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The Journal of Neuroscience, September 1, 1999, 19(17):7434-7449

Synaptic Control of Glycine and GABA_A Receptors and Gephyrin Expression in Cultured Motoneurons

Sabine Lévi¹, Dominique Chesnoy-Marchais², Werner Sieghart³, and Antoine Triller¹

¹ Laboratoire de Biologie Cellulaire de la Synapse Normale et Pathologique (Institut National de la Santé et de la Recherche Médicale U-497), ² Laboratoire de Neurobiologie (Centre National de la Recherche Scientifique URA-1867), Ecole Normale Supérieure, F-75005 Paris, France, and ³ University Clinic For Psychiatry, Department of Biochemical Psychiatry, A-1090 Vienna, Austria

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

We have evaluated the influence of the secretory phenotype of presynaptic boutons on the accumulation of postsynaptic glycine receptors (GlyRs), type A GABA receptors (GABA_ARs), and gephyrin clusters. The cellular distribution of these components was analyzed on motoneurons cultured either alone or with glycinergic and/or GABAergic neurons. In motoneurons cultured alone, we observed gephyrin clusters at nonsynaptic sites and in front of cholinergic boutons, whereas glycine and GABA_A receptors formed nonsynaptic clusters. These receptors are functionally and pharmacologically similar to those found in cultures of all spinal neurons. Motoneurons receiving GABAergic innervation from dorsal root ganglia neurons displayed postsynaptic clusters of gephyrin and GABA_AR but not of GlyR/ subunits. In motoneurons receiving glycinergic and GABAergic innervation from spinal interneurons, gephyrin, GlyR/, and GABA_AR formed mosaics at synaptic loci. These results indicate that (1) the transmitter phenotype of the presynaptic element determines the postsynaptic accumulation of specific receptors but not of gephyrin and (2) the postsynaptic accumulation of gephyrin alone cannot account for the formation of GlyR-rich microdomains.

Key words: dorsal root ganglia; GABA_A receptor; gephyrin; glycine receptor; motoneurons; picrotoxinin; presynaptic innervation; spinal neurons; strychnine

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

In the nervous system, certain ionotropic receptors accumulate at postsynaptic membrane-facing terminals enriched in the corresponding neurotransmitter. Such is the case for GlyR (Triller et al., 1985, 1987; Van den Pol and Gorcs, 1988), GABA_AR 6 and GABA_AR 3 subunits (Baude et al., 1992; Todd et al., 1996), and ionotropic glutamate receptors (Petralia and Wenthold, 1992; Craig et al., 1993; Aoki et al., 1994; Petralia et al., 1994). Other GABA_A and glutamate receptor subtypes are also present at nonsynaptic sites (Baude et al., 1992, 1994, 1995; Sur et al., 1995a). On the cytoplasmic side, peripheral membrane proteins bind and contribute to the clustering of various types of receptors. These include gephyrin for GlyR and some GABA_AR subtypes [see references in Vannier and Triller (1997) and Essrich et al. (1998)] and PDZ domain (initially identifed in PSD95, Disc Large, and Zonula Occludens 1 proteins) molecules for ionotropic and metabotropic glutamate receptors [see references in Sheng and Wyszynski (1997)]. These molecules are functionally homologous to rapsyn, which stabilizes the muscular nicotinic acetylcholine receptor (nAChR) [see references in Sanes (1997)]. Peripheral proteins anchor receptors by direct or indirect attachment to perisynaptic or subsynaptic cytoskeletal elements. An unresolved question is that of the involvement of presynaptic innervation in postsynaptic accumulation of transmitter receptors and associated proteins. We have examined this question for the postsynaptic accumulation of GlyR, GABA_AR, and gephyrin in spinal motoneurons.

Glycine and GABA are involved in postsynaptic inhibition through the activation of the chloride (Cl) channels associated with GlyR and GABA_AR. Both receptors belong to the nAChR superfamily (Betz, 1990). GlyR is a pentamer composed of  and  subunits (32) [see references in Vannier and Triller (1997)]. Gephyrin links GlyR through its  subunit to the subsynaptic cytoskeleton (Kirsch and Betz, 1995; Meyer et al., 1995). GABA_ARs are also pentamers. The 2, 3, 5, 3, and 2 subunit mRNAs are detected in motoneurons (Persohn et al., 1991; Wisden et al., 1991). A recent study has shown that gephyrin is involved in the stabilization of GABA_AR in the postsynaptic membrane (Essrich et al., 1998).

We have analyzed the distribution of gephyrin, GlyR/, and GABA_AR2/3 subunits on cultured motoneurons: (1) alone, establishing connections among themselves and therefore receiving cholinergic inputs; (2) with dorsal root ganglia (DRG) neurons to supply a GABAergic innervation, taking advantage of the fact that a subclass of DRG neurons expresses a GABAergic phenotype (Roy et al., 1991; Chauvet et al., 1995); or (3) with spinal interneurons to provide glycinergic and GABAergic innervations. We show that in the absence of inhibitory presynaptic innervation, motoneurons express GlyR and GABA_AR that are functional and form nonsynaptic clusters. In the presence of presynaptic innervation, these receptors accumulate specifically under boutons containing the corresponding neurotransmitter. In contrast, gephyrin accumulates under all synaptic terminals whether they contain acetylcholine (ACh), GABA, or glycine. Our results demonstrate that gephyrin alone is not able to sort GlyR and GABA_AR to synaptic sites and that glycinergic and GABAergic endings provide specific signals for accumulation of the corresponding receptors.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Motoneuron purification and culture. Motoneurons were purified from ventral spinal cords of embryonic day 15 Sprague Dawley rats (Janvier, Le Genest-sur-Isle, France) by a combination of metrizamide density-gradient centrifugation and immunopanning on dishes coated with the 192 antibody as previously described (Henderson et al., 1995). This antibody recognizes the low-affinity neurotrophin receptor p75^NTR, which is selectively expressed by motoneurons at this developmental stage (Chandler et al., 1984; Yan and Johnson, 1988) (Developmental Studies Hybridoma Bank, Iowa City, IA). Purified motoneurons (2 × 10³) were plated on polyornithine-laminin (Sigma, St. Louis, MO) precoated 12 mm coverslips in four-well plates (Nunc, Dannstadt, Germany). Culture medium was the Neurobasal-B27 medium combination (Life Technologies, Gaithersburg, MD) supplemented with 0.5 mM L-glutamine (Life Technologies), 25 µM -mercaptoethanol (Life Technologies), and 2% horse serum (v/v; Sigma). For certain experiments, motoneurons were cultured in the glycine-free MEM medium (Life Technologies) supplemented with vitamins and essential amino acids (except glycine) (Life Technologies), 1 mM glucose (Sigma), B27, 0.5 mM L-glutamine (Life Technologies), 25 µM -mercaptoethanol (Life Technologies), and 2% horse serum (v/v; Sigma). The amount of glycine in the horse serum was found to be 229 µM (Beckman 6300 amino acid analyzer), which gave a final concentration of 4.6 µM. To keep motoneurons alive, 1 ng/ml recombinant rat ciliary neurotrophic factor (CNTF; Peprotech, London) (Arakawa et al., 1990) and 100 pg/ml recombinant human glial cell line-derived neurotrophic factor (GDNF; Peprotech) (Henderson et al., 1994) were added to the culture medium. Cultures were kept at 37°C in 7.5% CO₂ for up to 11 d in vitro (DIV). The culture medium was renewed every 4 d.

