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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1998-6-4
pubmed:abstractText
Nicotinic acetylcholine receptors (AChRs) are clustered at high density in the postsynaptic membranes of skeletal neuromuscular junctions and cholinergic interneuronal synapses. A cytoplasmic protein, rapsyn, is essential for AChR clustering in muscle. Here, we asked whether rapsyn mediates neuronal AChR clustering at cholinergic synapses in a mammalian sympathetic ganglion, the superior cervical ganglion (SCG). Several observations supported this possibility: (1) AChR clusters containing the alpha3-5 and beta2 subunits, homologs of the muscle AChR subunits, are present at SCG synapses; (2) rapsyn RNA is readily detectable in the SCG; and (3) expression of recombinant rapsyn in heterologous cells induces aggregation of coexpressed neuronal AChR subunits. However, rapsyn protein was undetectable at ganglionic synaptic sites. Moreover, aggregates of neuronal AChRs induced in heterologous cells by full-length rapsyn remained intracellular, whereas rapsyn-induced clusters of muscle AChRs reached the cell surface. Additional studies revealed a second rapsyn RNA species in SCG generated by alternative splicing and competent to encode a novel short rapsyn isoform. However, this isoform clustered neither neuronal nor muscle AChRs in heterologous cells. Most telling, the number, size, and density of AChR clusters in SCG did not differ significantly between neonatal mice bearing a targeted mutation of the rapsyn gene and littermate controls. Thus, rapsyn is dispensable for clustering of ganglionic neuronal nicotinic AChRs.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0270-6474
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4166-76
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9592096-Amino Acid Sequence, pubmed-meshheading:9592096-Animals, pubmed-meshheading:9592096-Carrier Proteins, pubmed-meshheading:9592096-Cells, Cultured, pubmed-meshheading:9592096-Cholinergic Fibers, pubmed-meshheading:9592096-Gene Expression, pubmed-meshheading:9592096-Humans, pubmed-meshheading:9592096-Kidney, pubmed-meshheading:9592096-Membrane Proteins, pubmed-meshheading:9592096-Mice, pubmed-meshheading:9592096-Mice, Inbred C57BL, pubmed-meshheading:9592096-Mice, Knockout, pubmed-meshheading:9592096-Molecular Sequence Data, pubmed-meshheading:9592096-Motor Neurons, pubmed-meshheading:9592096-Muscle Proteins, pubmed-meshheading:9592096-Mutagenesis, pubmed-meshheading:9592096-RNA, Messenger, pubmed-meshheading:9592096-Receptors, Cholinergic, pubmed-meshheading:9592096-Receptors, Nicotinic, pubmed-meshheading:9592096-Superior Cervical Ganglion, pubmed-meshheading:9592096-Synapses
pubmed:year
1998
pubmed:articleTitle
Rapsyn clusters neuronal acetylcholine receptors but is inessential for formation of an interneuronal cholinergic synapse.
pubmed:affiliation
Department of Anatomy and Neurobiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't