a critical process for dividing or sprouting synaptic boutons (Figure 1l).42 These results suggested that Nwk reticulum is not directly linked to microtubules. However, Nwk reticulum at the bouton midline were partially colocalized with Actin-GFP signals, reinforcing previous reports that interactions between Nwk and the Actin cytoskeleton are important for structural and functional synaptic plasticity at the Drosophila larval NMJs.31 Neuroglian, the Drosophila L1 homolog shown to be involved with axon pathfinding, was present on both the presynaptic and postsynaptic terminals but was not colocalized with Nwk in Type 1b boutons (Figure 1m). In addition, Nwk reticulum partially colocalized with Hiw, shown to be related with FasII-independent synaptic plasticity (Figure 1o). Western blots from larval body wall muscle extracts of CS, nwk2 and nwk2/Df were probed sequentially with anti-Nwk or Mab-α-Tubulin (12G10) (Figure 1p). Two strong NWK bands of approximately 110 Kda that were clearly seen from CS body wall muscle extracts were not present in nwk2 or nwk2/Df body wall muscle extracts, even though similar intensities of α-Tubulin bands were detected. At least two abundant alternate splicing NWK variants are present in synapses in Drosophila larval NMJs. These precise and comparative localization patterns of Nwk reticulum suggest that NWK may be important for regulating synapse sizes and the trafficking of SV pools.
Localization of Nwk at synapse edges and reserve SVs were revealed by immuno-EM
Anti-Nwk immuno-EM analysis was performed to obtain further information regarding subsynaptic localization patterns of Nwk at synapses (Figure 2). Most silver- and gold-enhanced anti-Nwk particles were distributed at the edge of synapses (46.2%) or within SV pools (44.6%) in Type 1b synaptic boutons (Table 1 and Figure 2a). Two different types of SV pools at the presynaptic terminals of Drosophila NMJs have been suggested.26, 43, 44 The SVs involved with exocytosis present near the T-AZs are called the RRP.45 In contrast, SVs that are broadly distributed inside synaptic boutons are called the RP.26, 43, 45 At the EM levels, SVs near the T-AZs were considered as RRP.44 Therefore, the localization of Nwk particles in either the RRP or RP was further characterized. In this study, SVs present within 200 nm from the stub of T-AZs were considered to be in the RRP and were otherwise considered be in the RP. Among the 29 particles localized at the SV pools, 5 particles were present in the RRP and 24 particles in the RP (Figures 2c–e and Table 1). Synaptic terminals of Type Ib boutons in nwk2 NMJs processed simultaneously with CS NMJs showed significantly reduced numbers of NWK particles (Figure 2b). Even though three times more thin sections obtained from nwk2 NMJs than those of CS NMJs were examined, only three Nwk particles were observed at the presynaptic terminals and five particles at the postsynaptic terminals or muscles (Table 1). These immuno-EM results reinforced the subsynaptic distribution patterns of NWK at the edge of synapses and SV pools and suggesting possible roles of NWK in regulating synapse stability and transmission.
Synergistic phenotypes in the bouton numbers and branch extension in eag1;;nwk2 NMJs
Consistent with localization patterns of Nwk at the presynaptic terminals of Type 1 glutamtergic NMJs, several morphological phenotypes, including increased numbers of synaptic boutons, extended length of synaptic branches and reduced sizes of synaptic bouton area, were observed from nwk2 null mutant NMJs when those phenotypes from CS NMJs were compared (Figures 3a1,3b1 and 31–3k). The numbers of synaptic boutons in nwk2 NMJs were significantly increased compared with those in CS NMJs (CS, 112.0±3.27; nwk2, 148.2±3.22; nwk2/Df, 150.1±4.63) (Figure 3i). The increased numbers of synaptic boutons have been considered evidence of activity-dependent Hebbian plasticity.19 Mutations in eag, one of the voltage gated K+ channels, induce hyperexcitability in Drosophila larval NMJs (Figure 3c1). 19 The bouton number for eag1 NMJs (146.6±6) was not statistically distinguishable from that for nwk2 NMJs but was significantly increased compared with that for CS NMJs (Figures 3b1 and i). Similar phenotypes between eag1 and nwk2 mutant NMJs raised possibilities that eag and nwk might be present in the same signaling pathway regulating the development of synaptic boutons. To test this possibility, eag1;;nwk2 NMJs were generated and examined (Figures 3d1 and i). eag1;;nwk2 NMJs showed significantly increased bouton numbers (eag1;;nwk2, 181.4±5.06; eag1;;nwk2/Df, 179.5±5.56) compared with those in eag1or nwk2 NMJs (Figures 3d1 and i). Synergistic phenotypes observed in eag1;;nwk2 NMJs suggested that eag1 and nwk2 are present in parallel or different signal transduction pathways regulating bouton numbers at Type1 glutamatergic NMJs. This notion is supported by additional morphological phenotypes observed from nwk2 NMJs, such as elongated synaptic branches or decreased areas of boutons, that were not observed in eag1 NMJs (Figures 3j and k). The synaptic branch lengths in nwk2 or nwk2/Df NMJs (nwk2, 754.9±29.9 μm; nwk2/Df, 768.8±23.8 μm) were significantly increased compared with those of CS NMJs (CS, 617.4±25.1 μm). However, the synaptic branch length in eag1 NMJs (683.3±28.7 μm) was not significantly different from those of either CS or nwk mutant NMJs (Figure 3j). The length of eag and nwk double-mutant NMJs (eag1;;nwk2, 852.9±31.6 μm; eag1;;nwk2/Df, 882.7±28.7 μm) was significantly different from that of nwk NMJs (Figures 3d1 and j). These results suggested that eag and nwk may not act via the same signaling mechanisms regulating the numbers of synaptic boutons and NMJ length.
