|Home | About | Journals | Submit | Contact Us | Français|
Author contributions: H.W. and P.B. designed research; H.W., J.M.H., and W.-C.W. performed research; H.W., J.M.H., W.-C.W., and P.B. analyzed data; H.W. and P.B. wrote the paper.
Rapsyn-deficient myasthenic syndrome is characterized by a weakness in voluntary muscle contraction, a direct consequence of greatly reduced synaptic responses that result from poorly clustered acetylcholine receptors. As with other myasthenic syndromes, the general muscle weakness is also accompanied by use-dependent fatigue. Here, we used paired motor neuron target muscle patch-clamp recordings from a rapsyn-deficient mutant line of zebrafish to explore for the first time the mechanisms causal to fatigue. We find that synaptic responses in mutant fish can follow faithfully low-frequency stimuli despite the reduced amplitude. This is in part helped by a compensatory increase in the number of presynaptic release sites in the mutant fish. In response to high-frequency stimulation, both wild-type and mutant neuromuscular junctions depress to steady-state response levels, but the latter shows exaggerated depression. Analysis of the steady-state transmission revealed that vesicle reloading and release at individual release sites is significantly slower in mutant fish during high-frequency activities. Therefore, reductions in postsynaptic receptor density and compromised presynaptic release collectively serve to reduce synaptic strength to levels that fall below the threshold for muscle action potential generation, thus accounting for use-dependent fatigue. Our findings raise the possibility that defects in motor neuron function may also be at play in other myasthenic syndromes that have been mapped to mutations in muscle-specific proteins.
SIGNIFICANCE STATEMENT Use-dependent fatigue accompanies many neuromuscular myasthenic syndromes, including muscle rapsyn deficiency. Here, using a rapsyn-deficient line of zebrafish, we performed paired motor neuron target muscle patch-clamp recordings to investigate the mechanisms causal to this phenomenon. Our findings indicate that the reduced postsynaptic receptor density resulting from defective rapsyn contributes to weakness, but is not solely responsible for use-dependent fatigue. Instead, we find unexpected involvement of altered transmitter release from the motor neuron. Specifically, slowed reloading of vesicle release sites leads to augmented synaptic depression during repeated action potentials. Even at moderate stimulus frequencies, the depression levels for evoked synaptic responses fall below the threshold for the generation of muscle action potentials. The associated contraction failures are manifest as use-dependent fatigue.
Human congenital myasthenic syndromes often result from mutations in proteins that are key to synapse development and function. Examples include deficiencies in MuSK (Chevessier et al., 2004; Mihaylova et al., 2009; Maselli et al., 2010), Doc7 (Beeson et al., 2006; Müller et al., 2007; Selcen et al., 2008), agrin (Huzé et al., 2009), acetylcholine receptors (AChR) (Ohno et al., 1997; Engel et al., 2010), and acetylcholinesterase (AChE) (Ohno et al., 1998; Ishigaki et al., 2003). Zebrafish motility mutants have contributed richly to our understanding of many human neuromuscular diseases. For example, mutant lines for AChE (Behra et al., 2002; Downes and Granato, 2004), AChR (Sepich et al., 1998; Ono et al., 2001b), and choline acetyltransferase (Wang et al., 2008) have provided physiological models for myasthenic syndromes. Mutant lines for the P/Q calcium channel (Wen et al., 2013b) and α-subunit of the AChR (Walogorsky et al., 2012a; Walogorsky et al., 2012b) also provided new insights into human Lambert–Eaton syndrome and slow channel syndrome, respectively. These lines also served as experimental platforms for testing therapeutic agents that are either currently in use or in clinical trial. Much of this success is due to the ability to perform in vivo paired motor neuron target muscle patch-clamp recordings in the vertebrate zebrafish (Wen and Brehm, 2005, 2010). Together with quantitative measurements of swimming performance in zebrafish, it has been possible to link compromised motility to the mechanistic underpinnings.
A phenotypic consequence often shared among the different congenital forms of myasthenic syndromes is fatigue of voluntary movements after exercise (Yasaki et al., 2004). In the case of muscle rapsyn deficiency, the absence of high-density postsynaptic AChRs (Ohno et al., 2002) and the greatly reduced end-plate potentials (EPPs) (Engel, 2007) account for overall muscle weakness. However, this general reduction in amplitude cannot account for the additional fatigue that sets in at moderate- to high-frequency activity. In the present study, we explore for the first time the basis of use-dependent fatigue in an animal model for myasthenic syndrome.
