Abstract
Structural and functional plasticity induced by neuronal competition is a common feature of developing nervous systems. However, the rules governing how postsynaptic cells differentiate between presynaptic inputs are unclear. In this study, we characterized synaptic interactions following manipulations of tonic Ib or phasic Is glutamatergic motoneurons that coinnervate postsynaptic muscles of male or female Drosophila melanogaster larvae. After identifying drivers for each neuronal subtype, we performed ablation or genetic manipulations to alter neuronal activity and examined the effects on synaptic innervation and function at neuromuscular junctions. Ablation of either Ib or Is resulted in decreased muscle response, with some functional compensation occurring in the Ib input when Is was missing. In contrast, the Is terminal failed to show functional or structural changes following loss of the coinnervating Ib input. Decreasing the activity of the Ib or Is neuron with tetanus toxin light chain resulted in structural changes in muscle innervation. Decreased Ib activity resulted in reduced active zone (AZ) number and decreased postsynaptic subsynaptic reticulum volume, with the emergence of filopodial-like protrusions from synaptic boutons of the Ib input. Decreased Is activity did not induce structural changes at its own synapses, but the coinnervating Ib motoneuron increased the number of synaptic boutons and AZs it formed. These findings indicate that tonic Ib and phasic Is motoneurons respond independently to changes in activity, with either functional or structural alterations in the Ib neuron occurring following ablation or reduced activity of the coinnervating Is input, respectively.
SIGNIFICANCE STATEMENT Both invertebrate and vertebrate nervous systems display synaptic plasticity in response to behavioral experiences, indicating that underlying mechanisms emerged early in evolution. How specific neuronal classes innervating the same postsynaptic target display distinct types of plasticity is unclear. Here, we examined whether Drosophila tonic Ib and phasic Is motoneurons display competitive or cooperative interactions during innervation of the same muscle, or compensatory changes when the output of one motoneuron is altered. We established a system to differentially manipulate the motoneurons and examined the effects of cell type-specific changes to one of the inputs. Our findings indicate Ib and Is motoneurons respond differently to activity mismatch or loss of the coinnervating input, with the Ib subclass responding robustly compared with Is motoneurons.
Introduction
Functional and structural changes in neuronal circuits occur during development and in response to environmental stimuli, learning, and injury (Katz and Shatz, 1996; Destexhe and Marder, 2004; Foeller and Feldman, 2004; Lamprecht and LeDoux, 2004; Holtmaat and Svoboda, 2009). Disruptions of these plasticity pathways contribute to neurodevelopmental diseases and impair rewiring after brain injury, highlighting the importance of the underlying mechanisms (Luo and O'Leary, 2005; Melom and Littleton, 2011; Doll and Broadie, 2014; Nahmani and Turrigiano, 2014). In contrast to mammals, invertebrate nervous systems like that of Drosophila melanogaster are more stereotypical in their organization. Neuroblasts divide and differentiate in a specific order to generate fixed cellular lineages with genetically hardwired synaptic targets (Hartenstein and Campos-Ortega, 1984; Thomas et al., 1984; Johansen et al., 1989a; Bossing et al., 1996; Landgraf et al., 1997; Schmid et al., 1999; Hoang and Chiba, 2001; Yu et al., 2010; Harris et al., 2015; Lee, 2017; Shepherd et al., 2019). Although Drosophila display stereotypical neuronal connectivity, plasticity can occur throughout development and into adulthood. Structural plasticity is most prominent during metamorphosis, when larval neurons reorganize their processes and synaptic partners form functional adult circuits (Technau and Heisenberg, 1982; Truman, 1990; Schubiger et al., 1998; Lee and Luo, 1999; Marin et al., 2005; Williams and Truman, 2005; Alyagor et al., 2018; Mayseless et al., 2018). Alterations in connectivity also occur in response to changes in environmental stimuli or following acute or chronic manipulations of neuronal activity (Cash et al., 1992; Chang and Keshishian, 1996; Davis et al., 1998; Lnenicka et al., 2003; Sigrist et al., 2003; Berdnik et al., 2006; Hourcade et al., 2010; Matz et al., 2010; Golovin et al., 2019).
Although plasticity occurs broadly across neuronal circuits, the motor system has played an important role in defining mechanisms for activity-dependent structural changes in connectivity. Locomotion is an essential behavior in many animals and requires coordinated output from central pattern generators to orchestrate motoneuron (MN) firing patterns that activate specific muscles (Marder and Calabrese, 1996; Marder and Rehm, 2005). In vertebrates, individual muscle fibers receive transient innervation from many cholinergic motoneurons during early development (Sanes and Lichtman, 1999). As many as 10 distinct motor axons can innervate a single muscle fiber before an activity-dependent competition results in retention of only a single axon (Tapia et al., 2012). This axonal competition allows a large pool of identical motoneurons to transition from dispersed weak outputs to the muscle field to strong innervation of a smaller subset of muscles (Colman et al., 1997; Walsh and Lichtman, 2003; Turney and Lichtman, 2012).
Unlike vertebrate neuromuscular junctions (NMJs), early promiscuity in synaptic partner choice and subsequent synapse elimination does not occur in Drosophila. Instead, the larval motor system is composed of ∼36 motoneurons from four subclasses that are genetically programmed by specific transcription factors and guidance molecules to form stereotypical connections to the 30 muscles in each abdominal hemisegment (Hoang and Chiba, 2001; Clark et al., 2018). Although synaptic partner choice is hardwired, activity-dependent plasticity and homeostatic mechanisms have been characterized, making Drosophila an ideal system to study synaptic interactions between motor neurons (Davis et al., 1998; Sigrist et al., 2003; Guan et al., 2005; Yoshihara et al., 2005; Frank et al., 2006; Berke et al., 2013; Davis, 2013; Cho et al., 2015; Davis and Müller, 2015; Gaviño et al., 2015; Harris and Littleton, 2015; Böhme et al., 2019; Goel et al., 2019). Although individual muscles normally restrict innervation to a single neuron from each subclass, it is unclear whether motoneurons interact during innervation of the same muscle target or respond when the output of one motoneuron is altered. Therefore, we established a system to differentially manipulate the two primary glutamatergic inputs and characterized the subsequent effects on synaptic morphology and function. We found that only the tonic Ib motoneuron is capable of partially compensating following ablation or silencing of the phasic Is input.
Materials and Methods
Drosophila stocks.
Drosophila melanogaster were cultured on standard medium at 25°C. Genotypes used in this study include the following: w1118 [stock #3605, Bloomington Drosophila Stock Center (BDSC)]; 13× LexAop2-mCD8-GFP (stock #32204, BDSC); UAS-DsRed (stock #6282, BDSC); UAS-CD8-GFP (stock #32185, BDSC); UAS-Reaper (stock #5823, BDSC); UAS-TeTXLC (stock #28837, BDSC); UAS-NaChBac (stock #9469, BDSC); GMR27E09-GAL4 (stock #49227, BDSC); MN1-Ib-GAL4 (stock #40701, BDSC); and 6–58 Is-GAL4 (from Ellie Heckscher, University of Chicago, Chicago, IL). Animals of either sex were used depending on the genetic scheme.
