Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/197147
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSuárez, Elisabeth-
dc.contributor.authorBach González, Daniel-
dc.contributor.authorCadefau Surroca, Joan Aureli-
dc.contributor.authorPalacín Prieto, Manuel-
dc.contributor.authorZorzano Olarte, Antonio-
dc.contributor.authorGumà i Garcia, Anna Maria-
dc.date.accessioned2023-04-24T15:03:05Z-
dc.date.available2023-04-24T15:03:05Z-
dc.date.issued2001-05-25-
dc.identifier.issn0021-9258-
dc.identifier.urihttp://hdl.handle.net/2445/197147-
dc.description.abstractNeuregulins regulate the expression of acetylcholine receptor genes and induce development of the neuromuscular junction in muscle. In studying whether neuregulins regulate glucose uptake in muscle, we analyzed the effect of a recombinant neuregulin, (r)heregulin-beta1-(177-244) (HRG), on L6E9 muscle cells, which express the neuregulin receptors ErbB2 and ErbB3. L6E9 responded acutely to HRG by a time- and concentration-dependent stimulation of 2-deoxyglucose uptake. HRG-induced stimulation of glucose transport was additive to the effect of insulin. The acute stimulation of the glucose transport induced by HRG was a consequence of the translocation of GLUT4, GLUT1, and GLUT3 glucose carriers to the cell surface. The effect of HRG on glucose transport was dependent on phosphatidylinositol 3-kinase activity. HRG also stimulated glucose transport in the incubated soleus muscle and was additive to the effect of insulin. Chronic exposure of L6E9 cells to HRG potentiated myogenic differentiation, and under these conditions, glucose transport was also stimulated. The activation of glucose transport after chronic HRG exposure was due to enhanced cell content of GLUT1 and GLUT3 and to increased abundance of these carriers at the plasma membrane. However, under these conditions, GLUT4 expression was markedly down-regulated. Muscle denervation is associated with GLUT1 induction and GLUT4 repression. In this connection, muscle denervation caused a marked increase in the content of ErbB2 and ErbB3 receptors, which occurred in the absence of alterations in neuregulin mRNA levels. This fact suggests that neuregulins regulate glucose transporter expression in denervated muscle. We conclude that neuregulins regulate glucose uptake in L6E9 muscle cells by mechanisms involving the recruitment of glucose transporters to the cell surface and modulation of their expression. Neuregulins may also participate in the adaptations in glucose transport that take place in the muscle fiber after denervation.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Society for Biochemistry and Molecular Biology-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1074/jbc.M008100200-
dc.relation.ispartofJournal of Biological Chemistry, 2001, vol. 276, num. 21, p. 18257-18264-
dc.relation.urihttps://doi.org/10.1074/jbc.M008100200-
dc.rights(c) American Society for Biochemistry and Molecular Biology, 2001-
dc.sourceArticles publicats en revistes (Bioquímica i Biomedicina Molecular)-
dc.subject.classificationGlucosa-
dc.subject.classificationCèl·lules musculars-
dc.subject.classificationTransport biològic-
dc.subject.otherGlucose-
dc.subject.otherMuscle cells-
dc.subject.otherBiological transport-
dc.titleA novel role of neuregulin in skeletal muscle. Neuregulin stimulates glucose uptake, glucose transporter translocation and transporter expression in muscle cells-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec180145-
dc.date.updated2023-04-24T15:03:05Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Biologia Cel·lular, Fisiologia i Immunologia)
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)

Files in This Item:
File Description SizeFormat 
180145.pdf389.7 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.