Smaller synaptic boutons in nwk2 and eag1;;nwk2 NMJs
Another morphological phenotype in nwk2 NMJ was reduced bouton sizes. Bouton sizes in nwk2 NMJs (4.095±0.225 μm2, n=124; Figures 3b2 and k) were significantly smaller than those of CS (7.051±0.499 μm2, n=103; Figures 3a2 and k) or eag1 NMJs (8.127±0.507 μm2, n=103; Figures 3c2 and k) but similar to those of eag1;;nwk2 NMJs (3.650±0.154 μm2, n=154; Figures 3d2 and k). Consistently, typical transmission EM images taken from across the midlines of boutons in CS, nwk2, eag1 or eag1;;nwk2 NMJs showed that bouton sizes in nwk2 or eag1;;nwk2 were significantly smaller than those in CS or eag1 (Figures 4a–d). Further morphometric analysis by based on serial transmission EM images revealed that the average synaptic bouton length in nwk2 NMJs (3.18±0.25 μm, n=9) was similar to those in CS NMJs (3.99±0.26 μm, n=7) but significantly smaller than those of eag1 NMJs (4.43±0.41 μm, n=7; Figure 4e). The bouton surface area in nwk2NMJs (17.04±1.87 μm2) was significantly decreased, <70% of CS (29.90±4.46 μm2) or <60% of eag1 (25.93±2.19 μm2) (Figure 4f). The bouton volume in nwk2 NMJs (6.39±1.09 μm3) was reduced to <40% that in CS (17.37±4.07 μm3) or <50% that in eag1 NMJs (12.81±1.3 μm3) (Figure 4g). Compared with nwk2 NMJs, the bouton length and volume in eag1;;nwk2 NMJs were statistically identical, but the average bouton surface area (length=2.39±0.24 μm, surface area=9.74±1.81 μm2, volume=3.38±0.82 μm3, n=9) was not (Figures 4e–g). These results suggested that synaptic boutons in eag1;;nwk2 might be more spherical compared with the more elliptical boutons in nwk2. The normal development of sizes and shapes of synaptic boutons required the expression of Nwk.