Understanding the mechanisms causal to use-dependent fatigue is challenging because, intuitively, it would seem to point to presynaptic defects such as frequency-dependent synaptic depression. However, whereas mutations in muscle proteins are common among myasthenic syndromes, thus far, none has been reported to affect the function of the motor neuron. Paradoxically, the most common treatment of myasthenic syndromes involves agents that facilitate transmitter release (Engel, 2007), prompting us to revisit a presynaptic contribution to these syndromes. We set out to test directly for presynaptic defects in mediation of use-dependent fatigue using a rapsyn-deficient line of fish, twitch once (two). As with human myasthenic syndrome, these mutant fish exhibit pronounced fatigue (Ono et al., 2001a; Ono et al., 2002). Our studies further exploited the advantages offered by paired motor neuron target skeletal muscle recordings (Wen and Brehm, 2005, 2010), which revealed a compromised speed of reloading and release for active release sites at two motor neurons, resulting in exaggerated synaptic depression and behavioral fatigue. These findings provide the first insights into the mechanisms causal to use-dependent fatigue, a phenotype shared by multiple congenital myasthenic syndromes.
Electrophysiological experiments used either wild-type or homozygous two mutant (allele twoth26e; Granato et al., 1996) zebrafish (Danio rerio) of either sex at 72–96 h after fertilization. Paired in vivo electrophysiological recordings between the caudal primary (CaP) motor neuron and target fast skeletal muscle were performed as described previously (Wen and Brehm, 2005, 2010). The CaP soma was held at −80 mV under current clamp and action potentials were elicited with a 2 ms current injection. The muscle cells were briefly pretreated with 2 m formamide and held at −50 mV to help prevent contractions. Muscle miniature end-plate currents (mEPCs) and evoked end-plate currents (EPCs) were sampled at 100 kHz and filtered at 10 kHz. Data were acquired with EPC10/2 dual patch-clamp amplifier (List Electronics) under control by HEKA Patchmaster software. Data were analyzed using Igor Pro (WaveMetrics) and Mini-Analysis (SynaptoSoft) and are presented as mean ± SD unless otherwise indicated. Statistical comparisons were made with two-tailed t tests in Prism software (GraphPad).
The patch electrodes used for muscle voltage-clamp recordings were low resistance (2–3 MΩ) to minimize the errors associated with series resistance (Rs). Rs was estimated from the current response to a 10 mV step and monitored throughout the experiment. Experiments were terminated when Rs exceeded 10 MΩ. All synaptic currents were routinely 60% Rs compensated online, with the remaining 40% Rs correction performed offline (Traynelis, 1998; Wen et al., 2016). All of the sample traces shown in the figures were 60% compensated, but all of the tabulated data underwent the additional 40% offline compensation. Current-clamp recordings from dissociated muscles were performed to determine the resting potential and threshold for the action potential. Muscle cells were dissociated by first removing the larval skin and then incubating the larva in 60% L-15 + 25 mm Na-HEPES (M-L15; Life Technologies) with 20 mg/ml collagenase (Life Technologies) for ~90 min at 28°C. The larvae were washed in collagenase-free solution and triturated to dissociate individual muscle cells. Recordings were performed within 2 h of dissociation. Resting potentials were estimated using the initial break in under current clamp and not corrected for liquid junction potential.
We adopted a multinomial model of release developed by Silver to estimate the number of functional release sites and their release probability. This model describes the relationship between the mean and variance of EPCs, assuming uniform release probability across synapses (Silver et al., 1998; Silver, 2003; Wen et al., 2016).
The mean EPC amplitude (G) and associated coefficient of variation (CV) were determined at a stimulus frequency of 0.2 Hz for each individual cells. The mean unitary event amplitude (q) and the associated coefficient of variation (CVq) were determined on the basis of asynchronous unitary events during a 100 Hz, 20 s stimulation protocol. CVq determined in this way represented the total variability in quantal size. Because the intrasite quantal variability was shown to be very low at this synapse (Wen et al., 2016), CVq provided the approximation for intersite quantal variability (Silver et al., 1998; Silver, 2003). The number of functional release sites (N) was then estimated for each recording using Equation 1 (Silver et al., 1998; Silver, 2003):
The release probability for each release site (Pr) was next computed according to the binomial model using Equation 2:
Recent studies have revealed the contribution of reluctant vesicles to the total releasable pool (Trommershauser et al., 2003; Moulder and Mennerick, 2005). Such kinetic complexity would be expected to affect estimates of N and Pr if distinct vesicle pools are associated with individual release sites. We chose to use the multinomial model because it does not require the additional sorting and trafficking of vesicle populations with different release probability to distinct release sites.
