The formation of neuromuscular synapses requires a mutual exchange of signals between motor neurons and muscle fibers leading to the formation of a highly specialized postsynaptic membrane and a highly differentiated nerve terminal, which insure that synaptic transmission is fast, robust and reliable. We found that Lrp4 has a key role in this exchange, as it acts bi- directionally to coordinate neuromuscular synapse formation. Lrp4 not only binds neuronal Agrin, activating MuSK and stimulating postsynaptic differentiation, but also functions as a direct muscle-derived retrograde signal that is necessary and sufficient for presynaptic differentiation. How Lrp4 stimulates presynaptic differentiation is not understood. Here, we propose to identify the motor neuron receptor for Lrp4 as a first step to understand how Lrp4 induces the differentiation of motor nerve terminals. Our previous studies showed that Lrp4 induces the clustering of synaptic vesicle and active zone proteins, thereby organizing the machinery for release of neurotransmitter. Retrograde signals, however, also cause motor axons to terminate and form synapses: in the absence of Lrp4 or MuSK, motor axons fail to stop and instead grow throughout the muscle without forming synapses. Here, we propose to determine whether Lrp4 is itself a 'stop' signal that arrests motor axon growth or whether Lrp4-mediated activation of MuSK leads to the production of a novel signal that control motor axon growth. The experiments described here should provide new insights into the mechanisms that control presynaptic differentiation during development and maintain neuromuscular synapses in adults. As such, these studies are likely to shed new light into neuromuscular diseases, including amyotrophic lateral sclerosis, congenital myasthenia, myasthenia gravis and age-related muscle wasting, sacropenia.

Public Health Relevance

The formation of neuromuscular synapses requires a complex exchange of signals between motor neurons and developing muscle fibers leading to the formation of a highly specialized postsynaptic membrane and a highly differentiated nerve terminal. Lrp4 acts bi-directionally to coordinate synapse formation by binding neuronal Agrin, activating MuSK and stimulating postsynaptic differentiation, and in turn functioning as a muscle-derived retrograde signal that is necessary and sufficient for presynaptic differentiation. Defects in this signaling pathway are responsible for a variety of congenital neuromuscular disorders and could underlie or contribute to neurodegenerative diseases such as ALS. The experiments described here are designed to determine how motor neurons respond to Lrp4, stimulating presynaptic differentiation.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
4R37NS036193-19
Application #
9100935
Study Section
Neurodifferentiation, Plasticity, and Regeneration Study Section (NDPR)
Program Officer
Nuckolls, Glen H
Project Start
1998-02-01
Project End
2017-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
19
Fiscal Year
2016
Total Cost
Indirect Cost
Name
New York University
Department
Neurosciences
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Burden, Steven J; Huijbers, Maartje G; Remedio, Leonor (2018) Fundamental Molecules and Mechanisms for Forming and Maintaining Neuromuscular Synapses. Int J Mol Sci 19:
Hata, Katsusuke; Maeno-Hikichi, Yuka; Yumoto, Norihiro et al. (2018) Distinct Roles of Different Presynaptic and Postsynaptic NCAM Isoforms in Early Motoneuron-Myotube Interactions Required for Functional Synapse Formation. J Neurosci 38:498-510
Cantor, Sarah; Zhang, Wei; Delestrée, Nicolas et al. (2018) Preserving neuromuscular synapses in ALS by stimulating MuSK with a therapeutic agonist antibody. Elife 7:
Lee, Jennifer K; Hallock, Peter T; Burden, Steven J (2017) Abelson tyrosine-protein kinase 2 regulates myoblast proliferation and controls muscle fiber length. Elife 6:
Joseph, Giselle A; Lu, Min; Radu, Maria et al. (2017) Group I Paks Promote Skeletal Myoblast Differentiation In Vivo and In Vitro. Mol Cell Biol 37:
Remédio, Leonor; Gribble, Katherine D; Lee, Jennifer K et al. (2016) Diverging roles for Lrp4 and Wnt signaling in neuromuscular synapse development during evolution. Genes Dev 30:1058-69
Gomez, Andrea M; Froemke, Robert C; Burden, Steven J (2014) Synaptic plasticity and cognitive function are disrupted in the absence of Lrp4. Elife 3:e04287
Huijbers, Maartje G; Zhang, Wei; Klooster, Rinse et al. (2013) MuSK IgG4 autoantibodies cause myasthenia gravis by inhibiting binding between MuSK and Lrp4. Proc Natl Acad Sci U S A 110:20783-8
Yumoto, Norihiro; Kim, Natalie; Burden, Steven J (2012) Lrp4 is a retrograde signal for presynaptic differentiation at neuromuscular synapses. Nature 489:438-42
Zhang, Wei; Coldefy, Anne-Sophie; Hubbard, Stevan R et al. (2011) Agrin binds to the N-terminal region of Lrp4 protein and stimulates association between Lrp4 and the first immunoglobulin-like domain in muscle-specific kinase (MuSK). J Biol Chem 286:40624-30

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