Transgenic constructs.
To create the MN1-Ib LexA driver line, a 2736 bp fragment from the intronic region of the Dpr4 locus that was used to generate the GMR94G06 MN1-Ib-GAL4 driver line (stock #40701, BDSC) was PCR amplified and cloned into Invitrogen pCR8/GW/TOPO (Thermo Fisher Scientific). This was followed by an LR cloning step into the pBPLexA::p65Uw plasmid (catalog #26231, Addgene). The resulting construct was sent for injection into an attP40 donor site strain by BestGene.
Immunocytochemistry.
Third instar wandering larvae were reared at 25°C and dissected in hemolymph-like HL3.1 solution as following (in mm): 70 NaCl, 5 KCl, 1.5 CaCl2, 4 MgCl2, 10 NaHCO3, 5 trehalose, 115 sucrose, and 5 HEPES, pH 7.2. Larvae were fixed for 10 min in HL3.1 buffer with 4% formaldehyde and washed three times for 10 min with PBT (PBS containing 0.1% Triton X-100), followed by a 30 min incubation in block solution (5% NGS in PBT). Fresh block solution and primary antibodies were added. Samples were incubated overnight at 4°C and washed with two short washes and three extended 20 min washes in PBT. Secondary antibodies were added to block solution and were incubated at room temperature for 2 h or at 4°C overnight. Finally, larvae were rewashed and mounted in 80% glycerol. Antibodies used for this study include the following: mouse anti-BRP (Bruchpilot), 1:500 [stock #NC82, Developmental Studies Hybridoma Bank (DSHB)]; mouse anti-DLG (Discs large), 1:1000 (stock #4F3, DSHB); chicken anti-DLG, 1:500; DyLight 649 conjugated anti-HRP (horseradish peroxidase), 1:500 (catalog #123–605-021, Jackson ImmunoResearch); rabbit anti-GFP Alexa Fluor 488, 1:500 (catalog #G10362, Thermo Fisher Scientific); goat anti-mouse Alexa Fluor 546, 1:500 (catalog #A-11030; Thermo Fisher Scientific); and phalloidin-conjugated Alexa Fluor 555 or 657, 1:500 (Thermo Fisher Scientific). Immunoreactive proteins were imaged on a Zeiss Pascal confocal microscope (Carl Zeiss Microscopy) using either a 40× 1.3 numerical aperture (NA), a 63× 1.3 NA, or a 100× 1.3 NA oil-immersion objective (Carl Zeiss Microscopy). Images were processed using Zen software (Zeiss).
Motoneuron GAL4 driver screen.
The FlyLight Project image database of larval brain and ventral nerve cord (VNC) GFP expression provided by Gerry Rubin [Janelia Research Campus, Howard Hughes Medical Institute (HHMI)] was searched for GAL4 lines displaying restricted expression in small subsets of segmentally repeated neurons with GFP-labeled axons projecting from the VNC. Candidate lines meeting these criteria were obtained and crossed to UAS-CD8::GFP (stock #32185, BDSC) for immunostaining with DyLight 649-conjugated anti-HRP (Jackson ImmunoResearch), Alexa Fluor 555 phalloidin (Thermo Fisher Scientific), and rabbit anti-GFP Alexa Fluor 488 (Thermo Fisher Scientific). Confocal imaging was performed to classify labeled neurons based on their synaptic connectivity within the abdominal musculature.
Quantification of confocal images.
Imaris 9.2 software (Oxford Instruments) was used to identify BRP puncta to quantify active zone (AZ) number, and HRP labeling was used to quantify the synaptic bouton number from 3D image stacks through the NMJ. For DLG/HRP measurements, the 3D mask feature was used, and the software determined bouton volume within HRP staining and muscle subsynaptic reticulum (SSR) volume from DLG staining. Quantification was conducted at muscle 1 (M1) in abdominal segment A3. The n value refers to the number of NMJs analyzed, with no more than two NMJs analyzed per larvae. Animals used in each analysis were derived from at least three independent experimental crosses. All analysis was performed blind to genotype.
Live imaging of Ib and Is innervation and synaptic growth.
Live imaging was done under desflurane anesthesia at muscles M1 and M4 at abdominal segments A2–A4 as previously described (Akbergenova et al., 2018). Selected larvae were covered with halocarbon oil and a coverglass and were imaged. After imaging, larvae were placed in numbered chambers with food in a 25°C incubator. Larvae were imaged at the beginning of the first instar larval stage and during the subsequent 24 h interval with the same data acquisition settings. Confocal images were obtained on a Zeiss Axio Imager 2 equipped with a spinning-disk confocal head (model CSU-X1, Yokagawa) and ImagEM X2 EM-CCD camera (Hamamatsu). A pan-APOCHROMAT 63× objective with 1.40 NA from Zeiss (Carl Zeiss Microscopy) was used for imaging.
Electrophysiology.
Wandering third instar larvae were dissected in modified HL3.1 saline solution, as follows (in mm): 70 NaCl, 5 KCl, 0.3 CaCl2, 4 MgCl2, 10 NaHCO3, 5 trehalose, 115 sucrose, and 5 HEPES, pH 7.18. For electrophysiology and force recordings, larvae were pinned medial side up at the anterior and posterior ends, an incision was made alongthe midline, and the visceral organs were removed. All nerves emerging from the CNS were severed at the ventral nerve cord and the CNS, and the ventral nerve cord was removed. Excitatory junctional potentials (EJPs) were elicited by stimulating severed abdominal nerves. A Master 800 A.M.P.I. stimulator(A-M Systems) was used for stimulation via a suction electrode. EJPs were recorded using sharp glass microelectrodes containing a 2:1 mixture of 3 m potassium chloride/3 m potassium acetate with electrode resistances of40–80 MΩ. An Axoclamp 2B amplifier (Molecular Devices) was used for signal detection and digitized via a Digidata 1550 digitizer (Molecular Devices). Signals were acquired at 10 kHz using Clampex and were analyzed with Clampfit, MiniAnalysis, and Microsoft Excel. For physiology experiments involving MN1-Ib GAL4, MNIs GAL4, UAS-RPR, MN1-Ib>RPR, MNIs>RPR, UAS-TeTXLC, and MNIs> TeTXLC, the preparations were stained afterward to identify animals that had both Ib and Is innervation at muscle 1. Data were used only in cases where both inputs were present, or in situations where the specific loss of one input was expected (RPR experiments). For Ib>NaChBac and Is> NaChBac electrophysiology experiments, minimal stimulation protocols were used to verify both inputs were present. Experiments with only Ib input were discarded. All analysis was performed blind to genotype.
Muscle force contraction measurements.
Force recordings were obtained using an Aurora Scientific 403A Force Transducer System with a force transducer headstage, amplifier, and digitizer. Larvae were dissected ventral side up in HL3.1 saline containing 1.5 mm Ca2+. Nerve-evoked contractions were generated using stimulation bursts from a Master 8 Stimulator (A.M.P.I.). The duration of single impulses was 5 ms and interburst duration was kept constant at 15 s. Burst frequency was altered during each individual experiment. Digitized data were acquired using Dynamic Muscle Acquisition Software (DMC version 5.5, Aurora Scientific) and imported and processed in MATLAB using custom code. All analysis was performed blind to genotype.
