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Volume 17, Number 17, Issue of September 1, 1997 pp. 6534-6544
Copyright ©1997 Society for Neuroscience

Neural Agrin Induces Ectopic Postsynaptic Specializations in Innervated Muscle Fibers

Thomas Meier1, Dominik M. Hauser3, Matthias Chiquet4, Lukas Landmann2, Markus A. Ruegg3, and Hans R. Brenner1

Institutes of 1 Physiology and 2 Anatomy and 3  Biozentrum, University of Basel, CH-4051 Basel, Switzerland, and 4 Maurice E. Müller Institute for Biomechanics, University of Berne, CH-3010 Berne, Switzerland

ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
FOOTNOTES
REFERENCES

ABSTRACT

Neural agrin, in the absence of a nerve terminal, can induce the activity-resistant expression of acetylcholine receptor (AChR) subunit genes and the clustering of synapse-specific adult-type AChR channels in nonsynaptic regions of adult skeletal muscle fibers. Here we show that, when expression plasmids for neural agrin are injected into the extrasynaptic region of innervated muscle fibers, the following components of the postsynaptic apparatus are aggregated and colocalized with ectopic agrin-induced AChR clusters: laminin-beta 2, MuSK, phosphotyrosine-containing proteins, beta -dystroglycan, utrophin, and rapsyn. These components have been implicated to play a role in the differentiation of neuromuscular junctions. Furthermore, ErbB2 and ErbB3, which are thought to be involved in the regulation of neurally induced AChR subunit gene expression, were colocalized with agrin-induced AChR aggregates at ectopic nerve-free sites. The postsynaptic muscle membrane also contained a high concentration of voltage-gated Na+ channels as well as deep, basal lamina-containing invaginations comparable to the secondary synaptic folds of normal endplates. The ability to induce AChR aggregation in vivo was not observed in experiments with a muscle-specific agrin isoform. Thus, a motor neuron-specific agrin isoform is sufficient to induce a full ectopic postsynaptic apparatus in muscle fibers kept electrically active at their original endplate sites.

Key words: neuromuscular junction; MuSK; utrophin; rapsyn; laminin-beta 2; agrin beta -dystroglycan; ErbB receptor; acetylcholine receptor; sodium channel

INTRODUCTION

During the development of the neuromuscular junction (NMJ) a small region of the skeletal muscle fiber differentiates under the control of the motor neuron to form a postsynaptic apparatus. This structure is highly specialized in morphology and molecular composition and is thought to serve the stable aggregation of a high density of acetylcholine receptors (AChRs) in the synaptic muscle membrane (Fallon and Hall, 1994; Apel and Merlie, 1995; Carbonetto and Lindenbaum, 1995) and to induce the synthesis of a synapse-specific AChR subtype containing an epsilon -subunit (Brenner at al., 1990; Sanes et al., 1991).

Proteins of the postsynaptic apparatus implicated in the aggregation of AChRs include utrophin, a synapse-specific homolog of dystrophin (Ohlendieck et al., 1991; Bewick et al., 1992; Tinsley et al., 1992, 1994), alpha - and beta -dystroglycan (Ibraghimov-Beskrovnaya et al., 1992; Fallon and Hall, 1994), and rapsyn (Frail et al., 1988; Apel et al., 1995), thought to link AChRs to the cytoskeleton. Several lines of evidence indicate that the redistribution of AChRs to form postsynaptic aggregates is triggered by the protein agrin, a component of the synaptic basal lamina (BL; McMahan, 1990). Consistent with this hypothesis, bath-applied agrin induces in cultured myotubes the accumulation of AChRs and other molecules associated with normal NMJs (Wallace, 1989), and, in mice carrying a mutated agrin gene, muscle fibers fail to form functional endplates (Gautam et al., 1996). Agrin is characterized by alternatively spliced sites, termed A and B (y and z in rat agrin; Rupp et al., 1992) at the C-terminal end and, in the chick, the NtA domain at the N-terminal part (Ruegg et al., 1992; Denzer et al., 1995). In vitro, the most potent AChR-aggregating isoform of agrin is expressed by motor neurons and contains a four amino acid insert at the A splice site and an eight amino acid insert at the B splice site. In contrast, little or no AChR-aggregating activity is observed with the agrin isoform that lacks inserts at sites A and B and is expressed predominantly by non-neuronal cells, including muscle (for review, see Bowe and Fallon, 1995).

The AChR-aggregating function of agrin requires the synapse-specific receptor tyrosine kinase MuSK, which is tyrosine-phosphorylated by agrin isoforms active in AChR aggregation (Valenzuela et al., 1995; DeChiara et al., 1996; Glass et al., 1996). Similarly, phosphorylation of the AChR beta -subunit seems to be required for agrin-induced AChR aggregation (Wallace et al., 1991; Meier et al., 1995, 1996).

