Unknown

Dataset Information

0

Structural mechanisms of the agrin-LRP4-MuSK signaling pathway in neuromuscular junction differentiation.


ABSTRACT: The neuromuscular junction (NMJ) is the most extensively studied model of neuronal synaptogenesis. Acetylcholine receptor (AChR) clustering on the postsynaptic membrane is a cardinal event in the differentiation of NMJs. AChR clustering and postsynaptic differentiation is orchestrated by sophisticated interactions among three proteins: the neuron-secreted proteoglycan agrin, the co-receptor LRP4, and the muscle-specific receptor tyrosine kinase MuSK. LRP4 and MuSK act as scaffolds for multiple binding partners, resulting in a complex and dynamic network of interacting proteins that is required for AChR clustering. In this review, we discuss the structural basis for NMJ postsynaptic differentiation mediated by the agrin-LRP4-MuSK signaling pathway.

SUBMITTER: Zong Y 

PROVIDER: S-EPMC4627850 | biostudies-literature | 2013 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Structural mechanisms of the agrin-LRP4-MuSK signaling pathway in neuromuscular junction differentiation.

Zong Yinong Y   Jin Rongsheng R  

Cellular and molecular life sciences : CMLS 20121122 17


The neuromuscular junction (NMJ) is the most extensively studied model of neuronal synaptogenesis. Acetylcholine receptor (AChR) clustering on the postsynaptic membrane is a cardinal event in the differentiation of NMJs. AChR clustering and postsynaptic differentiation is orchestrated by sophisticated interactions among three proteins: the neuron-secreted proteoglycan agrin, the co-receptor LRP4, and the muscle-specific receptor tyrosine kinase MuSK. LRP4 and MuSK act as scaffolds for multiple b  ...[more]

Similar Datasets

| S-EPMC3278892 | biostudies-literature
| S-EPMC4564764 | biostudies-literature
| S-EPMC2933840 | biostudies-literature
| S-EPMC6650252 | biostudies-literature
| S-EPMC3422364 | biostudies-literature
| S-EPMC7403661 | biostudies-literature