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The Journal of Neuroscience, May 1, 1999, 19(9):3376-3383

Constitutively Active MuSK Is Clustered in the Absence of Agrin and Induces Ectopic Postsynaptic-Like Membranes in Skeletal Muscle Fibers

Graham Jones, Chris Moore, Said Hashemolhosseini, and Hans Rudolf Brenner

Department of Physiology, University of Basel, CH-4051 Basel, Switzerland


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

In skeletal muscle fibers, neural agrin can direct the accumulation of acetylcholine receptors (AChR) and transcription of AChR subunit genes from the subsynaptic nuclei. Although the receptor tyrosine kinase MuSK is required for AChR clustering, it is less clear whether MuSK regulates gene transcription. To elucidate the role of MuSK in these processes, we constructed a constitutively active MuSK receptor, MuSKneuTMuSK, taking advantage of the spontaneous homodimerization of the transmembrane domain of neuT, an oncogenic variant of the neu/erbB2 receptor. In the extrasynaptic region of innervated muscle fibers, MuSKneuTMuSK formed highly concentrated aggregates that colocalized with AChR clusters. Associated with MuSK-induced AChR clusters was a normal complement of synaptic proteins. Moreover, transcription of the AChR-epsilon subunit gene was increased, albeit via an indirect mechanism by MuSK-induced aggregation of erbB receptors and neuregulin. Although neural agrin was not required, the activity of MuSKneuTMuSK was nevertheless potentiated by ectopic expression of a muscle agrin isoform inactive in AChR clustering. To define the role of the kinase domain in the formation of a postsynaptic-like membrane, a second fusion receptor, neuneuTMuSK, which included the MuSK kinase but not the MuSK extracellular domain, was expressed. Significantly, neuneuTMuSK induced AChR clusters that colocalized with aggregates of endogenous MuSK. Taken together, it was concluded that the MuSK kinase domain is sufficient to initiate the recruitment of additional MuSK receptors, which then develop into highly concentrated aggregates by means of a positive feedback loop to induce a postsynaptic membrane in the absence of neural agrin.

Key words: agrin; muscle; MuSK; gene transcription; neuromuscular junction; rat


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

The formation of the developing neuromuscular junction (NMJ) involves the nerve-induced transcription of acetylcholine receptor (AChR) subunit genes in the subsynaptic nuclei of the muscle fiber and the aggregation of their gene products, the AChRs, at the subsynaptic membrane. Synapse formation is thought to be initiated by the release of agrin from the nerve terminal (McMahan, 1990). Agrin is expressed in several isoforms (Ruegg and Bixby, 1998). Isoforms expressed by neurons, but not those by other tissues, cluster AChRs expressed on the surface of cultured myotubes (Ruegg et al., 1992; Ferns et al., 1993) by the activation of the receptor tyrosine kinase MuSK (Glass et al., 1996). Because AChR clusters are induced independently of agrin in cultured myotubes by the addition of anti-MuSK antibodies (Xie et al., 1997; Hopf and Hoch, 1998), MuSK is likely to be part of an agrin receptor complex. However, it remains unclear whether MuSK can activate AChR gene transcription.

Synapse-specific transcription of AChR genes is thought to be induced by neuregulins (NRGs) activating erbB receptor tyrosine kinases, both of which are localized at the neuromuscular junction (for review, see Fischbach and Rosen, 1997). However, the agrin- and NRG-activated pathways may converge, because ectopic agrin can induce AChR gene transcription in nonsynaptic muscle regions (Jones et al., 1997), where it also aggregates muscle-derived NRGs and erbB receptors (Meier et al., 1997, 1998a; Rimer et al., 1998). Furthermore, AChR gene transcription in cultured myotubes induced by full-length agrin is dependent on the erbB-receptor pathway (Meier et al., 1998a).

Despite the evidence equating the biological activity of neural agrin with MuSK activation in subsynaptic differentiation, several inconsistencies remain unresolved. One question is how in extrasynaptic regions of innervated muscle fibers where MuSK is reported to be absent (Valenzuela et al., 1995), subsynaptic differentiation is initiated by agrin, and which pathways induce MuSK aggregation at mature ectopic postsynaptic-like membranes (Meier et al., 1997). Second, in cultured myotubes, activation of MuSK by neural agrin added in soluble form induces AChR clustering only but not AChR gene transcription (Jones et al., 1996). Rather, the stable attachment of agrin to a laminin substrate is required for gene transcription, consistent with the idea that agrin may have roles beyond MuSK activation. For example, signaling by agrin appears to involve integrins (Martin and Sanes, 1997). Finally, the role of an agrin-induced NRG/erbB receptor pathway via activation of MuSK is unclear, because localization of erbB receptors is absent in both rapsyn- and MuSK-deficient muscle, but localized transcription appears to be absent from the latter only (Gautam et al., 1995; Moscoso et al., 1995; DeChiara et al., 1996).

These problems were addressed by expressing in muscle fibers constitutively active chimeric constructs comprising combinations of the extra- and intracellular domains of MuSK and erbB2/neu separated by the transmembrane domain of neuT, an oncogenic variant of the erbB2/neu receptor (Bargmann et al., 1986). In this way, the roles of MuSK in various aspects of agrin-induced differentiation of the postsynaptic muscle membrane could be examined directly.


