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dc.contributor.authorNishimune, Hiroshi
dc.contributor.authorValdez, Gregorio
dc.contributor.authorJarad, George
dc.contributor.authorMoulson, Casey L.
dc.contributor.authorMüller, Ulrich
dc.contributor.authorMiner, Jeffrey H.
dc.contributor.authorSanes, Joshua R.
dc.description.abstractA prominent feature of synaptic maturation at the neuromuscular junction (NMJ) is the topological transformation of the acetylcholine receptor (AChR)-rich postsynaptic membrane from an ovoid plaque into a complex array of branches. We show here that laminins play an autocrine role in promoting this transformation. Laminins containing the 4, 5, and 2 subunits are synthesized by muscle fibers and concentrated in the small portion of the basal lamina that passes through the synaptic cleft at the NMJ. Topological maturation of AChR clusters was delayed in targeted mutant mice lacking laminin 5 and arrested in mutants lacking both 𝝰4 and 𝝰5. Analysis of chimeric laminins in vivo and of mutant myotubes cultured aneurally demonstrated that the laminins act directly on muscle cells to promote postsynaptic maturation. Immunohistochemical studies in vivo and in vitro along with analysis of targeted mutants provide evidence that laminin-dependent aggregation of dystroglycan in the postsynaptic membrane is a key step in synaptic maturation. Another synaptically concentrated laminin receptor, Bcam, is dispensable. Together with previous studies implicating laminins as organizers of presynaptic differentiation, these results show that laminins coordinate post- with presynaptic maturation.
dc.publisherThe Rockefeller University Press
dc.rightsAttribution–Noncommercial–Share Alike 3.0 Unported
dc.titleLaminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junction
dc.title.serialJournal of Cell Biology

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Attribution–Noncommercial–Share Alike 3.0 Unported
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