SynaptopHluorin experiments used two and the paralytic line relaxed (red ts25a; Granato et al., 1996) that were engineered to express synaptopHluorin in the CaP motor neuron (Wen et al., 2013a). Relaxed was used in the place of wild-type control to avoid small movement artifacts during image acquisition. Live confocal images of fluorescence changes during stimulation were acquired using a Yokogawa CSU-10 spinning disc (Solamere Technologies) with a Stanford Photonics Turbo 620 intensified CCD camera. Sequential images were acquired continuously at 67 ms intervals using Piper software control version 2.5.04 (Stanford Photonics). Ten image planes were acquired for each time point by quickly displacing the objective (W N-Achroplan 63×/0.9; Zeiss) in 1 μm increments using a piezo device mounted under the objective (Mipos 100; Piezo Systems), which allowed for sampling of many presynaptic terminals (10–20) during the experiment. The 10 images were projected to produce a single image for each time point. Images were analyzed using ImageJ, Microsoft Excel, and custom scripts written in Igor Pro 6.3. To determine the change in fluorescence for individual terminals, regions of interest (ROIs) were placed over responsive presynaptic nerve terminals, as revealed by 100 Hz stimulation and 50 mm NH4Cl application. An additional five ROIs were placed in adjacent areas that did not contain fluorescence signal to measure local background fluorescence. To correct for background, fluorescence from the five background ROIs were averaged and subtracted from each presynaptic terminal fluorescence. Fluorescence change (ΔF) was normalized to the baseline fluorescence before the stimulation (F0) to obtain ΔF/F0.
Fluorescence imaging used an LD C-Apochromat 40× objective on a Zeiss 710 confocal microscope. AChRs were labeled with Alexa Fluor 555-conjugated α-bungarotoxin (α-btx; Life Technologies) and AChE was labeled with fasciculin II (fasII; Alomone Laboratories) that was custom conjugated to Alexa Fluor 647 (Life Technologies). Both labels were microinjected into the bloodstream of live fish 20 min before imaging. Presynaptic terminals were identified by vesicle loading with FM1-43 (Life Technologies) as described previously (Li et al., 2003).
Muscle contraction was quantitated on the basis of length change in response to repetitive stimulation of the CaP motor neuron. The images of fast muscle cells were captured sequentially at 1000 frames/s using a Photonics Fastcam (Photron). The time-dependent changes in muscle length were quantitated frame by frame using Photron high-speed motion analysis tools. Reference points at both ends of a single muscle were chosen to track length change.
The zebrafish motility mutant two was unable to mount efficient, long-range swimming when stimulated. Instead of the strong initial bend and subsequent rhythmic swimming, two was able to generate only one to a few weak tail flips, reflecting use-dependent fatigue. The skeletal muscle of two was generally healthy in appearance, but labeling with α-btx revealed largely diffuse AChRs with only a few small clusters compared with wild-type muscle (Fig. 1A). The compromised clustering of AChRs in two stemmed from a mutation in rapsyn that led to its retention in the endoplasmic reticulum (Ono et al., 2002; Park et al., 2012). Despite the absence of receptor clusters in two, normal-appearing AChE clusters were identified on the basis of fasII label (Fig. 1A). These AChE clusters marked the site of functional synapses in both wild-type and two based on colocalization of FM1-43-labeled presynaptic vesicles (Fig. 1B). The finding that developmental acquisition of presynaptic function occurred in the absence of postsynaptic receptor clusters is consistent with a previously published study showing that transmitter release occurred in mutant fish lacking AChRs altogether (Li et al., 2003). In that study, however, it was not determined whether quantitative differences existed, which might signal a dependence of exocytosis on postsynaptic receptors.
We set out to explore neuromuscular transmission for defects that account for use-dependent fatigue. As a first step, we investigated whether receptor density or number might affect presynaptic function through use of synaptopHluorin, a sensitive indicator of exocytosis. SynaptopHluorin is formed by a fusion between the pH-dependent GFP and a vesicle-associated membrane protein (VAMP) (Miesenböck et al., 1998). While inside the vesicle, the fluorescence is quenched by the acidic environment, but upon fusion to the plasma membrane, synaptopHluorin takes on the characteristic GFP fluorescence. Therefore, increases in fluorescence (ΔF) that accompany stimulation of the motor neuron provide a direct readout of vesicle fusion and associated transmitter release. We created transgenic lines that expressed synaptopHluorin in the terminals of the CaP motor neuron of relaxed and two fish. The relaxed paralytic mutant line was used as the control to eliminate movement artifact associated with muscle contraction during image acquisition. Paralysis results from a mutation in the skeletal muscle dihydropyridine receptor in relaxed, which mediates the excitation-contraction coupling (Ono et al., 2001b; Schredelseker et al., 2005). Therefore, the mutation is far downstream of AChR activation. To insure that the mutation did not affect synaptic transmission, we quantitated the key functional fingerprints for comparison with wild-type fish. No significant differences in mEPC amplitude, EPC amplitude, or quantal content were found using low-frequency stimulation (Table 1; also see Koyama et al., 2011). In addition, the levels of steady-state depression in response to high-frequency stimulation showed no significant difference between relaxed and wild-type fish, validating its use as the control (Table 1).