    MATERIALS AND METHODS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Construction of MuSK and erbB2/neu fusion receptors. MuSK cDNA was amplified by RT-PCR from primary rat myotube poly(A+) RNA, and full-length cDNA was subcloned into the EcoRI and XbaI sites of p_myc, a pcDNA1 (Invitrogen, Carlsbad, CA)-based vector that includes five copies of the myc epitope (Meier et al., 1998b) to create pMuSK_myc. Rat neuT cDNA was isolated from the vector pSVneuT (Bargmann et al., 1986). The nomenclature adopted for this paper divides the receptor cDNA into extracellular, transmembrane, and intracellular/kinase domains. To construct pMuSKneuTneu, a region of the extracellular domain of MuSK between nucleotides 1416 and 1596 was amplified using the following PCR primers: MuSK1416_s, 5'-ggagtgcagcaagcttcccagc-3', which includes the HindIII site at position 1426, and MuSK1596_asNdeI 5'-ccgggcacatatgcaggcgagacggcgaaggaagacgtgga-3' (Microsynth, Balgach, Switzerland), which introduces an NdeI site (underlined) encoding a linker peptide AYV between the MuSK extracellular domain and the neuT transmembrane domain in the completed fusion receptor. The transmembrane domain and part of the intracellular domain of neuT was amplified using the following oligonucleotides: neuT1985_sNdeI 5'-ccggggcatatgtgacattcatcattgcaactgtagagggcgtc-3', which introduces an NdeI site and neuT2406_as 5'-gatgtcaggcagatgccc-3'. The resulting PCR product was digested with NdeI and XbaI (at nucleotide 2332) and subcloned with the HindIII- and NdeI-digested MuSK PCR product into pMuSK_myc digested with HindIII and XbaI. This fragment was then excised by digestion with EcoRI and XbaI and ligated with the intracellular region of neuT by digesting pSVneuT with XbaI and XhoI and subcloning into pCDNAI digested with EcoRI and XhoI. To construct pMuSKneuTMuSK_myc, the following PCR amplifications were performed: pMuSKneuTneu was amplified using MuSK1416_s and MuSKneuT_as 5'-cctccttcggcagcaatagattaggattccaacgacc-3', which included MuSK intracellular domain (underlined) and neuT transmembrane sequences; intracellular domains of MuSK were amplified using MuSK1663_s 5'-tattgctgccgaaggagg-3', which includes the same region as underlined in MuSKneuT_as and MuSK2727_as. The two PCR products were diluted, mixed, and reamplified using the flanking primers MuSK1416_s and MuSK2727_as. The resulting product was isolated and digested with HindIII and BlpI (at position 1812) and subcloned into pMuSK_myc digested with HindIII and BlpI. To construct pneuneuTMuSK, a fragment of neuT extending from the extracellular domain into the neuT transmembrane domain was amplified using the primers neu1886_s, 5'-gaggagggcatatgccag-3' and neuTM.Glu_as, 5'-ggacgccctctacagttgc-3'; the neuT transmembrane domain into the MuSK intracellular domain was amplified using the primers neuTM.Glu_s, 5'-gcaactgtagagggcgtcc-3', and MuSK1921_as, 5'-cctccttcagcatcttcacagccacc-3'. The resulting PCR products were diluted, mixed, and reamplified using neu1886_s and MuSK_as. The resulting PCR product was digested with the restriction endonucleases NdeI and BlpI and combined with pMuSK_myc digested with HindIII and BlpI and an neuT extracellular fragment HindIII/NdeI. The resulting constructs were then sequenced, and equivalent expression of MuSKneuTMuSK, MuSKneuTneu, and neuneuTMuSK was confirmed by immunoprecipitation and Western blot analysis of transfected Cos-1 cells.

Construction of pGFP-S6. To identify transfected myoblasts and injected muscle fibers, we constructed a green fluorescent protein (GFP) (Clontech, Palo Alto, CA) that was targeted into the nucleus. To do this, three nuclear localization signals (NLSs) present at the C terminus of the S6 protein (Schmidt et al., 1995) were fused to the C terminus of humanized GFP. An EcoRI restriction endonuclease site was introduced via PCR at the 3' end of cDNA encoding humanized GFP, which was then cloned 5' HindIII-EcoRI 3' into the vector pCMX-pI2 (Umesono et al., 1991). A 251 bp fragment of the cDNA encoding the three NLSs of protein S6 was amplified using the following primers: S6F 5'- aaagaattcaagaaacctaggaccaaagca-3', S6R 5'-tcaggatccctatttctgactggattcaga-3'. S6F includes the first NLS of S6, and S6R includes a stop codon. The resulting PCR product was digested with EcoRI and BamHI (underlined in S6F and S6R) and subcloned into the EcoRI-BamHI sites of pCMX-pI2/GFP to generate pGFP-S6.

Transfection of C2C12 myoblasts. For analysis of transcriptional activity of the -216epsilon subunit gene promoter (Jones et al., 1996), 1 × 105 C2C12 cells were passaged onto six-well plates that had been coated with either laminin alone or laminin with agrin as described (Meier et al., 1998a). Myoblasts were transfected with 800 ng of reporter plasmid DNA, 200 ng of the appropriate receptor plasmid, and 200 ng of pCH110 (Pharmacia BioTech Europe) using 5 µl FuGENE 6 (Roche Diagnostics Boehringer Mannheim, Mannheim, Germany) according to the manufacturer's instructions. Myotubes were analyzed 5 d after transfection. Results are averages of three dishes each from at least three independent transfections. For immunoprecipitation experiments, C2C12 myoblasts were transfected with 1 µg of the appropriate plasmid expression vector and allowed to differentiate for 5 d. Cells were lysed, and membrane proteins were immunoprecipitated as described (Meier et al., 1998a).

Injection of muscle fibers and immunohistochemistry. Single rat soleus fibers were injected as described previously (Jones et al., 1997; Meier et al., 1997) with 80 ng/µl pGFP-S6, 100 ng/µl pMuSKneuTMuSK_myc or pneuneuTMuSK_myc, and where applicable, 100 ng/µl pcAgrin7A0B0. Rats were killed 4 weeks later. For immunohistochemistry, muscles were frozen in prechilled isopentane and cut into 12 µm cross sections. Immunohistochemistry of unfixed cross sections was performed using antibodies and methods as described (Meier et al., 1997).

Quantitative TaqMan fluorescent real time PCR analysis of AChR-epsilon subunit RNA in injected muscles. Expression of GFP-S6 allowed direct visualization of injected fibers, the borders of which were marked before freezing. The injected and noninjected regions were then excised, and total RNA was extracted using the Qiagen RNeasy RNA extraction kit (Qiagen AG, Basel, Switzerland). First-strand cDNA was synthesized from 2 µg of total RNA primed with 250 ng of random hexamers (Roche Diagnostics Boehringer Mannheim) using Superscript reverse transcriptase (Life Technologies, Gaithersburg, MD). First-strand cDNA was purified using the High Pure PCR Product Purification Kit (Roche Diagnostics Boehringer Mannheim). The primers beta -actin sense 5'-ttcaacaccccagccatgt-3', anti-sense 5'-gtggtacgaccagaggcataca-3', AChR-epsilon subunit sense 5'-ccaacgactcacgccacat-3', and anti-sense 5'-ggcgcggcagtagctcta-3' were synthesized and flanked the TaqMan oligonucleotide probes beta -actin, 5'-(FAM)cgtagccatccaggctgtgttgtcc(TAMRA)-3' and AChR-epsilon , 5'-(FAM)ccctcggctgcgccagatttt(TAMRA)-3'. TaqMan PCR was performed using the TaqMan PCR Core Reagent Kit as described by the manufacturer (Perkin-Elmer Applied Biosystems), with the exception that MgCl2 was increased to 5 mM. AChR-epsilon subunit mRNA was quantitated relative to beta -actin mRNA using the comparative CT method. CT (threshold cycle) is defined as the cycle number at which the amount of amplified target passes a fixed threshold above baseline. Delta CT is the difference in threshold cycles between AChR-epsilon and beta -actin, calculated for RNA isolated from either injected or noninjected regions. Subtracting the Delta CT of the noninjected region from the Delta CT of the injected region gives the value Delta Delta CT, which when applied in the formula 2-Delta Delta CT, gives the amount of AChR-epsilon subunit RNA in injected muscle fibers, normalized to beta -actin, and relative to the noninjected region. To ensure that the Delta Delta CT calculation was valid, the efficiency with which both genes were amplified was examined and found to be the same.


