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大鼠大脑突触后位点超微水平上翻译元件的定位。

Localization of translational components at the ultramicroscopic level at postsynaptic sites of the rat brain.

作者信息

Asaki Chie, Usuda Nobuteru, Nakazawa Ayami, Kametani Kiyokazu, Suzuki Tatsuo

机构信息

Department of Neuroplasticity, Research Center on Aging and Adaptation, Shinshu University, 3-1-1 Asahi, Matsumoto 390-8621, Japan.

出版信息

Brain Res. 2003 May 16;972(1-2):168-76. doi: 10.1016/s0006-8993(03)02523-x.

Abstract

We investigated the localization of components of translational machinery and their regulators in the postsynaptic region. We examined several components, especially those involved in translational regulation: components of (1) MAPK-Mnk-eIF4E, (2) PI3-kinase-PDK-Akt/PKB-FRAP/mTOR-PHAS/4EBP, (3) p70S6K-S6 ribosomal protein and (4) eEF2 kinase/CaMKIII-eEF2 pathways. Western blotting detected all the components examined in the synaptic fractions, and their differential localization to the synaptic subcompartments: initiation or elongation factors, except for eIF5, were detected predominantly in the dendritic lipid raft fraction, which contained ER marker proteins. In contrast, most of their regulatory kinases were distributed to both the postsynaptic density (PSD) and the dendritic lipid raft fractions, or enriched in the former fraction. Localization of eIF4E at synaptic sites was further examined immunohistochemically at the electron microscopic level. The eIF-4E-immunoreactivity was localized to the postsynaptic sites, especially to the microvesicle-like structures underneath the postsynaptic membrane in the spine, some of which were localized in close proximity to PSD. These results suggest that the postsynaptic local translational system, in at least four major regulatory pathways, is similar to those in the perinuclear one, and that it takes place, at least partly, immediately beneath the postsynaptic membrane. The results also suggest the presence of ER-associated type of translational machinery at the postsynaptic sites.

摘要

我们研究了翻译机制及其调节因子在突触后区域的定位。我们检测了几种成分,特别是那些参与翻译调控的成分:(1)丝裂原活化蛋白激酶-锰激酶-真核生物翻译起始因子4E(MAPK-Mnk-eIF4E)、(2)磷脂酰肌醇-3激酶-丙酮酸脱氢酶激酶-蛋白激酶B/蛋白激酶B相关蛋白-脆性组氨酸三联体/哺乳动物雷帕霉素靶蛋白-富含脯氨酸的Akt底物/4E结合蛋白(PI3-kinase-PDK-Akt/PKB-FRAP/mTOR-PHAS/4EBP)、(3)p70核糖体蛋白S6激酶-S6核糖体蛋白和(4)真核生物延伸因子2激酶/钙调蛋白激酶Ⅲ-真核生物延伸因子2(eEF2 kinase/CaMKIII-eEF2)途径的成分。蛋白质免疫印迹法检测到在突触组分中检测的所有成分,以及它们在突触亚组分中的差异定位:除真核生物翻译起始因子5(eIF5)外,起始或延伸因子主要在含有内质网标记蛋白的树突脂质筏组分中检测到。相反,它们的大多数调节激酶分布在突触后致密部(PSD)和树突脂质筏组分中,或在前一组分中富集。在电子显微镜水平上,通过免疫组织化学进一步检测了真核生物翻译起始因子4E(eIF4E)在突触部位的定位。eIF-4E免疫反应性定位于突触后部位,特别是在脊柱突触后膜下方的微囊样结构中,其中一些位于靠近PSD的位置。这些结果表明,突触后局部翻译系统,至少在四个主要调节途径中,与核周的翻译系统相似,并且至少部分地发生在突触后膜的正下方。结果还表明在突触后部位存在内质网相关类型的翻译机制。

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