Real-time changes in synaptopHluorin fluorescence were measured with a spinning disk confocal microscope. The dim baseline fluorescence allowed selection of optimal image planes containing multiple synaptic terminals (Fig. 2A). To initiate exocytosis, the CaP motor neuron was stimulated at 100 Hz for 10 s to elicit increased fluorescence in the terminals (Fig. 2A). After termination of the stimulus, 50 mm NH4Cl was added to neutralize the lumen of all remaining vesicles rapidly (Fig. 2A–C). For both conditions, the change in fluorescence was quantitated as ΔF/F0. This allowed estimation of the fraction of vesicles participating in exocytosis during the 100 Hz, 10 s train, a protocol that leads to nearly complete functional depletion (Wen et al., 2010, 2013a). For each synaptic terminal, the fraction of vesicles released by the stimulus was quantitated as the ratio of fluorescence change associated with stimulus to that associated with NH4Cl treatment (Fig. 2D). Stimulus-driven increases in fluorescence were seen for both relaxed and two terminals, but the peak fluorescence levels were significantly smaller for two (Fig. 2A–C). The reduced level of stimulus-induced release in two was not due to a smaller total vesicle population, as revealed by the maximal fluorescence after the NH4Cl treatment (Fig. 2A–C). Rather, two releases only 14 ± 10% of the vesicles compared with 46 ± 18% for relaxed fish during the 100 Hz stimulation (Fig. 2D).
The finding of presynaptic involvement in rapsyn-deficient two fish prompted our further investigation into the causal mechanisms. For this purpose, we turned to paired patch-clamp recordings between the CaP motor neuron and target fast muscle (Wen and Brehm, 2005, 2010). The first measurements compared the unitary mEPCs in wild-type and two fish. Neither the frequency of occurrence (Table 2) nor the decay kinetics of spontaneous mEPCs differed between wild-type and two. However, the amplitudes were greatly reduced in two, reflecting the lowered AChR density (Fig. 3A, Table 2; Ono et al., 2002). Asynchronous unitary events provided an alternative means of estimating mEPC amplitude. Stimulation of the CaP motor neuron at 100 Hz for 20 s led to functional depletion and transition to asynchronous release that corresponded principally to unitary events (Fig. 3B; Wen et al., 2010, 2013a). The high frequency of occurrence permitted large numbers of unitary events to be collected for individual recordings. Both methods produced normally distributed amplitudes in wild-type, but the distribution for two was often right skewed, reflecting the inability to resolve the very small events (Fig. 3C; Wen et al., 2016). Therefore, we only included those two recordings in which a clear peak in the frequency versus amplitude distributions could be resolved. These relations were fit by Gaussian curves with a mean based on the peak value with the right side of the distribution fully resolved. The peak value was then used as the estimate for mean quantal size for two fish. Measurements based on spontaneous events and asynchronous unitary events yielded similar estimates of mean mEPC amplitude, with significantly lower values in all cases for two (Fig. 3D, Table 2).
Having determined the unitary synaptic responses, we turned to measurements of stimulus-evoked EPC amplitudes. Low-frequency 0.2 Hz stimulation was used to avoid the complications associated with synaptic depression (Fig. 4A; Wen et al., 2016). As with the unitary event amplitudes, the EPCs in two were significantly smaller than those in wild-type (Fig. 4A,B, Table 2). Importantly, the ~15-fold difference in mean mEPC amplitude between wild-type and two was greater than the ~6-fold difference in EPC amplitude. As an estimate of quantal content for both two and wild-type, the mean EPC amplitude was divided by the mean mEPC amplitude for each individual recording (Fig. 4C; Wen et al., 2016). The quantal content for wild-type ranged from ~7 to 18, with an overall average of 12.0 ± 2.6 compared with a much wider range of ~7 to 74 and larger average of 25.9 ± 16.9 for two (Fig. 4C, Table 2).