    RESULTS
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

Constitutive activation of MuSK induces ectopic AChR clusters

To examine the biological activity of MuSK independently of activation by agrin, we designed an activated MuSK receptor construct. This was performed by exploiting the neuT oncogene, in which a single point mutation in the transmembrane domain results in the spontaneous formation of active neuT homodimers. It is now apparent that although the transmembrane domain of the receptor tyrosine kinases is required for activity, correct biological signaling also involves dimerization of the extracellular and kinase domains (Siegel and Muller, 1996; Burke et al., 1997; Tzahar et al., 1997). On the basis of these findings, we reasoned that a MuSK receptor fusion construct, MuSKneuTMuSK, in which the MuSK extracellular and kinase domains were separated by a neuT transmembrane domain (for the nomenclature of the fusion constructs, see Fig. 1), would homodimerize yet retain MuSK biological activity.



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  		Figure 1.   Schematic of MuSK and neu/erbB2 receptor fusion constructs. The nomenclature adopted divides each receptor tyrosine kinase into extracellular, transmembrane (TM), and intracellular/kinase domains. Also shown is the C-terminal myc tag. The plasmid encoding each chimeric receptor is denoted by the prefix "p" and myc as suffix. Wild-type MuSK (rMuSK) is indicated as are each of the fusion receptor products encoded by each plasmid: MuSKneuTMuSK, MuSKneuTneu, and neuneuTMuSK.

In response to neural agrin, the MuSK kinase domain is only transiently phosphorylated over a time course of minutes (Glass et al., 1996), and a similar problem occurs with constitutive activation of the MuSK kinase domain. Therefore, because only those isoforms of agrin that induce AChR clustering also phosphorylate MuSK (Glass et al., 1996), AChR clustering in C2C12 myotubes was used to assay MuSKneuTMuSK activity. C2C12 myoblasts were transfected with pMuSKneuTMuSK_myc and pGFP-S6, which encodes nuclear-localized GFP. AChR clusters were induced on 80% of GFP-positive myotubes, which compared favorably with AChR clustering on myotubes transfected with pGFP-S6 but treated with neural agrin (94% AChR cluster/GFP colocalization). In contrast, in myoblasts transfected with pMuSKneuTneu_myc, which consists of the MuSK extracellular domain but the erbB2/neu kinase domain, only 3% of GFP-positive myotubes exhibited AChR clustering, the same as that seen for untreated myotubes transfected with pGFP-S6 alone (data not shown).

We next investigated whether activation of MuSK was sufficient to induce AChR clusters in the nerve-free region of innervated muscle fibers. To identify injected fibers, pMuSKneuTMuSK_myc was coinjected with pGFP-S6. Overexpression of constitutively active MuSKneuTMuSK induced approximately one AChR cluster per injected fiber [Fig. 2, MuSKneuTMuSK, and right panel, -cAgrin 7A0B0 (1.2 ± 0.1 AChR clusters/injected fiber; SEM, n = 9 muscles/200 fibers)]; they were similar in number and appearance to those induced by low levels of neural agrin. Similar findings were obtained with a chimera lacking a myc tag (data not shown). In contrast, ectopic expression of wild-type MuSK only rarely induced AChR clusters, which were small and point-like in appearance (data not shown).



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  		Figure 2.   Constitutive activation of MuSK is sufficient to induce ectopic, activity-resistant AChR clusters but is enhanced by a muscle agrin isoform, cAgrin7A0B0. In muscle fibers injected with pMuSKneuTMuSK_myc, generally one AChR cluster was recorded per injected fiber (MuSKneuTMuSK, AChR) and was associated with clusters of GFP-positive nuclei (GFP). cAgrin7A0B0 secreted from neighboring fibers increased the number of AChR clusters on pMuSKneuTMuSK_myc-injected fibers (MuSKneuTMuSK/cAgrin). In the example shown, three AChR clusters (arrows) are present in close proximity on the same injected fiber as seen by colocalization with clusters of GFP-positive nuclei. Analysis of the average number of AChR clusters per GFP-positive fiber showed that cAgrin7A0B0 increased the average number of MuSKneuTMuSK-induced AChR clusters per injected fiber more than twofold (right panel, +cAgrin 7A0B0; SEM, n = 4 muscles, 100 fibers) over that observed in muscle fibers injected with pMuSKneuTMuSK_myc alone (right panel, -cAgrin 7A0B0; SEM, n = 9 muscles, 200 fibers). Scale bar, 50 µm.

It was shown previously that the distribution of endogenous MuSK is coextensive with that of ectopic agrin deposits, independent of whether an active or an inactive isoform of agrin was expressed (Meier et al., 1997; D. M. Hauser and M. A. Ruegg, personal communication). This suggests that agrin may influence AChR clustering via two mechanisms: (1) by accumulating MuSK and (2) by phosphorylating MuSK. We were therefore interested to see whether an inactive muscle isoform of chick agrin influenced the appearance of MuSKneuTMuSK and/or AChR clusters. To do this, expression plasmids encoding either MuSKneuTMuSK or chick agrin, cAgrin7A0B0, were injected into neighboring muscle fibers. Although the morphology of the resulting AChR clusters remained similar to those induced by MuSKneuTMuSK alone (Fig. 2, MuSKneuTMuSK/cAgrin), cAgrin7A0B0 increased the average number of AChR clusters on pMuSKneuTMuSK_myc-injected fibers more than twofold, such that several AChR clusters were now present on each injected fiber examined [Fig. 2, right panel, +cAgrin 7A0B0 (2.6 ± 0.3 AChR clusters/injected fiber; SEM, n = 4 muscles/100 fibers)]. Thus, MuSKneuTMuSK induced ectopic AChR clusters independently of neural agrin, but this activity was enhanced by exogenous chick muscle agrin cAgrin7A0B0.

