QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

Vol. 17, Issue 11, 4709-4719, November 2006

This Article Abstract Full Text (PDF) Supplemental Material All Versions of this Article: E06-03-0253v1 17/11/4709    most recent Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Nunes, P. Articles by Stewart, B. A. Search for Related Content PubMed PubMed Citation Articles by Nunes, P. Articles by Stewart, B. A.

Synaptic Vesicle Mobility and Presynaptic F-Actin Are Disrupted in a N-ethylmaleimide–sensitive Factor Allele of Drosophila

Paula Nunes^*, Nicola Haines^*, Venkat Kuppuswamy, David J. Fleet, and Bryan A. Stewart^*

Departments of *Biology and Computer Science, University of Toronto, Mississauga, Ontario, Canada L5L 1C6

Submitted April 3, 2006; Accepted August 9, 2006
Monitoring Editor: Erika Holzbaur

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
N-ethylmaleimide sensitive factor (NSF) can dissociate the soluble NSF attachment receptor (SNARE) complex, but NSF also participates in other intracellular trafficking functions by virtue of SNARE-independent activity. Drosophila that express a neural transgene encoding a dominant-negative form of NSF2 show an 80% reduction in the size of releasable synaptic vesicle pool, but no change in the number of vesicles in nerve terminal boutons. Here we tested the hypothesis that vesicles in the NSF2 mutant terminal are less mobile. Using a combination of genetics, pharmacology, and imaging we find a substantial reduction in vesicle mobility within the nerve terminal boutons of Drosophila NSF2 mutant larvae. Subsequent analysis revealed a decrease of filamentous actin in both NSF2 dominant-negative and loss-of-function mutants. Lastly, actin-filament disrupting drugs also decrease vesicle movement. We conclude that a factor contributing to the NSF mutant phenotype is a reduction in vesicle mobility, which is associated with decreased presynaptic F-actin. Our data are consistent with a model in which actin filaments promote vesicle mobility and suggest that NSF participates in establishing or maintaining this population of actin.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
N-ethylmaleimide–sensitive factor (NSF) was isolated on the basis of its ability to restore vesicle trafficking between Golgi membranes after treatment by N-ethylmaleimide (Block et al., 1988). It was further shown that NSF can hydrolyze ATP and together with soluble NSF attachment protein (SNAP) this activity can dissociate the three-member protein complex known as the SNAP receptor (SNARE) complex (Whiteheart et al., 1992; Sollner et al., 1993a, 1993b; Whiteheart et al., 1994). In addition to this established NSF function, other studies indicate that NSF likely has multiple cellular roles. These studies include reports of non-SNARE binding partners for NSF (Xu et al., 1998; McDonald et al., 1999; Han et al., 2000; Cong et al., 2001; Muller et al., 2002; Martin et al., 2006), and the role NSF plays in trafficking postsynaptic glutamate receptor subunits in the mammalian CNS (Nishimune et al., 1998; Song et al., 1998). Altogether, these data indicate that NSF is potentially central to many different types of intracellular trafficking events, some of which do not require SNARE proteins.

We have taken a genetic approach to studying NSF using the fruit fly, Drosophila melanogaster. Drosophila has two NSF genes, comatose (which encodes the NSF1 protein) and NSF2 (Boulianne and Trimble, 1995; Pallanck et al., 1995), whose proteins are 80% identical and are functionally redundant. NSF1 is the predominant functional isoform in the adult fly nervous system, although NSF2 is functionally important in other tissues and throughout development (Golby et al., 2001). A null allele of NSF2 dies as first instar larvae (Golby et al., 2001), thus preventing examination of the easily accessible and widely studied third larval instar neuromuscular junction (NMJ). A dominant-negative NSF2 (NSF2^E/Q) transgene was generated by site-directed mutagenesis of a highly conserved amino acid within the D1 ATPase domain of the molecule (Stewart et al., 2001), and the mutation renders a molecule that is capable of binding MgATP but it hydrolyzes ATP less well (Whiteheart et al., 1994; Stewart et al., 2001). When expressed in neurons, NSF2^E/Q reduces synaptic strength, increases synaptic fatigue, and reduces size of the synaptic vesicle pool (Stewart et al., 2002), consistent with previous work on NSF (Kawasaki et al., 1998). Two unexpected findings emerged: first these changes occurred in the absence of detectable changes in SNARE complex abundance and second, the NSF2^E/Q transgene induced a marked overgrowth of the neuromuscular junction.

Developmental and ultrastructural studies (Stewart et al., 2005) further revealed that the NSF2^E/Q induced overgrowth phenocopies an expanded NMJ found at the embryonic synapse of the NSF2⁵⁵ loss-of-function allele and that the larval NSF2^E/Q NMJ has a reduced density of presynaptic active zones. Interestingly, there was no difference in the number of synaptic vesicles in the NSF2^E/Q nerve terminal compared with controls. This suggests the reduction in vesicle pool size is not due to an endocytosis defect because genuine mutations of endocytotic genes all show dramatically reduced number of vesicles (Zhang et al., 1998; Verstreken et al., 2002, 2003; Koh et al., 2004). To explain our data, we hypothesize that there is a decrease in the intrabouton mobility of vesicles in the NSF2^E/Q nerve terminal.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Fly Stocks
Drosophila melanogaster stocks were raised on Bloomington medium and crossed at room temperature or 25°C. UAS-Actin-GFP stocks were obtained from the Kyoto Stock Centre, UAS-Synaptotagmin-GFP (Zhang et al., 2002) was obtained from the Bloomington Stock Center, and UAS-moesin-GFP flies were the gift of D. Kiehart (Edwards et al., 1997). elav-Gal4 is a pan-neuronal driver that expresses in postmitotic neurons. elav^c155-Gal4 and elav^3A-Gal4 lines were used to drive UAS gene expression in the control background. A recombinant third chromosome carrying elav^3A-Gal4 and UAS-NSF2^E/Q is described in Stewart et al. (2002) and was used for NSF2^E/Q mutant experiments. We have previously shown that there is no effect of overexpressing wild-type NSF2 and that yw, UAS-NSF2^E/Q, and elav^3A-Gal4 are phenotypically equivalent with respect to NMJ overgrowth (Stewart et al., 2002, 2005). Unless otherwise stated, larvae resulting from a cross of elav^3A-Gal4 to UAS-Actin-GFP or UAS-Synaptotagmin-GFP are referred to as controls, whereas larvae from elav^3A-Gal4::UAS-NSF2^E/Q crossed to UAS-Actin-GFP or UAS-Synaptotagmin-GFP are referred to as mutants.