Statistical analysis.
Prism software (version 8.1.1; GraphPad Software), and FIJI/ImageJ software was used for statistical analysis. Statistical significance in two‐way comparisons was determined by a Student's t test, while one-way ANOVA parametric analysis was used when comparing more than two datasets. Statistical comparisons are made with control unless noted. Appropriate sample size was determined using a normality test. Data are presented as the mean ± SEM (*p < 0.05, **p < 0.01, ***p < 0.001, n.s. = not significant).
Results
Screen for Ib and Is motoneuron-specific GAL4 drivers
Four subclasses of motoneurons innervate the abdominal musculature in Drosophila, with each class defined by their synaptic partner choice, neurotransmitter or neuromodulator content, and biophysical and synaptic properties (Jan and Jan, 1976; Johansen et al., 1989a; Atwood et al., 1993; Lnenicka and Keshishian, 2000; Hoang and Chiba, 2001). Approximately 30 type Ib glutamatergic motoneurons are found per hemisegment and function as the primary driver of contraction for individual muscles. A single Ib motoneuron individually innervates a single muscle fiber, allowing for fine-tuning of specific locomotor programs. The Ib neuronal subclass has big synaptic boutons containing AZs with low release probability (Pr) that facilitate during high-frequency stimulation (Lnenicka and Keshishian, 2000; Peled and Isacoff, 2011; Melom et al., 2013; Newman et al., 2017; Akbergenova et al., 2018). We refer to the Ib subtype as tonic to denote the sustained firing during muscle contractions cycles, low release probability, and short-term facilitation. Three type Is glutamatergic motoneurons per hemisegment provide input to the ventral, lateral, or dorsal muscle groups, respectively. Each Is neuron innervates multiple fibers to coordinatethe contraction of functionally related muscles. In contrast to Ib motoneurons, Is motoneurons have smaller synaptic boutons and fewer AZs with higher Pr release sites that undergo depression during repetitive stimulation (Fig. 1A). We refer to the Is subtype as phasic to denote that it has stronger synapses that rapidly undergo depression, with a firing pattern that drives rapid coactivation of specific muscle groups. The remaining type II and III subclasses are neuromodulatory in nature (Gorczyca et al., 1993; Stocker et al., 2018).
To preferentially manipulate Ib and Is motoneurons, GAL4 lineswith subclass-specific expression were identified from the FlyLight Project (Jenett et al., 2012; Manning et al., 2012). and strains were provided by Ellie Heckscher (University of Chicago). The FlyLight collection consists of >5000 transgenic Drosophila lines with ∼3 kb of regulatory genomic DNA from candidate neuronal genes driving GAL4 expression. Images of membrane-tethered UAS-CD8-GFP driven by each GAL4 line in third instar brain lobes and VNC were provided by Gerry Rubin (Janelia Research Campus, HHMI). Candidate lines for further analysis were chosen on the basis of two criteria: (1) restricted expression of GFP in a single pair or a small subset of segmentally repeated abdominal neurons in the VNC; and (2) GFP expression in axons exiting the VNC as expected for motoneurons innervating peripheral musculature (Fig. 1B). Forty-two GAL4 driver lines were identified as promising candidates in the initial screen and subjected to further immunostaining to identify their synaptic targets. Six of these lines were verified as having restricted expression in a small subset of motoneurons (Table 1), including GAL4 drivers specific for Ib and Is motoneurons (Fig. 1C–F). Line GMR94G06 displayed restricted expression in the Ib motoneuron (MN1-Ib) that innervates muscle M1 (Fig. 1B–D). GMR94G06 contains regulatory DNA from the Dpr4 locus, which encodes a member of the cell surface Ig-containing proteins implicated in synaptic target recognition (Carrillo et al., 2015). Line GMR27F01 contained regulatory sequences from the Fmr1 gene and showed restricted expression in two Is motoneurons and a type II neuromodulatory neuron (Table 1). Line 6-58 displayed restricted expression in the Is motoneurons MNISN-Is and MNSNb/d-Is that innervate the ventral and dorsal muscles, respectively (Fig. 1E,F). To determine the gene regulatory region responsible for Is motoneuron expression in 6-58, which contained an unknown insertion site, plasmid rescue and reverse PCR was performed. The insertion site mapped to the 5′ UTR of the Dip-α gene. Like DPR4, DIP-α is a member of the Ig domain family of synaptic target recognition proteins and was previously found to be expressed in Is motoneurons (Ashley et al., 2019). The MN1-Ib driver GMR94G06 and an additional Is GAL4 driver line (GMR27E09, containing regulatory sequences from Fmr1) were independently identified in a recent study (Pérez-Moreno and O'Kane, 2019). We refer to the restricted GAL4 driver lines as MN1-Ib GAL4 and MNIs GAL4 in the remaining text. Together, they provide a toolkit to genetically manipulate the tonic Ib and phasic Is motoneuron subclasses that coinnervate muscle M1.
Establishment of MN1-Ib and MN-Is synaptic connections during development
MN1-Ib and MNIs drivers were used to fluorescently label the two neuronal subpopulations and establish the timing for M1 innervation, the most peripheral target of the dorsal abdominal musculature. MN1-Ib (formerly referred to as aCC) and MNIs (formerly referred to as RP2) were previously identified as pioneer neurons for the ISN nerve branch, being the first to exit the VNC toward the dorsal muscle field (Jacobs and Goodman, 1989; Johansen et al., 1989b; Lin et al., 1995; Sánchez-Soriano and Prokop, 2005). To colabel MN1-Ib and MNIs in the same animal, an MN1-Ib LexA driver line was generated by subcloning the 2736 bp genomic Dpr4 fragment from GMR94G06 into pBPLexA::p65Uw. This construct was used to generate transgenic animals containing MN1-Ib LexA, allowing independent LexA and GAL4 transgene expression in MN1-Ib and MNIs motoneurons. Serial intravital imaging through the cuticle of briefly anesthetized animals coexpressing MN1-Ib Lex; LexAop2-CD8-GFP and MNIs GAL4; UAS-DsRed was performed as previously described (Akbergenova et al., 2018). By the beginning of the first instar larval stage, all MN1-Ib motoneurons had correctly targeted M1 during late embryonic development, elaborating a growth cone-like projection over the muscle surface (Fig. 2A,B). In contrast, MNIs had a more variable time course of innervation, with the Is growth cone trailing behind MN1-Ib, often without targeting M1 in early first instars. By the end of the first instar larval stage, only 28% of MNIs motoneurons had innervated the muscle. MNIs innervation of M1 continued over the rest of larval development, with 72% of Is motoneurons innervating M1 by the third instar stage (abdominal segments 2–4; n = 7 larvae; Fig. 2C). The remaining M1 muscles lacked Is innervation. These data indicate that the Ib motoneuron innervates M1 before the arrival of Is, with the Is motoneuron forming synaptic contacts with the muscle later in development or failing to innervate the target completely.