Motoneuron and DRG neuron cocultures. DRG were dissected from embryonic day 15 (E15) mice, collected in PBS (120 mM, pH 7.4), and centrifuged for 5 min at 800 × g. The supernatant was discarded and replaced by the Neurobasal-B27 medium with 0.2% horse serum. One or two whole DRG explants were added to purified motoneurons plated the day before. The culture medium was completely replaced after 4 d, and cultures were maintained for up to 7 DIV.

Motoneuron and spinal interneuron cocultures. Primary cultures of spinal cord neurons were prepared from E15 Sprague Dawley rats as described previously (Béchade et al., 1996; Lévi et al., 1998). In parallel, ventral spinal cords were dissected and dissociated, and neurons were centrifuged on a 6.5% metrizamide cushion. The interface of the metrizamide cushion enriched in large motoneurons was collected. Neurons (2 × 10³) from the latter fraction were mixed with 10⁵ spinal neurons and plated on 12 mm glass coverslips. Cultures were maintained in the Neurobasal-B27 medium with 0.2% horse serum for up to 11 DIV.

Antibodies. The mAbs used in this study were as follows: (1) mAb7a, which recognizes gephyrin (1:200; Boehringer Mannheim, Mannheim, Germany) (Pfeiffer et al., 1984). Splice variants of gephyrin transcripts are widely expressed in the CNS (Kirsch et al., 1993a). Immunocytochemistry with mAb7a showed the same widespread distribution (Kirsch and Betz, 1993), suggesting that mAb7a has a broad spectrum of recognition for gephyrin. However, some heavy forms of gephyrin may not be detected by mAb7a (Kawasaki et al., 1997); (2) mAb4a, which binds to all GlyR  and  subunit isoforms (1:100; gift from H. Betz) (Pfeiffer et al., 1984; Schröder et al., 1991); (3) mAb bd17 directed against the GABA_A R2/3 subunits (10 µg/ml; Boehringer Mannheim) (Richards et al., 1987); (4) anti-Islet1 homeodomain protein (clone 2D6, 1:2; Developmental Studies Hybridoma Bank) (Ericson et al., 1992; Tsuchida et al., 1994); (5) anti-155 kDa rat neurofilament protein that specifically stains axons (clone 2H3, 1:2000; Developmental Studies Hybridoma Bank) (Dodd et al., 1988); (6) AP14, which detects MAP2A (1:50; gift from B. Riederer) (Binder et al., 1984); and (7) anti-synaptophysin (1:20; Boehringer Mannheim). As secondary antibodies, we used a carboxymethyl indocyanine-3 (CY3)-coupled affinity-purified goat anti-mouse IgG (1:200; Jackson Immunoresearch Laboratories, West Grove, PA). Polyclonal antibodies (pAbs) were also used: (1) rabbit anti-synapsin I (1:2000; gift from P. de Camilli) (De Camilli et al., 1983); (2) rabbit anti-glutamate decarboxylase of 67 kDa (GAD67, 1:2000; Chemicon, Temecula, CA) (Wong et al., 1974); (3) rabbit anti-MAP2 (1:250; Sigma); (4) rabbit antiserum raised against the rat GABA_AR3 subunit (5 µg/ml) (Todd et al., 1996); (5) rabbit anti-glutamate receptor 1 (GluR1, 10 µg/ml; Chemicon) (Wenthold et al., 1992); and (6) goat anti-choline acetyltransferase (ChAT, 1:500; Chemicon). The rabbit pAbs were recognized by a fluorescein (FITC)-conjugated affinity-purified goat anti-rabbit IgG (H+L) (1:200; Jackson Immunoresearch Laboratories). For double-staining of gephyrin and ChAT, mAb7a was recognized by an FITC-conjugated affinity-purified horse anti-mouse IgG (H+L) (1:200; Vector Laboratories, Burlingame, CA), and the goat pAb anti-ChAT was recognized by a CY3-conjugated affinity-purified donkey anti-sheep IgG (H+L) (1:200; Jackson Immunoresearch Laboratories).

Immunocytochemistry. For all immunodetections except that of mAb4a, cells were fixed with 4% (w/v) paraformaldehyde for 15 min. Cells were washed in PBS and permeabilized with 0.12% Triton X-100 in PBS with 0.12% (w/v) gelatin for 5 min. The permeabilized cells were incubated with primary antibodies overnight at 4°C. The next day, cells were washed in PBS and incubated with secondary fluorescent antibodies for 45 min at room temperature. For mAb4a immunocytochemistry, a methanol/acetic acid (95:5) mixture was used as fixative (10 min at 20°C). Cells were rinsed in PBS and incubated successively in primary and secondary antibodies as described above. For multiple-labeling experiments, antibodies were incubated simultaneously. For immunoperoxidase reactions, cells were incubated successively with the Islet1 mAb and the secondary biotinylated affinity-purified horse anti-mouse IgG (H+L) (1:200; Vector Laboratories) for 1 hr, rinsed in PBS, and then incubated with the ABC complex (1:200; Vector Laboratories) for 30 min. Peroxidase staining was obtained by incubating cells in a DAB-H₂O₂ reactant (Sigma). Peroxidase reactions were monitored under the microscope and stopped by washing with PBS.