Activation of the MuSK kinase domain initiates recruitment and aggregation of additional MuSK receptors

Endogenous MuSK colocalizes with ectopic neural (Meier et al., 1997) and muscle agrin isoforms (Hauser and Ruegg, personal communication), suggesting that agrin may be involved in the localization of MuSK to the NMJ. To examine the distribution of MuSKneuTMuSK in the absence of agrin, fibers injected with pMuSKneuTMuSK_myc were analyzed in frozen cross sections through the injected region. First, the distribution of MuSKneuTMuSK was determined by immunohistochemistry using antibodies that recognized the extracellular domain of MuSK (Meier et al., 1997) or the C-terminal myc tag. Intense myc immunoreactivity colocalized with AChR clusters, with only faint staining extending throughout the cytoplasm and around the remainder of the muscle fiber circumference (Fig. 3A, MuSKneuTMuSK, myc). MuSK immunoreactivity was similarly concentrated at AChR clusters (Fig. 3A, MuSKneuTMuSK, MuSK). In muscles injected with pMuSKneuTMuSK_myc and pcAgrin7A0B0, concentrated aggregates of MuSKneuTMuSK still colocalized with AChRs (data not shown). The formation of highly concentrated aggregates of MuSKneuTMuSK coincident with AChR clusters, both in the presence and absence of cAgrin7A0B0, thus implies a positive feedback loop, driven by the activation of MuSK itself. Furthermore, because MuSKneuTneu did not induce AChR clustering in injected muscle fibers (data not shown), the MuSK kinase domain was essential for this process. To directly test whether activation of the MuSK kinase was sufficient for the recruitment of MuSK, we constructed pneuneuTMuSK_myc, which includes the erbB2/neu extracellular domain and the MuSK kinase domain (Fig. 1). In contrast to MuSKneuTMuSK, neuneuTMuSK did not induce AChR clusters in C2C12 myotubes (data not shown), similar to a trkC/MuSK chimera, which also lacks the MuSK extracellular domain and is consistent with the idea that the MuSK extracellular domain is required for AChR clustering (Glass et al., 1997). Surprisingly, however, ectopic expression of neuneuTMuSK in innervated muscle fibers induced AChR clusters indistinguishable from those induced by MuSKneuTMuSK (Fig. 3B, neuneuTMuSK, AChR), suggesting that the MuSK extracellular domain must be supplied by endogenous MuSK. Indeed, both neuneuTMuSK, identified specifically by an anti-myc antibody (Fig. 3B, neuneuTMuSK, myc), and endogenous MuSK, identified by an antibody against the extracellular domain of MuSK (Fig. 3B, neuneuTMuSK, MuSK) (Meier et al., 1997), colocalized with AChR clusters.



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  		Figure 3.   A, Distribution of AChRs and MuSKneuTMuSK in injected fibers. MuSKneuTMuSK was identified using an antibody that recognized a C-terminal myc epitope (myc) (bottom panel). Highly concentrated deposits of MuSKneuTMuSK colocalized with AChR clusters (AChR). Similarly, by using an antibody that recognized the extracellular domain of MuSK, MuSK immunoreactivity was restricted to AChR clusters (MuSK). B, Ectopic expression of neuneuTMuSK, which includes the MuSK kinase domain but not the MuSK extracellular domain, recruits endogenous MuSK and induces AChR clusters in innervated muscle fibers. AChR clusters induced by neuneuTMuSK (AChR) colocalize with neuneuTMuSK (myc) and endogenous MuSK (MuSK), resolved using either anti-myc or anti-MuSK (extracellular domain) antibodies, respectively. Bottom panel, Summary of receptor recognition by anti-myc and anti-MuSK antibodies. Scale bar, 50 µm.

The association of neuneuTMuSK with endogenous MuSK receptors was confirmed by immunoprecipitation experiments. Extracts from C2C12 myotubes transfected with pneuneuTMuSK_myc were immunoprecipitated with an anti-myc antibody and analyzed by Western blotting using an anti-MuSK antibody that does not recognize neuneuTMuSK (Fig. 4, lane 2). A single band of 100 kDa was detected, corresponding to endogenous MuSK. A similar result is shown for C2C12 myotubes transfected with pMuSKneuTMuSK_myc (Fig. 4, lane 3). However, in myotubes transfected with pMuSKneuTneu_myc, no endogenous MuSK was co-immunoprecipitated. Instead, only MuSKneuTneu (120 kDa) was detected using an anti-MuSK antibody (Fig. 4, lane 4). Furthermore, because neither endogenous erbB2 nor erbB3 receptors were co-immunoprecipitated with neuneuTMuSK or MuSKneuTneu (data not shown), the chimeric receptors primarily formed homodimers. Together, these results suggested that activation of the MuSK kinase domain was required for the aggregation of endogenous MuSK receptors seen at ectopic AChR clusters.



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  		Figure 4.   neuneuTMuSK interacts with endogenous MuSK receptors in C2C12 myotubes. Lysates from C2C12 myotubes transfected with pGFP-S6 alone (lane 1), pneuneuTMuSK_myc (lane 2), pMuSKneuTMuSK_myc (lane 3), or pMuSKneuTneu_myc (lane 4) were immunoprecipitated with anti-myc antibody. Immunoprecipitated proteins were analyzed by Western blotting by incubation with an anti-MuSK antibody that recognized the extracellular domain of MuSK. Molecular weight markers indicated in kilodaltons.

MuSKneuTMuSK induces a postsynaptic membrane that includes a normal complement of synaptic proteins

Rapsyn, phosphotyrosine, and utrophin each colocalized with AChR clusters induced by MuSKneuTMuSK (data not shown). MuSKneuTMuSK also recruited laminin-beta 2 (Fig. 5, lam-beta 2), a synaptic component of the extracellular matrix potentially important in the differentiation of the presynaptic nerve terminal (Porter et al., 1995; Patton et al., 1997). Also present at ectopic AChR clusters was the postsynaptic membrane protein beta -dystroglycan (Fig. 5, beta -DG). beta -Dystroglycan binds noncovalently with the extracellular glycoprotein alpha -dystroglycan, and both are integral components of the dystrophin-associated protein complex (Tinsley et al., 1994). In addition, both neural and muscle agrin bind alpha -dystroglycan via domains not required for MuSK activation (Gesemann et al., 1996). In muscle fibers expressing MuSKneuTMuSK, no accumulation of endogenous muscle agrin was seen at MuSKneuTMuSK-induced AChR clusters (data not shown; see also Meier et al., 1997). However, ectopic expression of chick muscle agrin cAgrin7A0B0 resulted in deposits of cAgrin7A0B0 at AChR clusters in neighboring pMuSKneuTMuSK_myc-injected fibers (Fig. 5, cAgrin). Thus, additional binding sites for agrin are present at MuSKneuTMuSK-induced AChR clusters.