The synthesis of adult AChRs at the synapse in electrically active muscle is maintained by a factor that also is bound to the synaptic BL (Brenner et al., 1992; Jo and Burden, 1992; Herczeg et al., 1995). By inducing ectopic secretion of neural agrin from muscle fibers in vitro and in vivo, we have shown recently that neural agrin, immobilized presumably by attachment to the extracellular matrix, is sufficient to induce ectopic adult-type AChR aggregates (Jones et al., 1996, 1997). Given the functional similarities of ectopic agrin-induced AChR clusters to AChRs at normal mature endplate membrane, we now show that the neural agrin isoform cAgrin7A4B8 (Denzer et al., 1995) also induces the localized expression of structural components characteristic of a normal postsynaptic apparatus. In contrast, cAgrin7A0B0, an isoform lacking AChR-aggregating activity on cultured myotubes, failed to induce ectopic AChR aggregates in vivo. We propose that neural agrin alone is sufficient to induce all aspects of functional and structural postsynaptic differentiation in vivo and that this activity is restricted to agrin isoforms that normally are expressed by motor neurons.

MATERIALS AND METHODS

Agrin plasmids and muscle fiber injections. Full-length chick agrin constructs cAgrin7A4B8 and cAgrin7A0B0 (Denzer et al., 1995) and green fluorescence protein (GFP) were cloned into pcDNAI (Invitrogen, San Diego, CA), dissolved at 200 ng/µl in 150 mM KCl containing Fast Green FCF (25 mg/ml; Sigma, St. Louis, MO), back-filled into micropipettes, and pressure-injected under electrophysiological control into to the proximal endplate-free region of single soleus muscle fibers in rats anesthetized with Nembutal (1 ml/kg) (Jones et al., 1997). After the surgical cut was closed, animals were kept for 7 weeks. Injected soleus muscles remained innervated during the entire period. For analysis, excised soleus muscles were stained for AChR with rhodamine-alpha -bungarotoxin (Rh-alpha BGT; Molecular Probes, Eugene, OR) or for agrin with a polyclonal anti-chicken agrin antiserum (Gesemann et al., 1995) and BODIPY-conjugated goat anti-rabbit IgG (Molecular Probes). In some experiments the sciatic nerve was cut, and the soleus muscle was removed after 4 d. To obtain regenerated muscle preparations, we injected denervated rat soleus muscle with Notexin, and their endplate region was frozen 2 d later (Brenner et al., 1992). Unstimulated muscles were allowed to regenerate for 20 d. For analysis, all muscles were quick-frozen in prechilled isopentane and cryocut into 12 µm sections.

Immunohistochemistry and antibodies. Unfixed sections were rinsed briefly with PBS and preincubated for 5-10 min in PBS supplemented with 5% horse serum, 1% bovine serum albumin, and 0.1% Triton X-100. The following primary antibodies were diluted in 5% horse serum, 1% bovine serum albumin, and 0.01% Triton X-100 in PBS, as indicated in the references or data sheets, and sections were incubated for 2 hr at room temperature: anti-chick agrin (Reist et al., 1987), monoclonal antibody (mAb) 5B1; anti-rat agrin (Hoch et al., 1994), mAb AGR-435 (StressGen number 550); anti-laminin-beta 2 (Sanes et al., 1990), mAb C4; anti beta -dystroglycan (Bewick et al., 1992), mAb 8D5 (NovoCastra, Newcastle, UK); anti-utrophin (Bewick et al., 1992), mAb DRP1/12B6 (NovoCastra); anti-rapsyn (Froehner, 1984), mAb 1234; anti-phosphotyrosine, mAb 4G10 (Upstate Biotechnology); anti-ErbB2/Neu, Ab C-18 (Santa Cruz Biotechnology, Dr. Glaser AG, Switzerland); and anti-ErbB3, Ab C-17 (Santa Cruz Biotechnology); and anti-sodium channel (Dugandzija-Novakovic et al., 1995), polyclonal serum (Upstate Biotechnology, Lake Placid, NY). As control, anti-Na+ channel antibodies were preabsorbed with the peptide antigen as described (Dugandzija-Novakovic et al., 1995). For detection, FITC-labeled goat anti-mouse or goat anti-rabbit IgG (Jackson ImmunoResearch, West Grove, PA) was used. For triple staining, sections were photographed for Rh-alpha BGT labeling and reincubated with anti-chick agrin mAb 5B1, followed by Cy3-conjugated secondary antibody (Molecular Probes). This labeling was very intense and required an ~10 times shorter exposure time for documentation than the Rh-alpha BGT signal. To increase the sensitivity for the detection of ErbB2 and ErbB3 primary antibodies, we used unconjugated goat anti-rabbit IgG (Cappel, Cochranville, PA), followed by FITC-conjugated rabbit anti-goat IgG (Jackson ImmunoResearch). Immunofluorescence micrographs were taken on a Zeiss Axiophot microscope (Oberkochen, Germany) equipped with appropriate fluorescence filter sets.