For sequential mAb7a and mAb4a immunodetections, cells were fixed in a methanol/acetic acid (95:5) solution (10 min at 20°C), rinsed, and incubated with mAb4a (1:100, 1 hr). After washes, cells were treated with lissamine rhodamine-conjugated affinipure Fab fragment goat anti-mouse IgG (H+L) (1:50, 45 min; Jackson Immunoresearch Laboratories). They were then rinsed and incubated with unconjugated Fab fragment goat anti-mouse IgG (H+L) (1:50, 45 min; Jackson Immunoresearch Laboratories) to saturate still unbound mAb4a. Then they were incubated with mAb7a (1:200, 1 hr), which was further recognized by an FITC-conjugated affinity-purified horse anti-mouse IgG (H+L) (1:200, 45 min; Vector Laboratories). All incubations were performed at room temperature. Control cells were exposed to the same treatment except that they were incubated with only one of the primary antibodies.

In all experiments, the specificity of immunolabeling and the absence of antibody cross-reaction in double-staining experiments were controlled by omission of the primary antibodies. Cultures were observed with a standard or a confocal (Molecular Dynamics, Sunnyvale, CA) epifluorescence microscope. Fluorescent images were acquired on a Hamamatsu CCD camera (C5985) mounted on a Leica DMR/HCS microscope (objective 40 or 63×), and dual color images were obtained using Imagespace software (Molecular Dynamics). Images were prepared for printing using Adobe Photoshop software.

Quantitative analysis. Motoneuron purity was estimated by counting under phase contrast (objective 40×) the number of cells with nuclear peroxidase staining of Islet1. The proportions of cells displaying gephyrin-, GlyR/-, and GABA_AR3-immunoreactivity (IR) were determined by visual inspection using a standard fluorescence microscope (objective 63×). For each experiment, 36 ± 3 fields were analyzed. For these quantifications, data are expressed as means ± SEM of three independent experiments. Colocalization of gephyrin, GlyR/, or GABA_AR2/3 with synapsin was determined from double-staining experiments of synapsin and mAb7a, mAb4a, or mAbbd17. The quantifications were performed on images acquired with a Hamamatsu CCD camera and specific filters for FITC and CY3 fluorescences (Leica). This procedure was chosen because it allows a minimal bleed-through between FITC and CY3 channels, which was always found to be lower than 0.3%. Confocal microscopy was used to measure the surface area of gephyrin, GlyR/, and GABA_AR3 clusters. To improve accuracy, the quantification was performed by means of simple staining experiments. Immunopositive cells were displayed in the center of the digitized field, and all neurites within the field were computed. Excitation was obtained with an argon ion laser set at 514 nm for CY3 excitation, and the emitted light was filtered with a long-pass filter (530 nm). Pixel size and focus steps were 0.21 and 0.3 µm, respectively (objective 63×, numerical aperture 1.4), with images of 512 × 512 pixels. Digitized series of optical sections at different planes of focus were collected using a host computer (Indy, Silicon Graphics). The background noise was reduced, and the contrast was enhanced by applying a median (3 × 3 × 3) Gaussian filter. Maximum intensity projections were derived from these sections using Imagespace (Molecular Dynamics) software. The surface area of clusters was determined with NIH 1.52 software. The threshold intensity fluorescence was set manually for each cell to insure efficient detection and to avoid coalescence of clusters. An image-object was computed if it comprised at least three pixels. This analysis was performed on motoneurons cultured alone or in the presence of spinal interneurons, as well as on interneurons. Statistical analysis was performed using StatView F.4.11 software.

Electrophysiology. The experiments were performed at room temperature (20-23°C) between 6 and 8 DIV in the whole-cell configuration of the patch-clamp technique. Before recording, the culture medium was replaced by the external solution to be used during the experiment, which contained (in mM): 150 NaCl, 2.5 KCl, 1.8 CaCl₂, 1 MgCl₂, 20 glucose, and 10 HEPES-NaOH, pH 7.4. The internal solutions used to fill the recording electrode contained (in mM): either 145 CsCl, 1 MgCl₂, 10 EGTA, 1 CaCl₂, 3 ATP-Mg, 0.3 GTP-Na, and 10 HEPES-CsOH, pH 7.2, for internal solution A or 145 Cs methanesulfonate, 15 CsCl, 1 MgCl₂, 0.1 EGTA, 3 ATP-Mg, 0.3 GTP-Na, and 10 HEPES-CsOH, pH 7.2, for internal solution B. The culture dish was continuously perfused with the external solution. In addition, a fast perfusion system was used for rapid applications of glycine and modulators onto the recorded cell. All solutions applied via this system contained 0.2 µM tetrodotoxin. This system was made of glass syringes, Teflon taps, and Teflon tubing connected to two parallel glass barrels (one of them only containing glycine); lateral movements of this system were controlled by a computer-driven motor to apply the solution of the desired barrel to the cell [continuously perfused with one of the solutions of this system; for more details, see Chesnoy-Marchais (1996)]. For concentrations of glycine below 40 µM, successive responses recorded under identical conditions were quite stable when tested every 40 sec. For higher concentrations (80-160 µM), the interval between successive tests was longer (100 sec) to allow for recovery from desensitization. Stock solutions of strychnine (hemisulfate, Sigma) and picrotoxinin (Sigma) were prepared at 1 mM in water and at 100 mM in ethanol, respectively. In the experiments using picrotoxinin, the solutions applied by fast perfusion contained 1:1000 ethanol. When a modulator was applied "with preincubation," it was applied continuously between and during the successive glycine applications, that is, in both barrels of the fast perfusion. When applied "without preincubation," it was present only in the glycine-containing barrel.

Patch-clamp micropipettes were made from hard glass (Kimax 51); the shank of each pipette was covered with Sylgard, and the tip was fire-polished. Their resistance was close to 5 M. The cells were voltage-clamped by an EPC7 List amplifier, which was controlled by a TANDON 38620 computer, via a Cambridge Electronic Design (CED) 1401 interface, using CED patch- and voltage-clamp software. The current monitor output of the amplifier was filtered at 0.3 kHz before being sampled on-line at 0.6 kHz. The bath was connected to the ground via an agar bridge. Membrane potentials were corrected for junction potentials. The series resistance was routinely measured and compensated. The zero indicated on the current traces is the absolute zero current level.

