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本文引用的文献

1
Distinct trafficking and expression mechanisms underlie LTP and LTD of NMDA receptor-mediated synaptic responses.NMDA 受体介导的突触反应长时程增强和 LTD 的独特转运和表达机制。
Hippocampus. 2010 May;20(5):646-58. doi: 10.1002/hipo.20654.
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Delivery of AMPA receptors to perisynaptic sites precedes the full expression of long-term potentiation.AMPA 受体向突触周围位点的递送先于长时程增强的完全表达。
Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11388-93. doi: 10.1073/pnas.0802978105. Epub 2008 Aug 5.
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'Synaptic tagging' and 'cross-tagging' and related associative reinforcement processes of functional plasticity as the cellular basis for memory formation.“突触标记”“交叉标记”以及功能性可塑性的相关联合强化过程作为记忆形成的细胞基础。
Prog Brain Res. 2008;169:117-43. doi: 10.1016/S0079-6123(07)00007-6.
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Protein synthesis and neurotrophin-dependent structural plasticity of single dendritic spines.单个树突棘的蛋白质合成与神经营养因子依赖性结构可塑性
Science. 2008 Mar 21;319(5870):1683-7. doi: 10.1126/science.1152864. Epub 2008 Feb 28.
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Activin increases the number of synaptic contacts and the length of dendritic spine necks by modulating spinal actin dynamics.激活素通过调节脊髓肌动蛋白动力学来增加突触接触的数量和树突棘颈部的长度。
J Cell Sci. 2007 Nov 1;120(Pt 21):3830-7. doi: 10.1242/jcs.012450. Epub 2007 Oct 16.
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Changes in synaptic morphology accompany actin signaling during LTP.在长时程增强(LTP)过程中,突触形态的变化伴随着肌动蛋白信号传导。
J Neurosci. 2007 May 16;27(20):5363-72. doi: 10.1523/JNEUROSCI.0164-07.2007.
7
Identification of compartment- and process-specific molecules required for "synaptic tagging" during long-term potentiation and long-term depression in hippocampal CA1.在海马CA1区的长时程增强和长时程抑制过程中,确定“突触标记”所需的特定区室和过程的分子。
J Neurosci. 2007 May 9;27(19):5068-80. doi: 10.1523/JNEUROSCI.4940-06.2007.
8
The role of CaMKII as an F-actin-bundling protein crucial for maintenance of dendritic spine structure.钙调蛋白激酶II作为一种对维持树突棘结构至关重要的F-肌动蛋白成束蛋白的作用。
Proc Natl Acad Sci U S A. 2007 Apr 10;104(15):6418-23. doi: 10.1073/pnas.0701656104. Epub 2007 Apr 2.
9
Actin polymerization regulates the synthesis of PKMzeta in LTP.肌动蛋白聚合作用调节长时程增强中ζ-蛋白激酶M的合成。
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10
Protein kinase Mzeta enhances excitatory synaptic transmission by increasing the number of active postsynaptic AMPA receptors.蛋白激酶Mζ通过增加活性突触后AMPA受体的数量来增强兴奋性突触传递。
Hippocampus. 2006;16(5):443-52. doi: 10.1002/hipo.20171.

干扰肌动蛋白网络及其对体外脑片中海马CA1神经元长时程增强和突触标记的影响。

Interfering with the actin network and its effect on long-term potentiation and synaptic tagging in hippocampal CA1 neurons in slices in vitro.

作者信息

Ramachandran Binu, Frey Julietta U

机构信息

Department of Neurophysiology, Leibniz Institute for Neurobiology, 39118 Magdeburg, Germany.

出版信息

J Neurosci. 2009 Sep 30;29(39):12167-73. doi: 10.1523/JNEUROSCI.2045-09.2009.

DOI:10.1523/JNEUROSCI.2045-09.2009
PMID:19793974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6666138/
Abstract

Long-term potentiation (LTP) is a cellular correlate for memory formation, which requires the dynamic changes of the actin cytoskeleton. As shown by others, the polymerization of the actin network is important for early stages of LTP. Here, we investigated the role of actin dynamics in synaptic tagging and particularly in the induction of protein synthesis-dependent late-LTP in the CA1 region in hippocampal slices in vitro. We found that the inhibition of actin polymerization affects protein synthesis-independent early-LTP, prevents late-LTP, and interferes with synaptic tagging in apical dendrites of hippocampal CA1. The transformation of early-LTP into late-LTP was blocked by the application of the structurally different actin polymerization inhibitors latrunculin A or cytochalasin D. We suggest that the actin network is required for early "housekeeping" processes to induce and maintain early-LTP. Furthermore, inhibition of actin dynamics negatively interacts with the setting of the synaptic tagging complex. We propose actin as a further tag-specific molecule in apical CA1 dendrites where it is directly involved in the tagging/capturing machinery. Consequently, inhibition of the actin network prevents the interaction of tagging complexes with plasticity-related proteins. This results in the prevention of late-LTP by inhibition of the actin network during LTP induction.

摘要

长时程增强(LTP)是记忆形成的细胞关联物,它需要肌动蛋白细胞骨架的动态变化。正如其他人所表明的,肌动蛋白网络的聚合对于LTP的早期阶段很重要。在这里,我们研究了肌动蛋白动力学在突触标记中的作用,特别是在体外海马切片CA1区蛋白合成依赖性晚期LTP的诱导中的作用。我们发现,肌动蛋白聚合的抑制影响蛋白合成非依赖性早期LTP,阻止晚期LTP,并干扰海马CA1顶树突中的突触标记。应用结构不同的肌动蛋白聚合抑制剂Latrunculin A或细胞松弛素D可阻止早期LTP向晚期LTP的转变。我们认为,肌动蛋白网络对于诱导和维持早期LTP的早期“管家”过程是必需的。此外,肌动蛋白动力学的抑制与突触标记复合体的设置产生负相互作用。我们提出肌动蛋白是顶CA1树突中另一种标记特异性分子,它直接参与标记/捕获机制。因此,肌动蛋白网络的抑制阻止了标记复合体与可塑性相关蛋白的相互作用。这导致在LTP诱导期间通过抑制肌动蛋白网络来阻止晚期LTP。