Expression construct encoding the extracellular domain of Nsk2, the mouse homolog to MuSK. PCR was conducted according to the manufacturer's advice with Pwo-polymerase (Boehringer Mannheim, Mannheim, Germany). To distinguish expression constructs and recombinant protein, cDNA constructs are named with the prefix p, followed by the name of the recombinant protein they encode. PCR reactions were conducted on partial cDNA clones (provided by Dr. A. D. Reith, Ludwig Institute for Cancer Research, London, UK) encoding the extracellular domain of Nsk2 (Ganju et al., 1995). PCR products were ligated into pcDNAI (Invitrogen) containing a tag consisting of the constant region of mouse immunoglobulin (Fc), which was generated by restriction digestion of pcN257Fc (Denzer et al., 1997) with EcoRI and BamHI. The resulting construct, pNsk2Fc, was digested with EcoRI and XbaI restriction endonucleases and ligated into EcoRI/XbaI cut pcINEO expression vector (Promega, Madison, WI), giving rise to pINNsk2Fc. All PCR products used to generate expression constructs were sequenced to ensure that no mutations were introduced by DNA amplification.

Culturing and transfection of COS-7 and human embryonic kidney (HEK) 293 cells. COS-7 (Gluzman, 1981) cells were cultured in DMEM (Life Technologies, Gaithersburg, MD) supplemented with 10% newborn calf serum, 10 mM sodium pyruvate, 100 U/ml penicillin, and 100 µg/ml streptomycin. COS-7 cells were transiently transfected with pNsk2Fc, using the DEAE-dextran-based method (Cullen, 1987). HEK 293 cells were cultured in the same medium as described above and stably transfected with pINNsk2Fc according to Gorman et al. (1990). Stably transfected HEK 293 cells were selected with G418 (800 µg/ml), and surviving colonies were picked and stained intracellularly with FITC-conjugated goat anti-mouse IgG (Jackson ImmunoResearch). Colonies expressing high levels of recombinant Nsk2Fc were cloned subsequently by limited dilution.

Purification of recombinant Nsk2Fc. Transiently transfected COS-7 cells or stably transfected HEK 293 cells were grown in medium, as described above, in which the newborn calf serum was replaced by IgG-depleted fetal calf serum (Life Technologies). Supernatants usually were collected 3-6 d after transfection, and the conditioned medium was incubated with protein A-Sepharose (Pharmacia). The Sepharose beads were washed with 25 vol of 0.1 M sodium phosphate, pH 7.5. Column-bound proteins were eluted with 10 vol of 0.1 M glycine, pH 3.5. Fractions of 1.5 ml were collected and buffered immediately with 35 µl of 1 M Tris-HCl, pH 8.0. Aliquots of each fraction were analyzed on 10% SDS-PAGE, and proteins were visualized by silver staining (Morrisey, 1981). Fractions with high concentrations of Nsk2Fc were pooled and dialyzed three times against 1.5 l of PBS. Fractions with low concentration of Nsk2Fc were concentrated with the Centriplus concentrator (Amicon, Beverly, MA). Nsk2Fc concentration was determined according to Lowry et al. (1951) with the DC Protein assay kit (Bio-Rad Laboratories, Glattbrugg, Switzerland) and BSA as a standard. Furthermore, the relative intensity of Nsk2Fc and of known amounts of BSA was compared on silver-stained gels as an independent measure.

Anti-Nsk2 extracellular domain sera (anti-Nsk2Fc). Polyclonal antisera were raised in rabbits by injecting protein A-Sepharose-purified Nsk2Fc. For the first injection 70 µg of protein in complete Freund's adjuvant was used. For booster injections in 4-8 wk intervals, the same amount of Nsk2Fc was dissolved in incomplete Freund's adjuvant. This antiserum is referred to as anti-MuSK/Nsk2 to indicate the homology of MuSK cloned from Torpedo, human, rat, and chicken (Jennings et al., 1993; Valenzuela et al., 1995; DeChiara et al., 1996; Glass et al., 1996) with Nsk2 cloned in mouse (Ganju et al., 1995).

Electron microscopy. Plasmid-injected muscle was excised and fixed with 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer, pH 7.4, for 24 hr. Fixed muscle was stained for acetylcholinesterase (AChE) activity according to Koelle and Friedenwald (1949). Normal endplates as well as stained regions induced by ectopic agrin expression were identified under a dissecting microscope. Pieces of tissue (1-3 mm3) were cut from these areas and post-fixed overnight with 2% osmium tetroxide in 0.1 M sodium cacodylate buffer, pH 7.4. Tissue blocs were dehydrated with ethanol and propylene oxide and embedded in Epon; 1-µm-thick longitudinal sections were prepared. Semithin sections were counterstained with toluidine blue and inspected for AChE staining. Then ultrathin sections were prepared from positive areas, stained with uranylacetate and lead citrate, and viewed in a Hitachi 7100 electron microscope.