For NSF2 loss-of-function studies we first made a recombinant chromosome bearing elav^3A-Gal4::Df(3R)urd/TM3, P[w[+mC] = ActGFP]JMR2, Ser¹; the deficiency removes the NSF2 coding region. Second we constructed flies carrying UAS-Actin-GFP on the second chromosome and NSF2⁵⁵/TM3, P[w[+mC] = GAL4-twi.G]2.3, P[UAS-2xEGFP]AH2.3, Sb¹ Ser¹. NSF2⁵⁵ is a severe loss-of-function allele with a stop codon in the N-terminal domain of NSF2 at amino acid 130 (Golby et al., 2001). Crossing these two lines together, and selecting against the GFP balancer chromosomes, yields offspring that carry UAS-Actin-GFP; NSF2⁵⁵/elav^3A-Gal4:Df(3R)urd.

Live and Fixed Larval Preparations and Drug Administration
Wandering third instar larvae were dissected in HL3 physiological saline without calcium (Stewart et al., 1994), and all experiments were conducted in this saline. To minimize movements during image acquisition for fluorescence recovery after photobleaching (FRAP) experiments, the preparation was transferred to a drop of saline on a 3 x 4-inch Sylgard-coated glass slide, stretched out so that the surface of the body wall musculature was flat and immobilized using Nexaband tissue glue (WPI, Sarasota, FL). For fixed preparations, dissected larvae were covered with 4% EM-grade formaldehyde in phosphate-buffered saline (PBS) for 10 min and washed briefly in PBS.

For NSF2 loss-of-function analysis, first instar larvae were dissected as above with sharpened tungsten wire needles. They were fixed with 4% EM-grade formaldehyde in PBS for 10 min, washed briefly in PBS plus 0.1% Triton X-100 (PBT), incubated in antibody solution as indicated below, washed in PBT, and mounted in Vectashield (Vector Laboratories, Burlington, Ontario, Canada). Four UAS-Actin-GFP; NSF2⁵⁵/elav^3A-Gal4::Df(3R)urd and four UAS-Actin-GFP; NSF2⁵⁵/elav^3A-Gal4 first instar larvae were dissected on the same slide and processed simultaneously under identical conditions. This procedure was carried out twice, and the images shown in Figure 5 are representative of these two genotypes.

The primary antibodies used in this study were rabbit anti-GFP (1:1000, Invitrogen, Burlington, Ontario, Canada), rabbit anti-synaptotagmin (1:2000, gift of N. Reist) and Texas-red–conjugated goat anti-HRP (1:1000; ICN Biomedical, Irvine, CA). The secondary antibodies were goat anti-rabbit Alexa488 and goat anti-rabbit Alexa546 (1:1000, Invitrogen). Rhodamine-phalloidin (Sigma, Oakville, Ontario, Canada) was used at a dilution of 1:1500 in PBT.

Latrunculin A (Sigma) and jasplakinolide (Molecular Probes) were prepared as a 1 mM stock solution in DMSO, and swinholide A (Sigma) was prepared as a 1 mM stock in 100% ethanol. All stock solutions were kept at –20°C, and they were diluted in HL3 to make working solutions at the concentrations indicated in the text. We bath-applied these drugs by exchanging the HL3 solution for HL3 plus the drug; we let the drug incubate for 5 min before image collection and completed image acquisition within 60 min. The preparation was maintained in the drug containing solution throughout the experiment.

Imaging and FRAP
Images in this study were taken from the muscle 6/7 neuromuscular junction in abdominal segments 3 or 4 of wandering third instar larvae.

Live time-lapse images of actin-GFP signals were acquired using a 60x water immersion lens on a Nikon E600FN microscope (Mississauga, Ontario, Canada) equipped with filters appropriate for GFP excitation and emission. Images were acquired with a Hammamatsu ORCA ER camera (Bridgewater, NJ) operated with SimplePCI software (Compix, Sewickley, PA). An Uniblitz shutter (Vincent and Associates, Rochester, NY) was used to minimize the preparation's exposure to fluorescent light; images were acquired once every 15 s with 1-s exposure time per image. Still images were transformed into movies using SimplePCI (Compix) and digitally stabilized according to the methods described in Fleet and Weiss (2005).

Images of antibody- and phalloidin-labeled nerve terminals were acquired on a LSM510 (Carl Zeiss, Toronto, Ontario, Canada) confocal laser microscope using a 63x/NA 1.4 oil immersion lens. The pinhole on the microscope was set to acquire to images with a focal depth of 1.0 µm. The confocal gain and laser power were identical for both genotypes.

For FRAP analysis, an LSM510 (Carl Zeiss) confocal laser microscope equipped with a 100x/NA 1.0 Achroplan water immersion objective and a 200 mW Argon laser was used. The 488-nm line of the argon laser was set at 3–5% for GFP excitation, and emission was collected though a 505-nm long-pass filter. For Syt-GFP images 512 x 512-pixel frames were captured at zooms 8, 9, and 10 (0.02 µm/pixel) with a pinhole setting of 2.0 Airy units (2.4-µm optical sections). The scan speed was set at 6 (6.40 µs/pixel) for higher-quality images and at 12 (0.80 µs/pixel) for faster acquisition. Actin-GFP images were 256 x 256-pixel frames captured a zoom 5 or 6, and the scan speed was 10 (1.76 µs/pixel). Photobleaching was achieved by scanning a 12 x 30-pixel region of interest (ROI) 10 times at 100% laser power. A single frame was captured before the bleaching scan, and 59 frames were acquired every 1.0 s subsequently for Syt-GFP and once every 500 ms for actin-GFP.

For quantifying recovery values we used a recovery index (RI) was defined as follows:

(1)

where F_i, F_b, and F_p represent the initial fluorescence, bleached fluorescence, and plateau fluorescence values within the ROI, respectively. This ratio accounts for the differing fluorescence intensities encountered both before and after bleaching among various boutons and preparations. For soluble-GFP and actin-GFP, we normalized the plateau value to the initial value (% recovery); because these two species move rapidly, there is some uncertainty about the lowest bleach level and therefore F_b cannot be measured as accurately.

F-actin Fractionation
Brains from 10 wandering third instar larva were dissected in HL3 solution and incubated in 100 µl HL3 with or without 5 µM swinholide A for 20 min at room temperature. Tissue was then transferred into 100 µl of actin stabilization buffer (Cytoskeleton Inc., Denver, CO; 50 mM PIPES, pH 6.9, 50 mM NaCl, 5 mM MgCl₂, 5 mM EGTA, 5% glycerol, 0.1% Nonidet P40, 0.1% Triton X-100, 0.1% Tween 20, 0.1% -mercaptoethanol, 1 mM ATP, and 1 tablet/50 ml complete protease inhibitor [Roche]) and homogenized with 10 strokes of a glass microtissue grinder. After a 10-min room temperature incubation, samples were spun at 1,000 x g for 2 min to remove large debris, and the resulting supernatants were then spun at 100,000 x g for 1 h at 22°C in a Beckman optima XL-100K ultracentrifuge with Sw55-Ti rotor and adaptors. Supernatants were carefully removed and pellets were resuspended in SDS sample buffer. Aliquots of samples before ultracentrifugation and the supernatants and pellet after ultracentrifugation were boiled and then separated on 10% SDS-polyacrylamide gels and transferred to PVDF membrane. Actin was detected with mAb JLA20 used at 1:50 dilution (Developmental Studies Hybridoma Bank, University of Iowa, Iowa City, IA) and an HRP-coupled secondary (Bio-Rad, Mississauga, Ontario, Canada) followed by chemiluminescent detection (ECL Plus, Amersham, Baie d'Urfe, Quebec, Canada). Blots were scanned and digitized with a Molecular Dynamics Phosphoimager (Sunnyvale, CA). Band intensities were compared with known amounts of nonmuscle actin (Cytoskeleton Inc.) run on the same gel and quantified using ImageJ (NIH).