This ~2-fold higher quantal content for two could result from either a higher release probability for a similar number of release sites or a larger number of release sites. To distinguish between these possibilities, we used EPC fluctuation analysis to estimate the number of functional release sites (N) and the Pr for each release site (Silver et al., 1998; Silver, 2003; Wen et al., 2016). For this purpose, the mean and variance associated with both mEPC and EPC amplitude were measured for individual cells, as described above, and a multinomial model of release was applied (see Materials and Methods). Estimates of N for wild-type ranged from 8 to 21 with an average of 13.6 ± 3.2, whereas those from two ranged from 16 to 102 with an average of 42.3 ± 27.6 (Fig. 4D, Table 2). Estimates of Pr ranged from ~0.7 to 1 with a mean value of 0.9 ± 0.1 for wild-type. Estimates for two Pr were lower, ranging from ~0.3 to 0.9 with a mean value of 0.7 ± 0.2 (Fig. 4E, Table 2). Therefore, the higher quantal content for two fish resulted from a larger number of release sites, counterbalancing a mild reduction in release probability.
A higher quantal content for two fish was at odds with impaired exocytosis determined using synaptopHluorin as the optical indicator (Fig. 2). Paired recordings made during bouts of repetitive stimulation that corresponded to rhythmic swimming provided a resolution to this apparent paradox. At stimulus frequencies between 20 and 100 Hz, the EPCs showed a stereotypic depression within the first several responses in both wild-type and two fish (Fig. 5A; Wen et al., 2016). There was no difference in the time course of depression onset at any of the frequencies tested (Fig. 5A). However, the levels of depression achieved after the first few stimuli were significantly greater in two recordings. Comparisons using paired-pulse ratios between the second and the first EPC amplitudes revealed a greater depression for two at 20, 50, and 100 Hz (Table 2). For each recording, the level of steady-state depression was determined on the basis of the mean steady-state amplitude computed for the last 25 EPCs of a train of 30 stimuli divided by the amplitude of the first EPC of the stimulus train. At 20, 50, and 100 Hz, the ratios for all recordings were all significantly lower in two, indicating greater synaptic depression (Fig. 5B, Table 2). Therefore, the increased quantal content that was determined at low-frequency stimulation cannot compensate sufficiently for the depression occurring during repetitive stimulation. The exaggerated steady-state depression is consistent with the observed decrease in optically determined exocytosis in two fish (Fig. 2).
Next, we sought to identify the mechanism(s) causal to greater synaptic depression and compromised exocytosis in two. Vesicle availability at the release sites is central to continued release in the face of repetitive stimulation. Both the size of readily releasable vesicle pool (RRP) and the rate at which individual release sites are replenished with new releasable vesicles after prior release could potentially affect the levels of depression (Del Castillo and Katz, 1954; Elmqvist and Quastel, 1965; von Gersdorff and Matthews, 1997; Zucker and Regehr, 2002). We adopted an approach developed for the neuromuscular junction (NMJ) and subsequently applied to central neurons to estimate both parameters (Elmqvist and Quastel, 1965; Schneggenburger et al., 1999; Thanawala and Regehr, 2013; Wen et al., 2016). This method is based on the assumption that the steady-state release is sustained by the balance between vesicle release and replenishment at the release sites. When the cumulative release is plotted versus time, the slope provides a direct measurement of the rate at which release sites are replenished with new vesicles (referred to as reloading rate from here on) and the y-intercept approximates the RRP size (Elmqvist and Quastel, 1965; Schneggenburger et al., 1999; Thanawala and Regehr, 2013; Neher, 2015; Wen et al., 2016).
The CaP was stimulated at 100 Hz for 300 ms, the peak EPC amplitudes were converted to quantal content, and then the accumulated quantal content was plotted against time during the stimulus train for both wild-type and two fish. Data points corresponding to steady-state responses were fitted using linear regression and back extrapolated to time 0 (Fig. 6A). The y-intercept provided an estimate of the size of the RRP available at the onset of stimulation, which corresponded to 19.4–42.5 vesicles in wild-type versus 19.0–140.4 vesicles for two. This would seemingly point to a larger RRP at two synapses, but the estimated number of release sites was also higher, on average, for two. Moreover, estimates of the RRP and release site number bore a direct relationship for individual recordings (Fig. 6B). Upon correction for differences in release site number, the RRP in two averaged 1.5 ± 0.5 vesicles per site at 100 Hz, which was only slightly smaller than the 2.2 ± 0.3 for wild-type (Fig. 6C, Table 2). The RRP sizes estimated from 20, 50, and 100 Hz were similar, suggesting that there was minimal new recruitment of vesicles during the first few EPCs (Fig. 6C). Therefore, the estimates likely represented the entire pool of readily releasable vesicles before stimulation. For both wild-type and two, the pool of one or two readily releasable vesicles would deplete within the first few responses and could not account for the differences in steady-state levels of depression.