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Gephyrin, GlyR, and GABA_AR cellular distribution in motoneurons cultured alone

Motoneurons were purified by a combination of metrizamide density-gradient and immunopanning techniques (Henderson et al., 1995). As estimated by immunoperoxidase staining of the motoneuronal embryonic marker Islet1 (Ericson et al., 1992), 89.2 ± 1.3% of the cells had a motoneuronal phenotype (Fig. 1A). The remaining cells corresponded to Islet1-negative but p75 low-affinity neurotrophin receptor- and L14 lectin-positive motoneurons (Henderson et al., 1993). Double-immunofluorescence experiments with antibodies against MAP2 and 155 kDa neurofilament protein were performed to label dendrites and axons, respectively. These experiments showed that at 7 DIV, motoneurons are polarized with somato-dendritic and axonal compartments (Fig. 1B). We used the mAb7a and mAb4a antibodies to stain gephyrin and GlyR/ subunits, respectively (Pfeiffer et al., 1984), whereas GABA_AR3 subunit was recognized by a previously characterized pAb (Todd et al., 1996). The gephyrin, GlyR/, and GABA_AR3 formed puncta on somata and dendrites as shown in double-labeling experiments with anti-MAP2 antibodies (Fig. 1C-E). A few scattered spots of gephyrin were also detected along the length of some axons (data not shown). Clusters of GlyR/ and GABA_AR3 were not detected in axons. However, in some neurons, clusters of GlyR/ (Fig. 1D) or GABA_AR3 (Fig. 1E) were detected at the level of the axon-hillock. Confocal optical sections revealed small, round or ellipsoidal clusters of gephyrin at membrane areas in contact with the coverslip (Fig. 1F1 exemplifies a neuron with a large number of clusters) as well as at distance from it (Fig. 1F2). Numerous bright spots of GlyR/ (Fig. 1G1) and GABA_AR3 (data not shown) were also detected at the substrate-neuron interface as well as at a distance from it. On some cells, GlyR/-IR (Fig. 1G2) and GABA_AR3-IR (Fig. 1K1, arrow) formed large patches at the neuronal surface.

View larger version (59K): [in this window] [in a new window]   Figure 1.   Gephyrin, GlyR, and GABAAR distribution on motoneurons cultured alone. A, Immunoperoxidase showing the nuclear staining of the embryonic motoneuronal marker Islet1. B, Double-staining of the dendritic protein MAP2 (green) and the axon-enriched 155 kDa neurofilament protein (red). C-E, Presence of clusters (arrows) of gephyrin (C, red), GlyR/ (D, red), or GABAAR3 (E, green) on MAP2-IR somato-dendritic compartment (green in C, D; red in E). GlyR/ clusters are also accumulated at the level of axon-hillock (arrowhead in D). F, G, Confocal visualization of Geph-IR (F1-2) and GlyR/-IR (G1-2), respectively. Discontinuous Geph-IR (arrows) at the cell-to-substrate contact (F1) and at a distance from the coverslip (F2). GlyR/ forms clusters at the cell-to-substrate contact (arrows in G1) and occasionally displays a continuous labeling (arrows in G2) on sections passing through the nucleus. H, I, Double-immunofluorescence showing that Geph-IR clusters (H1, I1) accumulate in front of synapsin-IR boutons (arrowheads in H2) displaying ChAT-IR (arrowheads in I2). Geph-IR clusters (H1, I1) are also detected at nonsynaptic sites (arrows). In contrast, GlyR/ (J1) and GABAAR2/3 (K1) do not concentrate at synaptic sites (arrowheads in J1-2 and K1-2, respectively). Insets in H2, I2, J2, and K2 show superimposed images of H1-H2, I1-I2, J1-J2, and K1-K2, respectively. ChAT, Choline acetyltransferase; GABAAR2/3, GABAAR2/3 subunits-IR; GABAAR3, GABAAR3 subunits-IR; Geph, gephyrin-IR; GlyR/, GlyR/ subunits-IR; MAP2, dendritic marker; NF, NF155 Kda-IR; Syn, synapsin-IR. Scale bar: A, B, 50 µm; C-K2, 10 µm.

The relationships of these receptor components to presynaptic endings were analyzed in double-staining experiments in which the synaptic boutons were identified with a pAb against synapsin. For these experiments, we used the mAb bd17 directed against GABA_AR2/3 subunits (Richards et al., 1987) because the anti-synapsin Ab is a pAb. Synapsin-positive endings were detected over somata and/or dendrites of many motoneurons and could correspond to autapses or may originate from other motoneurons. On these cells, gephyrin-IR clusters were found on the soma and neurites at synaptic and nonsynaptic loci (Fig. 1H1-H2). Almost all presynaptic specializations were facing gephyrin-IR clusters. These postsynaptic gephyrin-IR clusters were larger than those observed at nonsynaptic loci and extend all along the synaptic contact (Fig. 1H1). To verify that presynaptic boutons in these pure cultures of motoneurons were cholinergic, we immunostained for ChAT (Fig. 1I1-2). We found that after 11 DIV, almost all boutons were ChAT-positive and that 90.2 ± 3.8% (10 cells encompassing 199 boutons) of these boutons were apposed to gephyrin-IR clusters (Fig. 1I1-2). In contrast, most GlyR/ (Fig. 1J1-2) and GABA_AR2/3 (Fig. 1K1--2) clusters were detected at the cell surface at sites that were not facing presynaptic boutons. Because glycine was present at high concentration (400 µM) in the culture medium, it may be involved in the clustering of gephyrin. To examine this issue, motoneurons were cultured in glycine-depleted medium. This medium was not completely glycine free because the added serum contributed to a final concentration of 4.6 µM (see Materials and Methods). However, this low concentration is shown to activate <2% of the GlyR channels (see Fig. 3). With this low amount of glycine, we found that motoneurons had postsynaptic and nonsynaptic clusters of gephyrin (data not shown), similar to motoneurons cultured in a glycine-rich medium.

The question remains of the association of large gephyrin clusters postsynaptic to cholinergic synapses with GlyR/-IR. This was approached by sequential detection of gephyrin (Fig. 2A1) and GlyR/ (Fig. 2A2) on motoneurons cultured alone for 7 DIV. We found that large gephyrin-IR clusters were not associated with GlyR/-IR, suggesting that gephyrin microdomains postsynaptic to cholinergic afferences do not recruit GlyR/ at this site. In contrast, many small, round-shaped clusters of gephyrin found at nonsynaptic loci colocalized with GlyR/-IR clusters of comparable size and shape.

View larger version (139K): [in this window] [in a new window]   Figure 2.   Simultaneous detection of gephyrin-IR (A1, A3, A5) and GlyR/-IR (A2, A4, A6) on motoneurons cultured alone for 7 DIV. Motoneurons display large and small, round-shaped Geph-IR clusters. Large Geph-IR clusters do not colocalize with GlyR/-IR (crossed arrows). Most (arrowheads) but not all (arrows) small Geph-IR clusters colocalize with GlyR/-IR clusters. Geph, Gephyrin-IR; GlyR/, GlyR/ subunits-IR. A1-2, Pairs of digitized images acquired with CCD camera (A1, FITC channel; A2, TRITC channel). A3-4, A5-6, Higher magnification of the plain and dotted outlined regions in A1-2, respectively. Scale bar: A1-2, 10 µm; A3-4, A5-6, 1.2 µm.

