Department of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX 77555, USA.
J Mol Neurosci. 2012 Jun;47(2):340-5. doi: 10.1007/s12031-012-9753-1. Epub 2012 Apr 11.
Mammalian target of rapamycin (mTOR) signaling plays a critical role in the regulation of activity-dependent protein synthesis in neurons. It is well established that the GTPase-activating protein tuberous sclerosis complex proteins (2TSC2) is an upstream inhibitor of mTOR. In this study, we show that glutamate stimulation down-regulates TSC2 protein in cortical cultures via NMDA receptor (NMDAR) activation. Interestingly, the mTOR-specific inhibitor rapamycin blocks the glutamate-induced TSC2 down-regulation. This finding suggests that NMDAR activation evokes an mTOR-mediated negative regulation of TSC2. In addition, we also show that the glutamate-induced down-regulation of TSC2 protein is blocked by proteasome inhibitor MG132, indicating the involvement of proteasome-mediated protein degradation. We propose that the NMDAR activation stimulates an mTOR-proteasome pathway to degrade TSC2 protein.
哺乳动物雷帕霉素靶蛋白(mTOR)信号通路在调节神经元中活性依赖的蛋白质合成中起着关键作用。已有研究证实,GTP 酶激活蛋白结节性硬化复合物蛋白(TSC2)是 mTOR 的上游抑制剂。在本研究中,我们发现谷氨酸刺激通过 NMDA 受体(NMDAR)的激活来下调皮质培养物中的 TSC2 蛋白。有趣的是,mTOR 特异性抑制剂雷帕霉素阻断了谷氨酸诱导的 TSC2 下调。这一发现表明,NMDAR 的激活引发了 mTOR 介导的 TSC2 的负调控。此外,我们还发现,谷氨酸诱导的 TSC2 蛋白下调被蛋白酶体抑制剂 MG132 阻断,表明涉及蛋白酶体介导的蛋白质降解。我们提出,NMDAR 的激活刺激了 mTOR-蛋白酶体途径来降解 TSC2 蛋白。