The second candidate for conferring differences in steady-state depression level between wild-type and two resided in the reloading rates. The slope of the fitted cumulative release versus time relationship provided an estimate of the number of vesicles reloaded in the whole cell per unit time (Fig. 6A). The slope values were highly variable in two, but, again, correlated well with the estimated number of release sites for individual cells (Fig. 6D). After correction for differences in release site numbers, the mean reloading rates at each release site for two were significantly slower than wild-type at all frequencies tested (Fig. 6E, Table 2). Two fish reload each site at a rate of 0.012 vesicle/ms at 100 Hz, less than half of the wild-type rate (0.027 vesicles/ms). It took, on average, 83 ms to equip a release site with a new releasable vesicle in the mutant fish, compared with 37 ms for wild-type. Therefore, the slower reloading rate for the release sites forms the basis for greater steady-state depression in two fish. The reloading rates for both wild-type and two increased with stimulus frequency (Fig. 6E, Table 2), reflecting calcium-dependent vesicle recruitment, which was greater at shorter interval action potentials (Dittman and Regehr, 1998; Stevens and Wesseling, 1998; Wang and Kaczmarek, 1998; Sakaba and Neher, 2001; Wen et al., 2016). This feature of reloading accounted well for the shallow frequency dependence of depression over the range of 20–100 Hz (Fig. 5).
Direct measurements of EPC amplitude recovery time course from steady-state levels of depression provided an independent test for slowed reloading in two fish (Fig. 7). For this purpose, a conventional protocol was used wherein the steady-state level of release was established using a 300 ms, 100 Hz train, followed by a single test stimulus delivered at variable intervals after termination of the train (Varela et al., 1997; von Gersdorff et al., 1997; Silver et al., 1998; Wang and Kaczmarek, 1998; Hallermann et al., 2010; McElvain et al., 2015; Fig. 7A). The extent of recovery was measured as the ratio of the test EPC to the first response of the train. The recovery of EPC amplitude followed a biexponential time course in both two (Fig. 7B) and wild-type (Fig. 7B; Wen et al., 2016). The slow time constants for two (2.81 s) and wild-type (2.65 s) were similar, but the fast component was significantly slower for two (143.5 ms) compared with wild-type (43.1 ms). Another difference is reflected in the projected fractional recovery curves. The wild-type asymptotically approaches unity whereas the two projects to 0.9, suggesting the presence of an even slower component of recovery in two. The 3.3-fold slower recovery for two, specifically in the high-frequency domain, supports the idea that slowed reloading is the principal factor governing enhanced synaptic depression in two fish at high-activity levels such as those involved in swimming behavior.
As a test of the idea that the greater synaptic depression seen in two could contribute to muscle fatigue through action potential failure, we calculated the predicted depolarization associated with consecutive responses for both wild-type and two fish (Fig. 8A,B). For this purpose, we used the amplitudes for each EPCs recorded at 20 Hz to predict the corresponding EPP amplitudes. Should the EPP fail to reach threshold for a muscle action potential (−29.4 ± 3.0 mV, n = 8 cells), then the muscle would likely fail to contract. The conversion from current to voltage took into account the passive membrane properties through recordings of miniature EPP (mEPP) amplitudes. The mEPPs in wild-type averaged 13.2 ± 2.0 mV at the resting potential of −65 mV (n = 6 cells). The mEPPs could not be fully resolved in two due to their much smaller amplitudes. However, the absence of any differences in passive muscle membrane properties between wild-type and two (resistance, capacitance, and resting potential; Table 2) permitted a means of estimation on the basis of mEPC amplitude ratios. Using the ratio of mean current amplitudes, the mean mEPP amplitude for two was 0.9 mV. The quantal content for both wild-type and two was then used to predict the EPP amplitude for each of the responses during the 20 Hz train (Fig. 8A,B). For wild-type recordings, the average predicted EPP for all 30 stimuli exceeded threshold for an action potential (Fig. 8A). However, the predicted values for two, although variable for the first few EPPs, consistently fell below threshold for the subsequent stimuli during the train (Fig. 8B). It could be argued that the reduced receptor density in two alone could account for the failure to follow high-frequency stimulation without the help of the slower reloading rate. To test for a direct dependence of the differences in reloading rates in placing the steady-state levels subthreshold for action potential generation, we selected the cells with high level of compensatory increase in the number of release sites and estimated EPP amplitude using either the wild-type or two reloading rate (Fig. 8B, inset). The predicted levels of EPP would reach threshold for muscle action potentials during 20 Hz if these cells were reloading the release sites at the rate of wild-type, but fall below threshold using the two reloading rate. Therefore, despite a compensatory increase in release site numbers, the slowed reloading, together with reduced receptor density, drive the levels of depression to subthreshold values.