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  		Figure 5.   MuSKneuTMuSK-induced AChR clusters include a normal complement of postsynaptic proteins. AChR clusters were identified (AChR) and examined for the presence of laminin-beta 2 (lam-beta 2), beta -dystroglycan (beta -DG), and NaCh. In muscles injected with pMuSKneuTMuSK and pcAgrin7A0B0, deposits of cAgrin7A0B0 at AChR clusters were observed (cAgrin, arrow). Scale bar, 50 µm.

We also examined whether voltage-activated Na+-channels (NaChs) were present. Unlike the AChR channels, which aggregate early in synapse formation and become localized to the crests of the postsynaptic folds (Fertuck and Salpeter, 1976), NaChs aggregate late in the maturation of the postsynaptic membrane (Lupa et al., 1993), and they are concentrated in the troughs of the postsynaptic folds (Boudier et al., 1992), suggesting that the aggregation and localization of NaChs are regulated differently to the AChRs (Colledge and Froehner, 1998). However, NaChs also colocalized with MuSKneuTMuSK-induced AChR clusters (Fig. 5, NaCh). Therefore, clustering of NaChs is also regulated by MuSK.

Activation of MuSK aggregates erbB receptors and NRGs

We next asked whether MuSK, in the absence of neural agrin, induced the assembly of the erbB/NRG signaling pathway. Indeed, using an antibody specific for the mammalian AChR-epsilon subunit, we found that AChR clusters were of the adult AChR subtype (Fig. 6, AChR-epsilon ) and that such AChR clusters contained aggregates of NRGs (Fig. 6, NRG), erbB2 (Fig. 6, erbB2), and erbB3 receptors (data not shown). To ascertain whether this was reflected in increased gene transcription, AChR-epsilon subunit mRNA from the region of injected muscle expressing MuSKneuTMuSK was quantified using a real-time RT-PCR assay. To increase the sensitivity of this assay, we used muscles that had been co-injected with pMuSKneuTMuSK_myc and pcAgrin7A0B0. Ectopic expression of pcAgrin7A0B0 alone did not increase AChR-epsilon subunit mRNA in the injected region (1.15 ± 0.1, SEM; n = 3 muscles), whereas expression of pMuSKneuTMuSK_myc and pcAgrin7A0B0 increased AChR-epsilon subunit mRNA by up to fourfold (3.8 ± 0.3, SEM; n = 3 muscles). The close agreement between these results and those from similar experiments using neural agrin (Jones et al., 1997; Meier et al., 1997; Rimer et al., 1998) is consistent with the hypothesis that MuSKneuTMuSK activates AChR gene transcription by organizing the erbB/NRG pathway.



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  		Figure 6.   MuSKneuTMuSK-induced AChR clusters include the AChR-epsilon subunit and colocalize with the erbB2 receptor tyrosine kinase and NRGs. AChR clusters were identified (AChR) and examined for the presence of the AChR-epsilon subunit (AChR-epsilon ), NRGs (NRG), or erbB2 (erbB2). Scale bar, 50 µm.

We next sought to test this hypothesis further in cultured C2C12 myotubes, which have proved to be a convenient and reliable model for examining the regulation of AChR gene transcription by agrin (Jones et al., 1996; Meier et al., 1998a). Initially, we compared the transcriptional activation imparted by activation of either the MuSK or erbB2/neu kinase domains. For this purpose, an AChR-epsilon subunit promoter reporter plasmid, pLCF216epsilon (Jones et al., 1996), was cotransfected with either pMuSKneuTneu_myc or pMuSKneuTMuSK_myc. Surprisingly, unlike in innervated muscle fibers, no significant increase in luciferase activity was induced by MuSKneuTMuSK (Fig. 7, MuSK). In contrast, MuSKneuTneu clearly activated transcription, with luciferase activity increased approximately fivefold over that seen for MuSKneuTMuSK or in control cultures (Fig. 7, neu).



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  		Figure 7.   MuSK does not directly increase transcription of the AChR-epsilon subunit gene in C2C12 myotubes. The transcriptional activity of the MuSK and erbB2/neu kinase domains was directly compared by culturing C2C12 myoblasts on a laminin substrate. Myoblasts were transfected with either pLCF216epsilon (control: con) or pLCF216epsilon with pMuSKneuTMuSK_myc (MuSK) or pMuSKneuTneu_myc (neu), a chimeric receptor that included the erbB2/neu kinase domain. The role of MuSK in AChR transcription was investigated further by culturing C2C12 myoblasts on a substrate of neural mini-agrin cN257C21B8 adhered to laminin (B8). The requirement for erbB2/neu was tested by cotransfecting a dominant-negative erbB2/neu mutant into myoblasts similarly cultured on a laminin/cN257C21B8 substrate (B8, neu KM). Mini-agrin cN257C21B0 (B0), which does not phosphorylate MuSK or induce AChR clustering, did not increase transcription. Also shown is the transcriptional activity of a saturating amount of soluble NRG (NRG).

The role of MuSK in neural agrin-induced AChR transcription in cultured C2C12 myotubes was therefore reexamined using a truncated form of neural agrin, mini-agrin cN257C21B8. In cN257C21B8, the N-terminal laminin-binding domain of agrin is linked to a minimal C-terminal 21 kDa fragment that is sufficient for MuSK phosphorylation, AChR clustering, and binding of the putative agrin receptor (Gesemann et al., 1995, 1996; Meier et al., 1998b). In innervated muscle fibers, cN257C21B8 induces AChR-epsilon subunit gene transcription as well as aggregation of NRG and erbB2 (Meier et al., 1998b). Importantly, in contrast to full-length neural agrin, the truncated mini-agrin lacks the N-terminal heparan sulfate glycosaminoglycan (GAG) side chains that are required for binding of NRG (Meier et al., 1998a), thus excluding transcriptional activation independent of MuSK activation via GAG-attached NRGs.

As with full-length agrin (Jones et al., 1997), mini-agrin cN257C21B8 bound to a laminin substrate (Fig. 7, B8), but not when added directly to the culture supernatant (data not shown), increased AChR-epsilon subunit promoter activity in a quantitatively similar manner to MuSKneuTneu (Fig. 7, neu) or saturating NRG (Fig. 7, NRG). The induction of transcription by mini-agrin cN257C21B8 was abolished by the expression of a dominant negative erbB2/neu receptor (Fig. 7, B8 neu KM), which inhibits NRG-dependent activation of intracellular pathways (Wallasch et al., 1995). In contrast, an inactive mini-agrin isoform, cN257C21B0, which does not induce AChR clustering, failed to increase AChR-epsilon subunit gene transcription (Fig. 7, B0). Thus, in C2C12 myotubes, activated MuSK was not sufficient by itself to activate AChR gene transcription directly. Instead, transcription activated by MuSK required the NRG/erbB pathway, dependent on interaction with substrate-bound agrin or a related molecule, a condition that in innervated muscle fibers may be met by a native basal lamina component.