Since phasic Is motoneurons have stronger synapses with higher Pr active zones than their tonic Ib counterparts at the third instar stage (Kurdyak et al., 1994; Lnenicka and Keshishian, 2000; Lu et al., 2016; Newman et al., 2017; Genç and Davis, 2019; Karunanithi et al., 2020), we examined Is synaptic maturation given their shorter developmental time window compared with the pre-existing Ib input. Presynaptic bouton and AZ number at motoneuron NMJs increase throughout larval development to help maintain normal levels of depolarization during the rapid expansion of muscle size during this period. This synaptic growth is accompanied by expansion in the size of the postsynaptic density (PSD) and glutamate receptor fields (Zito et al., 1999; Akbergenova et al., 2018). To examine glutamate receptor field formation and maturation at developing Ib and Is synapses, we followed M4 innervation during early larval development (Fig. 2D). The Ib and Is inputs arrive at distinct positions on M4, allowing unambiguous identification of neuronal subclass without having to genetically label the motoneurons, as required for M1. Live imaging was performed in developing larvae expressing RFP-tagged GluRIIA and GFP-tagged GluRIIB under the control of their endogenous promotors (Rasse et al., 2005). Glutamate receptors at the NMJ are tetramers, with three essential subunits and a fourth subunit of either GluRIIA or GluRIIB (Schuster et al., 1991; Petersen et al., 1997; Marrus et al., 2004; Featherstone et al., 2005; Qin et al., 2005). As observed at M1, MN4-Ib innervation preceded MNIs arrival at M4, with 18% of M4 fibers completely lacking Is innervation at the third instar stage (abdominal segments A2–A4, n = 9 larvae). Although Is innervation of M4 was delayed compared with Ib, the fractional rate of synapse addition was elevated at Is terminals during consecutive days of imaging as quantified by the appearance of new GluRIIA/GluRIIB-positive PSDs (MN4-Ib, 1.46-fold increase; MNIs, 1.86-fold increase; n = 11, p = 0.0014; Fig. 2E,F). Overall, the delayed innervation by Is resulted in a reduced PSD number at M4 compared with Ib (day 1: MN4-Ib, 31.9 ± 3.3 AZs; MNIs, 16.5 ± 2.6 AZs; day 2: MN4-Ib, 46.5 ± 4.9 AZs; MNIs, 29.9 ± 4.5 AZs; n = 11, p = 0.0014; Fig. 2F). Although the Is motoneuron formed fewer synapses than Ib, the average PSD size defined by the GluRIIB area in first instar larvae was 69% larger than those of the corresponding Ib input (MN4-Ib: 0.215 ± 0.004 µm2, n = 1006 PSDs; MNIs: 0.363 ± 0.013 µm2, n = 399 PSDs; p = 1.2 × 10−8; Fig. 2G,H). Given that PSD maturation is activity dependent at NMJs (Schmid et al., 2008; Petzoldt et al., 2014; Akbergenova et al., 2018), these data suggest that PSDs may develop faster at the stronger Is AZs than PSDs apposed to weaker Ib AZs. Alternatively, the postsynaptic muscle may compartmentalize the delivery of PSD material to Is versus Ib synapses such that Is sites are favored for the accumulation of glutamate receptors incorporating the IIB subunit.
To further characterize the differences in postsynaptic receptor composition between MN4-Ib and MNIs, GluRIIA PSD levels were assayed to determine whether they were also proportionally increased when apposed to MNIs AZs. No difference in GluRIIA PSD accumulation at MN4-Ib versus MNIs first instar synapses was found (MN4-Ib: 6268 ± 881.9 GluRIIA fluorescent intensity units, n = 25; Is: 7767 ± 1040, n = 25; p = 0.73). A key feature of Drosophila PSD maturation is a change in the ratio of GluRIIB and GluRIIA subunit-containing receptors during development (Schmid et al., 2008). Comparative analysis of the GluRIIB/GluRIIA ratio revealed that it was shifted in favor of the GluRIIB subunit at PSDs apposed to MNIs AZs (3.19 ± 0.4 ratio, n = 25) versus MN4-Ib AZs (2.12 ± 0.27 ratio, n = 25; p = 0.03; Fig. 2I). These data suggest that different synaptic inputs innervating the same muscle can display distinct PSD glutamate receptor subunit incorporation. Overall, we conclude that PSDs form at a slightly elevated rate at MNIs connections during this early growth window and that they preferentially accumulate the GluRIIB subunit versus the GluRIIA variant.
A central pathway regulating synaptic maturation at Drosophila NMJs is mediated through muscle secretion of Glass Bottom Boat (Gbb), a bone morphogenetic protein (BMP) ligand that acts on presynaptic BMP receptors to activate a SMAD-dependent transcriptional synaptic growth program (Aberle et al., 2002; Marqués et al., 2002; McCabe et al., 2003; Ball et al., 2010; Rodal et al., 2011; Berke et al., 2013). To determine whether Ib and Is motoneurons were equally sensitive to Gbb signaling given their different innervation time course, we assayed synapse formation and growth of MN4-Ib and MNIs at M4 in Gbb mutants (Fig. 3A). As previously observed, loss of Gbb reduced the synaptic growth of Ib motoneurons innervating M4 compared with controls (control MN4-Ib NMJ area: 182.8 ± 21.6 µm2, n = 11 NMJs from 5 larvae; Gbb MN4-Ib NMJ area: 56.2 ± 5.8 µm2, n = 21 NMJs from 8 larvae; p = 0.0001; Fig. 3B). Although synaptic growth was reduced, 100% of M4 muscles displayed Ib synaptic innervation. In contrast, synaptic innervation from the Is motoneuron was reduced in Gbb mutants, with only 48% of M4 muscles containing Is innervation compared with 82% in controls (Fig. 3C). In cases where the Is motoneuron innervated M4 in Gbb, similar reductions in synaptic growth compared with Ib were observed (control Is NMJ area: 102.2 ± 11.3 µm2, n = 7 NMJs from 5 larvae; Gbb Is NMJ area: 33.8 ± 4.0 µm2, n = 16 NMJs from 8 larvae; p = 0.0006; Fig. 3B). These data indicate the Gbb pathway promotes synaptic growth in tonic Ib motoneurons but is not required for target innervation. In contrast, the loss of Gbb signaling in phasic Is motoneurons decreases synaptic growth and also reduces the percentage of muscles with Is innervation.