RESULTS

Rat muscle fibers were induced to express the neural chicken agrin isoform cAgrin7A4B8 in their extrasynaptic region by intracellular injection of expression plasmids (Jones et al., 1997). In culture, recombinant cAgrin7A4B8 is capable of inducing AChR aggregates, and it binds to the BL component laminin (Denzer et al., 1997). On its secretion from the injected fibers, such agrin presumably became attached to extracellular matrix. Each site secreting agrin was associated, both in the injected as well as in adjacent fibers, with ectopic nerve-free clusters of AChRs. We have shown previously that they contain synapse-specific adult-type AChR channels (Jones et al., 1997). Close inspection of agrin-expressing sites showed that agrin immunoreactivity on the fiber surface extended over a distance of approximately three to five fiber diameters. Within the agrin-positive regions, smaller but stronger deposits of agrin often were seen that closely matched AChR clusters (see, for example, Fig. 8A). Thus, although AChR clusters were always associated with agrin-secreting sites, they did not extend over the entire length of the deposit. As with normal endplates, the agrin-induced ectopic AChR clusters were resistant to electrical muscle activity, because the fibers were innervated during the entire time of the experiment, i.e., up to 7 weeks. AChR clusters were absent from the noninjected regions distant from the injection sites (data not shown).
Fig. 8. The induction of ectopic synapse-like specializations by agrin depends on the presence of amino acid inserts at the A and B splice sites. Shown are en face views of superficial rat soleus muscle fibers stained for agrin and AChRs after injection of cAgrin7A4B8 (A, B) and cAgrin7A0B0 (C, D) expression plasmids, respectively. Live muscle was stained for ectopically expressed agrin (A, C) and AChRs (B, D). Expression of cAgrin7A4B8, but not cAgrin7A0B0, induces the expression of ectopic AChR aggregates. Note that the distribution of agrin7A4B8 labeling exceeds the distribution of ectopic AChRs (arrow in A). Scale bar, 50 µm.
[View Larger Version of this Image (86K GIF file)]

To investigate whether cAgrin7A4B8 is sufficient to induce a postsynaptic apparatus that is also structurally similar to that of normal endplates, we have conducted a detailed study on the molecules assembled at ectopic agrin-induced AChR clusters. To this end, sites of cAgrin7A4B8 expression in rat soleus muscle were localized by staining the entire muscle with rhodamine-labeled alpha -bungarotoxin (Rh-alpha BGT). Sections subsequently were stained for chick agrin and the endogenous rat agrin. As shown in Figure 1A, cAgrin7A4B8 was not confined to the surface of the injected fiber but was associated also with adjacent fibers, and at such deposits AChR aggregates were found (Fig. 1B; see also Fig. 8A,B). However, agrin deposits extended further along the fiber circumferences than did AChR clusters. The anti-chick agrin antibodies did not cross-react with rat agrin present at the original, normal endplates of the muscle (Fig. 1C,D). Conversely, the mAb 435 (Hoch et al., 1994), while staining rat agrin at original endplates (Fig. 1G,H), did not stain ectopic chick agrin deposits (Fig. 1E,F). These results suggest that AChR aggregation at ectopic sites in adult muscle fibers is not accompanied by a significant accumulation of muscle (rat) agrin.

Fig. 1. Intracellular injection of cDNA constructs encoding neural chick agrin into the endplate-free region of rat soleus muscle induces the aggregation of AChRs, but not of (muscle) rat agrin. Individual muscle fibers were injected with an expression plasmid encoding cAgrin7A4B8 at extrasynaptic regions (top). Analysis of sections from ectopic sites revealed that regions expressing chick agrin (A) contained ectopic AChR aggregates (B). Note that there is no obvious correlation between the amount of expressed chick agrin and aggregated AChRs, because both regions with strong chick agrin expression (arrows) as well as regions with much weaker agrin expression, possibly at neighboring fibers, induced the accumulation of AChRs. Antibodies raised against chick agrin did not cross-react with rat agrin, because original endplates were not stained (C, D). With the use of a monoclonal antibody specific for rat agrin (Hoch et al., 1994), endogenous muscle agrin was not detected at AChR-positive sites induced by ectopic chick agrin (E, F). The same antibody, however, stained rat agrin at original endplates (G, H). Scale bar, 35 µm.
[View Larger Version of this Image (49K GIF file)]

Ectopic agrin induces accumulation of several synaptic proteins

Normal endplates are characterized by the accumulation of specific molecules in the postsynaptic apparatus of the muscle fiber. In synaptic BL, these components include, in addition to agrin and AChE, a laminin isoform containing the beta 2 chain (Hunter et al., 1989; Sanes et al., 1990). We have shown previously that AChE activity is tightly colocalized with agrin-induced ectopic AChR clusters (Jones et al., 1997). Full-length cAgrin7A4B8 binds to laminin-beta 2 (Denzer et al., 1997) and to alpha -dystroglycan (Bowe et al., 1994; Campanelli et al., 1994; Gee et al., 1994; Sugiyama et al., 1994; Gesemann et al., 1996). We therefore asked whether cAgrin7A4B8 would induce accumulation of laminin-beta 2 or dystroglycans at ectopic AChR aggregates. As shown in Figure 2, laminin-beta 2 clearly was enriched at ectopic AChR clusters. Similarly, beta -dystroglycan, which originates from the same precursor protein as alpha -dystroglycan and remains strongly associated with it (for review, see Henry and Campbell, 1996), and the cytoplasmic NMJ-specific utrophin also were colocalized at AChR aggregates (Fig. 2). As with normal endplates (data not shown), the distribution of laminin-beta 2 and utrophin was confined almost entirely to AChR aggregates, whereas beta -dystroglycan merely was enriched at such sites. The ectopic AChR clusters were also positive for the binding sites recognized by the lectin Vicia villosa-B4 agglutinin (VVA-B4; data not shown). Such N-acetylgalactosaminyl-terminated saccharides have been proposed to play a role in agrin-mediated AChR clustering (Martin and Sanes, 1995).
Fig. 2. Expression of chick neural agrin in extrasynaptic regions causes the accumulation of synapse-specific components of the extracellular matrix and the dystrophin-associated glycoprotein complex in muscle membrane. Staining for laminin-beta 2 (A) and utrophin (E) are colocalized with ectopic AChR aggregates (B, F). In contrast, beta -dystroglycan (C, arrows) is present throughout the myofiber circumference but is increased at ectopic AChR aggregates (D, arrows). The distribution of all three molecules with respect to AChR clusters is similar to that of original nerve-induced endplates. Scale bar, 35 µm.
[View Larger Version of this Image (67K GIF file)]

