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Synaptic activity at calcium-permeable AMPA receptors induces a switch in receptor subtype.钙通透性AMPA受体处的突触活动会诱导受体亚型的转换。
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Selective acquisition of AMPA receptors over postnatal development suggests a molecular basis for silent synapses.在出生后的发育过程中对AMPA受体的选择性获取表明了沉默突触的分子基础。
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Dendritic and postsynaptic protein synthetic machinery.树突状和突触后蛋白合成机制。
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Metabotropic glutamate receptor-initiated translocation of protein kinase p90rsk to polyribosomes: a possible factor regulating synaptic protein synthesis.代谢型谷氨酸受体引发蛋白激酶p90rsk向多核糖体的转位:调节突触蛋白合成的一个可能因素。
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Synaptic coexistence of AMPA and NMDA receptors in the rat hippocampus: a postembedding immunogold study.大鼠海马中AMPA和NMDA受体的突触共存:包埋后免疫金标研究
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在分离的神经元树突内刺激谷氨酸受体蛋白合成及膜插入。

Stimulation of glutamate receptor protein synthesis and membrane insertion within isolated neuronal dendrites.

作者信息

Kacharmina J E, Job C, Crino P, Eberwine J

机构信息

Departments of Pharmacology and Psychiatry, and Neurology, University of Pennsylvania Medical Center, Philadelphia, PA 19104-6084, USA.

出版信息

Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11545-50. doi: 10.1073/pnas.97.21.11545.

DOI:10.1073/pnas.97.21.11545
PMID:11027353
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC17237/
Abstract

The selective subcellular localization of mRNAs to dendrites and the recent demonstration of local protein synthesis have highlighted the potential role of postsynaptic sites in modulation of cell-cell communication. We show that epitope-tagged subunit 2 of the ionotopic glutamate receptor, GluR2, mRNA transfected into isolated hippocampal neuronal dendrites is translated in response to pharmacologic stimulation. Further, confocal imaging of N-terminally labeled GluR2 reveals that the newly synthesized GluR2 protein can integrate into the dendritic membrane with the N terminus externally localized. These data demonstrate that integral membrane proteins can be synthesized in dendrites and can locally integrate into the cell membrane.

摘要

mRNA在树突中的选择性亚细胞定位以及近期关于局部蛋白质合成的证明,突出了突触后位点在调节细胞间通讯中的潜在作用。我们发现,转染到分离的海马神经元树突中的离子型谷氨酸受体GluR2的表位标记亚基2 mRNA,会响应药理刺激而被翻译。此外,对N端标记的GluR2进行共聚焦成像显示,新合成的GluR2蛋白能够整合到树突膜中,且N端位于细胞外部。这些数据表明,整合膜蛋白能够在树突中合成,并能在局部整合到细胞膜中。