Role of MN1-Ib and MNIs in muscle excitability and contraction
To determine the relative contributions of Ib and Is motoneurons in muscle excitability, simultaneous electrophysiological recordings were performed at third instar larval muscles M1 and M2 in HL3.1 saline solution containing 0.3 mm extracellular Ca2+. A minimal stimulation protocol was used to isolate MN1-Ib or MNIs, as MNIs innervates both muscles compared with MN1-Ib (Fig. 4A). By increasing the current applied to the larval nerve through the stimulating electrode, responses following the activation of one or both motor axons could be isolated in cases where dual innervation was present. The average EJP amplitude recorded at M1 when both Ib and Is inputs were active was 24.2 ± 1.7 mV (n = 22; Fig. 4B,C). When Ib or Is was individually recruited during minimal stimulation, reduced responses of similar amplitude at M1 were observed (MN1-Ib: 11.8 ± 1.6 mV, n = 22; MNIs: 12.4 ± 1.4 mV, n = 22), indicating that each neuron provides similar drive to M1 following single action potentials (Fig. 4B,C). Given that MN1-Ib has more AZs compared with MNIs at M1 (Fig. 2F), these results are consistent with MNIs motoneurons having higher Pr per AZ as previously described (Lu et al., 2016; Newman et al., 2017; Genç and Davis, 2019).
To examine the contribution of MN1-Ib and MNIs for muscle contractility, nerve-evoked bodywall contraction force was recorded with a force transducer attached to the head of dissected larvae (Fig. 4D). To isolate contraction force mediated predominantly by the dorsal muscle group (M1, M2, M3, M9, and M10), third instar larvae were dissected along the ventral midline. Severed abdominal nerves were placed in a suctionelectrode, and the nerve bundle was stimulated at increasing frequencies in HL3.1 saline containing 1.5 mm extracellular Ca2+ as previously described (Ormerod et al., 2016). Control MN1-Ib and MNIs GAL4 larval preparations showed increasing contraction force when a 0.1 ms simulation was ramped from 1 to 150 Hz for 600 ms (Fig. 4E). To determine the contribution of each motoneuron subclass for contractile force, MN1-Ib or MNIs was ablated by expressing the cell death gene reaper (UAS-RPR) to induce apoptosis (Whiteet al., 1994, 1996; Goyal et al., 2000). Expression of UAS-RPR with MN1-Ib or MNIs GAL4 resulted in elimination of the corresponding motoneuron class. Ablation of MNIs removed phasic input to all dorsal and ventral muscles and resulted in a robust reduction in contractile force over the entire frequency distribution, including a 53% decrease in maximum force following 150 Hz stimulation (MNIs GAL4: 5.4 ± 0.2 mN, n = 7; MNIs> UAS-RPR: 2.5 ± 0.1 mN, n = 8; p = 0.009; Fig. 4F) and a 65% decrease in minimal contractile force following a single action potential (MNIs GAL4: 0.2 ± 0.02 mN, n = 7; MNIs>RPR: 0.07 ± 0.02 mN, n = 7; p = 0.0009; Fig. 4G). Ablation of MN1-Ib eliminated tonic input only to M1, leaving innervation of the other dorsal muscles by their respective Ib and Is neurons intact. Loss of MN1-Ib caused a less severe defect, resulting in a 25% decrease in contractile force at 150 Hz (MN1-Ib GAL4: 5.5 ± 0.2 mN, n = 7; MN1-Ib>UAS-RPR: 4.1 ± 0.2 mN, n = 7; p = 0.022; Fig. 4F) and a 33% decrease at 1 Hz (MN1-Ib GAL4: 0.21 ± 0.02 mN, n = 7; MN1-Ib>UAS-RPR: 0.14 ± 0.01 mN, n = 7; p = 0.068; Fig. 4G). Although it is difficult to directly compare the contributions of Ib versus Is ablation in force contraction assays given that Is innervates multiple muscles, these findings suggest that both motoneuron subclasses contribute to muscle contraction force, with the phasic Is input providing the drive for both excitability and contraction.
Lack of Ib and Is synaptic competition during NMJ development
Given the role of Ib and Is motoneuron inputs in driving muscle excitability, we examined whether interactions between the inputs occurred during larval development that shaped their axonal arbor expansion and AZ number when they coinnervated M1 or M4. If Ib and Is neurons competed for synaptic growth signals emanating from the muscle, or suppressed the growth of the coinnervating input, competitive interactions should generate a negative correlation between Ib and Is synapse number. If the two inputs display cooperative interactions during growth, for example by coactivating the muscle to release more synaptogenic factors, one would expect a positive correlation. Similarly, if both inputs were independent and growing only in response to muscle size, a positive correlation would be expected. Ib and Is synaptic terminals were identified following anti-DLG immunostaining. DLG is a component of the postsynaptic muscle SSR and is prominent around presynaptic Ib boutons compared with Is (Lahey et al., 1994). Synapse number was quantified for wandering third instar larvae by immunolabeling for the core AZ T-bar component BRP (Wagh et al., 2006; Fouquet et al., 2009). Synaptic bouton number was determined using anti-HRP immunostaining, which provides a neuron-specific membrane label. No correlation was observed between Ib and Is AZ number per NMJ at M1 (r = −0.11, n = 29, p = 0.57, Pearson R; Fig. 5A) or between Ib and Is inputs at M4 (Pearson R = −0.10, n = 19, p = 0.69; Fig. 5B). Similarly, no correlation for Ib versus Is bouton number at M1 (Pearson R = 0.15, n = 29, p = 0.44; Fig. 5C) or M4 (Pearson R = 0.13, n = 19, p = 0.60; Fig. 5D) was found. We also quantified synaptic interactions between MN4-Ib and MNIs at M4 in Gbb mutants. Although the absence of Gbb signaling leads to decreased synapse number for both MNIs and MN4-Ib motoneurons, there was no correlation between NMJ area of Ib and Is in Gbb mutants (Pearson R = 0.13, n = 10, p = 0.73). These data are consistent with Ib and Is motoneurons forming synapses on the muscle without obvious competitive or cooperative interactions that shape their connectivity during development.
As described above, ∼30% of larval M1 muscles lack Is innervation. This natural variation provided an opportunity to examine whether growth of the coinnervating MN1-Ib motoneuron was altered at mature third instar NMJs when MNIs innervation was absent. Lack of Is innervation did not result in any change in M1 muscle surface area (coinnervation: 46,661 ± 1457 µm2, n = 16; Ib only: 48,206 ± 1170 µm2, n = 8; p = 0.66, ANOVA). Although the total AZ number was reduced at M1 in the absence of Is innervation (Ib only: 285.8 ± 29.7 AZs, n = 10; coinnervation: 389.7 ± 17.3 AZs, n = 13; F(5,60) = 62.05, p = 0.0068; Fig. 6A), the AZ number contributed solely by the MN1-Ib input was not significantly altered whether Is was absent (285.8 ± 29.7 Ib AZs, n = 10) or present (329.1 ± 15.8 Ib AZs, n = 13; F(5,60) = 62.05; p = 0.66; Fig. 6A). Likewise, no change in synaptic bouton number in MN1-Ib motoneurons was observed whether MNIs was absent (18.0 ± 4.3 Ib boutons, n = 8) or present (19.1 ± 4.4 Ib boutons, n = 16; F(5,66) = 60.73, p = 0.99; Fig. 6B). In addition, the NMJ area of MN4-Ib terminals in Gbb mutants was not altered if MNIs was present (52.8 ± 8.4 µm2, n = 10) or absent (57.4 ±7.0 µm2, n = 16; p = 0.68). We conclude that synaptic growth of Ib motoneurons is not altered when Is innervation is lacking.
