Abstract

The 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.

Highlights

  • Insulin-like growth factors (IGFs) and associated signaling pathways play a central role in regulating skeletal muscle growth in mammals [1,2]

  • Stimulation of the cellular responses to IGF-I are mediated through the IGF-I receptor via the PI3K/AKT/mTOR pathway [8], with the availability of IGFs regulated by the insulin-likegrowth factor binding proteins (IGFBPs)

  • Cluster I comprised genes predominantly expressed in mono-nucleated cells and included IGF binding proteins (IGFBPs)-5.1 and 5.2, IGFBP-6, IGFBP-rP1, IGFBP-2.2, MRF4 and IGF-II

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Summary

Introduction

Insulin-like growth factors (IGFs) and associated signaling pathways play a central role in regulating skeletal muscle growth in mammals [1,2]. Stimulation of the cellular responses to IGF-I are mediated through the IGF-I receptor via the PI3K/AKT/mTOR pathway [8], with the availability of IGFs regulated by the insulin-likegrowth factor binding proteins (IGFBPs). IGFBP-5 regulates the differentiation of C2C12 myoblasts through binding to IGF-II [17], whereas IGFBP-2 inhibits IGF-I stimulated cell proliferation and DNA synthesis, and is considered a negative regulator of growth [18]. Basic fibroblast growth factor (bFGF) affects IGF signalling by inhibiting differentiation [19,20,21] and promoting cell proliferation [22]. In addition to stimulation by IGFs, the PI3K/AKT/mTOR pathway has recently been shown to be nutritionally regulated, in that mTORC1 phosphorylation is dependant on amino acid availability [23]. Several amino acid signalling pathways have been identified including vps34 [26], recombination activating proteins (Rags) [27,28] and the ste-20 related mitogen-activated protein kinase kinase kinase kinase 3 (MAP4K3) [29]

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