Agrin-induced tyrosine phosphorylation of AChRs and their interaction with rapsyn reduce their lateral mobility and seem to be required for agrin-induced receptor aggregation. To see whether the agrin-induced aggregation of AChRs at ectopic sites might follow a similar mechanism, we double-stained Rh-alpha BGT-labeled ectopic receptors with antibodies for rapsyn and phosphotyrosine (Fig. 3). As with normal endplates, AChR aggregates induced by extrasynaptically expressed agrin also stained for rapsyn and tyrosine-phosphorylated proteins. Thus, secretion of cAgrin7A4B8 from innervated muscle fibers at ectopic sites is sufficient to induce the colocalized accumulation of specific components at three different levels of normal endplates: muscle BL, membrane, and cytoplasm.

Fig. 3. Colocalization of rapsyn and phosphotyrosine with AChR aggregates induced by ectopic neural chick agrin. Staining for rapsyn (A) and phosphotyrosine-containing proteins (P-Tyr; C) is colocalized with ectopic AChR aggregates (B, D). Scale bar, 35 µm.
[View Larger Version of this Image (84K GIF file)]

The receptor tyrosine kinase MuSK colocalizes with cAgrin7A4B8

The muscle-specific receptor tyrosine kinase, MuSK, is required for the formation of the NMJ. Several lines of evidence indicate that MuSK is part of a signal-transducing receptor complex activated by agrin (Glass et al., 1996). In innervated muscle MuSK is concentrated at synapses, whereas after denervation it is expressed along the entire length of the muscle fiber (Valenzuela et al., 1995). To study the distribution of MuSK in injected rat muscle, we generated a polyclonal serum specific for the extracellular domains of Nsk2, the mouse homolog of MuSK. This antiserum recognized Nsk2 in cultured C2C12 myotubes (data not shown), and it stained normal rat endplates (Fig. 4A,B). No staining was observed with the preimmune serum (Fig. 4C,D) or the secondary antibody alone (data not shown). Expression of cAgrin7A4B8 in extrasynaptic regions clearly induced MuSK/Nsk2 protein. All of the ectopic AChR clusters were also MuSK/Nsk2-positive (data not shown), but like ectopic cAgrin7A4B8, MuSK/Nsk2 protein also could be resolved in fiber regions adjacent to the agrin-induced AChR clusters (Fig. 4E,F). In fact, re-staining sections with anti-chick agrin antibodies showed that MuSK/Nsk2 protein was well colocalized with anti-chick agrin immunoreactivity (Fig. 4G-I, J-L). Thus, the colocalization of MuSK/Nsk2 and agrin is not sufficient to induce the accumulation of AChRs along the entire length of ectopic agrin deposits.
Fig. 4. Accumulation of MuSK at original endplates (A-D) and at agrin-induced ectopic AChR clusters (E-L). Antibodies produced against Nsk2, the mouse homolog of MuSK, but not preimmune serum (Pre-IS), stained original endplates identified with Rh-alpha BGT (A-D). E-F, G-I, J-L, Three examples of ectopic MuSK accumulation. E-F, Agrin-induced ectopic MuSK-aggregates (E, arrow) do not induce AChR aggregates along their entire length. Triple-staining protocols revealed that extrasynaptic MuSK (G, J) more closely followed the distribution of ectopically expressed chick agrin (I, L) than AChR aggregates (H, K). G-I, Arrows show sites at which expression of both cAgrin7A4B8 and MuSK is not associated with AChR clusters, whereas another site in a neighboring muscle fiber contained AChRs (stars). J-L, AChR aggregates are located at sites with elevated expression of MuSK and chick agrin (arrows). In a neighboring myofiber a reduced level of MuSK staining matches the distribution of chick agrin (arrowheads) but is not colocalized with AChRs. Note that intracellular labeling for chick agrin (L) indicates that this muscle fiber was injected with the agrin expression construct. Scale bars: in A-F, 35 µm; in G-L, 50 µm.
[View Larger Version of this Image (112K GIF file)]