Reduced synapse areas in nwk2 and eag1;;nwk2 synaptic boutons
Synapses are electron-dense parallel membrane structures usually harboring T-AZs surrounded by SVs at the presynaptic terminals (Figures 4a–d). The area of total synapses in CS (0.364±0.022 μm2, n=133) was similar to that in eag1 (0.383±0.023 μm2, n=113). In addition, the average total synaptic area was similar in nwk2 (0.229±0.015 μm2, n=83) and eag1;;nwk2boutons (0.213±0.019 μm2, n=64), even though they were significantly smaller than those in CS or eag1 boutons (Figure 4h). Previous studies in synapses in Drosophila larval Type 1b boutons suggested that synapses are ever changing structures undergoing emerging, strengthening, maturing, weakening or other processes. Studies in brp (Drosophila homolog of human active zone protein ELSK/CAST/ERC) loss-of-function mutants showed that T-AZs at synapses were essential for maintaining activity-dependent release of SVs, rather than spontaneous release of SVs.39, 40 These studies suggested that synapses without a T-AZ may be silent, while one or more T-AZs may be active synapses undergoing activity-dependent SV exocytosis. Therefore, the synapses in each genotype were further divided by the numbers of T-AZs present. In this analysis, 25% of CS synapses, 22% of nwk2 synapses, 18% of eag1 synapses and 34% of eag1;;nwk2 synapses lacked a T-AZ and were considered silent synapses, while 63% of CS synapses, 65% of nwk2 synapses, 64% of eag1 synapses and 59% of eag1;;nwk2 synapses were with one T-AZ. In addition, 11% of CS synapses, 12% of nwk2 synapses, 19% of eag1 synapses and 6% of eag1;;nwk2 synapses had two or more T-AZs. The areas of silent synapses in nwk2 (0.090±0.009 μm2) and eag1;;nwk2 (0.096±0.012 μm2) boutons were <50–60% of those in CS (0.163±0.017 μm2) and eag1 (0.187±0.024 μm2) boutons (Figure 4i). However, the area of synapses with one T-AZ in eag1;;nwk2 (0.252±0.022 μm2) boutons was only significantly different from those in CS (0.352±0.02 μm2) or eag1 (0.348±0.02 μm2) boutons (Figure 4j). The areas of synapses with one T-AZ in nwk2(0.293±0.022 μm2) were not significantly different from those of CS, eag1 or eag1;;nwk2. The areas of synapses with two T-AZs in nwk2 boutons were significantly reduced, to ~60% of those in CS or eag1 boutons (Figure 4k, CS, 0.793±0.0669 μm2; nwk2; 0.462±0.0486 μm2; eag1, 0.709±0.0663 μm2; eag1;;nwk2; 0.482±0.0989 μm2). These EM morphometry results showed that Nwk has important roles in maintaining synapses at the proper sizes, and they explain why nwk2 mutants showed reduced evoked junctional current in a previous study.31
FasII levels at synaptic boutons were increased at nwk NMJs
Another phenotype observed from NMJs in hyperexcitability mutant is decreased FasII localization at boutons.20 Downregulation of FasII at boutons by increased neuronal activities, hypomorphic mutations in fasII or activation of mitogen-activated protein kinase-RAS signaling in NMJs resulted in increased numbers of boutons.46 Given that Nwk acts via a signaling mechanism different from that of canonical Hebbian plasticity, FasII localization at boutons of nwk2 NMJs might be different from those of boutons of eag1 NMJs. Indeed, FasII localization at boutons in nwk2 NMJs was significantly increased compared with boutons in CS or eag1 NMJs (Figures 5a–c). Relative FasII immunoreactivity at the NMJs in nwk2 or nwk2/Df mutants was 120.3±2.6 or 119.4±2.1, respectively, an increase of ~40% compared with those in CS (86.3±1.3). FasII levels in eag1;;nwk2 NMJs (98.3±1.5) were increased by ~30% compared with those in eag1 NMJs (74.4±1.8) and decreased by~20% compared with those in nwk2 or nwk2/Df (Figure 4d). These adjusted FasII levels in eag1;;nwk2 NMJs reinforced our hypothesis that Nwk is a component of a signaling mechanism that is different from canonical Hebbian plasticity.
Genetic interaction between Nwk and FasII in regulating synaptic morphology
The synaptic bouton number (61.0±3.33) and branch length (399.6±17.0 μm) in fasIIe76 NMJs were <50% of those in CS or nwk2 NMJs (Figures 3g1). However, the synaptic boutons of fasIIe76 (13.18±0.93 μm2, n=82) were twice as large as those of CS (Figures 3g2 and k). Further, fasIIe76/+ NMJs expressed FasII protein at ~55% of the level observed in CS NMJs and had similar average numbers of synaptic boutons (141.8±5.64) as eag1 and nwk2 NMJs (Figures 3e1 and i). The branch length and bouton area in fasIIe76/+ NMJs were not significantly different from those of CS or eag1 NMJs (Figures 3e1). These results suggested that reduced FasII at NMJs is enough to induce increased bouton numbers but not sufficient to extend the length of synaptic branches. Increased FasII localization at boutons of nwk2 NMJs (Figure 5) and compensatory localization patterns between Nwk and FasII at boutons of CS NMJs (Figure 1c) suggested that Nwk and FasII may have complementary roles in regulating synaptic plasticity. To gain insight into unknown mechanisms underlying synaptic plasticity by FasII and Nwk, FasII protein levels in nwk2 NMJs were genetically regulated by recombining fasIIe76 mutant chromosomes. When FasII expression was reduced to 10% of CS, the numbers of synaptic boutons and bouton midline areas in fasIIe76;;nwk2 (118.1±4.22; 729±0.471 μm2, n=102) were not significantly different from those of CS (Figures 3h1). These results suggested that fasIIe76 and nwk2 mutations mutually suppressed the opposing phenotypes when 10% of the normal level of FasII was expressed. Only the length of synaptic branches of fasIIe76;;nwk2 (732.8±40.4 μm) was similar to those of nwk2 NMJs. When FasII expression was reduced to 55% of CS, the bouton numbers of fasIIe76/+;;nwk2 (132.6±4.73) and fasIIe76/+;;nwk2/Df (131.4±6.92) NMJs were similar to those of fasIIe76/+ and nwk2 mutants (Figures 3f1 and i). However, the synaptic branch lengths of fasIIe76/+;;nwk2 (781.0±54.8 μm) and fasIIe76/+;;nwk2/Df (821.4±34.1 μm) were similar to those of nwk2 mutants. In addition, the bouton midline areas of fasIIe76/+;;nwk2 (6.638±0.41 μm2, n=128) were similar to those of fasIIe76/+ (Figures 3f2 and k).
