Department of Cellular and Molecular Physiology (H166), Pennsylvania State University College of Medicine, 500 University Drive, Hershey, Pennsylvania 17033, USA.
Endocrinology. 2011 Jan;152(1):151-63. doi: 10.1210/en.2010-0248. Epub 2010 Nov 24.
Bacterial infection decreases skeletal muscle protein synthesis via inhibition of the mammalian target of rapamycin (mTOR), a key regulator of translation initiation. To better define the mechanism by which muscle mTOR activity is decreased, we used an in vitro model of C2C12 myotubes treated with endotoxin [lipopolysaccharide (LPS)]and interferon (IFN)-γ to determine whether stable lipophilic pyruvate derivatives restore mTOR signaling. Myotubes treated with a combination of LPS and IFNγ down-regulated the phosphorylation of the mTOR substrates S6 kinase-1 and 4E binding protein-1. The phosphorylation of ribosomal protein S6 was decreased, whereas phosphorylation of elongation factor-2 was enhanced; all results consistent with defects in both translation initiation and elongation. LPS/IFNγ decreased protein synthesis 60% in myotubes. Treatment with methyl or ethyl pyruvate partially protected against the LPS/IFNγ-induced fall in mTOR signaling. The protective effect of ethyl and methyl pyruvate could not be replicated by an equimolar amount of sodium pyruvate. Although LPS/IFNγ treated myotubes were initially IGF-I responsive, prolonged exposure (≥ 17 h) resulted in IGF-I resistance at the level of mTOR despite normal IGF-I receptor phosphorylation. Ethyl pyruvate treatment restored IGF-I sensitivity as evidenced by the left shift in the IGF-I dose-response curve and maintained IGF-I responsiveness for a prolonged period of time. Ethyl pyruvate also restored IGF-I-stimulated protein synthesis in LPS/IFNγ-treated myotubes. Cotreatment with N-acetyl cysteine or ascorbic acid also preserved IGF-I sensitivity and mTOR activity. The data suggest that the combination of LPS and IFNγ inhibits mTOR activity and that prolonged exposure induces IGF-I resistance in myotubes. Lipophilic pyruvate derivatives and antioxidants show promise at rescuing mTOR activity and muscle protein synthesis by maintaining IGF-I sensitivity in this model.
细菌感染通过抑制哺乳动物雷帕霉素靶蛋白(mTOR)来减少骨骼肌蛋白合成,mTOR 是翻译起始的关键调节剂。为了更好地定义肌肉 mTOR 活性降低的机制,我们使用了用内毒素 [脂多糖(LPS)] 和干扰素(IFN)-γ处理的 C2C12 肌管的体外模型,以确定稳定的亲脂性丙酮酸盐衍生物是否恢复 mTOR 信号。用 LPS 和 IFNγ 处理的肌管下调了 mTOR 底物 S6 激酶-1 和 4E 结合蛋白-1 的磷酸化。核糖体蛋白 S6 的磷酸化减少,而伸长因子-2 的磷酸化增强;所有结果均与翻译起始和延伸均存在缺陷一致。LPS/IFNγ 使肌管中的蛋白质合成降低了 60%。用甲基或乙基丙酮酸盐处理可部分防止 LPS/IFNγ 引起的 mTOR 信号下降。LPS/IFNγ 处理的肌管最初对 IGF-I 有反应,但延长暴露(≥17 小时)导致 mTOR 对 IGF-I 产生抗性,尽管 IGF-I 受体磷酸化正常。尽管用等摩尔量的丙酮酸钠不能复制乙基和甲基丙酮酸的保护作用,但乙基丙酮酸处理可恢复 IGF-I 敏感性,表现为 IGF-I 剂量反应曲线向左移位,并可延长 IGF-I 敏感性。乙基丙酮酸还可恢复 LPS/IFNγ 处理的肌管中 IGF-I 刺激的蛋白质合成。用 N-乙酰半胱氨酸或抗坏血酸共同处理也可保持 IGF-I 敏感性和 mTOR 活性。数据表明,LPS 和 IFNγ 的组合抑制了 mTOR 活性,并且延长暴露会导致肌管中 IGF-I 产生抗性。亲脂性丙酮酸衍生物和抗氧化剂有望通过维持该模型中的 IGF-I 敏感性来恢复 mTOR 活性和肌肉蛋白质合成。