Ablation of MNIs triggers increased evoked release from the remaining MN1-Ib input
Although no structural compensation was observed in MN1-Ib when MNIs was absent, functional changes in neurotransmitter release could occur in the absence of increased release sites. In addition, a mismatch in neuronal activity between inputs during development could result in unique forms of plasticity compared with when a motoneuron was missing. To generate an input imbalance, MN1-Ib or MNIs GAL4 drivers were used to express several well characterized UAS transgenes that alter neuronal activity (Simpson, 2009; Venken et al., 2011; Yoshihara and Ito, 2012; Pauls et al., 2015). To decrease neurotransmitter release and synaptic output, a transgene encoding tetanus toxin light chain (UAS-TeTXLC) was expressed to cleave the v-SNARE n-Synaptobrevin and to eliminate evoked synaptic transmission (Sweeney et al., 1995). A transgene encoding a bacterial voltage-gated Na+ channel (UAS-NaChBac) that enhances depolarization was used to constitutively increase neuronal excitability (Nitabach et al., 2006). To compare the effects of reduced or enhanced activity with the complete absence of each input, Reaper expression (UAS-RPR) was used to ablate MN1-Ib or MNIs. None of the manipulations altered M1 muscle surface area (F(10,175) = 2.129, p = 0.66, n = 6–29/genotype), indicating that muscle growth is not affected by ablation or activity changes in MN1-Ib or MNIs motoneurons (see Fig. 8A). For all experimental manipulations, the Ib motoneuron was labeled with MN1-Ib LexA, and LexAop-GFP in the background for unambiguous identification of the two inputs following immunostaining with the pan-neuronal marker anti-HRP (Ib and Is) and anti-GFP (Ib only). Synaptic development (see Figs. 8–10, 12–13), synaptic function (see Fig. 11A) and muscle contraction force (see Fig. 11B–D) were analyzed in controls and compared with Ib and Is motoneurons expressing the transgenes with their respective GAL4 driver.
We first examined whether the ablation of each motoneuron subclass altered the synaptic structure of the remaining input. The expression of UAS-RPR with either MN1-Ib GAL4 or MNIs GAL4 resulted in the elimination of the respective motoneuron compared with controls (Fig. 7A–E). Membrane fragments immunopositive for GFP from the MN1-Ib LexA, LexAop-GFP labeling were often observed near M1 in MN1-Ib GAL4> UAS-RPR larvae (Fig. 7D), suggesting that cell death and membrane fragmentation occurred after the initial stages of axonal pathfinding. Genetic ablation of the Is motoneuron in MNIs GAL4>UAS-RPR larvae did not result in a change in MN1-Ib AZ (F(10,183) = 52.42, p = 0.999; see Fig. 9A) or bouton number (F(10,185) = 29.99, p = 0.999; see Fig. 9B), similar to conditions where MNIs naturally failed to innervate M1 in control larvae.
To determine whether MN1-Ib altered its functional properties without changes in the number of release sites, electrophysiology was performed at third instar M1 muscles to measure Ib-evoked release when Is innervation was present in controls versus when Is was ablated with UAS-RPR. Although no structural changes were identified at MN1-Ib NMJs, a functional change in the output of the motoneuron was observed. The evoked EJP response triggered by MN1-Ib activation was increased 24% at M1 muscles when MNIs input was ablated (15.4 ± 1.0 mV, n = 11) versus when MNIs was present (11.8 ± 1.6 mV, n = 22; F(10,58) = 5.30, p = 0.05; see Fig. 11A). This compensation did not result in complete recovery of the evoked output observed when both inputs were present (control Is-GAL4: 25.9 ± 1.5 mV, n = 10). In addition, contractile force was still decreased following MNIs ablation, as previously noted (Fig. 4E–G; also see Fig. 11B,D). These data suggest that the muscle is capable of detecting loss of the Is input and increasing synaptic output from the remaining Ib motoneuron, resulting in a partial rescue of muscle excitability.
To examine whether Is motoneurons displayed similar functional compensation, genetic ablation of the Ib motoneuron was performed using MN1-Ib GAL4; UAS-RPR. As previously described, M1 occasionally lacked MNIs input because of natural variation in controls. As such, MN1-Ib ablation resulted in M1 having no synaptic innervation (42%) or only MNIs innervation (58%). Larvae with Is innervation at M1 following ablation of the Ib motoneuron displayed a dramatic decrease in the number of total AZs (control: 332.1 ± 13.5 AZs, n = 25; Ib>RPR: 67.7 ± 8.4 AZs, n = 11; F(10,183) = 35.17, p < 0.0001; Fig. 8B) and synaptic boutons (control: 28.8 ± 1.4, n = 25; Ib> RPR: 11.0 ± 2.1, n = 11; F(10,183) = 19.47, p < 0.0001; Fig. 8C), given the larger number of synapses normally contributed by the MN1-Ib input. However, the loss of MN1-Ib did not trigger changes in the number of Is AZs (Fig. 9C) or Is synaptic boutons (Fig. 9D) compared with Is innervation when MN1-Ib was present. In contrast to the functional increase in evoked release in tonic Ib neurons following ablation of Is, the loss of MN1-Ib did not trigger a compensatory increase in evoked output from the remaining MNIs motoneuron (see Fig. 11A). We conclude that compensatory structural or functional changes do not occur in the phasic Is input following loss of the tonic Ib motoneuron at M1. In contrast, loss of Is results in functional changes in the coinnervating Ib input that partially compensates for the reduced evoked response.
Imbalances in MN1-Ib or MNIs neuronal activity reveal structural plasticity of tonic Ib inputs
To examine the consequences of activity perturbations between Ib and Is motoneurons at M1 NMJs during development, manipulations were performed to increase or decrease synaptic output of one of the two neurons. Expression of UAS-TeTXLC in either the Ib or Is input blocked evoked synaptic transmission from the affected motoneuron, reducing EJP amplitude recorded physiologically to the level observed when only the Ib or Is motoneuron were recruited during minimal stimulation (see Fig. 11A). Silencing the Is motoneuron in MNIs GAL4; UAS-TeTXLC larvae resulted in structural changes at the NMJ (Fig. 10A,C), with an increase in the total number of AZs(control: 396.3 ± 14.6 AZs, n = 15; MNIs >TeTXLC: 465.0 ± 14.7 AZs, n = 18; F(10,183) = 35.17, p = 0.0187; Fig. 8B) and synaptic boutons (control: 41.2 ± 2.7, n = 15; Is>TeTXLC: 50.9 ± 2.7, n = 18; F(10,183) = 19.47, p = 0.028; Fig. 8C). This enhanced synaptic growth was due to increases occurring in the coinnervating MN1-Ib input (Fig. 9A,B), with no changes observed in the affected MNIs (Fig. 9C,D). In particular, MN1-Ib displayed a large increase in AZ number when Is was silenced compared with when Is was present or ablated (Is present: 314 ± 12.9, n = 15; Is ablated: 326.6 ± 14.4, n = 14; Is silenced: 402.7 ± 13.0, n = 18; F(10,183) = 35.17, p = 0.0187). Although the number of release sites increased in MN1-Ib following the silencing of MNIs (MNIs>TeTXLC), electrophysiology (Fig. 11A) and contraction (Fig. 11B,D) assays indicated that these structural changes were insufficient to induce increased excitability or contractility of the muscle. We conclude that the complete absence of the Is input leads to a functional increase in release from the coinnervating tonic Ib input without a change in the number of release sites. In contrast, when Is is present but functionally silent, the Ib input displays a distinct response with a structural change that includes more release sites, but the overall functional output of the motoneuron remains unaltered.