Our NMJ morphology analysis results suggested that three morphological aspects examined in this study could be regulated by different signaling mechanisms. We can suggest that FasII is downstream of Nwk in regulating the numbers and sizes of synaptic boutons but either is upstream in the regulation of synaptic branch length or does not participate in this process. Further studies with other mutants showing altered morphologies will reveal more details of the signaling mechanisms.
nwk synapses showed impaired RRPs at T-AZs
The localization of Nwk with SVs at the confocal microscopic level (Figure 1) and EM level (Figure 2) suggested that Nwk may have important roles in regulating SV trafficking or transmission. Electrophysiological studies showed that the quantal contents of nwk2 NMJs were ~50% less than those of CS, although the amplitude of miniature excitatory junctional currents or quantal sizes were slightly increased without changes in frequency of miniature excitatory junctional currents.31 Even though the ~50% decrease in the numbers of synapses and T-AZs in nwk2 boutons may contribute to reduced synaptic transmission in nwk2 NMJs, the numbers of synaptic boutons in nwk2 NMJs were increased by ~40%. These results suggested that other defects caused by loss of Nwk at synaptic terminals may exist. Thus we further examined whether SV pools in nwk2, eag1 or eag1;;nwk2 boutons were altered.
First, we examined whether Mab-Synapsin signals in nwk2 boutons were altered (Figures 6a–d). When nwk2, eag1 or eag1;;nwk2 boutons were compared with CS, only nwk2 boutons appeared to have reduced Synapsin immunoreactivity. eag1 boutons showed stronger signals and eag1;; nwk2 boutons showed signals similar to those of CS. These results suggested that Nwk may be critical for maintaining normal SV pools at the presynaptic terminals.
Next, we examined whether RRP and RP were altered in nwk2 boutons by performing EM (Figures 6e–h). In this study, the RRP and RP were defined as SVs within 200 nm or at 200–400 nm, respectively, from the stub of T-AZs. The numbers of SVs in the RRP (6.44±0.27) or RP (10.83±0.53) in nwk2 were significantly less than those of CS (RRP, 11.49±0.28; RP, 24.115±0.77). The RRPs of eag1 (12.72±0.38) and eag1;;nwk2 (12.43±0.30) were significantly increased compared with that of CS. However, only the RP of eag1 (28.21±0.91) was significantly increased compared with that of CS. The RP of eag1;;nwk2 (23.26±0.82) was similar to that of CS (Figure 6i). These results suggested that Nwk is critical for maintaining the RRP and RP. In addition, the reduction in SVs induced by the loss of Nwk at the presynaptic terminals might be offset by increased neural activity, which is known to strengthen synaptic connections.
Nwk formed a protein complex with DSypt1 and Synapsin
Reduced Synapsin immunoreactivities together with reduced RRP and RP at nwk mutant synapses suggested that NWK and Synapsin may present at the same protein complexes. To investigate this possibility, we performed Mab-Synpasin immunoprecipitation and proved precipitates with rabbit anti-Nwk or anti-DSypt1 antibodies (Figure 6j). There were clear one Nwk and two DSypt1 bands when Mab-Synapsin precipitates were separated. Consistent with a previous report,47 three Synapsin bands were clearly detected. These results suggested that NWK formed a protein complex with DSypt1 and Synapsin and regulates SV trafficking and transmission.