Data Analysis
All images were analyzed using the Zeiss LSM-510 software or the open-source application ImageJ 1.32j. All statistical tests and curve fitting were performed using Prism 4.0 (GraphPad Software, San Diego, CA) using tests indicated in the text. We chose p < 0.05 as the level of statistical significance, and unless otherwise indicated, data are presented as mean ± SEM throughout the text. Figures were assembled using the open-source application Inkscape.

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Reduced Synaptic Vesicle Mobility in NSF2^E/Q Boutons
To test the hypothesis that the NSF2^E/Q has altered synaptic vesicle mobility, we applied FRAP analysis to control and NSF2^E/Q larval NMJs. We used a synaptotagmin-GFP (Syt-GFP) fusion protein to label synaptic vesicles and photobleached small regions of single synaptic boutons and then measured the movement of the GFP signal back into the bleached area (Figure 1).

View larger version (38K): [in this window] [in a new window]   Figure 1. FRAP analysis of synaptic vesicle mobility. (a) An image of Syt-GFP within the nerve terminal boutons of a control (elav3A-Gal4 x UAS-SytGFP) Drosophila larva. Colored shapes indicated the regions from which mean fluorescence intensities were taken and are shown in subsequent panels. (b) Time sequence of the same bouton before (0), immediately after photobleaching (1), 10 s (10), and 60 s (60) after bleaching. The arrow indicates the 12 x 30-pixel region that was bleached. (c) SytGFP expression in a mutant (elav3A-Gal4::UAS-NSF2E/Q x UAS-SytGFP) larva shown at the same time intervals as in panel b; the arrow indicates the region that was photobleached. The inset shows the area (purple square) from which mean fluorescence intensity was measured. (d) The time course of changes in fluorescence intensity for the colored regions indicated in panels a and c. The red line represents the region within the bleach zone, and the blue line a region adjacent to the bleach zone; the pink line is the average intensity of the whole target bouton, and the green line is the average intensity of a neighboring bouton. The purple line represents the bleached region in the mutant bouton shown in c. (e) Each colored line represents the mean fluorescence intensity from the cross-section indicated by the white rectangle in panel a, at times 0, 1, 10, 30, and 60 s. Scale bar, (a) 2.5 µm.

View larger version (24K): [in this window] [in a new window]   Figure 2. Summary of FRAP analysis. (a) The time course of fluorescence intensity changes. The symbols represent the mean value from each of control and NSF2E/Q boutons at each time point. Error bars, SEM. Lines are best fit to the one-phase exponential equation y = A(1 – e(–k/x)) + B. (b) Summary of recovery index values, where the bars represent the mean value and the error bars the SEM for each of the genotypes and conditions indicated. The right axis, % recovery, applies only to the pair of sol-GFP bars. Sample size: n = number of boutons is indicated on each bar; the number of larvae were control, 9; NSF2E/Q, 6; fixed, 2; control CD8-GFP, 2; NSF2E/Q CD8-GFP, 2; control sol-GFP, 2; and NSF2E/Q sol-GFP, 2.

Fitting the FRAP recovery curve with a one-phase exponential equation (Figure 2) yielded a time constant for recovery of 3.5 ± 0.2 s in the control samples, whereas it was 6.3 ± 0.4 s in the mutant samples. The difference between the genotypes is significant (F test, p < 0.001). This indicates that the vesicles in the control nerve terminal move at a faster rate than those moving within the mutant nerve terminal. Thus, our FRAP analysis of vesicle mobility shows that the NSF2^E/Q transgene substantially impairs both the extent and the rate of vesicle movement within individual presynaptic boutons.

Swinholide Impairs Vesicle Mobility in Control Terminals, Whereas Latrunculin Restores Vesicle Mobility in NSF2^E/Q Terminals
To determine if there is a relationship between vesicle mobility and presynaptic actin, in a separate set of trials we applied the F-actin severing drug swinholide A, the F-actin–depolymerizing drug latrunculin A, and the F-actin–stabilizing drug jasplakinolide (Bubb et al., 1995; Spector et al., 1999) to control and NSF2^E/Q nerve terminals. First, swinholide (Figure 3a) and latrunculin (unpublished data) both lead to redistribution of actin-GFP within a few minutes (see also NonUniform Distribution of Actin below), whereas there was no change in Syt-GFP distribution upon application of the drug, or up to 40 min afterward. When we measured the FRAP recovery index for nontreated control preparations, we found a mean value of 62.6 ± 2.1 (n = 20 from 5 larvae) and for control preparations treated with 5 µM swinholide a value of 49.3 ± 2.5 (n = 41 from 3 larvae), and for control preparations treated with 10 µM latrunculin a value of 54.8 ± 2.2 (n = 43 from 7 larvae) was found. The value for NSF2^E/Q nontreated nerve terminals was 24.8 ± 1.7 (n = 58 from 10 larvae) and for NSF2^E/Q swinholide- and latrunculin-treated terminals the respective values were 30.7 ± 2.9 (n = 23 from 3 larvae) and 46.6 ± 2.4 (n = 36 from 4 larvae). After application of 10 µM jasplakinolide, the FRAP recovery index was 61.6 ± 1.3 (n = 27 from 2 larvae) in the controls and 32.7 ± 1.3 (n = 23 from 2 larvae) in NSF2^E/Q boutons.

View larger version (39K): [in this window] [in a new window]   Figure 3. Effect of swinholide and latrunculin on vesicle mobility. (a) Images of actin-GFP and Syt-GFP before and after application of 5 µM swinholide. The normally punctate distribution of actin is abolished after drug treatment (the scale bar for actin-GFP image is 2 µm), whereas the donut-shaped synaptotagmin signal remains virtually unchanged. This image was taken 40 min after application of swinholide (scale bar for Syt-GFP image is 1.5 µm) (b) Summary of recovery index values in the absence of drug or in the presence of 5 µM swinholide (Swi), 10 µM latrunculin (Lat), or 10 µM jasplakinolide (Jas), where the bars represent the mean value and the error bars the SEM for each of the genotypes and conditions indicated. Sample size (n = number of boutons) is indicated on each bar; the number of larvae were as follows: control no drug, 5; control + Swi, 3; control + Lat, 7; control + Jas, 2; NSF2E/Q, 5; NSF2E/Q + Swi, 3; NSF2E/Q + Lat, 4; and NSF2E/Q + Jas, 2.

