Kanazawa Takumi, Taneike Ikue, Akaishi Ryuichiro, Yoshizawa Fumiaki, Furuya Norihiko, Fujimura Shinobu, Kadowaki Motoni
Department of Applied Biological Chemistry, Faculty of Agriculture, Niigata University, Ikarashi, Niigata 950-2181, Japan.
J Biol Chem. 2004 Feb 27;279(9):8452-9. doi: 10.1074/jbc.M306337200. Epub 2003 Nov 10.
Autophagy, a major bulk proteolytic pathway, contributes to intracellular protein turnover, together with protein synthesis. Both are subject to dynamic control by amino acids and insulin. The mechanisms of signaling and cross-talk of their physiological anabolic effects remain elusive. Recent studies established that amino acids and insulin induce p70 S6 kinase (p70(S6k)) phosphorylation by mTOR, involved in translational control of protein synthesis. Here, the signaling mechanisms of amino acids and insulin in macroautophagy in relation to mTOR were investigated. In isolated rat hepatocytes, both regulatory amino acids (RegAA) and insulin coordinately activated p70(S6k) phosphorylation, which was completely blocked by rapamycin, an mTOR inhibitor. However, rapamycin blocked proteolytic suppression by insulin, but did not block inhibition by RegAA. These contrasting results suggest that insulin controls autophagy through the mTOR pathway, but amino acids do not. Furthermore, micropermeabilization with Saccharomyces aureus alpha-toxin completely deprived hepatocytes of proteolytic responsiveness to RegAA and insulin, but still maintained p70(S6k) phosphorylation by RegAA. In contrast, Leu(8)-MAP, a non-transportable leucine analogue, did not mimic the effect of leucine on p70(S6k) phosphorylation, but maintained the activity on proteolysis. Finally, BCH, a System L-specific amino acid, did not affect proteolytic suppression or mTOR activation by leucine. All the results indicate that mTOR is not common to the signaling mechanisms of amino acids and insulin in autophagy, and that the amino acid signaling starts extracellularly with their "receptor(s)," probably other than transporters, and is mediated through a novel route distinct from the mTOR pathway employed by insulin.
自噬是一种主要的大量蛋白水解途径,与蛋白质合成一起参与细胞内蛋白质周转。两者均受氨基酸和胰岛素的动态调控。它们生理合成代谢作用的信号传导及相互作用机制仍不清楚。最近的研究表明,氨基酸和胰岛素通过mTOR诱导p70 S6激酶(p70(S6k))磷酸化,这与蛋白质合成的翻译控制有关。在此,研究了氨基酸和胰岛素在与mTOR相关的巨自噬中的信号传导机制。在分离的大鼠肝细胞中,调节性氨基酸(RegAA)和胰岛素协同激活p70(S6k)磷酸化,这被mTOR抑制剂雷帕霉素完全阻断。然而,雷帕霉素阻断了胰岛素对蛋白水解的抑制作用,但未阻断RegAA的抑制作用。这些相反的结果表明,胰岛素通过mTOR途径控制自噬,而氨基酸则不然。此外,用金黄色葡萄球菌α毒素进行微透化处理完全剥夺了肝细胞对RegAA和胰岛素的蛋白水解反应性,但仍维持RegAA对p70(S6k)的磷酸化作用。相比之下,亮氨酸类似物Leu(8)-MAP不能模拟亮氨酸对p70(S6k)磷酸化的作用,但能维持其蛋白水解活性。最后,系统L特异性氨基酸BCH不影响亮氨酸对蛋白水解的抑制作用或mTOR激活。所有结果表明,mTOR并非氨基酸和胰岛素在自噬信号传导机制中的共同因素,并且氨基酸信号传导始于细胞外,其“受体”可能不是转运体,而是通过一条不同于胰岛素所采用的mTOR途径的新途径介导。