Developing skeletal muscle cells express functional muscarinic acetylcholine receptors coupled to different intracellular signaling systems

dc.contributor.authorFurlan, Ingrid
dc.contributor.authorGodinho, Rosely Oliveira [UNIFESP]
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.date.accessioned2016-01-24T12:38:04Z
dc.date.available2016-01-24T12:38:04Z
dc.date.issued2005-10-01
dc.description.abstract1 This study analyzed the expression of muscarinic acetylcholine receptors (mAChRs) in the rat cultured skeletal muscle cells and their coupling to G protein, phospholipase C and adenylyl cyclase (AC).2 Our results showed the presence of a homogeneous population of [H-3]methyl-quinuclidinyl benzilate-binding sites in the membrane fraction from the rat cultured muscle (K-D = 0.4 nM, B-max = 8.9 fmol mg protein(-1)). Specific muscarinic binding sites were also detected in denervated diaphragm muscles from adult rats and in myoblasts isolated from newborn rats.3 Activation of mAChRs with carbachol induced specific [S-35]GTP gamma S binding to cultured muscle membranes and potentiated the forskolin-dependent stimulation of AC. These effects were totally inhibited by 0.1-1 mu M atropine.4 in addition, mAChRs were able to stimulate generation of diacylglycerol (DAG) in response to acetylcholine, carbachol or selective mAChR agonist oxotremorine-M.5 the carbachol-dependent increase in DAG was inhibited in a concentration-dependent manner by mAChR antagonists atropine, pirenzepine and 4-DAMP mustard.6 Finally, activation of these receptors was correlated with increased synthesis of acetylcholinesterase, via a PKC-dependent pathway.7 Taken together, these results indicate that expression of mAChRs, coupled to G protein and distinct intracellular signaling systems, is a characteristic of noninnervated skeletal muscle cells and may be responsible for trophic influences of acetylcholine during formation of the neuromuscular synapse.en
dc.description.affiliationUniversidade Federal de São Paulo, Dept Pharmacol, Div Cellular Pharmacol, Escola Paulista Med, BR-04044020 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Pharmacol, Div Cellular Pharmacol, Escola Paulista Med, BR-04044020 São Paulo, Brazil
dc.description.sourceWeb of Science
dc.format.extent389-396
dc.identifierhttp://dx.doi.org/10.1038/sj.bjp.0706329
dc.identifier.citationBritish Journal of Pharmacology. London: Nature Publishing Group, v. 146, n. 3, p. 389-396, 2005.
dc.identifier.doi10.1038/sj.bjp.0706329
dc.identifier.issn0007-1188
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/28475
dc.identifier.wosWOS:000232317400010
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofBritish Journal of Pharmacology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectmuscarinic acetylcholine receptorsen
dc.subjectdiacylglycerolen
dc.subjectcyclic AMPen
dc.subjectskeletal muscleen
dc.subjectG proteinen
dc.subjectdevelopmenten
dc.titleDeveloping skeletal muscle cells express functional muscarinic acetylcholine receptors coupled to different intracellular signaling systemsen
dc.typeinfo:eu-repo/semantics/article
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