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白藜芦醇通过促进 mTOR 和 DEPTOR 之间的相互作用来抑制 mTOR 信号通路。

Resveratrol inhibits mTOR signaling by promoting the interaction between mTOR and DEPTOR.

机构信息

Department of Pharmacology, University of Texas Health Science Center, San Antonio, Texas 78229-3900, USA.

出版信息

J Biol Chem. 2010 Nov 19;285(47):36387-94. doi: 10.1074/jbc.M110.169284. Epub 2010 Sep 17.

Abstract

Resveratrol (RSV) is a naturally occurring polyphenol that has been found to exert antioxidant, anti-inflammatory, and neuroprotective properties. However, how RSV exerts its beneficial health effects remains largely unknown. Here, we show that RSV inhibits insulin- and leucine-stimulated mTOR signaling in C2C12 fibroblasts via a Sirt1-independent mechanism. Treating C2C12 cells with RSV dramatically inhibited insulin-stimulated Akt, S6 kinase, and 4E-BP1 phosphorylation but had little effect on tyrosine phosphorylation of the insulin receptor and activation of the p44/42 MAPK signaling pathway. RSV treatment also partially blocked mTOR and S6 kinase phosphorylation in TSC1/2-deficient mouse embryonic fibroblasts, suggesting the presence of an inhibitory site downstream of TSC1/2. Knocking out PDK1 or suppressing AMP-activated protein kinase had little effect on leucine-stimulated mTOR signaling. On the other hand, RSV significantly increased the association between mTOR and its inhibitor, DEPTOR. Furthermore, the inhibitory effect of RSV on leucine-stimulated mTOR signaling was greatly reduced in cells in which the expression levels of DEPTOR were suppressed by RNAi. Taken together, our studies reveal that RSV inhibits leucine-stimulated mTORC1 activation by promoting mTOR/DEPTOR interaction and thus uncover a novel mechanism by which RSV negatively regulates mTOR activity.

摘要

白藜芦醇(RSV)是一种天然存在的多酚,已被发现具有抗氧化、抗炎和神经保护作用。然而,RSV 如何发挥其有益的健康作用在很大程度上仍然未知。在这里,我们表明 RSV 通过一种 Sirt1 非依赖性机制抑制 C2C12 成纤维细胞中胰岛素和亮氨酸刺激的 mTOR 信号。用 RSV 处理 C2C12 细胞可显著抑制胰岛素刺激的 Akt、S6 激酶和 4E-BP1 磷酸化,但对胰岛素受体的酪氨酸磷酸化和 p44/42 MAPK 信号通路的激活几乎没有影响。RSV 处理还部分阻断了 TSC1/2 缺陷型小鼠胚胎成纤维细胞中 mTOR 和 S6 激酶的磷酸化,表明 TSC1/2 下游存在一个抑制位点。敲除 PDK1 或抑制 AMP 激活的蛋白激酶对亮氨酸刺激的 mTOR 信号几乎没有影响。另一方面,RSV 显著增加了 mTOR 与其抑制剂 DEPTOR 之间的结合。此外,在通过 RNAi 抑制 DEPTOR 表达水平的细胞中,RSV 对亮氨酸刺激的 mTOR 信号的抑制作用大大降低。总之,我们的研究揭示了 RSV 通过促进 mTOR/DEPTOR 相互作用抑制亮氨酸刺激的 mTORC1 激活,从而揭示了 RSV 负调控 mTOR 活性的新机制。

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