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核糖体蛋白S6的突触驱动磷酸化在活跃突触与树突和细胞体之间受到丝裂原活化蛋白激酶(MAPK)和磷脂酰肌醇-3激酶/哺乳动物雷帕霉素靶蛋白(PI3K/mTOR)信号通路的差异调节。

Synaptically driven phosphorylation of ribosomal protein S6 is differentially regulated at active synapses versus dendrites and cell bodies by MAPK and PI3K/mTOR signaling pathways.

作者信息

Pirbhoy Patricia Salgado, Farris Shannon, Steward Oswald

机构信息

Reeve-Irvine Research Center, University of California, Irvine, California 92697, USA.

Department of Neurobiology and Behavior, Center for the Neurobiology of Learning and Memory, University of California, Irvine, California 92697, USA.

出版信息

Learn Mem. 2017 Jul 17;24(8):341-357. doi: 10.1101/lm.044974.117. Print 2017 Aug.

Abstract

High-frequency stimulation of the medial perforant path triggers robust phosphorylation of ribosomal protein S6 (rpS6) in activated dendritic domains and granule cell bodies. Here we dissect the signaling pathways responsible for synaptically driven rpS6 phosphorylation in the dentate gyrus using pharmacological agents to inhibit PI3-kinase/mTOR and MAPK/ERK-dependent kinases. Using phospho-specific antibodies for rpS6 at different sites (ser235/236 versus ser240/244), we show that delivery of the PI3-kinase inhibitor, wortmannin, decreased rpS6 phosphorylation throughout the somatodendritic compartment (granule cell layer, inner molecular layer, outer molecular layer), especially in granule cell bodies while sparing phosphorylation at activated synapses (middle molecular layer). In contrast, delivery of U0126, an MEK inhibitor, attenuated rpS6 phosphorylation specifically in the dendritic laminae leaving phosphorylation in the granule cell bodies intact. Delivery of the mTOR inhibitor, rapamycin, abolished activation of rpS6 phosphorylation in granule cell bodies and dendrites, whereas delivery of a selective S6K1 inhibitor, PF4708671, or RSK inhibitor, SL0101-1, attenuated rpS6 phosphorylation throughout the postsynaptic cell. These results reveal that MAPK/ERK-dependent signaling is predominately responsible for the selective induction of rpS6 phosphorylation at active synapses. In contrast, PI3-kinase/mTOR-dependent signaling induces rpS6 phosphorylation throughout the somatodendritic compartment but plays a minimal role at active synapses. Collectively, these results suggest a potential mechanism by which PI3-kinase/mTOR and MAPK/ERK pathways regulate translation at specific subcellular compartments in response to synaptic activity.

摘要

内侧穿通通路的高频刺激会在活化的树突域和颗粒细胞体中引发核糖体蛋白S6(rpS6)的强烈磷酸化。在这里,我们使用药理学试剂抑制PI3激酶/mTOR和MAPK/ERK依赖性激酶,剖析负责齿状回中突触驱动的rpS6磷酸化的信号通路。使用针对不同位点(ser235/236与ser240/244)的rpS6的磷酸特异性抗体,我们发现PI3激酶抑制剂渥曼青霉素的递送降低了整个体树突区室(颗粒细胞层、内分子层、外分子层)中的rpS6磷酸化,尤其是在颗粒细胞体中,同时保留了活化突触(中分子层)处的磷酸化。相反,MEK抑制剂U0126的递送特异性减弱了树突板层中的rpS6磷酸化,而颗粒细胞体中的磷酸化保持完整。mTOR抑制剂雷帕霉素的递送消除了颗粒细胞体和树突中rpS6磷酸化的激活,而选择性S6K1抑制剂PF4708671或RSK抑制剂SL0101-1的递送减弱了整个突触后细胞中的rpS6磷酸化。这些结果表明,MAPK/ERK依赖性信号主要负责在活跃突触处选择性诱导rpS6磷酸化。相反,PI3激酶/mTOR依赖性信号诱导整个体树突区室中的rpS6磷酸化,但在活跃突触中起最小作用。总的来说,这些结果提示了一种潜在机制,通过该机制PI3激酶/mTOR和MAPK/ERK途径响应突触活动调节特定亚细胞区室中的翻译。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35e3/5516686/6460e3f37dab/PirbhoyLM044974f01.jpg

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