cAgrin7A4B8-induced postsynaptic specializations show signs of maturation

Maturation of the neuromuscular synapse is characterized by the accumulation of voltage-gated Na+ channels, the aggregation of myonuclei that selectively transcribe AChR genes, and the generation of postsynaptic folds. Earlier work has shown that some aspects of synapse maturation are found at cAgrin7A4B8-induced ectopic sites (Jones et al., 1997). To complete these studies, we now have examined, using an anti-peptide antiserum, the distribution of voltage-gated Na+ channels and the formation of membrane infoldings at agrin-induced ectopic AChR clusters. Accumulation of Na+ channel labeling was seen at ectopic cAgrin7A4B8-expressing sites, and it also colocalized with ectopic AChR aggregates (Fig. 5E,F). At some sites, however, accumulations of Na+ channels extended beyond AChR clusters (Fig. 5G-I).
Fig. 5. Voltage-gated Na+ channels (Na-Ch) are aggregated at extrasynaptic regions by expression of neural chick agrin. Antisera specific for Na+ channels specifically labeled endplates (A, B). Preabsorption with immunogenic peptide (C) inhibits the staining at endplates (D). The distribution of Na+ channel immunoreactivity is shown for two extrasynaptic sites of muscle fibers injected with agrin expression plasmids (E, F, G-I). The general outline of Na+ channel immunoreactivity (E, arrows) follows ectopic AChR aggregates (F, arrows). In some cases, however, the distribution of Na+ channels (G, arrow) was not confined to the site of extrasynaptic AChRs (H) induced by agrin (I). Scale bars: in A-F, 35 µm; in G-I, 50 µm.
[View Larger Version of this Image (111K GIF file)]

The ultrastructure of muscle fibers at ectopic agrin-induced AChR clusters was examined in the electron microscope. Marking such sites histochemically for AChE activity enabled us to localize them readily in thin sections. AChE-stained sections, indeed, contained deep sarcolemmal invaginations that contained BL comparable to those at normal endplates (Fig. 6). Such invaginations were associated with numerous mitochondria and morphologically distinct nuclei.

Fig. 6. Ultrastructure of postsynaptic specializations induced by ectopic expression of agrin in rat soleus muscle. Before being processed for electron microscopy, muscle injected with agrin cDNA expression constructs was sectioned longitudinally and stained for cholinesterase activity. A, Normal endplate in injected muscle shown as control. Note polymorphic nucleus (n) next to heavily stained synaptic folds and adjacent nerve terminal (t). B, A normal extrasynaptic muscle fiber nucleus (n) is lens-shaped and tightly fits in between smooth sarcolemma and myofibrils; z, Z-band of myofibrils. C, A region expressing ectopic agrin is characterized by deep, cholinesterase-positive membrane folds and underlying polymorphic nuclei. D, Higher magnification of the region boxed in C showing sarcolemmal invaginations, which contain basal lamina (arrows). Scale bars: in A-C, 1.9 µm; in D, 0.5 µm.
[View Larger Version of this Image (146K GIF file)]

Aggregation of ErbB receptors

At normal synapses AChR subunit gene transcription in the subsynaptic nuclei of the muscle fiber is thought to be induced by neuregulin-mediated phosphorylation of members of the ErbB family of receptor tyrosine kinases (Martinou et al., 1991; Falls et al., 1993; Chu et al., 1995). Both neuregulins and ErbBs are concentrated at the NMJ (Altiok et al., 1995; Goodearl et al., 1995; Jo et al., 1995; Moscoso et al., 1995; Sandrock et al., 1995). However, ectopic agrin alone can induce the synthesis and aggregation of functional adult subtype AChR channels (Jones et al., 1996, 1997). One way in which agrin might induce AChR gene transcription via the neuregulin/ErbB pathway is by inducing the binding of a muscle-derived neuregulin to synaptic BL and by concentrating ErbB receptors in synaptic muscle membrane. Therefore, we stained sections containing ectopic agrin with antibodies for ErbB2 and ErbB3. Indeed, both receptors could be observed readily at agrin-induced ectopic AChR clusters (Fig. 7), but staining intensity appeared weaker than at denervated endplates (data not shown). The lower staining intensity at agrin-injected sites could be attributable to a lower level of ErbB accumulation by the ectopic agrin than by the nerve or to ErbB immunoreactivity associated with perisynaptic cells present at the denervated endplates. To distinguish between these possibilities, we destroyed denervated soleus muscle, including perisynaptic cells, and allowed regeneration of new fibers inside their old BL sheaths in the absence of nerve. Under the regulation of neural factors associated with the old synaptic BL, such fibers form new functional endplates (Brenner et al., 1992; Jo et al., 1992) that include a high concentration of ErbBs (Zhu et al., 1995). Two to three weeks after muscle damage, ErbB2 and ErbB3 were observed at such sites, and the staining intensity was similar to ectopic agrin-induced sites (data not shown).
Fig. 7. ErbB2 (A) and ErbB3 (C) receptors are colocalized with cAgrin7A4B8-induced AChR aggregates (B, D) at extrasynaptic regions of innervated rat muscle fibers. Shown is labeling of sections with specific antibodies and Rh-alpha BGT (B, D). Scale bar, 50 µm.
[View Larger Version of this Image (104K GIF file)]

Taken together, these experiments demonstrate that an agrin isoform that normally is expressed by motor neurons is sufficient to induce the differentiation of a postsynaptic apparatus, the morphology of which closely resembles that of mature endplates.