Our data indicate that in cultured motoneurons that do not receive glycinergic and GABAergic functional innervation, one can observe clusters of gephyrin, GlyR/, and GABA_AR2/3. Gephyrin accumulates in front of synaptic cholinergic boutons, and these postsynaptic gephyrin clusters hardly recruit GlyR/ and GABA_AR2/3 (for quantification, see Fig. 8).

Functional and pharmacological properties of GlyR and GABA_AR in motoneurons cultured alone

In an attempt to understand the different localizations of GlyRs and gephyrin in motoneurons cultured alone (in particular the absence of GlyRs at gephyrin-rich synaptic loci), we investigated the functional and pharmacological properties of the receptors of these cells. Glycine (applied at 10-320 µM by a fast perfusion system) evoked responses in all the motoneurons recorded in the whole-cell configuration of the patch-clamp technique (n > 50). A concentration-response curve obtained from a single motoneuron is illustrated in Figure 3A. The response (recorded here for an inward driving force of 20 mV only) was already detectable at 10 µM glycine. Raising the concentration increased the peak response and revealed some desensitization. For each cell in which a complete curve was obtained, the concentration dependence of the peak response was fitted by a Hill equation (Fig. 3A, right graph and legend). The EC₅₀, Hill coefficient (n_H), and maximum response (I_max) values thus derived were then averaged for two series of motoneurons (Fig. 3C, bars labeled MN1 and MN2; see legend); EC₅₀ and n_H were always close to 40 µM and 2, respectively. For comparison, identical experiments (Fig. 3B) were performed on cultured neurons from the whole spinal cord (spinal neuron). The physiological properties of neurons in both types of cultures were almost identical (Fig. 3C). For example, the mean EC₅₀ and n_H values found using internal solution A were 37.1 ± 7.4 µM (4) and 1.92 ± 0.19 (4) for purified motoneurons (MN2), and 38.3 ± 8.5 µM (6) and 2.25 ± 0.20 (6) for cultures of all spinal neurons (SN), respectively. The I_max values were more variable and usually slightly larger for purified motoneurons, which can be explained by their greater surface area.

View larger version (38K): [in this window] [in a new window]   Figure 3.   Comparison of the functional and pharmacological properties of GlyRs in cultures of purified motoneurons and all spinal neurons. A-C, Concentration-response curves in both types of cultures (purified motoneurons: A, C, bars labeled MN; cultures of all spinal neurons: B, C, bars labeled SN). The internal solution and membrane potential were solution A and 20 mV (A-C, bars labeled MN2 and SN) or solution B and 70 mV(C, bars labeled MN1). The left traces in A or B show superimposed current recordings obtained during successive applications of glycine at increasing concentrations (10-160 µM). The right graph in A or B (obtained from the corresponding left traces) shows for each cell the fit of the concentration dependence of the peak response by a Hill equation: y = Imax/(1 + (EC50/x)nH). The values and corresponding errors given by the computer for EC50, nH, and Imax for each of these cells were, respectively, 46.7 ± 3.4 µM, 1.92 ± 0.16 and 0.744 ± 0.035 nA in A, and 47.7 ± 0.9 µM, 2.16 ± 0.06 and 0.833 ± 0.011 nA in B. C, Mean values and SD for these three parameters, derived from several such experiments performed in different cells under identical conditions. D, Voltage dependence of the responses of purified motoneurons to glycine (internal solution A). Glycine (10 µM) was applied for 2 sec at different test potentials, using long voltage jumps from the holding potential (20 mV) toward the test potential (the voltage jump beginning 0.8 sec before each glycine application). Left graphs, Normalized I-V curves for three different motoneurons, obtained by dividing each glycine response by the response of the corresponding cell at 60 mV. Right traces, Records obtained in one of these cells during voltage jumps to 80 and +80 mV. E, Strychnine sensitivity of glycine responses (internal solution A, holding potential 20 mV). Left panel, Mean values of the percentage of inhibition of the peak glycine responses by strychnine (50 or 500 nM applied with preincubation) in cultures of purified motoneurons (white bars) and in cultures of all spinal neurons (hatched bars). The glycine concentration was either 40 µM (close to the EC50) or 100 µM. Middle panel, Effect of strychnine applied with preincubation first at 50 nM, then at 500 nM, on the response to glycine (40 µM) of a purified motoneuron (MN). Right panel, Effect of 500 nM strychnine, applied first without preincubation, then with preincubation, on the response to glycine (100 µM) in a culture of all spinal neurons (SN).

The voltage-sensitivity of glycine responses of motoneurons cultured alone was investigated. The I-V curves of the responses to 10 µM glycine obtained from three motoneurons with symmetrical chloride concentrations are illustrated in Figure 3D. As shown by the plot of the normalized responses of these cells and by the records obtained in one of them for two symmetrical driving forces, the voltage dependence was clearly nonlinear, favoring outward responses. The reversal potential was close to E_Cl (here 0 mV); this was confirmed in an experiment using asymmetrical chloride concentrations (internal solution B), bringing the reversal potential to 50 mV (data not shown).

The blocking effect of the classical GlyR antagonist strychnine was investigated in the two types of cultures. In motoneurons cultured alone, when strychnine was applied with preincubation (both between and during glycine applications) at either 50 or 500 nM, the peak responses to 40 µM glycine were reduced by 52.8 ± 5.3% (5) or 96.2 ± 1.1% (5), respectively (Fig. 3E, white bars and records labeled MN). The responses recorded in cultures of all spinal neurons showed a similar strong sensitivity to strychnine (Fig. 3E, hatched bars). For all neurons studied, when strychnine was applied without preincubation (i.e., only with glycine), its blocking effect was apparently much lower. This is illustrated for the effect of 500 nM strychnine on the response to 100 µM glycine in a culture of all spinal neurons (Fig. 3E, traces labeled SN), and the results were confirmed in four similar experiments (relatively small blockade between 21 and 44%). The requirement for preincubation with strychnine was confirmed in motoneurons cultured alone (the peak response to 40 µM glycine, which could be completely blocked by 500 nM strychnine with preincubation, was only reduced by 60 ± 11% (3) without preincubation).

