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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-104

Willmann, R; Pun, S; Stallmach, L; Sadasivam, G; Santos, A F; Caroni, P; Fuhrer, C (2006). Cholesterol and lipid microdomains stabilize the postsynapse at the neuromuscular junction. The EMBO Journal, 25(17):4050-4060.

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Abstract

Stabilization and maturation of synapses are important for development and function of the nervous system. Previous studies have implicated cholesterol-rich lipid microdomains in synapse stabilization, but the underlying mechanisms remain unclear. We found that cholesterol stabilizes clusters of synaptic acetylcholine receptors (AChRs) in denervated muscle in vivo and in nerve-muscle explants. In paralyzed muscles, cholesterol triggered maturation of nerve sprout-induced AChR clusters into pretzel shape. Cholesterol treatment also rescued a specific defect in AChR cluster stability in cultured src(-/-);fyn(-/-) myotubes. Postsynaptic proteins including AChRs, rapsyn, MuSK and Src-family kinases were strongly enriched in lipid microdomains prepared from wild-type myotubes. Microdomain disruption by cholesterol-sequestering methyl-beta-cyclodextrin disassembled AChR clusters and decreased AChR-rapsyn interaction and AChR phosphorylation. Amounts of microdomains and enrichment of postsynaptic proteins into microdomains were decreased in src(-/-);fyn(-/-) myotubes but rescued by cholesterol treatment. These data provide evidence that cholesterol-rich lipid microdomains and SFKs act in a dual mechanism in stabilizing the postsynapse: SFKs enhance microdomain-association of postsynaptic components, whereas microdomains provide the environment for SFKs to maintain interactions and phosphorylation of these components.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Brain Research Institute
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:6 September 2006
Deposited On:11 Feb 2008 12:12
Last Modified:28 Nov 2013 02:11
Publisher:Nature Publishing Group
ISSN:0261-4189
Publisher DOI:10.1038/sj.emboj.7601288
Related URLs:http://www.nature.com/emboj/journal/v25/n17/abs/7601288a.html
PubMed ID:16932745
Citations:Web of Science®. Times Cited: 30
Google Scholar™
Scopus®. Citation Count: 31

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