We next examined the consequences of silencing MN1-Ib activity with TeTXLC (Fig. 10A,B). Similar to when MN1-Ib was ablated, the coinnervating MNIs did not display structural (Fig. 9C,D) or functional (Fig. 11A–C) compensation, indicating the Is motoneuron is less capable of compensatory synaptic plasticity when the coinnervating Ib motoneuron is ablated or silenced. In contrast to the lack of change in the Is input, silencing MN1-Ib (Ib>TeTXLC) triggered several structural changes to its own morphology. First, a striking reduction in AZ number was found, with a 30% decrease in release sites in MN1-Ib motoneurons lacking evoked transmission (UAS-TeTXLC: 333.6 ± 21.2 AZs, n = 14; MN1-Ib GAL4: 281.6 ± 11.9 AZs, n = 25; MN1-Ib>TeTXLC: 215.3 ± 13.6 AZs, n = 15; F(10,183) = 52.42, p = 0.001; Fig. 9A). Second, there was a change in the anatomy of the MN1-Ib axon at the NMJ, with the appearance of synaptic filopodial-like protrusions (Fig. 10A–C). This phenotype was never observed in controls (average protrusions per MN1-Ib NMJ: UAS-TeTXLC: 0, n = 14; MN1-Ib GAL4: 0, n = 25; MN1-Ib>TeTXLC: 7.2 ± 2.4, n = 16; F(4,83) = 9.921, p = 0.0001; Fig. 10D). Similar filopodial-like protrusions were described previously at early first instar NMJs during the initial stages of synapse formation in wild-type animals, but never at mature third instar NMJs (Akbergenovaet al., 2018). Such protrusions were not observed in silenced Is motoneurons or in Ib motoneurons following Is silencing (Fig. 10A–D), indicating that MN1-Ib and MNIs react differently to changes in their own activity.
A final morphologic change at silenced MN1-Ib NMJs was a decrease in postsynaptic SSR membrane revealed by anti-DLG staining (Fig. 12A–D). SSR volume compared with presynaptic NMJ volume (anti-HRP staining) was reduced by 50% on average at MN1-Ib>TeTXLC NMJs compared with controls (F(2,54) = 11.70, p = 0.0079; Fig. 12D). Together, the reduced AZ number, decreased muscle SSR volume, and increased synaptic filopodial-like protrusions suggest that silenced MN1-Ib motoneurons maintain an immature state with reduced AZ formation and a failure to properly induce normal postsynaptic specializations. These defects are not observed at silenced Is phasic synapses, indicating that the Is motoneuron class is less sensitive to activity changes and any potential compensatory responses triggered from the muscle.
To determine whether enhanced activity of either of the two motoneuron subclasses would induce structural or functional changes, the NaChBac depolarizing Na+ channel was expressed in either MN1-Ib or MNIs (Fig. 13A–C). NaChBaC expression has been previously demonstrated to enhance membrane depolarization by increasing Na+ conductance (Pauls et al., 2015). Consistent with enhanced excitability and increased burst spiking in affected motoneurons, trains of EJPs in response to a single stimulus were often recorded from M1 in larvae expressing NaChBac (50% of MN1-Ib motoneurons; 38% of MN1s motoneurons; Fig. 13D). Although expression of the channel-enhanced excitability, it did not result in structural (Figs. 8, 9) or functional (Figs. 11, 13E) changes in synaptic properties of MN1-Ib>NaChBac or MNIs>NaChBac larvae. No alterations of the Ib or Is input were observed in either condition. Similarly, increased activity in either motoneuron class did not trigger any obvious structural competition between the inputs. We conclude that NMJ plasticity is more sensitive to manipulations that reduce presynaptic release versus those that enhance membrane excitability, and that these changes preferentially manifest within the tonic Ib subclass of motoneurons.
Discussion
To characterize how changes in the presence or activity of tonic Ib versus phasic Is motoneurons alter NMJ development and function in Drosophila, we identified GAL4 drivers specific for each class that innervate M1 and used them to alter the balance of input to the muscle. Our data indicate that Ib and Is motoneurons largely form independent inputs that make similar contributions to muscle excitability and contractile force. The Ib subclass was capable of structural and functional changes following manipulations that altered their output or that of the coinnervating Is motoneuron (Fig. 14A–D). These changes were observed only during conditions when neuronal activity was decreased or when the Is input was ablated. Functional increases in evoked release without enhanced synapse number were observed in Ib motoneurons following ablation of Is (Fig. 14B). In contrast, morphologic changes that increased AZ number without enhancing evoked release occurred when Is synaptic output was blocked with tetanus toxin (Fig. 14C). While Ib motoneurons were capable of several forms of plastic change following reduced input to the muscle, Is motoneurons were insensitive to manipulations of their own activity or that of the Ib input. Unlike the plasticity observed in Ib neurons following reduction in synaptic drive to the muscle, enhancing excitability of either the Ib or Is input was ineffective at triggering changes in either motoneuron class. These data indicate that reductions in activity from either input trigger a structural or functional change primarily from the tonic Ib motoneuron subclass.
The stereotypical connectivity found in the abdominal musculature of Drosophila larvae suggest that individual muscles normally allow synaptic innervation from only a single motoneuron of each subclass (Hoang and Chiba, 2001). However, expanded postsynaptic target choice has been observed following muscle loss induced by laser ablation or genetic mutation, with the affected Ib motoneuron targeting inappropriate nearby muscles without altering the innervation pattern of the correctly targeted Ib neuron (Sink and Whitington, 1991; Keshishian et al., 1994; Chang and Keshishian, 1996). Similarly, ablation of some motoneurons can result in axonal spouting from neighboring connections that targetthe deinnervated muscle (Chang and Keshishian, 1996). Misexpression of synaptic cell surface proteins can also alter target choice for some Ib and Is motoneurons (Lin and Goodman, 1994; Kose et al., 1997; Shishido et al., 1998; Ashley et al., 2019). In addition, silencing neuronal activity during development has been demonstrated to induce ectopic NMJs formed primarily by type II neuromodulatory neurons (Keshishian et al., 1994; Jarecki and Keshishian, 1995; White et al., 2001; Lnenicka et al., 2003; Mosca et al., 2005; Carrillo et al., 2010; Vonhoff and Keshishian, 2017). We did not observe any axonal sprouting onto M1 from other motoneurons that resulted in altered target choice when MN1-Ib or MNIs was ablated or silenced in our experiments. Given that M1 is the most dorsal muscle of the abdominal musculature, axons from other motoneurons are not present in the direct vicinity, so any signals released from M1 might be insufficient to attract additional innervation. We did find evidence that M1 may attempt to promote synaptic innervation when MN1-Ib was silenced withtetanus toxin. Under these conditions, the MN1-Ib terminal maintained an immature-like state with the presence of filopodial-like extensions (Fig. 14D). This effect was observed only in Ib motoneurons, highlighting differences in how Is terminals interact with or respond to signals from the muscle. We and others have observed similar filopodial-like extensions at newly forming NMJ connections in late embryos and early first instar larvae (Halpern et al., 1991; Broadie and Bate, 1993; Ritzenthaler et al., 2000; Ritzenthaler and Chiba, 2003; Kohsaka and Nose, 2009; Akbergenova et al., 2018). These presynaptic filopodial processes contain elevated levels of the Cacophony N-type Ca2+ channel and interact with GluRIIA-rich myopodia, with some progressing to form new synapses during early development (Akbergenova et al., 2018). Because of the lack of reinforcement signals caused by the absence of synaptic activity in silenced MN1-Ib motoneurons, we hypothesize that these processes fail to properly drive AZ assembly and new synapse formation. Indeed, a role for neuronal activity in regulating synaptogenic filopodial stabilization has been characterized in the Drosophila visual system (Sheng et al., 2018; Özel et al., 2019).