These predictions were tested directly by measuring contractions in fast muscle during repetitive stimulation of the CaP motor neuron. Changes in muscle length provided a metric for the ability of muscle cells to follow action potentials generated in the CaP. Fast muscle from wild-type fish was able to contract faithfully to each stimulus up to 100 Hz (Fig. 8C). However, none of the two muscle cells was able to follow faithfully any frequencies >1 Hz. Higher-frequency stimulation resulted in contraction failures, usually after the first, but always well within the first few stimuli (Fig. 8C). On these bases, we conclude that the reduced overall EPC amplitude resulting from the combination of lowered receptor density and greater depression are causal to use-dependent fatigue in swimming seen in two.
Although zebrafish are perhaps best known for their contributions to developmental processes, there is much precedent attesting to new insights into vertebrate neuromuscular physiology (Sepich et al., 1998; Ono et al., 2001b; Behra et al., 2002; Downes and Granato, 2004; Wang et al., 2008). This should come as no surprise given the highly conserved structure and function of all vertebrate neuromuscular junctions. To our knowledge, the only evidence for thinking that fundamental differences might exist between mammals and lower vertebrates was the calcium channel isoform mediating neuromuscular transmission. On the basis of pharmacology, frogs were thought to use N types (Sano et al., 1987; Katz et al., 1995; Thaler et al., 2001), as opposed to mammals, which use P/Q type channels (Uchitel et al., 1992). However, we determined recently that zebrafish also use P/Q type channels, making it likely that all vertebrate motor neurons use this channel type (Wen et al., 2013b). Zebrafish neuromuscular junction also demonstrated synaptotagmin 7 as the mediator of asynchronous synaptic transmission (Wen et al., 2010), a process first identified at frog neuromuscular junctions (Eccles et al., 1941; Feng, 1941). Subsequently, a role for synaptotagmin 7 in mediating asynchronous release was established for central synapses (Bacaj et al., 2013), further underscoring the importance of zebrafish in revealing general principles of synapse function.
Zebrafish motility mutants have also provided new insights into human diseases such as myasthenic syndromes. In the context of the present study, zebrafish motility mutant two paved the way for identifying rapsyn deficiency as a form of congenital myasthenic syndrome (Ono et al., 2001a; Ohno et al., 2002; Ono et al., 2002; Richard et al., 2003). This human syndrome ranks highly in clinical relevance on the bases of frequency of occurrence and severity (Newsom-Davis, 2005; Lorenzoni et al., 2012). The muscle weakness associated with mutant two fish was ascribed to small-amplitude unitary and evoked synaptic responses resulting from reduced receptor density (Ono et al., 2002). Although reduced synaptic potentials could account for general muscle weakness, they could not fully account for the fatigue associated with repetitive movements in afflicted humans (Ohno et al., 1997; Ohno et al., 2002) and two fish (Ono et al., 2002). Electromyography from humans afflicted with myasthenic syndrome revealed decrementing electrical responses and associated fatigue at frequencies as low as several hertz (Yasaki et al., 2004; Lorenzoni et al., 2012). What was causal to these decrementing responses has remained an open question until now.
In two fish, both optical measurement of exocytosis from the motor neuron terminals and patch-clamp measurements of evoked synaptic currents in muscle indicate compromised transmitter release during repetitive stimulation. The synaptopHluorin experiments indicated a significantly reduced amount of exocytosis in two fish during a 100 Hz train and paired CaP motor neuron target muscle recordings indicated significant increases in the levels of steady-state depression. Both results place the locus of dysfunction in the motor neuron, which was unexpected given the locus of postsynaptic mutant rapsyn. The presynaptic defect in transmitter release, together with the greatly reduced receptor density, is causal to postsynaptic depolarizations that fall below threshold for contractions during repetitive activity. This is reflected in our predictions of muscle action potential failures and our direct measurements of muscle shortening during repetitive stimulation. Only at very low frequencies that do not lead to depression can contractions follow motor neuron action potentials faithfully in two fish.