Distribution of Actin in the Nerve Terminal
To assess the distribution of actin within the nerve terminal we expressed an UAS-Actin-GFP transgene in neurons of the control and NSF2^E/Q genotypes. We could easily identify GFP fluorescence within the CNS and in the presynaptic nerve terminal. Interestingly, the GFP signal within control synaptic boutons was not uniform, but rather very punctate in appearance (Figure 4a). In contrast, actin-GFP distribution in the NSF2^E/Q boutons was predominantly uniform with many fewer punctate concentrations of GFP found throughout the nerve terminal. These data indicate there is a substantial alteration in actin distribution within the mutant nerve terminals.

View larger version (85K): [in this window] [in a new window]   Figure 4. Altered actin distribution and localization of F-actin in NSF2E/Q boutons. (a) Images are of actin-GFP distribution in control and NSF2E/Q nerve terminals. In controls the GFP signal shows a nonuniform punctate appearance, whereas in the NSF2E/Q nerve terminal it is much more diffuse. (b) Single-slice confocal images of control actin-GFP–expressing nerve terminal labeled with phalloidin reveals that the actin-GFP puncta correspond to filamentous actin. Most of the phalloidin signal in this image is postsynaptic, corresponding to the subsynaptic reticulum of the muscle; however, the presynaptically expressed GFP coincides with phalloidin labeling. (c) Similar image of actin-GFP expressing NSF2E/Q boutons. This image was selected because it shows the exclusion of phalloidin signal from the actin-GFP signal, marked by the double arrowhead, whereas there are some GFP concentrations that do coincide with phalloidin, marked by the single arrowheads. (d) Colocalization of actin-GFP with synaptotagmin. Control nerve terminals expressing actin-GFP were immunostained with an antibody against Drosophila synaptotagmin. The two signals overlap to a great extent, but there are some areas in which the GFP signal is seen in the absence of Syt labeling. Scale bars, 4 µm.

View larger version (89K): [in this window] [in a new window]   Figure 5. Altered actin distribution in an NSF2 loss-of-function allele. (a and b) First instar larval NMJs from Df(3R)urd/+ and Df(3R)urd/NSF255 expressing actin-GFP. Clear concentrations of the actin-GFP signal can be seen in the controls (arrows), but these are absent in the loss-of-function allele. Images were acquired at the same confocal settings. Scale bar, 10 µm. (c and d) A second pair of NMJs shown at higher magnification and double-labeled with the neural marker anti-HRP. Clear actin-GFP puncta are visible (arrows) within the Df(3R)urd/+ NMJs, whereas in the Df(3R)urd/NSF255 boutons the actin-GFP appears diffuse and the puncta are not apparent.

In control preparations we also examined the distribution of actin-GFP relative to synaptic vesicles using an antibody against the synaptic vesicle protein, synaptotagmin. Our results showed that the two signals colocalize to a great extent (Figure 4d). This result is in accord with the knowledge that synaptic vesicles occupy a large volume within Drosophila nerve terminal boutons, and they often occupy an outer ring of the synaptic bouton with an empty center. The actin-GFP concentrations also appear primarily in an outer ring. These data place actin in the correct subcellular location to influence synaptic vesicle movement.

Rapid Movement of Actin within the Nerve Terminal
To expand our examination of actin within presynaptic boutons, we made time-lapse movies of the actin-GFP signals from live larval NMJs. We surprisingly observed that the punctate structures seen in the fixed preparation were not stable but rather constantly moving in living preparations (Figure 6; Supplementary Videos 1 and 2). In contrast, actin-GFP dynamics seemed reduced in the NSF2^E/Q terminals (Supplementary Videos 3 and 4).

View larger version (20K): [in this window] [in a new window]   Figure 6. Presynaptic actin is dynamic. (a) Time-lapse image sequence of actin-GFP expressed in a control nerve terminal. The time elapsed from the beginning of the sequence is indicated in the top left corner. The punctate actin structures indicated by the triangles at time zero have moved laterally by the end of the series, whereas the puncta indicated by the arrow at time 60 increases in brightness and then disappears by time 240. Finally, at time 330 some actin-GFP, at the double triangle, appears to splinter off a larger puncta and move down and out of the bouton. (b) A frequency distribution of the SD of individual pixels over the time series of image

We further we utilized this technique to examine the effects of swinholide, latrunculin, and jasplakinolide. Time-lapse imaging of NMJs treated with jasplakinolide showed that all GFP movement ceased upon application (unpublished data), whereas NMJs treated with the other two drugs show dispersion of the actin-GFP puncta. We quantitated four jasplakinolide-treated images series and five each for latrunculin and swinholide; the results are shown in Figure 6b. As expected, the individual pixel data show that the drug-treated samples have markedly less variation in fluorescence intensity over time, and thus nearly all of the pixels have small SDs. The mean of the SDs (±95% confidence interval) was 3.2 ± 0.02 for the jasplakinolide-treated samples, 2.1 ± 0.03 for the swinholide-treated sample, and 2.0 ± 0.01 for latrunculin-treated sample. ANOVA of the control, mutant, and control plus drug-treated cells revealed significant variation among them (p < 0.0001), and post-tests showed each group to be different from each other (p < 0.001 for each comparison).

To examine the possibility that the observations we made on actin-GFP were inadvertently due to the overexpression of actin within the nerve terminal, we used a moesin-GFP transgene as a reporter of actin at the synapse. This transgene contains only the actin-binding domain of moesin, fused to GFP, and it has been used in prior studies as a reporter of actin in living tissue (Edwards et al., 1997). Just as we saw with the actin-GFP, the moesin-GFP reporter shows a punctate nonuniform distribution within synaptic boutons, and time-lapse imaging of moesin-GFP also shows rapid movement within the boutons (unpublished data). This result substantiates the fact that actin-GFP is being incorporated into the normal actin biochemical pathway and that our observations with actin-GFP are not an artifact due to overexpression of actin.