Low sensitivity of glycine responses to picrotoxinin (PTX) is usually considered to be indicative of the presence of  subunits in functional heteromeric receptors (Pribilla et al., 1992; Pistis et al., 1997). Therefore, the blocking effect of a high concentration of PTX (100 µM, applied with preincubation) on the responses to glycine of motoneurons cultured alone was investigated. The responses to 40 µM glycine, recorded at 20 mV in four experiments with internal solution A, were reduced by only 44 ± 10%. In addition, the responses to 100 µM glycine, recorded between 30 and 90 mV in three other experiments with internal solution B, were reduced by only 26-28%, confirming the low sensitivity to PTX of GlyR in motoneurons.

In conclusion, the nonsynaptic GlyRs of motoneurons cultured alone retain the main pharmacological properties of the receptors found in cultures of all spinal neurons.

Cultured neurons from embryonic spinal cord (Ransom et al., 1977), as well as motoneurons from slices of embryonic or neonatal rat spinal cord (Gao and Ziskind-Conhaim, 1995), display chloride responses not only to glycine but also to GABA. The responses to 5 or 10 µM GABA were tested in motoneurons cultured alone (data not shown). Large responses of at least 0.8 nA were recorded for a driving force of only 20 mV (four cells). These responses were little affected (reduced by only 9.5 ± 7.6% in three experiments using 5 µM GABA) by a concentration of strychnine (500 nM applied with preincubation) that almost completely blocked glycine responses. In contrast, these GABA responses were almost completely blocked (result qualitatively confirmed in three cells) by a low concentration of bicuculline (10 µM) known to be ineffective on glycine responses (Lewis and Faber, 1993). Thus motoneurons cultured alone also display functional GABA_A receptors.

Cellular distribution of gephyrin, GlyR, and GABA_AR in motoneurons cocultured with dorsal root ganglia

Initially, embryonic DRG explants were added to purified motoneurons to provide a glutamatergic presynaptic innervation to motoneurons. To our surprise, we found that a large proportion of DRG neurons were GAD67-positive, indicating the presence of GABAergic neurons in the culture. These results were consistent with previous reports showing that embryonic (Roy et al., 1991; Chauvet et al., 1995) and adult (Schoenen et al., 1989; Roy et al., 1991; Chauvet et al., 1995) DRG neurons express a GABAergic phenotype. In our cultures, the colocalization of GAD67-IR puncta with synaptophysin-IR over Islet1-positive neurons indicate that DRG differentiate GABAergic synapses impinging on motoneurons. Gephyrin formed clusters on somata and neurites of motoneurons that accumulated in front of synapsin-IR profiles (Fig. 4A1-2). Most clusters of gephyrin were adjacent to GAD-positive boutons (Fig. 4B1-2), which were also synaptophysin positive (data not shown). Occasionally, gephyrin-IR clusters were detected in front of synaptophysin-positive but GAD-negative terminals (data not shown). On Islet1-positive motoneurons, GABA_AR2/3 were present in front of synapsin-positive boutons (Fig. 4C1-2); some clusters were also detected at nonsynaptic loci as described in vivo (Todd et al., 1996). Gephyrin was also detected at the level of GABA_AR3 clusters (Fig. 4D1-2). The GlyR/ staining pattern was identical to that observed on motoneurons cultured alone. GlyR/-IR clusters were present on the soma and along the length of the dendrites of motoneurons (Fig. 4E1). These GlyR/ clusters did not form under synapsin-positive varicosities (Fig. 4E1-2) or under GAD-IR blobs (Fig. 4F1-2). In some instances, a diffuse GlyR/-IR was observed over the soma and dendrites (Fig. 4F1).

View larger version (136K): [in this window] [in a new window]   Figure 4.   Gephyrin and GABAAR but not GlyR form postsynaptic clusters on motoneurons cocultured with DRG neurons. In all pairs of images, motoneurons are identified by the nuclear Islet1 staining. A, B, Geph-IR is concentrated in front of synapsin-IR boutons (arrowheads in A1-2) displaying GAD-IR (arrowheads in B1-2). C, D, GABAAR2/3 accumulate at synaptic (arrowheads in C1-2) and nonsynaptic loci (crossed arrow in C1-2). Geph-IR clusters colocalize with GABAAR3 clusters (arrowheads in D1-2). E, F, GlyR/ (E1, F1) form clusters (arrowheads) that are not adjacent to synapsin-IR (E1-2, crossed arrows) or GAD-IR (F1-2, crossed arrows) boutons. GABAAR2/3, GABAAR2/3 subunits-IR; GABAAR3, GABAAR3 subunits-IR; GAD, GAD67-IR; Geph, gephyrin-IR, GlyR/, GlyR/ subunits-IR; Isl, Islet1-IR; Syn, synapsin-IR. A1-A2, B1-B2, C1-C2, D1-D2, E1-E2, F1-F2, Pairs of digitized images acquired with CCD camera (A1, B1, C1, D1, E1, F1, TRITC channel; A2, B2, C2, D2, E2, F2, FITC channel). Scale bar, 10 µm.

These results again indicate that gephyrin accumulates under synaptic boutons, but when these boutons are GABAergic there is also a postsynaptic accumulation of GABA_AR2/3 but not of GlyR/.

Cellular distribution of gephyrin, GlyR, and GABA_AR in motoneurons cocultured with spinal interneurons

Dissociated spinal interneurons were cocultured with motoneurons to supply glycinergic and GABAergic innervation to motoneurons. In these cultures, motoneurons were identified by the Islet1 nuclear staining. At the somatic and dendritic surface, gephyrin, GlyR/, and GABA_AR2/3 formed numerous patches in front of synapsin-IR boutons (Fig. 5A1-2, B1-2, C1-2). A few synapsin-stained endings (Fig. 5A1-2, B1-2, C1-2, crossed arrows) did not colocalize with these receptor components; they may correspond to excitatory synapses (O'Brien et al., 1997). These data indicate that gephyrin, GlyR/, and GABA_AR2/3 clusters present at the periphery of motoneurons innervated by spinal interneurons face synaptic boutons.