3D HVEM tomography revealed T-AZ architectures of CS and nwk2 synapses at high resolution
To investigate SV localization patterns and synaptic architecture at three dimensions, CS and nwk2 synapses in Type 1b boutons were analyzed by 3D HVEM tomography. Examples of unprocessed HVEM images of CS and nwk2 synapses are shown in Figures 7a and b. Using 121 tilted images, 3D ultrastructures of synapses (Figures 7c and d) and T-AZs (Figures 7e and f) of CS and nwk2 were generated by IMOD.37 Because fewer SVs with enlarged sizes were observed from nwk2, we further quantified the 3D distribution patterns of SVs in RRPs. Consistent with conventional EM results (Figures 6e–h), significantly fewer SVs presented at RRP (CS, 138.0±9.0; nwk2, 91.0±6.8, P<0.01). The graphs showing SVs numbers based on distances from the stub of T-AZs suggested that no SVs were docked to T-AZs in nwk2. However, more SVs localized from 100 to 140 nm from T-AZs in nwk2 than in CS. In addition, SV size distribution results (Figure 7i) revealed that SVs in nwk2 were significantly larger than those in CS (nwk2, 42.69±0.45; CS, 39.40±0.315 nm, P<0.001). The 3D ultrastructural differences at synapses and T-AZs between CS and nwk2 were clearly visualized by 3D rotation videos (Supplementary Video Clips 1). Significantly fewer but enlarged SVs were present in the RRPs in nwk2 synapses.
In order to investigate the unknown in vivo functions of proteins containing SH3 and F-BAR domains in synaptic plasticity and transmission, we took advantage of Drosophila NMJs and available nwk mutants. Nwk is a Drosophila homolog of MEGAP, one of the proteins responsible for mental retardation in humans; Nwk was initially discovered by temperature-sensitive paralysis behavior of adult flies.31 Although genetic and physical interactions between Nwk and components of endocytosis, such as Dap160 and Dynamin,48 and actin cytoskeleton regulators, such as Wiskott–Aldrich syndrome protein31 and CDC42,49 have been reported, the localization patterns of Nwk at synaptic boutons appear to be different from localization patterns of the above-mentioned proteins. Thus we hypothesized that Nwk may directly or indirectly interact with other synaptic or cytoskeletal components. In addition, by performing immunohistochemistry to confirm partial colocalization of Nwk with DAP160 (Figure 1j),48 we also observed via confocal microscopy that Nwk partially colocalized (Figures 1e and f) and formed protein complexes (Figure 6j) with Synapsin and DSypt1. Furthermore, we found that Synapsin immunoreactivities at nwk synaptic boutons were significantly reduced (Figures 6a–d). These findings are highly intriguing because recent studies have shown that Synapsin, the most abundant presynaptic phosphoprotein in Drosophila, has a pivotal role in regulating SV trafficking at synaptic terminals by forming protein complexes with Dap16050 in glutamatergic NMJs. The defects of RRP and RP in nwk mutant synapses were further confirmed by performing transmission EM analysis (Figures 6e–i) and HVEM 3D tomography (Figures 7a–i). Thus it is possible that Nwk is actively participating in SV trafficking at RRP and RP via interactions with Synapsin, DSypt1 (Figure 6i), Dap160,50 Dynamin48 and other interacting proteins that have yet to be identified.
Another phenotype in nwk loss-of-function mutants that was able to be identified by this study’s use of HVEM 3D tomography was that of enlarged SVs (Figures 7a–i). Because we used 1 μm thick sections for examining size and distribution of SVs at nwk mutant and control synapses and as 20 nm gold particles were used to create a list of fiducial points and size standards for SVs, our HVEM 3D analysis results did not contain biased data originating from measuring diameters of sectioned SVs when 50–100 nm of thin sections were used for conventional transmission EM analysis as described by Kim et al.51 Recently, it has been shown that an F-BAR domain in Nwk binds to and remodels membranes to form concave membrane structures.52 Therefore, it is possible that Nwk may regulate SV recycling both directly, by interacting with synaptic membranes, and indirectly, through its binding partners, such as Synapsin, DSypt1, Dap160 and Dynamin. Thus loss of Nwk at synapses might induce enlarged SVs compared with control synapses.
