Defective Neuromuscular Synaptogenesis in Agrin-Deficient Mutant Mice

Medha Gautam, Peter G. Noakes, Lisa M. Moscoso, Fabio Rupp, Richard H. Scheller, John P. Merlie, Joshua R. Sanes

Cell · 1996 · 925 citations · 46 references

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Concepts

TL;DR

Motor axons induce acetylcholine receptor clustering at neuromuscular synapses, a process orchestrated by the motoneuron‑derived protein agrin. In agrin‑deficient mice, postsynaptic AChR clusters are markedly reduced, yet residual differentiation indicates a second nerve‑derived signal, and abnormal nerve branching and presynaptic development are also observed.

Abstract

During neuromuscular synapse formation, motor axons induce clustering of acetylcholine receptors (AChRs) in the muscle fiber membrane. The protein agrin, originally isolated from the basal lamina of the synaptic cleft, is synthesized and secreted by motoneurons and triggers formation of AChR clusters on cultured myotubes. We show here that postsynaptic AChR aggregates are markedly reduced in number, size, and density in muscles of agrin-deficient mutant mice. These results support the hypothesis that agrin is a critical organizer of postsynaptic differentiation. However, some postsynaptic differentiation does occur in the mutant, suggesting the existence of a second nerve-derived synaptic organizing signal. In addition, we show that intramuscular nerve branching and presynaptic differentiation are abnormal in the mutant, phenotypes which may reflect either a distinct effect of agrin or impaired retrograde signaling from a defective postsynaptic apparatus.

References

46