View larger version (120K): [in this window] [in a new window]   Figure 5.   Gephyrin, GlyR, and GABAAR distribution on motoneurons cocultured with spinal neurons. In all pairs of images, motoneurons are identified by the nuclear Islet1 staining. A-C, Accumulation of Geph (A2), GlyR/ (B2), and GABAAR2/3 (C2) in front of most (arrowheads) but not all (crossed arrows) synapsin-IR boutons (A1, B1, C1). D-F, Double-staining of GAD (D1, E1, F1) and Geph (D2); GlyR/ (E2) or GABAAR2/3 (F2) show closely apposed signals (arrowheads). Some Geph and GlyR/ spots are not adjacent to GAD-IR boutons (crossed arrows in D1-2, E1-2, respectively). G, H, Double-immunofluorescence showing that most GABAAR3-IR spots (arrowheads in G1, H1) are associated with Geph-IR (G2) and GlyR/-IR (H2) clusters. Few Geph-IR clusters do not colocalize with GABAAR3-IR (crossed arrows in G1-2). GABAAR2/3, GABAAR2/3 subunits-IR; GABAAR3, GABAAR3 subunits-IR; GAD, GAD67-IR; Geph, gephyrin-IR; GlyR/, GlyR/ subunits-IR; Isl, Islet1-IR; Syn, synapsin-IR. A1-A2, B1-B2, C1-C2, D1-D2, E1-E2, F1-F2, G1-G2, H1-H2, Pairs of digitized images acquired with CCD camera (A1, B1, C1, D1, E1, F1, G1, H1, FITC channel; A2, B2, C2, D2, E2, F2, G2, H2, TRITC channel). Scale bar, 10 µm.

Previous reports have shown that in the ventral horn of the spinal cord in vivo, boutons containing both glycine and GABA are presynaptic to gephyrin-IR synapses (Triller et al., 1987; Todd et al., 1996; Colin et al., 1998) and that corelease of these two neurotransmitters occurs (Jonas et al., 1998). Furthermore, some GABA_AR and GlyR clusters are colocalized in front of GABAergic terminals (Bohlhalter et al., 1994; Todd et al., 1996). The relationship of gephyrin, GlyR/, and GABA_AR2/3 to GABAergic axons was therefore analyzed. Gephyrin (Fig. 5D2) and GlyR/ (Fig. 5E2) clusters were often apposed to GAD-positive terminals (Fig. 5D1, E1). However, gephyrin and GlyR/ clusters were not always adjacent to GAD-IR profiles, suggesting that some of them are apposed to boutons enriched in glycine only. In contrast, all somato-dendritic GABA_AR2/3-IR clusters detected on motoneurons were apposed to GAD-IR boutons (Fig. 5F1-2). Simultaneous experiments in which GABA_AR3 was detected with gephyrin or with GlyR/ indicated that most but not all GABA_AR3-IR clusters were also immunoreactive for gephyrin (Fig. 5G1-2) or GlyR/ (Fig. 5H1-2). This raised the question regarding whether gephyrin is able to accumulate receptors other than GlyR and GABA_AR. This was determined by examining the cellular distribution of the GluR1 subunit of AMPA receptors on neurons cultured for 11 DIV (Fig. 6). The large majority of gephyrin clusters did not colocalize with GluR1 clusters (Fig. 6A1-2). However, we found that 9.8 ± 2.2% (10 cells for a total of 422 gephyrin clusters) of gephyrin clusters were associated with GluR1-IR. Similarly, most GlyR/ clusters were not stained for GluR1 clusters (Fig. 6B1-2). However, 8.0 ± 1.5% (10 cells for a total of 713 GlyR/ clusters) of GlyR/ clusters colocalized with GluR1-IR. For this quantification, we selected neurons with large numbers of GluR1 clusters. Interestingly, these neurons had a lower count of gephyrin and GlyR clusters.

View larger version (105K): [in this window] [in a new window]   Figure 6.   Comparison of GluR1-IR with gephyrin- or GlyR/-IR clusters on spinal interneurons. Spinal neurons immunolabeled at 11 DIV for GluR1 (A1, B1) and Geph (A2) or GlyR/ (B2). Most Geph- or GlyR/-IR (arrowheads) and GluR1-IR (crossed arrows) do not colocalize. Few Geph- and GlyR/-IR clusters colocalized with GluR1-IR (arrows). Geph, gephyrin-IR; GluR1, glutamate receptor subunit GluR1; GlyR/, GlyR/ subunits-IR. A1-A2, B1-B2, Pairs of digitized images acquired with CCD camera (A1, B1, FITC channel; A2, B2, TRITC channel). A3-4, B3-4, Higher magnification of a region outlined in A1-2, B1-2, respectively. Scale bar, A1-2, B1-2, 10 µm; A3-4, B3-4, 2.5 µm.

These data indicate that gephyrin, GABA_AR2/3, and GlyR/ can be detected at the same synapse on motoneurons apposed to GABAergic terminals. Some synapses had only one of these two receptors. Few gephyrin-IR synapses were associated with a noninhibitory receptor subunit, i.e., GluR1.

Quantification of gephyrin, GlyR, and GABA_AR-IR

The proportion of cells displaying immunoreactivity for gephyrin, GlyR/, and GABA_AR3 was determined at 7 DIV on motoneurons cultured alone or with spinal interneurons (Table 1). The immunoreactivity corresponding to GlyR/ and GABA_AR3 was present at the neuronal surface and had a clustered or diffuse distribution. The latter could only be observed when motoneurons were cultured alone. Diffuse staining of gephyrin was never observed on motoneurons cultured alone, therefore indicating that diffuse GlyR/ and GABA_AR3 are not associated with gephyrin. We found that the percentage of motoneurons displaying immunoreactivity for either gephyrin or GABA_AR3 increased when interneurons were added to the culture. In contrast, the presence of interneurons in the culture decreased the number of motoneurons with GlyR/-IR.

View this table: [in this window] [in a new window]   Table 1.   Percentage of motoneurons with gephyrin, GlyR/, and GABAAR3 immunoreactivity

The mean surface areas of gephyrin, GlyR/, and GABA_AR3 clusters were determined at 7 DIV on maximum intensity projections of a series of confocal sections spanning the whole thickness of the neuronal somata. The quantifications were performed on motoneurons cultured alone or with interneurons and on interneurons of the latter coculture (Table 2). We found that the presence of interneurons increased significantly the surface area of GlyR/, GABA_AR3, and gephyrin clusters on motoneurons. On motoneurons cultured alone for 7 DIV, most GlyR/ and GABA_AR2/3 clusters were nonsynaptic, but when cultured with interneurons they were detected in front of synaptic contacts (see Fig. 8). The GlyR/, GABA_AR3, and gephyrin clusters were slightly but significantly smaller on motoneurons cultured with interneurons than on interneurons themselves.