Fractionation of Actin
To complement the above findings, we measured the relative amounts of filamentous actin in the NSF2^E/Q and control neurons with a biochemical approach. Using larval brain homogenates as our starting material, we utilized high-speed centrifugation to separate filamentous and monomeric actin, followed by SDS-PAGE and Western blotting. We analyzed five independently prepared samples; in three of these we used the yw strain as the control genotype, whereas in the other two we used elavGal4x UAS-NSF2^WT as the control. In each of the five trials there was an equal amount of actin found in the input homogenates in both the control and NSF2^E/Q genotypes but there was less actin in the high-speed pellet prepared from NSF2^E/Q samples than in controls (Figure 7). From three paired trials, there was 27, 29, and 30% of total actin in the yw pellet compared with 8, 11, and 14% in the NSF2^E/Q strain. In the elav-Gal4x UAS-NSF2^WT strain there was 27.5 and 33% of the actin was in the pellet compared with 11 and 5% for the NSF2^E/Q strain (Figure 7b). Therefore, on average we found two thirds less actin in the pellet from the mutant samples. To be certain that the signal observed in the pellet fraction genuinely represents actin filaments, we pretreated the larval brains with 5 µM swinholide A and found that there was no longer actin in the high-speed pellet (Figure 7c). Therefore, this fractionation data indicates that there is less F-actin in the NSF2^E/Q brain and corresponds to our imaging data at the NMJ.

View larger version (33K): [in this window] [in a new window]   Figure 7. Actin Fractionation. (a) Larval brain homogenates were examined for actin before and after high-speed centrifugation by SDS-PAGE and Western blotting. This image is an example Western blot showing the input and the supernatant and pellet fractions. The input homogenates from elav-Gal4 x NSF2WT and elav-Gal4 x NSF2E/Q samples were equivalent but the amount of actin found in the pellet appears less for the NSF2E/Q sample. (b) Quantification of the amount of actin in high-speed pellet, expressed as a percentage of the input actin, for each of five trials. In all trials, the black bars represent the elav-Gal4 x NSF2E/Q result. For trials 1, 2, and 3 the open bars represent data obtained from yw controls, whereas for trials 4 and 5 the hatched bars represent data from elav-Gal4 x UAS-NSF2WT controls. (c) Pretreatment of larval brain homogenates eliminates actin detected in the pellet fraction. Twenty brains were dissected from elav-Gal4 x UAS-NSF2WT larvae, 10 were incubated in HL3 alone, and 10 were incubated in HL3 plus 5 µM swinholide followed by centrifugation, SDS-PAGE, and Western blotting. There was no detectable signal in the pellet samples that were pretreated with swinholide, indicating the signal in untreated samples arises from F-actin. This blot is representative of two independent trials with swinholide pretreatment.

Before examining live preparations we first established our FRAP parameters on actin-GFP synaptic boutons that were fixed in 3.7% formaldehyde. We found we could bleach a small section of the synaptic bouton using our microscope with 15 scans of a small region of interest at 100% laser power. In the fixed preparations fluorescence did not reappear in the bleached area, indicating there is no spontaneous recovery of GFP fluorescence.

We next applied FRAP analysis to live preparations of control and NSF2^E/Q larvae that were untreated or treated with 5 µM swinholide (Figure 8). In the untreated control boutons we observed that the fluorescence intensity returned to 57.9 ± 2.5% (n = 17 from 3 larvae) of its original value. In contrast, untreated NSF2^E/Q boutons showed substantially more recovery, returning to 77.8 ± 1.5% (n = 17 from 3 larvae). This result suggests that there is more G-actin actin within the NSF2^E/Q boutons than in controls. This idea is substantiated by our finding that recovery increases to 77.4 ± 5.0% (n = 19 from 3 larvae) after swinholide treatment of control boutons. In mutant boutons, actin mobility is unchanged after swinholide, with the recovery level being 81.9 ± 1.2% (n = 16 from 3 larvae) after treatment.

View larger version (63K): [in this window] [in a new window]   Figure 8. Frap analysis of actin-GFP. (a) Images of control (elav3A-Gal4 x Actin-GFP) and NSF2E/Q (elav3A-Gal4::UAS-NSF2E/Q x UAS-Actin-GFP) nerve terminals expressing actin-GFP subjected to FRAP. Arrow indicates the region that was photobleached, 0 indicates before photobleaching, 0.5 is immediately after photobleaching, and 10 and 20 are 10 and 20 s after photobleaching. Scale bar, 5 µm. (b) The time course of recovery of actin-GFP signal after photobleaching, where the symbols represent the mean value and the bars the SEM at each time point. The line is the best fit of the one-phase exponential equation y = A(1 – e(–k/x)) + B to the recovery data points. Scale bar, 2 µm. (c) Summary of the % recovery values obtained for control and NSF2E/Q boutons, in the absence or presence of 5 µM swinholide. Sample size (n = number of boutons) is indicated on each bar, from three larvae each.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
In this article we report that a transgene designed to impair NSF activity leads to a substantial reduction in synaptic vesicle mobility. This impairment is associated with altered distribution and polymerization of presynaptic actin. Application of actin-filament–disrupting drugs decreases synaptic vesicle mobility in control boutons but does not further reduce movement in NSF2^E/Q boutons. Three independent lines of evidence indicate that there is a reduction in actin filaments within NSF2^E/Q boutons, and FRAP analysis of actin indicates an increase in the proportion of G-actin. Altogether these data suggest first that F-actin promotes intrabouton vesicle mobility and second that NSF may have a role in establishing or maintaining actin filaments.

Synaptic Vesicles Are Mobile in the Resting Nerve Terminal
Although previous reports have used optical methods to examine synaptic vesicle mobility, our analysis provides new insight into this process. We found a high rate of synaptic vesicle mobility at the unstimulated Drosophila larval NMJ, with time constants of recovery measuring 3–4 s. Our results are most similar to those reported for the ribbon-type synapse of goldfish retinal bipolar cells (Holt et al., 2004), where vesicle recovery times after photobleaching are also less than 1 min, but our results are in contrast to the lack of mobility reported for vesicles at the frog NMJ and hippocampal cultured neurons (Henkel et al., 1996; Kraszewski et al., 1996). The differences may reflect genuine biological differences between types of synapses; the Drosophila NMJ is a high-output synapse, whereas hippocampal synapses are not. Also, the dependence on Synapsins is different. While Synapsin mutants of Drosophila are viable and have normal neurotransmission at the larval NMJ (Godenschwege et al., 2004), in vertebrates Synapsin is known to link vesicles to actin and to be important for normal synaptic release (Rosahl et al., 1995; Hilfiker et al., 2005).

Some of the inconsistencies between our data and the previous reports may also arise from technical differences. The clearest divergence between our approach and the previous reports is in the vesicle label used. We used a genetically encoded marker for synaptic vesicles, whereas the previous studies have relied on uptake of FM1-43. Because loading of such dyes requires substantial synaptic vesicle exo- and endocytosis, it is not possible to examine synapses that have not been recently activated, whereas we examined vesicle mobility in the resting preparation. A further complication associated with FM1-43 is that it may incorporate into nonvesicle cisternae (Richards et al., 2000), which would present an obstacle to measuring synaptic vesicle mobility. One previous report using a genetically encoded VAMP-GFP construct found low vesicle mobility (Estes et al., 2000), but in that case a very long photobleaching time of 25 s was used. In our hands, photobleaching exceeding 1 s led to substantial photodamage (Nunes and Stewart, unpublished results). It therefore seems likely that photodamage was a contributing factor to the low vesicle mobility of this previous report.

