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An increase in essential amino acid availability upregulates amino acid transporter expression in human skeletal muscle

机译:必需氨基酸可用性的增加会上调人体骨骼肌中的氨基酸转运蛋白表达

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Essential amino acids (EAA) stimulate skeletal muscle mammalian target of rapamycin complex 1 (mTORC1) signaling and protein synthesis. It has recently been reported that an increase in amino acid (AA) transporter expression during anabolic conditions is rapamycin-sensitive. The purpose of this study was to determine whether an increase in EAA availability increases AA transporter expression in human skeletal muscle. Muscle biopsies were obtained from the vastus lateralis of seven young adult subjects (3 male, 4 female) before and 1-3 h after EAA ingestion (10 g). Blood and muscle samples were analyzed for leucine kinetics using stable isotopic techniques. Quantitative RT-PCR, and immunoblotting were used to determine the mRNA and protein expression, respectively, of AA transporters and members of the general AA control pathway [general control nonrepressed (GCN2), activating transcription factor (ATF4), and eukaryotic initiation factor (eIF2) α-subunit (Ser52)]. EAA ingestion increased blood leucine concentration, delivery of leucine to muscle, transport of leucine from blood into muscle, intracellular muscle leucine concentration, ribosomal protein S6 (Ser240/244) phosphorylation, and muscle protein synthesis. This was followed with increased L-type AA transporter (LAT1), CD98, sodium-coupled neutral AA transporter (SNAT2), and proton-coupled amino acid transporter (PAT1) mRNA expression at 1 h (P 0.05) and modest increases in LAT1 protein expression (3 h post-EAA) and SNAT2 protein expression (2 and 3 h post-EAA, P 0.05). Although there were no changes in GCN2 expression and eIF2α phosphorylation, ATF4 protein expression reached significance by 2 h post-EAA (P 0.05). We conclude that an increase in EAA availability upregulates human skeletal muscle AA transporter expression, perhaps in an mTORC1-dependent manner, which may be an adaptive response necessary for improved AA intracellular delivery.
机译:必需氨基酸(EAA)刺激雷帕霉素复合物1(mTORC1)信号传导和蛋白质合成的骨骼肌哺乳动物靶标。最近有报道说,合成代谢条件下氨基酸(AA)转运蛋白表达的增加对雷帕霉素敏感。这项研究的目的是确定EAA利用率的增加是否会增加人骨骼肌中AA转运蛋白的表达。在摄入EAA(10 g)之前和之后1-3小时,从7名年轻成年受试者(3名男性,4名女性)的股外侧肌获得了活组织检查。使用稳定的同位素技术分析血液和肌肉样品的亮氨酸动力学。定量RT-PCR和免疫印迹分别用于测定AA转运蛋白和一般AA调控途径的成员的mRNA和蛋白质表达[一般控制非阻遏(GCN2),激活转录因子(ATF4)和真核起始因子( eIF2)α-亚基(Ser52)]。 EAA摄入增加了血液亮氨酸的浓度,亮氨酸向肌肉的运输,亮氨酸从血液向肌肉的运输,细胞内肌肉亮氨酸的浓度,核糖体蛋白S6(Ser240 / 244)磷酸化和肌肉蛋白合成。随后在1小时时L型AA转运蛋白(LAT1),CD98,钠偶联中性AA转运蛋白(SNAT2)和质子偶联氨基酸转运蛋白(PAT1)mRNA表达增加(P <0.05),且LAT1蛋白表达(EAA后3小时)和SNAT2蛋白表达(EAA后2和3小时,P <0.05)。尽管GCN2表达和eIF2α磷酸化没有变化,但是ATF4蛋白表达在EAA后2 h达到显着水平(P <0.05)。我们得出的结论是,EAA可用性的增加可能以mTORC1依赖的方式上调了人类骨骼肌AA转运蛋白的表达,这可能是改善AA细胞内传递所必需的适应性反应。

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