Induction of postsynaptic specializations in vivo is splice-dependent

On cultured myotubes AChR aggregation induced by bath-applied agrin is observed only with agrin isoforms containing amino acid inserts at splice sites A and B (for review, see Bowe and Fallon, 1995). However, when presented in a cell-attached form, rat agrin lacking inserts at sites A and B was shown to have some AChR-aggregating activity (Campanelli et al., 1991; Ferns et al., 1992, 1993). To address whether the agrinA0B0 isoform, when expressed in a physiological context, would have such aggregating activity, we also injected cDNA constructs encoding cAgrin7A0B0 into extrasynaptic fiber regions. Staining of cAgrin7A0B0-expressing fibers with anti-chick agrin antibodies showed no obvious difference in expression levels to fibers expressing cAgrin7A4B8 (Fig. 8), except that the robust deposits sometimes seen on cAgrin7A4B8-injected fibers and colocalized with AChR clusters were not observed. As documented before (see Fig. 1), cAgrin7A4B8 deposited at the ectopic sites was more extended than the clusters of AChRs it induced (Fig. 8, arrow). Unlike in the cAgrin7A4B8-expressing and adjacent muscle fibers, where AChR clusters were always observed, AChR clusters were never detected after expression of cAgrin7A0B0 neither in the injected nor in their neighboring fibers. Hence, the activity of agrin to induce AChR aggregation in vivo is strictly dependent on the presence of amino acid inserts at site A and/or site B.

DISCUSSION

The "agrin hypothesis" (McMahan, 1990) states that agrin synthesized by motor neurons and released at their endings is crucial for the differentiation of the subsynaptic apparatus in myofibers. When added to cultured myotubes that express AChRs constitutively, agrin triggers the redistribution of surface AChRs in myotube membranes to form AChR aggregates. Colocalized with these are components seen also at the normal postsynaptic specializations and thought to be involved in their stabilization (see references in the introductory remarks). The potential of agrin to induce AChR clusters in electrically active muscle in vivo where AChR expression is suppressed (Lømo and Rosenthal, 1972; Goldman et al., 1988; Kues et al., 1995) has not been investigated.

To assess the role of agrin as the neural mediator of postsynaptic differentiation in vivo, we have induced the local expression of full-length agrin at extrasynaptic regions of innervated muscle fibers. The agrinA4B8 isoform used in this study is abundantly expressed by chick and rat motor neurons (Hoch et al., 1993; Smith and O'Dowd, 1994; Ma et al., 1994; Stone and Nikolics, 1995). Our experiments demonstrate that ectopic neural agrin can induce ectopic AChR clusters in vivo. The origin of the stronger deposits of agrin often seen within the extended region of agrin immunoreactivity and closely matching AChR clusters is not clear (see, for example, Fig. 8A). Because agrin attaches to laminin (Denzer et al., 1997) and laminin-beta 2 is closely colocalized with AChR clusters, agrin may become bound preferentially at such sites. Our experiments further demonstrate that agrin alone can induce the differentiation of an ectopic postsynaptic-like structure locally, containing molecular components of normal postsynaptic specializations. Because the fibers remained innervated at their original endplates during the entire experiment, the differentiation was activity-resistant. Combined with our previous results that ectopic agrin is sufficient to induce the functional elements of normal endplate membrane, i.e., clusters of adult-type AChR channels and AChE activity (Jones et al., 1997), the present data support our hypothesis that nerve-derived agrin acts as the key neural mediator for differentiation of functional subsynaptic specializations in electrically active muscle fibers.

Distribution of MuSK at sites of ectopic AChR aggregation

It has been demonstrated recently that agrin-induced AChR clustering requires MuSK, a muscle-specific protein tyrosine kinase that might be part of the agrin receptor complex (DeChiara et al., 1996; Glass et al., 1996). Moreover, recent findings show that MuSK accumulates at nerve-muscle contacts even in rapsyn-deficient mice (Apel et al., 1997). Nevertheless, AChRs are not accumulated at the nerve-muscle contacts in the rapsyn-deficient mice (Gautam et al., 1995). These results strongly suggest that motor neurons induce the formation of a primary MuSK-containing scaffold and that the formation of this scaffold is rapsyn-independent, whereas the aggregation of AChRs is rapsyn-dependent. We now have found that, as with normal endplates, myofiber regions that express cAgrin7A4B8 showed accumulation of MuSK at sites of agrin deposition. These results show that neural agrin alone is sufficient to localize MuSK to specific sites and they suggest that accumulation of MuSK at nerve-muscle contacts may be induced by neural agrin. Our results that the colocalization of agrin and MuSK does not necessarily codistribute with AChRs, rapsyn, or utrophin also support the conclusion of Apel et al. (1997) that localization of MuSK does not require rapsyn. In addition, our results suggest that MuSK aggregation does not suffice to stabilize AChR aggregates. Accumulation of AChRs may depend on additional factors, which may be limited in abundance. Such limitation might restrict the growth of the AChR cluster---analogous to the perisynaptic regions of denervated fibers, which do not accept innervation by a transplanted foreign nerve (Lømo et al., 1984).