Actin in the Presynaptic Nerve Terminal
To date, the role actin plays in the nerve terminal is unclear, particularly with respect to exocytosis (Doussau and Augustine, 2000). Differing reports ascribe inhibitory (Wang et al., 1996; Bernstein et al., 1998; Morales et al., 2000), positive (Kuromi and Kidokoro, 1998; Cole et al., 2000; Sakaba and Neher, 2003), or supportive (Sankaranarayanan et al., 2003) roles in synaptic vesicle mobilization. The data herein support the idea that actin filaments promote intrabouton mobility of synaptic vesicles. Like Sankaranarayanan et al. (2003), we also found no disruption of the synaptic vesicle cluster after application of actin-depolymerizing drugs. However, when we examined movement of vesicles within a bouton, we did find a role for actin. Thus, actin is a cytoskeletal element important for short travel distances within a bouton.

Previous studies have examined the presynaptic distribution of actin at the synapse. At the frog neuromuscular junction (Dunaevsky and Connor, 2000; Richards et al., 2004), and the lamprey reticulospinal synapse (Shupliakov et al., 2002) actin appears excluded from active zones, whereas at synapses of hippocampal cells in culture actin localizes with and surrounds the vesicle cluster (Sankaranarayanan et al., 2003). Our fixed preparations of actin show a high degree of colocalization with synaptic vesicles, most like the hippocampal synapse; this observation is made more important by our finding that actin is very dynamic within presynaptic cytoplasm.

The Nerve Terminal Cytoskeleton Is Dynamic
We were surprised to find the nonuniform distribution of actin-GFP. These concentrations of actin correspond to filamentous actin, and we were further surprised to observe that puncta move dynamically within and between nerve terminal boutons. It seems likely that the images we see represent the rapid polymerization and depolymerization of actin, but the biological function of this activity is not certain. In some respects these observations are similar to those made on mast cell vesicle movement (Merrifield et al., 1999), in that actin comet tails have a role in pushing vesicles away from the plasma membrane toward the interior of the cell. Presently, we do not favor this model for the synaptic vesicle movement we measured here because the actin-stabilizing drug jasplakinolide stops actin-GFP puncta movement but it did not have an effect on our FRAP measurements of vesicle movement.

NSF2^E/Q Disrupts Vesicle Mobility and F-Actin
We have reported that expression of NSF2^E/Q in neurons leads to a reduction in the size of the vesicle pool that could be measured physiologically (Stewart et al., 2002). One potential explanation of this phenotype is disruption of endocytosis or generally reduced vesicle delivery to the nerve terminal. Both of these alternatives predict fewer vesicles in the boutons. Indeed, electron microscopic studies of bona fide endocytosis mutants show a clear and obvious reduction in the vesicle population (Zhang et al., 1998; Verstreken et al., 2002, 2003; Koh et al., 2004). However, when we examined the nerve terminal ultrastructure of the NSF2^E/Q larvae, we found no alteration in the total number of vesicles (Stewart et al., 2005). These data support the notion that there is not a major defect in endocytosis. We therefore proposed that a defect in intrabouton vesicle mobility may be at the heart of the observed phenotype. That possibility was directly tested here, and indeed we found that vesicles in the NSF2^E/Q nerve terminal are about half as mobile as those in controls.

Because our previous genetic data revealed that coexpression of actin or several actin regulators suppresses the NMJ overgrowth phenotype associated with NSF2^E/Q expression (Laviolette et al., 2005), we investigated the state of actin within the NSF2^E/Q nerve terminal. Three of our data sets indicate that there is reduced F-actin at the NSF2^E/Q nerve terminal. First, we showed that the punctate actin-GFP signal in controls corresponds to F-actin, that these puncta are reduced in the NSF2^E/Q boutons, and that phalloidin staining is likewise reduced in the NSF2^E/Q line; second, we used a centrifugation approach to separate F-actin, and we found that there is less F-actin in protein pellets prepared from NSF2^E/Q brain homogenates compared with controls; and third, we showed an increased mobility of actin-GFP in NSF2^E/Q boutons by FRAP analysis. We ruled out potential confounding effects of transgene expression by showing the similarity of actin-GFP distribution in a genuine NSF2 loss-of-function allele compared with that in the NSF2^E/Q allele. The convergence of these independent data sets leads to the conclusion that F-actin is disrupted in the nerve terminal of the NSF alleles, and we suggest that this is a major factor contributing to the NSF2 mutant phenotypes.

We have previously reported on diverse neural phenotypes associated with NSF2^E/Q expression that include physiological and developmental perturbation (Stewart et al., 2002, 2005). The present finding of F-actin disruption helps to reconcile the previous observations. The reduction in vesicle mobility, which we link to the reduced amount of F-actin, is consistent with the reduction in vesicle pool size and synaptic strength that we previously described (see also Cole et al., 2000). Additionally, the hypersprouting phenotype is also consistent with a reduction in F-actin because Drosophila NMJs show hypersprouting when LIM kinase is down-regulated (Ang et al., 2006) and mammalian neurons show greater neurite extension when actin dynamics are perturbed by increasing the activity of ADF/cofilin, an F-actin–depolymerizing factor (Endo et al., 2003). Therefore, despite the apparent divergence of some of our earlier observations, these can now be explained by the unifying observation that disruption of F-actin in the NSF2^E/Q allele underlies both the physiological and developmental phenotypes.

What is the relationship between NSF and actin? Because NSF is likely involved in many SNARE-dependent vesicular trafficking steps, one possibility is that manipulation of NSF simply impairs delivery of a cargo to the plasma membrane that is required for correct actin biochemistry and this then leads to the phenotypes we observe. Two pieces of evidence argue against this possibility. First, among SNARE-related genes the NMJ overgrowth phenotype is specific to NSF2 alleles; mutation in either of the Drosophila SNAREs Syntaxin 1A or n-Synaptobrevin, which also dramatically impair neurotransmitter release, do not cause NMJ overgrowth (Stewart et al., 2000), whereas NSF2⁵⁵ loss-of-function and NSF2^E/Q alleles do (Stewart et al., 2002, 2005). Second, mutations in Drosophila kinesin, which globally reduce vesicle traffic to the nerve terminal, do not cause NMJ overgrowth but rather they have reduced NMJ morphology (Hurd and Saxton, 1996). Therefore, these examples are not consistent with a general reduction in vesicle trafficking leading to NSF-like phenotypes. An alternative possibility is that NSF is involved, solely or with molecular partners, in regulating actin polymerization. There has been no previous finding of a direct biochemical interaction between NSF and actin, so it therefore seems more likely that the chaperone-like activity of NSF may regulate an upstream actin-regulatory or -stabilizing protein. The recent report of physical interaction between betaPix and NSF (Martin et al., 2006) suggests a novel pathway linking NSF to p21-activated kinase (PAK) regulated actin dynamics. Interestingly, actin biochemistry is also disturbed in a temperature-sensitive NSF allele in Dictyostelium (Thompson and Bretscher, 2002), indicating the relationship between actin and NSF is not unique to our particular mutations.