Many forms of plasticity, including synapse elimination at mammalian NMJs, ocular dominance plasticity, and cerebellar climbing fiber pruning, require Hebbian-like input imbalances to trigger synaptic interactions (Wiesel and Hubel, 1963, 1965; Sherman and Spear, 1982; Colman et al., 1997; Sanes and Lichtman, 1999; Walsh and Lichtman, 2003; Turney and Lichtman, 2012; Hashimoto and Kano, 2013; Tomàs et al., 2017; Wilson et al., 2019). As such, we were interested to see whether changes in the activity of Ib or Is motoneurons that created an imbalance between the output of the two neurons could drive unique changes compared with when one input was missing. In the case of the Ib neuron, this was indeed observed. In the absence of Is input, either because of natural variation in innervation in control animals or following ablation with UAS-RPR, there was no structural response in terms of adding additional release sites. However, the loss of Is triggered a functional increase in evoked release from the Ib neuron (Fig. 14B). In contrast, when an activity imbalance was created by expressing tetanus toxin in the Is neuron, Ib displayed structural plasticity that increased the number of release sites (Fig. 14C). Although the underlying molecular pathways that mediate the two distinct responses are unknown, the results suggest that the physical presence of Is likely alters the signaling systems responsible for triggering compensation in Ib motoneurons in response to reduced muscle drive.
For every manipulation we made beyond increasing excitability of the neurons, a response from the tonic Ib class was detected, while the phasic Is motoneuron displayed less plasticity. Since each muscle is innervated by a single Ib motoneuron, this plasticity may allow more robust and local regulation of muscle function. Although the Is did not show plastic change in response to manipulation of its activity or the coinnervating Ib in our experiments, we cannot rule out that Is neurons are capable of such plasticity but display less sensitivity to putative muscle-derived retrograde signals. Given that Is neurons innervate multiple muscles compared with Ib, it is also possible that small plastic changes occurring in Is are not synapse specific and are distributed over a larger population of AZs onto multiple muscles, resulting in little effect at any single postsynaptic target. Similar differences in homeostatic plasticity in Ib versus Is motoneurons have been described following reduced postsynaptic muscle glutamate receptor function, with the Ib motoneuron showing a more robust upregulation of presynaptic release compared with Is (Newman et al., 2017; Li et al., 2018; Cunningham and Littleton, 2019a,b). Although homeostatic plasticity has been observed in Is motoneurons in low extracellular Ca2+ (Genç and Davis, 2019), the elevated Pr of Is synapses may occlude further functional increases in release output in higher [Ca2+] normally found in larval hemolymph. Together, these results indicate that tonic Ib motoneurons express distinct plasticity mechanisms that can be triggered by reduced muscle function that are less robust or lacking in the phasic Is subclass. Whether the differential plasticity found in our study is linked directly to the tonic or phasic properties of Ib and Is motoneurons, or is under separate regulatory control, will require further investigation.
An important question moving forward is to identify mechanisms that control structural and functional plasticity in Ib motoneurons. Similarly, defining why the Is fails to respond to many of the same manipulations is poorly understood. Whether homeostatic plasticity mechanisms triggered in response to acute or chronic reduction in glutamate receptor function are also activated following the absence or functional silencing of presynaptic inputs as described here is unknown. Several molecular pathways contributing to homeostatic plasticity have been described at the NMJ (Davis, 2006, 2013; Bergquist et al., 2010; Müller et al., 2011, 2012; Müller and Davis, 2012; Younger et al., 2013; Frank, 2014; Wang et al., 2014, 2016; Davis and Müller, 2015; Gaviño et al., 2015; Kiragasi et al., 2017; Li et al., 2018; Ortega et al., 2018; Böhme et al., 2019; Goel et al., 2019; Gratz et al., 2019; Frank et al., 2020). Beyond Drosophila, studies in crustacean motor systems have shown that long-term alterations in activity can induce cell type-specific changes in tonic or phasic motoneuron structure or release properties (Atwood and Wojtowicz, 1986; Lnenicka et al., 1986, 1991; Govind and Walrond, 1989; Lnenicka and Atwood, 1989; Hong and Lnenicka, 1993; Wojtowicz et al., 1994). Given that tonic and phasic neurons are abundant in the nervous systems of both invertebrates and vertebrates (Schultz, 2001; Atwood and Karunanithi, 2002; Zucker and Regehr, 2002; Millar and Atwood, 2004; Ventimiglia and Bargmann, 2017), it will be interesting to determine whether such properties play a key role in defining their capacity for plastic change. The tools described here provide an opportunity to identify the distinct transcriptional profiles of each neuronal subclass in Drosophila to identify candidate mechanisms that mediate the differential plasticity responses of tonic Ib and phasic Is motoneurons.
Footnotes
The authors declare no financial or conflicts of interests.
This work was supported by National Institutes of Health (NIH) Grants NS-40296 and MH-104536 to J.T.L. N.A.A.-S. was supported in part by NIH Predoctoral Training Grant T32-GM-007287. We thank Ellie Heckscher and Gerry Rubin for sharing fly lines. We also thank the Bloomington Drosophila Stock Center (Indiana University, Bloomington, IN; NIH Grant P40-OD-018537), the Drosophila Genome Resource Center (Indiana University, Bloomington, IN; NIH Grant 2P40-OD-010949-10A1), the TRiP Center at Harvard Medical School (Boston, MA; NIH/National Institute of General Medical Sciences Grant R01-GM-084947), the Developmental Studies Hybridoma Bank (University of Iowa, Iowa City, IA), and the Vienna Drosophila Resource Center (Vienna, Austria) for providing the strains used in this study. In addition, we thank the staff and students in the Cold Spring Harbor Laboratory Drosophila Neurobiology course and members of the Littleton laboratory for sharing resources and advice.
- Correspondence should be addressed to J. Troy Littleton at troy{at}mit.edu
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