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dc.contributor.authorBower, Neil I.
dc.contributor.authorJohnston, Ian A.
dc.date.accessioned2011-12-05T17:03:53Z
dc.date.available2011-12-05T17:03:53Z
dc.date.issued2010-06-14
dc.identifier.citationBower , N I & Johnston , I A 2010 , ' Transcriptional regulation of the IGF signaling pathway by amino acids and insulin-like growth factors during myogenesis in Atlantic salmon ' , PLoS One , vol. 5 , no. 6 , e11100 . https://doi.org/10.1371/journal.pone.0011100en
dc.identifier.issn1932-6203
dc.identifier.otherPURE: 1728067
dc.identifier.otherPURE UUID: 93d790bb-e1f3-49d4-90a8-af1ef3c9e69c
dc.identifier.otherWOS: 000278741100014
dc.identifier.otherScopus: 77955233471
dc.identifier.otherORCID: /0000-0002-7796-5754/work/47136033
dc.identifier.urihttps://hdl.handle.net/10023/2092
dc.description.abstractThe insulin-like growth factor signalling pathway is an important regulator of skeletal muscle growth. We examined the mRNA expression of components of the insulin-like growth factor (IGF) signalling pathway as well as Fibroblast Growth Factor 2 (FGF2) during maturation of myotubes in primary cell cultures isolated from fast myotomal muscle of Atlantic salmon (Salmo salar). The transcriptional regulation of IGFs and IGFBP expression by amino acids and insulin-like growth factors was also investigated. Proliferation of cells was 15% d(-1) at days 2 and 3 of the culture, increasing to 66% d(-1) at day 6. Three clusters of elevated gene expression were observed during the maturation of the culture associated with mono-nucleic cells (IGFBP5.1 and 5.2, IGFBP-6, IGFBP-rP1, IGFBP-2.2 and IGF-II), the initial proliferation phase (IGF-I, IGFBP-4, FGF2 and IGF-IRb) and terminal differentiation and myotube production (IGF2R, IGF-IRa). In cells starved of amino acids and serum for 72 h, IGF-I mRNA decreased 10-fold which was reversed by amino acid replacement. Addition of IGF-I and amino acids to starved cells resulted in an 18-fold increase in IGF-I mRNA indicating synergistic effects and the activation of additional pathway(s) leading to IGF-I production via a positive feedback mechanism. IGF-II, IGFBP-5.1 and IGFBP-5.2 expression was unchanged in starved cells, but increased with amino acid replacement. Synergistic increases in expression of IGFBP5.2 and IGFBP-4, but not IGFBP5.1 were observed with addition of IGF-I, IGF-II or insulin and amino acids to the medium. IGF-I and IGF-II directly stimulated IGFBP-6 expression, but not when amino acids were present. These findings indicate that amino acids alone are sufficient to stimulate myogenesis in myoblasts and that IGF-I production is controlled by both endocrine and paracrine pathways. A model depicting the transcriptional regulation of the IGF pathway in Atlantic salmon muscle following feeding is proposed.
dc.format.extent14
dc.language.isoeng
dc.relation.ispartofPLoS Oneen
dc.rights© 2010 Bower, Johnston. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en
dc.subjectMuscle-cell differentiationen
dc.subjectTrout oncorhynchus-mykissen
dc.subjectFactor binding protein-5en
dc.subjectFactor-II receptoren
dc.subjectSkeletal-muscleen
dc.subjectGene-expressionen
dc.subjectIn-vitroen
dc.subjectPhosphatidylinositol 3-kinaseen
dc.subjectMessenger-RNAen
dc.subjectC2C12 myoblastsen
dc.subjectQH426 Geneticsen
dc.subject.lccQH426en
dc.titleTranscriptional regulation of the IGF signaling pathway by amino acids and insulin-like growth factors during myogenesis in Atlantic salmonen
dc.typeJournal articleen
dc.contributor.sponsorBBSRCen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. Scottish Oceans Instituteen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Marine Alliance for Science & Technology Scotlanden
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0011100
dc.description.statusPeer revieweden
dc.identifier.grantnumberBB/D015391/1en


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