Effects of Swinholide and Latrunculin
We found that both latrunculin and swinholide effectively dispersed the presynaptic actin-GFP puncta and that neither had an effect on the localization of synaptic vesicles. When we measured vesicle mobility we found reduced mobility in the treated boutons. Somewhat surprisingly we found that latrunculin partially restored mobility in the mutant line, whereas swinholide had no effect. We think that this result can be explained by the differing modes of action of these drugs. Although they both affect F-actin, they do so in different ways: Swinholide is an actin-severing agent that cuts actin filaments and stabilizes actin dimers, whereas latrunculin sequesters actin monomers and F-actin depolymerizes under endogenous actin cycling (Bubb et al., 1995; Spector et al., 1999; Fenteany and Zhu, 2003). It therefore seems likely that latrunculin cannot affect stable actin filaments, whereas swinholide should affect both stable and cycling actin. Therefore, the ability of latrunculin to partially restore vesicle mobility in the mutant is likely linked to its G-actin buffering capability. Because our actin-GFP FRAP data indicates that there is more G-actin within the NSF2^E/Q boutons, application of latrunculin would remove the excess G-actin and potentially free some vesicular/actin interaction sites, allowing the vesicles to move upon available, albeit reduced, actin filaments. We currently do not know the nature of the interaction sites, but these could be provided by vesicle-associated myosin, for example.

Altogether our data indicate that NSF may play a central role in vesicular trafficking not only through its energetic disassembly of SNARE complexes, but also by fine-tuning the actin cytoskeleton. Future studies aimed at determining the molecular interactions between NSF and the signaling pathways that regulate actin will greatly inform us about the expanding role of NSF in vesicular trafficking.

	ACKNOWLEDGMENTS

 
We thank L. Pallanck and D. Kiehart for providing fly stocks, N. Reist for anti-synaptotagmin antibodies, and Jingguo Ma and Sara Seabrooke for technical assistance. This work was financially supported by grants from Canadian Institutes for Health Research, Natural Sciences and Engineering Research Council of Canada, and a Premier's Research Excellence Award and the Canada Research Chairs Program to B.A.S.

	Footnotes

 
The online version of this contains supplemental material at MBC Online (http://www.molbiolcell.org).

This article was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E06-03-0253) on August 16, 2006.

Address correspondence to: Bryan Stewart (bstewart{at}utm.utoronto.ca)

	REFERENCES

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Ang, L. H., Chen, W., Yao, Y., Ozawa, R., Tao, E., Yonekura, J., Uemura, T., Keshishian, H., Hing, H. (2006). Lim kinase regulates the development of olfactory and neuromuscular synapses. Dev. Biol 293, 178–190.[CrossRef][Medline]

Bernstein, B. W., DeWit, M., Bamburg, J. R. (1998). Actin disassembles reversibly during electrically induced recycling of synaptic vesicles in cultured neurons. Mol. Brain Res 53, 236–250.[Medline]

Block, M. R., Glick, B. S., Wilcox, C. A., Wieland, F. T., Rothman, J. E. (1988). Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport. Proc. Natl. Acad. Sci. USA 85, 7852–7856.[Abstract/Free Full Text]

Boulianne, G. L. and Trimble, W. S. (1995). Identification of a second homolog of N-ethylmaleimide-sensitive fusion protein that is expressed in the nervous system and secretory tissues of Drosophila. Proc. Natl. Acad. Sci. USA 92, 7095–7099.[Abstract/Free Full Text]

Bubb, M. R., Spector, I., Bershadsky, A. D., Korn, E. D. (1995). Swinholide—A microfilament disrupting marine toxin that stabilizes actin dimers and severs actin-filaments. J. Biol. Chem 270, 3463–3466.[Abstract/Free Full Text]

Cole, J. C., Villa, B. R., Wilkinson, R. S. (2000). Disruption of actin impedes transmitter release in snake motor terminals. J. Physiol 525, Pt 3579–586.[Abstract/Free Full Text]

Cong, M., Perry, S. J., Hu, L. A., Hanson, P. I., Claing, A., Lefkowitz, R. J. (2001). Binding of the beta2 adrenergic receptor to N-ethylmaleimide-sensitive factor regulates receptor recycling. J. Biol. Chem 276, 45145–45152.[Abstract/Free Full Text]

Doussau, F. and Augustine, G. J. (2000). The actin cytoskeleton and neurotransmitter release: an overview. Biochimie 82, 353–363.[Medline]

Dunaevsky, A. and Connor, E. A. (2000). F-actin is concentrated in nonrelease domains at frog neuromuscular junctions. J. Neurosci 20, 6007–6012.[Abstract/Free Full Text]

Edwards, K. A., Demsky, M., Montague, R. A., Weymouth, N., Kiehart, D. P. (1997). GFP-moesin illuminates actin cytoskeleton dynamics in living tissue and demonstrates cell shape changes during morphogenesis in Drosophila. Dev. Biol 191, 103–117.[CrossRef][Medline]

Endo, M., Ohashi, K., Sasaki, Y., Goshima, Y., Niwa, R., Uemura, T., Mizuno, K. (2003). Control of growth cone motility and morphology by LIM kinase and Slingshot via phosphorylation and dephosphorylation of cofilin. J. Neurosci 23, 2527–2537.[Abstract/Free Full Text]

Estes, P. S., Ho, G. L., Narayanan, R., Ramaswami, M. (2000). Synaptic localization and restricted diffusion of a Drosophila neuronal synaptobrevin–green fluorescent protein chimera in vivo. J. Neurogenet 13, 233–255.[Medline]

Fenteany, G. and Zhu, S. T. (2003). Small-molecule inhibitors of actin dynamics and cell motility. Curr. Topics Med. Chem 3, 593–616.

Fleet, D. J. and Weiss, Y. (2005). Optical flow estimation. In: Mathematical Models for Computer Vision: The Handbook, ed. O. Faugeras. New York: Springer, 239–258.