In addition to regulating SV size and trafficking, our NMJ and synapse morphometric analysis results provided several lines of evidence supporting that Nwk regulates synaptic plasticity of glutamatergic NMJs in a manner different from activity-dependent Hebbian plasticity. Previous studies have shown one of the classical examples of Hebbian plasticity, in which increased neuronal activity in NMJs reduces FasII localization at synaptic boutons, resulting in both an increase in the number of synaptic boutons and branch elongation.19, 22 However, the findings of this study, which supported that genetically increased neuronal activity in nwk2 mutant NMJs resulted in significantly more synaptic boutons and branch elongations (Figure 3) and that the levels of FasII in nwk2 mutants were significantly higher than those of CS (Figure 5), suggested that Nwk may exist in a different signaling pathway from that of Hebbian plasticity.
The evidence presented in this study is important because most psychiatric and neurological diseases, ranging from autism and mental retardation to dementia, are reported to be accompanied by altered synaptic structures and functions.1 The association of MEGAP and mental retardation has been revealed in the process of identifying genes that are linked with distal chromosome 3p deletion syndrome (3p-syndrome) patients with severe mental retardation.3, 53 Similar to Nwk, MEGAP expression was observed in the embryonic central nervous systems of mice54 and high expression was found in the hippocampus, amygdala, piriform cortex, posterior parietal associative area and the dentate gyrus of adult mouse brains.3 In addition, similar to Nwk, MEGAP binds strongly to the phosphoinositide-rich membrane and is involved in the formation of filopodia.52 In the synaptogenesis stage, MEGAP has an important role in synapse selection, and consequently, the loss of MEGAP function results in a decrease in the number of neuron spines.55 Thus, although it has not been elucidated to date whether MEGAP expresses at presynaptic or postsynaptic terminals or both, it is possible that MEGAP may regulate SV size and distribution in neuron spines at glutamatergic synapses of the mouse central nervous system, especially at the hippocampus, resulting in mental retardation phenotypes in human patients3 and mouse knockout models.55, 56 Thus further studies in Nwk and MEGAP will reveal unknown molecular and cellular functions of SH3 and F-BAR domain proteins in synaptic plasticity and mental retardation.
van Spronsen M, Hoogenraad CC . Synapse pathology in psychiatric and neurologic disease. Curr Neurol Neurosci Rep 2010; 10: 207–214.
Turrigiano GG . The self-tuning neuron: synaptic scaling of excitatory synapses. Cell 2008; 135: 422–435.
Endris V, Wogatzky B, Leimer U, Bartsch D, Zatyka M, Latif F et al. The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation. Proc Natl Acad Sci USA 2002; 99: 11754–11759.
Jin P, Alisch RS, Warren ST . RNA and microRNAs in fragile X mental retardation. Nat Cell Biol 2004; 6: 1048–1053.
Gabellini D, Green MR, Tupler R . When enough is enough: genetic diseases associated with transcriptional derepression. Curr Opin Genet Dev 2004; 14: 301–307.
Belmonte MK, Allen G, Beckel-Mitchener A, Boulanger LM, Carper RA, Webb SJ . Autism and abnormal development of brain connectivity. J Neurosci 2004; 24: 9228–9231.
Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS et al. The spectrum of mutations in UBE3A causing Angelman syndrome. Hum Mol Genet 1999; 8: 129–135.
Zoghbi HY . Postnatal neurodevelopmental disorders: meeting at the synapse? Science 2003; 302: 826–830.
Turrigiano GG, Nelson SB . Homeostatic plasticity in the developing nervous system. Nat Rev Neurosci 2004; 5: 97–107.
Vitureira N, Goda Y . The interplay between Hebbian and homeostatic synaptic plasticity. J Cell Biol 2013; 203: 175–186.
Toyoizumi T, Kaneko M, Stryker MP, Miller KD . Modeling the dynamic interaction of hebbian and homeostatic plasticity. Neuron 2014; 84: 497–510.
Desai NS . Homeostatic plasticity in the CNS: synaptic and intrinsic forms. J Physiol 2003; 97: 391–402.
Abbott LF, Regehr WG . Synaptic computation. Nature 2004; 431: 796–803.
O'Rourke NA, Weiler NC, Micheva KD, Smith SJ . Deep molecular diversity of mammalian synapses: why it matters and how to measure it. Nat Rev Neurosci 2012; 13: 365–379.
Koh YH, Gramates LS, Budnik V . Drosophila larval neuromuscular junction: molecular components and mechanisms underlying synaptic plasticity. Microsc Res Tech 2000; 49: 14–25.
Keshishian H . Is synaptic homeostasis just wishful thinking? Neuron 2002; 14: 481–482.
Packard M, Mathew D, Budnik V . Wnts and TGF-β in synaptogenesis: old friends signaling at new places. Nat Rev Neurosci 2003; 4: 113–120.