Exploration into the mechanisms causal to the augmented steady-state depression levels in rapsyn-deficient fish pointed to compromised reloading rates for release sites. Unlike some central neurons (Saviane and Silver, 2006), the steady-state transmission at the zebrafish NMJ is not sustained by a large pool of RRP vesicles. Our measurement of the RRP size in both wild-type and two fish yielded estimates of one or two RRP vesicles at each release site, similar to estimates for both mouse calyx of Held and NMJ (Schneggenburger et al., 1999; Ruiz et al., 2011). Therefore, the RRP was depleted in both wild-type and rapsyn mutant fish within the first few stimuli before the establishment of the steady-state transmission. The steady-state levels were determined exclusively by the reloading rate of release sites, which differed significantly between wild-type and mutant fish. When expressed as rate of reloading per release site, the mutant fish were half those of wild-type. Although the bases for this lowered reloading rate is not known, a previous study in wild-type fish might offer potential mechanistic insights (Wen et al., 2016). Both variance analyses and recovery curves for wild-type fish have revealed the coexistence on the individual muscles of two kinetically distinct release sites that are ~60-fold different in their reloading rates. The fast class followed high-frequency stimulation without failure, whereas a slow class dropped out due to an inability to reload after depletion of the RRP. Therefore, the reloading rate of the fast zones sets the steady-state levels of response during high-frequency stimulation. Our estimates from the recovery time course for the mutant fish also point to the existence of at least two different kinetic components of release. The slow components are similar in wild-type and mutant, but the fast time constant is approximately three times slower, on average, in the mutant. Interpreted in the context of our model, the reloading rates for the fast sites are compromised, which leads to slowed recovery and greater depression.
Altered presynaptic function in response to the muscle rapsyn mutation is not only reflected in the slowed reloading, but also in an increase in the number of release sites. Compensatory increases in transmitter release caused by reduced numbers of postsynaptic receptors have been observed at both fly (Petersen et al., 1997) and mammalian (Plomp et al., 1992) NMJs and are thought to suggest retrograde signaling between the target muscle and the motor neuron. Recordings from intercostal synapse of humans afflicted with myasthenia gravis have also pointed to compensatory increases in quantal content (Cull-Candy et al., 1980). Functional compensation in the form of increased numbers of release sites helped to counter the reduced postsynaptic receptor density in two. Without such compensation, even low-frequency movements might not be possible. Indeed, in some human cases, the density of AChRs was so low that the associated synaptic potential failed to generate a muscle action potential even at rest (Engel, 2007). We observed that the level of compensatory increases in release site numbers varied widely for two fish. It is important to note that, even in fish with high levels of compensation, the membrane potential would be predicted to fall below threshold for action potential generation due to the slowed reloading rate. Moreover, if the reloading followed the wild-type rate, then these fish would be predicted to sustain movement for moderate frequencies such as 20 Hz despite the lowered receptor density. This further supports the idea that the slowed reloading rate in two, acting in concert with the reduced postsynaptic receptor density, are causal to the failure to follow high-frequency activity.
Our identification of a potential source of phenotypic variability in motility dysfunction may cast light on rapsyn deficiency in humans. If the same determinants of synaptic function shown here also hold for human myasthenic syndromes, this may help to account for the variability in phenotypic severity (Abicht et al., 2012). There are >20 different rapsyn mutations identified to date, all of which are thought, but not shown, to compromise postsynaptic receptor clustering (Hantaï et al., 2004). It is not clear that the different mutations are equivalent in either severity or associated compensation. For example, in afflicted individuals, even the identical mutations are not always a predictor of the phenotypic severity (Maselli et al., 2003; Burke et al., 2004). A rapsyn mutation that leads to a severe phenotype can be asymptotic in another person, pointing to additional factors in the disease state. Our present findings open the door to the idea that phenotypic variability among individuals could reflect levels of presynaptic compensation. Furthermore, should the compensation be proportional to the receptor density and associated activity, as suggested by studies on flies (Petersen et al., 1997; DiAntonio et al., 1999), this would potentially explain the phenotypic variability.
A second idea raised by our finding of great variability in compensation between individual recordings relates to the susceptibility of certain muscle groups to dystrophic function in humans (Lorenzoni et al., 2012). The ability of a motor neuron to compensate could depend on either the size of the target muscle field or on the class of motor neuron (Jessell, 2000; Lee and Pfaff, 2001). Should the specific motor neuron type dictate the balance between depression and compensation, it is possible that some affected muscle types would go undetected as a result of increased motor neuron compensation. Therefore, it becomes important to consider motor neuron function as well as target muscle when interpreting the factors causal to synaptic dysfunction.
This work was supported by the Muscular Dystrophy Association and the National Institutes of Health (P.B.). We thank James Maylie for advice about offline series resistance compensation and Michael Linhoff for Alexa Fluor 647-conjugated fasII.
The authors declare no competing financial interests.