Duckworth W C, Bennett R G, Hamel F G
Research Service, Veterans Affairs Medical Center, Omaha, Nebraska, USA.
Biochem Biophys Res Commun. 1998 Mar 17;244(2):390-4. doi: 10.1006/bbrc.1998.8276.
Insulin decreases cellular protein degradation, but the mechanism of this action is poorly understood. We have shown that insulin can have an inhibitory effect on the action of the proteasome in vitro, which requires the presence of insulin degrading enzyme (IDE). In this study we have used an antibody which inhibits the activity of IDE to show that IDE is required for insulin inhibition of protein degradation in intact cells. The anti-IDE antibody blocked the insulin effect on cellular degradation of proteins prelabeled with radioactive amino acids. The anti-IDE antibody also decreased insulin inhibition of proteasome degradation of a specific substrate in intact cells. These data suggest that insulin works intracellularly via IDE to inhibit protein degradation by the proteasome. Thus, IDE may function as an intracellular mediator for insulin effects on protein degradation. This is a novel signal transduction mechanism for peptide hormones.
胰岛素可减少细胞内蛋白质降解,但其作用机制尚不清楚。我们已经表明,胰岛素在体外对蛋白酶体的作用具有抑制作用,这需要胰岛素降解酶(IDE)的存在。在本研究中,我们使用了一种抑制IDE活性的抗体,以表明IDE是胰岛素抑制完整细胞中蛋白质降解所必需的。抗IDE抗体阻断了胰岛素对用放射性氨基酸预标记的蛋白质细胞降解的作用。抗IDE抗体还降低了胰岛素对完整细胞中特定底物蛋白酶体降解的抑制作用。这些数据表明,胰岛素通过IDE在细胞内发挥作用,抑制蛋白酶体介导的蛋白质降解。因此,IDE可能作为胰岛素对蛋白质降解作用的细胞内介质。这是一种肽类激素的新型信号转导机制。