Koh YH . Drosophila as a model organism for investigating molecular and cellular etiologies underlying complex neurological disorders in humans. J Asia Pac Entomol 2006; 9: 75–84.
Budnik V, Zhong Y, Wu CF . Morphological plasticity of motor axons in Drosophila mutants with altered excitability. J Neurosci 1990; 10: 3754–3768.
Schuster CM, Davis GW, Fetter RD, Goodman CS . Genetic dissection of structural and functional components of synaptic plasticity. I. Fasciclin II controls synaptic stabilization and growth. Neuron 1996; 17: 641–654.
Schuster CM, Davis GW, Fetter RD, Goodman CS . Genetic dissection of structural and functional components of synaptic plasticity. II. Fasciclin II controls presynaptic structural plasticity. Neuron 1996; 17: 655–667.
Davis GW, Schuster CM, Goodman CS . Genetic analysis of the mechanisms controlling target selection: target-derived Fasciclin II regulates the pattern of synapse formation. Neuron 1996; 19: 561–573.
Ljaschenko D, Ehmann N, Kittel RJ . Hebbian plasticity guides maturation of glutamate receptor fields in vivo. Cell Rep 2013; 3: 1407–1413.
Kim E, Sheng M . PDZ domain proteins of synapses. Nat Rev Neurosci 2004; 5: 771–781.
Rizzoli SO, Betz WJ . Synaptic vesicle pools. Nat Rev Neurosci 2005; 6: 57–69.
Kidokoro Y, Kuromi H, Delgado R, Maureira C, Oliva C, Labarca P . Synaptic vesicle pools and plasticity of synaptic transmission at the Drosophila synapse. Brain Res Brain Res Rev 2004; 47: 18–32.
Tejedor FJ, Bokhari A, Rogero O, Gorczyca M, Zhang J, Kim E et al. Essential role for dlg in synaptic clustering of Shaker K+ channels in vivo. J Neurosci 1997; 17: 152–159.
Koh YH, Popova E, Thomas U, Griffith LC, Budnik V . Regulation of DLG localization at synapses by CaMKII-dependent phosphorylation. Cell 1999; 98: 353–363.
Thomas U, Kim E, Kuhlendahl S, Koh YH, Gundelfinger ED, Sheng M et al. Synaptic clustering of the cell adhesion molecule fasciclin II by discs-large and its role in the regulation of presynaptic structure. Neuron 1997; 19: 787–799.
Paradis S, Sweeney ST, Davis GW . Homeostatic control of presynaptic release is triggered by postsynaptic membrane depolarization. Neuron 2001; 30: 737–749.
Coyle I, Koh YH, Lee W-CM, Slind J, Fergestad T, Littleton JT et al. Nervous Wreck, an adaptor protein that interacts with WASP, regulates synapse growth in Drosophila. Neuron 2004; 41: 512–534.
Kim AY, Seo JB, Kim WT, Choi HJ, Kim S-Y, Morrow G et al. The pathogenic human Torsin A in Drosophila activates the unfolded protein response and increases susceptibility to oxidative stress. BMC Genomics 2015; 16: 338.
Lee DW, Seo JB, Ganetzky B, Koh YH . ΔFY mutation in human Torsin A induces locomotor disability and abberant synaptic structures in Drosophila. Mol Cells 2009; 27: 89–97.
Zhang B, Koh YH, Beckstead RB, Budnik V, Ganetzky B, Bellen HJ . Synaptic vesicle size and number are regulated by a Clathrin adaptor protein required for endocytosis. Neuron 1998; 21: 1465–1475.
Roos J, Kelly RB . Dap160, a neural-specific Eps15 homology and multiple SH3 domain-containing protein that interacts with Drosophila dynamin. J Biol Chem 1998; 273: 19108–19119.
Schneider CA, Rasband WS, Eliceiri KW . NIH Image to ImageJ: 25 years of image analysis. Nat Methods 2012; 9: 671–675.
Kremer JR, Mastronarde DN, McIntosh JR . Computer visualization of three-dimensional image data using IMOD. J Struct Biol 1995; 116: 71–76.
Koh YH, Lehfield K, Ganetzky B . A Drosophila model of early-onset torsion dystonia suggests impairments in transforming growth factor-β signaling. Hum Mol Genet 2004; 13: 2019–2030.
Wagh DA, Rasse TM, Asan E, Hofbauer A, Schwenkert I, Durrbeck H et al. Bruchpilot, a protein with homology to ELKS/CAST, is required for structural integrity and function of synaptic active zones in Drosophila. Neuron 2006; 49: 833–844.