View this table: [in this window] [in a new window]   Table 2.   Quantification of GlyR/, GABAAR3, and gephyrin clusters surface areas (µm2)

The proportion of synapses apposed to gephyrin, GlyR/, or GABA_AR2/3 clusters and the proportion of nonsynaptic clusters were quantified on images collected with a CCD camera and are shown for motoneurons cultured alone for 3, 7, and 11 DIV (Fig. 7). Whether or not the gephyrin-, GlyR/-, and GABA_AR2/3-IR were adjacent to synapsin-IR, the proportion of apposition varied depending on the nature of the postsynaptic marker and stage of maturation (Fig. 8). The same analysis was performed on motoneurons cultured with interneurons (data not shown). The mean number of synaptic boutons increased significantly at the surface of motoneurons cultured with or without interneurons during maturation, indicating a progressive establishment of synaptic connections (Table 3). The mean numbers of gephyrin, GlyR/, or GABA_AR2/3 clusters per cell were not significantly different on motoneurons cultured alone, regardless of the stage in culture. In contrast, when motoneurons were cocultured with interneurons, the mean numbers of gephyrin, GlyR/, or GABA_AR2/3 clusters per cell increased significantly during the formation of synaptic contacts (between 3 and 7 DIV). On motoneurons cultured with interneurons, the number of gephyrin clusters was much smaller than the sum of GlyR/ and GABA_AR2/3 clusters. This indicates that a large proportion of postsynaptic aggregates were composed of mosaics of receptors, as already seen by double-labeling experiments (Fig. 5G1-2, H1-2). The level of synaptic localization of the postsynaptic markers was further quantified on motoneurons cultured alone (Fig. 8A1-3) or in the presence of interneurons (Fig. 8B1-3). When motoneurons were cultured alone, the proportion of synapses showing gephyrin clusters was already high (77.7 ± 6.5%) at 3 DIV and varied little until 11 DIV (90.1 ± 3.1%), whereas the proportion of nonsynaptic gephyrin clusters per cell decreased progressively during maturation (Fig. 8A1). In contrast, only 9-14% of synapses formed between motoneurons were apposed to GlyR/ clusters at any of the stages analyzed, and the proportion of nonsynaptic clusters decreased slightly between 7 and 11 DIV (Fig. 8A2). The percentage of synapses with GABA_AR2/3 clusters increased slightly during maturation to 36.1 ± 3.9% at 11 DIV, whereas that of nonsynaptic GABA_AR2/3 clusters decreased in parallel (Fig. 8A3). The scheme was different when motoneurons were cocultured with interneurons. The proportion of synapses showing gephyrin clusters increased significantly between 3 and 7 DIV and then remained stable until the end of the experiment, whereas the proportion of nonsynaptic gephyrin clusters decreased dramatically between 3 and 7 DIV (Fig. 8B1). The evolution of the level of synaptically and nonsynaptically localized GlyR/ (Fig. 8B2) and GABA_AR2/3 (Fig. 8B3) clusters was a mirror image of what was found on motoneurons cultured alone.

View larger version (86K): [in this window] [in a new window]   Figure 7.   Relationships during in vitro maturation of gephyrin, GlyR, and GABAAR with synaptic terminals on motoneurons cultured alone. Motoneurons double-stained for synapsin and gephyrin (A1-2, B1-2, C1-2), synapsin and GlyR/ (D1-2, E1-2, F1-2), and synapsin and GABAAR2/3 (G1-2, H1-2, I1-2) at 3, 7, and 11 DIV (left, middle, and right columns, respectively). A-C, At 3 DIV, Geph-IR clusters accumulate in front of most but not all synaptic boutons. Numerous Geph-IR clusters are also detected at nonsynaptic loci. At 7 and 11 DIV, the number of postsynaptic Geph-IR clusters increased, and the number of nonsynaptic Geph-IR clusters decreased. D-F, At all stages, most GlyR/ clusters are detected at nonsynaptic sites. G-I, At 3 and 7 DIV, few GABAAR2/3 clusters are in front of synapsin-IR terminals. Their number increases at 11 DIV. Arrows, Apposed synapsin and postsynaptic markers (Geph, GlyR/, or GABAAR2/3); crossed arrows, presence of synapsin-IR but not of the above-mentioned postsynaptic markers; arrowheads, presence of Geph-, GlyR/-, or GABAAR2/3-IR clusters without adjacent synapsin-IR. GABAAR2/3, GABAAR2/3 subunits-IR; Geph, gephyrin-IR; GlyR/, GlyR/ subunits-IR; Syn, synapsin-IR. A1-A2, B1-B2, C1-C2, D1-D2, E1-E2, F1-F2, G1-G2, H1-H2, I1-I, Pairs of digitized images acquired with CCD camera (A1, B1, C1, D1, E1, F1, G1, H1, I1, FITC channel; A2, B2, C2, D2, E2, F2, G2, H2, I2, TRITC channel). Scale bar, 10 µm.

View larger version (36K): [in this window] [in a new window]   Figure 8.   Quantifications of the synaptic localization of gephyrin, GlyR, and GABAAR on motoneurons cultured alone (A1-3) or with spinal interneurons (B1-3). In each case, the open bars give the proportion of synapses with the indicated postsynaptic IR (Gephyrin, GlyR/, or GABAAR2/3), and the filled bars give the proportion of nonsynaptic clusters per cell. Gephyrin, GlyR/, and GABAAR2/3 clusters were classified as synaptic when adjacent to synapsin-IR. Results are means (± SEM) from 10-18 cells. The levels of significance (ANOVA, Scheffé F test) are indicated by one (p < 0.05), two (p < 0.01), or three (p < 0.001) symbols. , Significance between 3 and 7 DIV; ¥, significance between 7 and 11 DIV; $, significance between 3 and 11 DIV.

View this table: [in this window] [in a new window]   Table 3.   Quantifications of the mean numbers of synapses and of gephyrin, GlyR, and GABAAR clusters per cell during in vitro maturation

These data suggest that the presynaptic glycinergic and/or GABAergic innervation supplied by interneurons (1) increases the number, size, and synaptic localization of GlyR/, GABA_AR2/3, and gephyrin clusters and (2) controls negatively the number of nonsynaptic clusters of receptors.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Role of presynaptic innervation in the formation of GlyR and GABA_AR microdomains

The role of presynaptic innervation in the formation of postsynaptic clusters was investigated on motoneurons cultured alone, with DRG, or with spinal interneurons. On motoneurons cultured alone, GlyR/ and GABA_AR2/3 formed nonsynaptic clusters. Therefore, clustering is independent of the corresponding presynaptic innervation, a situation comparable to that found in muscle (Kuromi and Kidokoro, 1984). Some motoneurons also expressed large patches of diffuse GlyR/ and GABA_AR3. GlyR and GABA_AR-IR were present on the somato-dendritic compartment, suggesting that targeting of receptors does not depend on innervation.

When motoneurons were contacted by GABAergic boutons, GABA_AR2/3 accumulated in front of these boutons, and the nonsynaptic GABA_AR3 disappeared. Nonsynaptic GlyR