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

MuSK kinase domain activation recruits additional MuSK receptors

It is thought that a prerequisite for the assembly of the postsynaptic muscle membrane is the formation of a MuSK scaffold (Apel et al., 1997; Glass and Yancopoulos, 1997). The observation that MuSKneuTMuSK was not distributed evenly around the circumference of the muscle fiber, but instead was concentrated at AChR clusters independently of agrin, showed that the formation of such a MuSK scaffold is an activity intrinsic to active MuSK. Previous reports have shown that the MuSK ectodomain interacts with rapsyn (Apel et al., 1997), whereas the kinase domain is required for phosphorylation of the AChR-beta subunit (Glass et al., 1997), and that both domains are required for AChR clustering. In results presented here, a chimeric receptor lacking the MuSK ectodomain, neuneuTMuSK, induced ectopic AChR clusters by recruiting endogenous MuSK receptors. Therefore, the primary event in the recruitment of MuSK to a developing scaffold is the activation of the kinase domain, which, given that these experiments were done in the extra-synaptic region of innervated muscle fibers, precedes the formation of AChR clusters. The recruitment of MuSK via a positive feedback loop might be particularly important for the induction by neural agrin of ectopic AChR clusters in the extra-synaptic region of innervated muscles fibers, where MuSK expression is low but not absent (C. Moore and H. R. Brenner, unpublished observations).

The reasons for the failure of neuneuTMuSK to induce AChR clusters in C2C12 myotubes remain unclear. One possible reason is that the extracellular matrix differs between cultured C2C12 myotubes and innervated muscle fibers. In addition, it should also be remembered that direct injection of plasmid DNA is an extremely efficient method of transfecting muscle fibers. This might be important in achieving a concentrated point source of neuneuTMuSK, thereby facilitating the recruitment of endogenous MuSK receptors and the formation of AChR clusters.

The ligand-independent activation of MuSK described here is similar to the formation of active MuSK homodimers by activating antibodies (Xie et al., 1997; Hopf and Hoch, 1998). It could also explain the occasional small AChR clusters on a low number of myofibers in mice deficient for agrin (Gautam et al., 1996), arising through spontaneous association of MuSK homodimers that in the absence of agrin would occur only with low frequency. The formation of such foci of endogenous MuSK could be promoted by the elevated level of MuSK expression in fetal and neonatal myotubes (Valenzuela et al., 1995; Bowen et al., 1998). It is possible that in denervated muscle, the formation of dense patches of AChR clusters (Ko et al., 1977) is attributable to increased levels of MuSK, which leads to the ligand-independent formation of active homodimers.

Activation of MuSK in injected muscle fibers was sufficient to induce localized deposits of laminin-beta 2. Interestingly, no accompanying accumulation of endogenous muscle agrin was observed. Thus, because laminin present in the muscle basal lamina binds agrin (Denzer et al., 1997), this indicates that laminin-beta 2 is aggregated at the NMJ independently of its binding to agrin. In the context of laminin 11 (alpha 5beta 2gamma 1), laminin-beta 2 is a stop signal for motor neurons at the NMJ (Patton et al., 1997). This would explain why, in agrin-deficient mice, innervating neurons do sometimes stop and differentiate at sites opposing agrin-independent AChR clusters (Gautam et al., 1996), whereas in MuSK-deficient mice neither AChR clusters nor examples of an arborized innervating motor neuron are observed (DeChiara et al., 1996). However, laminin-beta 2 is unlikely to be the only MuSK-induced retrograde signal. The differentiation of the presynaptic nerve terminal is also affected in rapsyn-deficient mice (Gautam et al., 1995), despite the presence in the synaptic basal lamina of laminin-beta 2 and agrin, which is also a stop signal for motor neurons (Campagna et al., 1995).

MuSK-induced AChR clustering potentiated by muscle agrin

Ectopic expression of a chick muscle cAgrin7A0B0 isoform facilitated, but was not essential for, AChR clusters induced by MuSKneuTMuSK. Because agrin does not directly interact with MuSK (Glass et al., 1996), the modulation of MuSK activity by muscle cAgrin7A0B0 must require an additional protein. This protein is probably distinct from the putative agrin receptor, which is not recognized by isoforms of agrin lacking amino acid inserts at the B slice site (i.e., B0) (Gesemann et al., 1996). A strong candidate for this role is alpha -dystroglycan, which binds to both neural and muscle agrin (Bowe et al., 1994; Gee et al., 1994; Gesemann et al., 1996). In addition, agrin binding to alpha -dystroglycan potentiates agrin-induced AChR clustering (Jacobson et al., 1998). Furthermore, beta -dystroglycan, which associates with alpha -dystroglycan and is central to the dystrophin-associated protein complex, was concentrated at MuSKneuTMuSK-induced AChR clusters (Fig. 5), as it is at the NMJ (Ervasti and Campbell, 1993).

The requirement of MuSK for synaptic gene transcription

Drawing together results obtained from innervated muscle fibers and cultured myotubes, it was concluded that AChR-epsilon subunit gene transcription, which at the NMJ occurs only from the subsynaptic nuclei in response to innervation (Brenner et al., 1990; Witzemann et al., 1991), was increased indirectly by MuSK via activation of the erbB/NRG pathway. This conclusion contrasts with data from neonatal rapsyn knock-out mice, in which MuSK remains accumulated and transcripts encoding AChR alpha - and gamma -subunits are elevated, despite the absence of erbB receptors from the postsynaptic membrane (Gautam et al., 1995; Moscoso et al., 1995). However, high resolution in situ hybridization in neonatal rat muscle with AChR alpha -subunit mRNA-specific probes shows that in developing endplate regions, the high level of alpha -subunit mRNA, unlike epsilon -subunit mRNA, may originate from unfused myoblasts (Brenner et al., 1990).

