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The actions of exogenous leucine on mTOR signalling and amino acid transporters in human myotubes.

BMC physiology (2011-06-28)
Petra Gran, David Cameron-Smith
ABSTRACT

The 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. Human 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. mTOR 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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
ECO TWEEN® 20, viscous liquid
Sigma-Aldrich
TWEEN® 20, Low-peroxide; Low-carbonyls
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TWEEN® 20, viscous liquid
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TWEEN® 20, for molecular biology, viscous liquid
Sigma-Aldrich
TWEEN® 20, Low-peroxide; Low-carbonyls
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TWEEN® 20, BioXtra, viscous liquid
Sigma-Aldrich
TWEEN® 20, viscosity 250-450 mPa.s (25 °C)