Godenschwege, T. A. (2004). Flies lacking all synapsins are unexpectedly healthy but are impaired in complex behaviour. Eur. J. Neurosci 20, 611–622.[CrossRef][Medline]

Golby, J. A., Tolar, L. A., Pallanck, L. (2001). Partitioning of N-ethylmaleimide-sensitive fusion (NSF) protein function in Drosophila melanogaster: dNSF1 is required in the nervous system, and dNSF2 is required in mesoderm. Genetics 158, 265–278.[Abstract/Free Full Text]

Han, S. Y., Park, D. Y., Park, S. D., Hong, S. H. (2000). Identification of Rab6 as an N-ethylmaleimide-sensitive fusion protein-binding protein. Biochem. J 352, Pt 1165–173.

Henkel, A. W., Simpson, L. L., Ridge, R. M., Betz, W. J. (1996). Synaptic vesicle movements monitored by fluorescence recovery after photobleaching in nerve terminals stained with FM1-43. J. Neurosci 16, 3960–3967.[Abstract/Free Full Text]

Hilfiker, S., Benfenati, F., Doussau, F., Nairn, A. C., Czernik, A. J., Augustine, G. J., Greengard, P. (2005). Structural domains involved in the regulation of transmitter release by synapsins. J. Neurosci 25, 2658–2669.[Abstract/Free Full Text]

Holt, M., Cooke, A., Neef, A., Lagnado, L. (2004). High mobility of vesicles supports continuous exocytosis at a ribbon synapse. Curr. Biol 14, 173–183.[CrossRef][Medline]

Hurd, D. D. and Saxton, W. M. (1996). Kinesin mutations cause motor neuron disease phenotypes by disrupting fast axonal transport in Drosophila. Genetics 144, 1075–1085.[Abstract]

Kawasaki, F., Mattiuz, A. M., Ordway, R. W. (1998). Synaptic physiology and ultrastructure in comatose mutants define an in vivo role for NSF in neurotransmitter release. J. Neurosci 18, 10241–10249.[Abstract/Free Full Text]

Koh, T. W., Verstreken, P., Bellen, H. J. (2004). Dap160/intersectin acts as a stabilizing scaffold required for synaptic development and vesicle endocytosis. Neuron 43, 193–205.[CrossRef][Medline]

Kraszewski, K., Daniell, L., Mundigl, O., DeCamilli, P. (1996). Mobility of synaptic vesicles in nerve endings monitored by recovery from photobleaching of synaptic vesicle–associated fluorescence. J. Neurosci 16, 5905–5913.[Abstract/Free Full Text]

Kuromi, H. and Kidokoro, Y. (1998). Two distinct pools of synaptic vesicles in single presynaptic boutons in a temperature-sensitive Drosophila mutant, shibire. Neuron 20, 917–925.[CrossRef][Medline]

Laviolette, M. J., Nunes, P., Peyre, J. B., Aigaki, T., Stewart, B. A. (2005). A genetic screen for suppressors of Drosophila NSF2 neuromuscular junction overgrowth. Genetics 170, 779–792.[Abstract/Free Full Text]

Martin, H. G., Henley, J. M., Meyer, G. (2006). Novel putative targets of N-ethylmaleimide sensitive fusion protein (NSF) and alpha/beta soluble NSF attachment proteins (SNAPs) include the Pak-binding nucleotide exchange factor betaPIX. J. Cell. Biochem 10.100/jcb.20998.

McDonald, P. H., Cote, N. L., Lin, F. T., Premont, R. T., Pitcher, J. A., Lefkowitz, R. J. (1999). Identification of NSF as a beta-arrestin1-binding protein. Implications for beta2-adrenergic receptor regulation. J. Biol. Chem 274, 10677–10680.[Abstract/Free Full Text]

Merrifield, C. J., Moss, S. E., Ballestrem, C., Imhof, B. A., Giese, G., Wunderlich, I., Almers, W. (1999). Endocytic vesicles move at the tips of actin tails in cultured mast cells. Nat. Cell Biol 1, 72–74.[CrossRef][Medline]

Morales, M., Colicos, M. A., Goda, Y. (2000). Actin-dependent regulation of neurotransmitter release at central synapses. Neuron 27, 539–550.[CrossRef][Medline]

Muller, J. M., Shorter, J., Newman, R., Deinhardt, K., Sagiv, Y., Elazar, Z., Warren, G., Shima, D. T. (2002). Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion. J. Cell Biol 157, 1161–1173.[Abstract/Free Full Text]

Nishimune, A., Isaac, J. T., Molnar, E., Noel, J., Nash, S. R., Tagaya, M., Collingridge, G. L., Nakanishi, S., Henley, J. M. (1998). NSF binding to GluR2 regulates synaptic transmission. Neuron 21, 87–97.[CrossRef][Medline]

Pallanck, L., Ordway, R. W., Ramaswami, M., Chi, W. Y., Krishnan, K. S., Ganetzky, B. (1995). Distinct roles for N-ethylmaleimide-sensitive fusion protein (NSF) suggested by the identification of a second Drosophila NSF homolog. J. Biol. Chem 270, 18742–18744.[Abstract/Free Full Text]

Richards, D. A., Guatimosim, C., Betz, W. J. (2000). Two endocytic recycling routes selectively fill two vesicle pools in frog motor nerve terminals. Neuron 27, 551–559.[CrossRef][Medline]

Richards, D. A., Rizzoli, S. O., Betz, W. J. (2004). Effects of wortmannin and latrunculin A on slow endocytosis at the frog neuromuscular junction. J. Physiol 557, 77–91.[Abstract/Free Full Text]

Rosahl, T. W., Spillane, D., Missler, M., Herz, J., Selig, D. K., Wolff, J. R., Hammer, R. E., Malenka, R. C., Sudhof, T. C. (1995). Essential functions of synapsins I and II in synaptic vesicle regulation. Nature 375, 488–493.[CrossRef][Medline]

Sakaba, T. and Neher, E. (2003). Involvement of actin polymerization in vesicle recruitment at the calyx of Held synapse. J. Neurosci 23, 837–846.[Abstract/Free Full Text]

Sankaranarayanan, S., Atluri, P. P., Ryan, T. A. (2003). Actin has a molecular scaffolding, not propulsive, role in presynaptic function. Nat. Neurosci 6, 127–135.[CrossRef][Medline]

Shupliakov, O., Bloom, O., Gustafsson, J. S., Kjaerulff, O., Low, P., Tomilin, N., Pieribone, V. A., Greengard, P., Brodin, L. (2002). Impaired recycling of synaptic vesicles after acute perturbation of the presynaptic actin cytoskeleton. Proc. Natl. Acad. Sci. USA 99, 14476–14481.[Abstract/Free Full Text]

Sollner, T., Bennett, M. K., Whiteheart, S. W., Scheller, R. H., Rothman, J. E. (1993a). A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion. Cell 75, 409–418.[CrossRef][Medline]

Sollner, T., Whiteheart, S. W., Brunner, M., Erdjument-Bromage, H., Geromanos, S., Tempst, P., Rothman, J. E.