In summary, we have shown that activation of the MuSK kinase domain initiates a positive feedback loop whereby additional MuSK receptors are recruited, resulting in concentrated foci of MuSK that then induce AChR clusters. Although this process did not require neural agrin, inactive muscle agrin facilitated the activity of MuSKneuTMuSK. Because this agrin isoform does not bind the putative agrin receptor, different domains within agrin can independently modulate the activity of MuSK. Furthermore, MuSK is likely to be important in the differentiation of the innervating motor neuron (laminin-beta 2) and later events in the maturation of the postsynaptic membrane (NaChs). Finally, MuSK indirectly activates synaptic gene transcription at the NMJ by assembly of the NRG/erbB pathway.


    FOOTNOTES

Received Dec. 18, 1998; revised Feb. 16, 1999; accepted Feb. 19, 1999.

This work was supported by grants from the Ott-Fonds of the Swiss Academy of Medical Sciences (G.J.), the Swiss National Science Foundation, the Helmut Horten Stiftung, and the Sandoz Stiftung (H.R.B.). We thank Dr. M. A. Ruegg for agrin expression constructs and comments on this manuscript, and D. Hauser for the anti-Nsk2/MuSK antibody.

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


    REFERENCES
TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

  • Apel ED, Glass DJ, Moscoso LM, Yancopoulos GD, Sanes JR (1997) Rapsyn is required for MuSK signaling and recruits synaptic components to a MuSK-containing scaffold. Neuron 18:623-635[ISI][Medline].
  • Bargmann CI, Hung M-C, Weinberg R (1986) Multiple independent activations of the neu oncogene by a point mutation altering the transmembrane domain of p185. Cell 45:649-657[ISI][Medline].
  • Boudier J-L, Treut TL, Jover E (1992) Autoradiographic localization of voltage-dependent sodium channels on the mouse neuromuscular junction using I125-alpha scorpion toxin. II. Sodium channel distribution on postsynaptic membranes. J Neurosci 12:454-466[Abstract].
  • Bowe MA, Deyst KA, Leszyk JD, Fallon JR (1994) Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans. Neuron 12:1173-1180[ISI][Medline].
  • Bowen DC, Park JS, Bodine S, Stark JL, Valenzuela DM, Stitt TN, Yancopoulos GD, Lindsay RM, Glass DJ, DiStefano PS (1998) Localization and regulation of MuSK at the neuromuscular junction. Dev Biol 199:309-319[ISI][Medline].
  • Brenner HR, Witzemann V, Sakmann B (1990) Imprinting of acetylcholine receptor message RNA accumulation in mammalian neuromuscular synapses. Nature 344:544-547[Medline].
  • Burke CL, Lemmon MA, Coren BA, Engelman DM, Stern DF (1997) Dimerization of the p185neu transmembrane domain is necessary but not sufficient for transformation. Oncogene 14:687-696[ISI][Medline].
  • Campagna JA, Ruegg MA, Bixby JL (1995) Agrin is a differentiation-inducing "stop-signal" for motorneurons in vitro. Neuron 15:1365-1374[ISI][Medline].
  • Colledge M, Froehner SC (1998) Signals mediating ion channel clustering at the neuromuscular junction. Curr Opin Neurobiol 8:357-363[ISI][Medline].
  • DeChiara TM, Bowen DC, Valenzuela DM, Simmons MV, Poueymirou WT, Thomas S, Kinetz E, Compton DL, Rojas E, Park JS, Smith C, DiStefano PS, Glass DJ, Burden SJ, Yancopoulos GD (1996) The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo. Cell 85:501-512[ISI][Medline].
  • Denzer AJ, Brandenberger R, Gesemann M, Chiquet M, Ruegg MA (1997) Agrin binds to the nerve-muscle basal lamina via laminin. J Cell Biol 137:671-683[Abstract/Free Full Text].
  • Ervasti JM, Campbell KP (1993) Dystrophin and the membrane skeleton. Curr Opin Cell Biol 5:82-86[Medline].
  • Ferns MJ, Campanelli JT, Hoch W, Scheller R, Hall Z (1993) The ability of agrin to cluster AChRs depends on alternative splicing and on cell surface proteoglycans. Neuron 11:491-502[ISI][Medline].
  • Fertuck HC, Salpeter MM (1976) Quantitation of junctional and extrajunctional acetylcholine receptors by electron microscope autoradiography after 125I-alpha bungarotoxin binding at the mouse neuromuscular junction. J Cell Biol 69:144-158[Abstract/Free Full Text].
  • Fischbach GD, Rosen KM (1997) ARIA: a neuromuscular junction neuregulin. Annu Rev Neurosci 20:429-458[ISI][Medline].
  • Gautam M, Noakes PG, Mudd J, Nichol M, Chu GC, Sanes JR, Merlie JP (1995) Failure of postsynaptic specialization to develop at neuromuscular junctions of rapsyn-deficient mice. Nature 377:232-236[Medline].
  • Gautam M, Noakes PG, Moscoso L, Rupp F, Scheller RH, Merlie JP, Sanes JR (1996) Defective neuromuscular synaptogenesis in agrin-deficient mutant mice. Cell 85:525-535[ISI][Medline].
  • Gee SH, Montanaro F, Lindenbaum MH, Carbonetto S (1994) Dystroglycan-alpha , a dystrophin-associated glycoprotein, is a functional agrin receptor. Cell 77:675-686[ISI][Medline].
  • Gesemann M, Denzer AJ, Ruegg MA (1995) Acetylcholine receptor-aggregating activity of agrin isoforms and mapping of the active site. J Cell Biol 128:625-636[Abstract/Free Full Text].
  • Gesemann M, Cavalli V, Denzer AJ, Brancaccio A, Schumacher B, Ruegg MA (1996) Alternative splicing of agrin alters its binding to heparin, dystroglycan, and the putative agrin receptor. Neuron 16:755-767[ISI][Medline].
  • Glass DJ, Yancopoulos GD (1997) Sequential roles of agrin, MuSK and rapsyn during neuromuscular junction formation. Curr Biol 7:379-384.
  • Glass DJ, Bowen DC, Stitt TN, Radziejewski C, Bruno J, Ryan TE, Gies DR, Shah S, Mattsson K, Burden SJ, DiStefano PS, Valenzeula DM, DeChiara TM, Yancopoulos GD (1996) Agrin acts via a MuSK receptor complex. Cell 85:513-523[ISI][Medline].