Accumulation of Na+ channels and the formation of ectopic junctional membrane folds

At the normal neuromuscular synapse, Na+ channels are located in the depth of the secondary synaptic folds (Flucher and Daniels, 1989), i.e., spatially separate from the AChR clusters, utrophin, and rapsyn (Bewick et al., 1992), which are localized at the crests of folds. They also are anchored to the cytoskeleton by an apparently distinct mechanism involving ankyrin (Srinivasan, 1988; Flucher and Daniels, 1989). In the present experiments with ectopic cAgrin7A4B8, aggregates of voltage-gated Na+ channels were not always colocalized closely with AChR clusters, but they were observed exclusively at or near agrin-induced AChR aggregates. This is in agreement with earlier observations showing that immobilized, but not soluble, agrin induces Na+ channel aggregates on cultured myofibers (Lupa and Caldwell, 1991; Sharp and Caldwell, 1996). The dependence of Na+ channel aggregation on agrin immobilization also may explain apparently conflicting results by Corfas and Fischbach (1993) that Na+ channels in cultured chick myotubes are induced by ARIA/heregulin, but not by soluble agrin. As proposed here and previously (Jones et al., 1996, 1997) for agrin-induced AChR gene expression, agrin attached to BL may stimulate the muscle fiber to secrete neuregulin and/or modify the BL in such a way as to provide binding sites for muscle-derived NRG. Such NRG aggregates would, in turn, induce the ectopic Na+ channel aggregates.

Formation of endplate membrane in electrically active fibers?

The formation of ectopic endplate structures by neural agrin in innervated muscle fibers is striking, because adult muscle fibers, if innervated, will not accept innervation by a foreign nerve (Jansen et al., 1973). The reason for the "resistance" to hyperinnervation seems to be electrical muscle activity, because muscles paralyzed by a blockade of impulse conduction in the original nerve do accept hyperinnervation by a foreign nerve (Cangiano et al., 1980). Indeed, signals acting from electrically inactive muscle (Rassendren et al., 1992) on the nerve seem to play a key role in the sprouting of motor axons in partially denervated muscle, and innervation can be prevented if the denervated muscle is kept active by chronic stimulation (Jansen et al., 1973). These observations, together with the apparent absence of MuSK from extrasynaptic regions of innervated muscle (Valenzuela et al., 1995), raise the question of how in our experiments ectopic agrin could have induced postsynaptic differentiation on active, innervated fibers. The possibility of fiber damage and degeneration on plasmid injection, potentially resulting in susceptibility to innervation, was excluded in control experiments (our unpublished data). Nevertheless, it remains possible that the muscle was transiently receptive to innervation and MuSK was upregulated as a consequence of tissue manipulation during muscle exposure for plasmid injection. Another possibility is that, even in innervated muscle, some MuSK might be expressed in nonsynaptic segments, as suggested by low levels of MuSK mRNA detected in extrasynaptic regions of normal rat soleus muscle (our unpublished data). Extrasynaptic MuSK then may become "trapped" by the neural agrin deposited at ectopic sites of agrin-secreting fibers, causing the formation of a primary MuSK-based scaffold. Therefore, our finding that, in innervated muscle, agrin alone could form ectopic synaptic membrane is consistent with the notion that secretion of agrin from the terminals of transplanted foreign motor axons may depend entirely on (inductive or permissive) signals supplied by inactive muscle only. In the present experiments agrin was supplied irrespective of muscle activity, consistent with the idea that active muscle per se can accept innervation if it is supplied with the appropriate neural factor(s). The present experiments suggest that, for synaptic differentiation of the muscle fiber, this factor is agrin. For motor nerve terminal differentiation, it again may be agrin, because in immobilized form agrin provides stop and differentiation signals for outgrowing motor neurites in vitro (Campagna et al., 1995).

FOOTNOTES

Received April 29, 1997; revised June 9, 1997; accepted June 11, 1997.

  

This work was supported by grants from the Swiss National Science Foundation and from the Swiss Foundation for Research on Muscle Diseases to H.R.B. and M.A.R. We thank Dr. S. Froehner for anti-rapsyn mAb 1234 and Dr. R. Levinson for anti-Na+ channel antiserum. The excellent technical assistance by Ms. M. Lichtsteiner, V. Gaschen (Berne), and Mr. B. Schumacher is gratefully acknowledged. We also thank Dr. B. Hunziker (Berne) for providing EM facilities and G. Jones for comments on this manuscript.

Correspondence should be addressed to Dr. Hans Rudolf Brenner, Department of Physiology, University of Basel, Vesalgasse 1, CH-4051 Basel, Switzerland.


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