Abstract

BackgroundThe branched-chain amino acid (BCAA) leucine has been identified to be a key regulator of skeletal muscle anabolism. Activation of anabolic signalling occurs via the mammalian target of rapamycin (mTOR) through an undefined mechanism. System A and L solute carriers transport essential amino acids across plasma membranes; however it remains unknown whether an exogenous supply of leucine regulates their gene expression. The aim of the present study was to investigate the effects of acute and chronic leucine stimulation of anabolic signalling and specific amino acid transporters, using cultured primary human skeletal muscle cells.ResultsHuman myotubes were treated with leucine, insulin or co-treated with leucine and insulin for 30 min, 3 h or 24 h. Activation of mTOR signalling kinases were examined, together with putative nutrient sensor human vacuolar protein sorting 34 (hVps34) and gene expression of selected amino acid transporters. Phosphorylation of mTOR and p70S6K was transiently increased following leucine exposure, independently to insulin. hVps34 protein expression was also significantly increased. However, genes encoding amino acid transporters were differentially regulated by insulin and not leucine.ConclusionsmTOR signalling is transiently activated by leucine within human myotubes independently of insulin stimulation. While this occurred in the absence of changes in gene expression of amino acid transporters, protein expression of hVps34 increased.

Highlights

  • The branched-chain amino acid (BCAA) leucine has been identified to be a key regulator of skeletal muscle anabolism

  • Cultures stimulated for 3 h displayed increased mammalian target of rapamycin (mTOR) expression under all treatment conditions, with the greatest increase observed with insulin stimulation (2.0-fold; P < 0.001)

  • While these actions appear transient at the leucine dose utilised, activation of mTOR and p70 ribosomal S6 kinase (p70S6K) occurred at physiologically relevant concentrations independently of insulin stimulation

Read more

Summary

Introduction

The branched-chain amino acid (BCAA) leucine has been identified to be a key regulator of skeletal muscle anabolism. The aim of the present study was to investigate the effects of acute and chronic leucine stimulation of anabolic signalling and specific amino acid transporters, using cultured primary human skeletal muscle cells. Various cell models have examined the anabolic potential of the branched chain amino acid (BCAA), leucine, to stimulate skeletal muscle growth via mammalian target of rapamycin (mTOR) signalling [7,8,3,9,10]. Recent evidence from rodent models suggests that it is the activity of Vps which is the primary modulator of leucine-stimulated mTOR signalling in rat muscle [28]. It has been previously demonstrated that human vacuolar protein sorting 34 (hVps34) is required for nutrient activation of p70S6K, via mTOR signalling [29]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call