  • Glass DJ, Apel ED, Shah S, Bowen DC, DeChiara TM, Stitt TN, Sanes JR, Yancopoulos GD (1997) Kinase domain of the muscle-specific receptor tyrosine kinase (MuSK) is sufficient for phosphorylation but not clustering of acetylcholine receptors: required role for the MuSK ectodomain? Proc Natl Acad Sci USA 94:8848-8853[Abstract/Free Full Text].
  • Hopf C, Hoch W (1998) Dimerization of the muscle-specific kinase induces tyrosine phosphorylation of acetylcholine receptors and their aggregation on the surface of myotubes. J Biol Chem 273:6467-6473[Abstract/Free Full Text].
  • Jacobson C, Montanaro F, Lindenbaum M, Carbonetto S, Ferns M (1998) alpha -Dystroglycan functions in acetylcholine receptor aggregation but is not a coreceptor for agrin-MuSK signaling. J Neurosci 18:6340-6348[Abstract/Free Full Text].
  • Jones G, Herczeg A, Ruegg MA, Lichtsteiner M, Kroger S, Brenner HR (1996) Substrate-bound agrin induces expression of acetylcholine receptor epsilon -subunit gene in cultured mammalian muscle cells. Proc Natl Acad Sci USA 93:5985-5990[Abstract/Free Full Text].
  • Jones G, Meier T, Lichtsteiner M, Witzemann V, Sakmann B, Brenner HR (1997) Induction by agrin of ectopic and functional postsynaptic-like membrane in innervated muscle. Proc Natl Acad Sci USA 94:2654-2659[Abstract/Free Full Text].
  • Ko PK, Anderson MJ, Cohen MW (1977) Denervated skeletal muscle fibres develop discrete patches of high acetylcholine receptor density. Science 196:540-542[Abstract/Free Full Text].
  • Lupa MT, Krzemien DM, Schaller KL, Caldwell JH (1993) Aggregation of sodium channels during development and maturation of the neuromuscular junction. J Neurosci 13:1326-1336[Abstract].
  • Martin PT, Sanes JR (1997) Integrins mediate adhesion to agrin and modulate agrin signalling. Development 124:3909-3917[Abstract].
  • McMahan UJ (1990) The agrin hypothesis. Cold Spring Harb Symp Quant Biol 55:407-418[Medline].
  • Meier T, Hauser DM, Chiquet M, Landmann L, Ruegg MA, Brenner HR (1997) Neural agrin induces ectopic postsynaptic specializations in innervated muscle fibers. J Neurosci 17:6534-6544[Abstract/Free Full Text].
  • Meier T, Masciulli F, Moore C, Schoumacher F, Eppenberger U, Denzer AJ, Jones G, Brenner HR (1998a) Agrin can mediate AChR gene expression in muscle by aggregation of muscle-derived neuregulins. J Cell Biol 141:715-726[Abstract/Free Full Text].
  • Meier T, Marangi PA, Moll J, Hauser DM, Brenner H-R, Ruegg MA (1998b) A minigene of neural agrin encoding the laminin-binding and acetylcholine receptor-aggregating domains is sufficient to induce postsynaptic differentiation in muscle fibres. Eur J Neurosci 10:3141-3152[ISI][Medline].
  • Moscoso LM, Chu GC, Gautam M, Noakes PG, Merlie JP, Sanes JR (1995) Synapse-associated expression of an acetylcholine receptor-inducing protein, ARIA/heregulin and its putative receptors, ErbB2 and ErbB3, in developing mammalian muscle. Dev Biol 172:158-169[ISI][Medline].
  • Patton BL, Miner JH, Chiu AY, Sanes JR (1997) Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice. J Cell Biol 139:1507-1521[Abstract/Free Full Text].
  • Porter BE, Weis J, Sanes JR (1995) A motorneuron-selective stop signal in the synaptic protein S-laminin. Neuron 14:549-559[ISI][Medline].
  • Rimer M, Cohen I, Lømo T, Burden SJ, McMahan UJ (1998) Neuregulins and erbB receptors at neuromuscular junctions and at agrin-induced postsynaptic-like apparatus in skeletal muscle. Mol Cell Neurosci 12:1-15[ISI][Medline].
  • Ruegg MA, Bixby JL (1998) Agrin orchestrates synaptic differentiation at the vertebrate neuromuscular junction. Trends Neurosci 21:22-27[ISI][Medline].
  • Ruegg MA, Tsim KWK, Horton SE, Kroger S, Escher G, Gensch EM, McMahan UJ (1992) The agrin gene codes for a family of basal lamina proteins that differ in function and distribution. Neuron 8:691-699[ISI][Medline].
  • Schmidt C, Lipsius E, Kruppa J (1995) Nuclear and nucleolar targeting of human ribosomal protein S6. Mol Biol Cell 6:1875-1885[Abstract].
  • Siegel PM, Muller WJ (1996) Mutations affecting conserved cysteine residues within the extracellular domain of neu promote receptor dimerization and activation. Proc Natl Acad Sci USA 93:687-696.
  • Tinsley JM, Blake DJ, Zuellig RA, Davies KE (1994) Increasing complexity of the dystrophin-associated complex. Proc Natl Acad Sci USA 91:8703-8313.
  • Tzahar E, Pinkas-Kramarski R, Moyer JD, Klapper LN, Alroy I, Levkowitz G, Shelly M, Henis S, Eisenstein M, Ratzkin BJ, Sela M, Andrews GC, Yarden Y (1997) Bivalence of EGF-like ligands drives the ErbB signaling network. EMBO J 16:4938-4950[ISI][Medline].
  • Umesono K, Murakami KK, Thompson CC, Evans RM (1991) Direct repeats as selective response elements for the thyroid hormone, retinoic acid, and vitamin D3 receptors. Cell 65:1255-1266[ISI][Medline].
  • Valenzuela DM, Stitt TN, DiStefano PS, Rojas E, Mattsson K, Compton DL, Nunez L, Park JS, Stark JL, Gies DR, Thomas S, Beau MML, Fernald AA, Copeland NG, Jenkins NA, Burden SJ, Glass DJ, Yancopoulos GD (1995) Receptor tyrosine kinase specific for the skeletal muscle lineage: expression in embryonic muscle, and at the neuromuscular junction, and after injury. Neuron 15:573-584[ISI][Medline].
  • Wallasch C, Weiss FU, Niederfellner G, Jallal B, Issing W, Ullrich A (1995) Heregulin-dependent regulation of HER2/neu oncogenic signalling by heterodimerization ith HER3. EMBO J 14:4267-4275[ISI][Medline].
  • Witzemann V, Brenner HR, Sakmann B (1991) Neural factors regulate AChR subunit mRNAs at rat neuromuscular junctions J Cell Biol 114:125-141[Abstract/Free Full Text].
  • Xie M-H, Yuan J, Adams C, Gurney A (1997) Direct demonstration of MuSK involvement in acetylcholine receptor clustering through identification of agonist ScFv. Nat Biotechnol 15:768-771[ISI][Medline].

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