Kittel RJ, Wichmann C, Rasse TM, Fouquet W, Schmidt M, Schmid A et al. Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release. Science 2006; 312: 1051–1054.
Koh TW, Verstreken P, Bellen HJ . Dap160/Intersectin acts as a stabilizing scaffold required for synaptic development and vesicle endocytosis. Neuron 2004; 43: 193–205.
Roos J, Hummel T, Ng N, Klambt C, Davis GW . Drosophila Futsch regulates synaptic microtubule organization and is necessary for synaptic growth. Neuron 2000; 26: 371–382.
Delgado R, Maureira C, Oliva C, Kidokoro Y, Labarca P . Size of vesicle pools, rates of mobilization, and recycling at neuromuscular synapses of a Drosophila mutant, shibire. Neuron 2000; 28: 941–953.
Roche JP, Packard MC, Moeckel-Cole S, Budnik V . Regulation of synaptic plasticity and synaptic vesicle dynamics by the PDZ protein Scribble. J Neurosci 2002; 22: 6471–6479.
Alabi AA, Tsien RW . Synaptic vesicle pools and dynamics. Cold Spring Harb Perspect Biol 2012; 4: a013680.
Koh YH, Ruiz-Canada C, Gorczyca M, Budnik V . The Ras1–mitogen-activated protein kinase signal transduction pathway regulates synaptic plasticity through Fasciclin II-mediated cell adhesion. J Neurosci 2002; 22: 2496–2504.
Klagges BR, Heimbeck G, Godenschwege TA, Hofbauer A, Pflugfelder GO, Reifegerste R et al. Invertebrate synapsins: a single gene codes for several isoforms in Drosophila. J Neurosci 1996; 16: 3154–3165.
O'Connor-Giles KM, Ho LL, Ganetzky B . Nervous wreck interacts with thickveins and the endocytic machinery to attenuate retrograde BMP signaling during synaptic growth. Neuron 2008; 58: 507–518.
Rodal AA, Motola-Barnes RN, Littleton JT . Nervous wreck and Cdc42 cooperate to regulate endocytic actin assembly during synaptic growth. J Neurosci 2008; 28: 8316–8325.
Winther ÅME, Vorontsova O, Rees KA, Näreoja T, Sopova E, Jiao W et al. An endocytic scaffolding protein together with Synapsin regulates synaptic vesicle clustering in the Drosophila neuromuscular junction. J Neurosci 2015; 35: 14756–14770.
Kim SJ, Atwoodb HL, Cooper RL . Assessing accurate sizes of synaptic vesicles in nerve terminals. Brain Res 2000; 877: 209–217.
Stanishneva-Konovalova TB, Kelley CF, Eskin TL, Messelaar EM, Wasserman SA, Sokolova OS et al. Coordinated autoinhibition of F-BAR domain membrane binding and WASp activation by Nervous Wreck. Proc Nat Acad Sci USA 2016; 113: E5552–E5561.
Gunnarsson C, Bruun CF . Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3-p26.1. Am J Med Genet A 2010; 152A: 3110–3114.
Waltereit R, Kautt S, Bartsch D . Expression of MEGAP mRNA during embryonic development. Gene Expr Patterns 2008; 8: 307–310.
Carlson BR, Lloyd KE, Kruszewski A, Kim I-H, Rodriguiz RM, Heindel C et al. WRP/srGAP3 facilitates the initiation of spine development by an inverse F-BAR domain, and its loss impairs long-term memory. J Neurosci 2011; 31: 2447–2460.
Bacon C, Endris V, Andermatt I, Niederkofler V, Waltereit R, Bartsch D et al. Evidence for a role of srGAP3 in the positioning of commissural axons within the ventrolateral funiculus of the mouse spinal cord. PLoS ONE 2011; 6: e19887.
The Korea Basic Science Institute kindly provided HVEM and IMOD analysis. This work was carried out with the support of the Cooperative Research Program for Agriculture Science & Technology Development (Project title: Elucidation the health improvement effects of boiled silk worm larvae, Project No.: PJ010828012017), the Rural Development Administration and the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (No. 2015R1D1A3A01018497).
The authors declare no conflict of interest.
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Hur, J., Lee, S., Kim, A. et al. Regulation of synaptic architecture and synaptic vesicle pools by Nervous wreck at Drosophila Type 1b glutamatergic synapses. Exp Mol Med 50, e462 (2018). https://doi.org/10.1038/emm.2017.303