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AMPA 受体与突触可塑性:化学家视角。

AMPA receptors and synaptic plasticity: a chemist's perspective.

机构信息

Department of Pharmaceutical Chemistry, University of California, San Francisco, California, USA.

出版信息

Nat Chem Biol. 2010 Feb;6(2):89-97. doi: 10.1038/nchembio.298.

DOI:10.1038/nchembio.298
PMID:20081822
Abstract

The ability of the mammalian brain to undergo experience-based adaptations is among its most important and fascinating properties. Such plasticity is reflected in the capacity of neuronal activity to continuously modify the neural circuitry that underlies thought, feeling and behavior. The locus of this plasticity occurs at the level of synapses, the specialized junctions where one neuron receives chemical signals from another. Synaptic connections become stronger or weaker in response to specific patterns of activity. This activity drives regulated changes in the neurotransmitter released by presynaptic neurons and in the receptors localized on postsynaptic neurons. Detailed studies of these receptors have advanced our understanding of synaptic plasticity. However, many key questions remain unresolved, and over the past decade innovative chemical approaches have emerged to tackle them. Here we review these chemical tools and their application to unraveling the molecular basis of synaptic plasticity.

摘要

哺乳动物大脑具有基于经验的适应能力,这是其最重要和最迷人的特性之一。这种可塑性反映在神经元活动不断改变潜在思想、感觉和行为的神经回路的能力上。这种可塑性的发生位置在突触水平,即一个神经元从另一个神经元接收化学信号的专门连接处。突触连接会根据特定的活动模式变得更强或更弱。这种活动驱动了由前神经元释放的神经递质和位于后神经元上的受体的调节变化。对这些受体的详细研究增进了我们对突触可塑性的理解。然而,仍有许多关键问题尚未解决,在过去十年中,创新的化学方法已经出现来解决这些问题。在这里,我们回顾这些化学工具及其在揭示突触可塑性的分子基础方面的应用。

相似文献

1
AMPA receptors and synaptic plasticity: a chemist's perspective.AMPA 受体与突触可塑性:化学家视角。
Nat Chem Biol. 2010 Feb;6(2):89-97. doi: 10.1038/nchembio.298.
2
Regulation of AMPA receptors during synaptic plasticity.突触可塑性过程中AMPA受体的调节
Trends Neurosci. 2002 Nov;25(11):578-88. doi: 10.1016/s0166-2236(02)02270-1.
3
AMPA receptor trafficking at excitatory synapses.AMPA受体在兴奋性突触处的转运。
Neuron. 2003 Oct 9;40(2):361-79. doi: 10.1016/s0896-6273(03)00640-8.
4
AMPA receptor trafficking: a road map for synaptic plasticity.AMPA受体转运:突触可塑性的路线图。
Mol Interv. 2003 Oct;3(7):375-85. doi: 10.1124/mi.3.7.375.
5
Role of AMPA receptor endocytosis in synaptic plasticity.AMPA 受体胞吞作用在突触可塑性中的作用。
Nat Rev Neurosci. 2001 May;2(5):315-24. doi: 10.1038/35072500.
6
Regulation of AMPA receptor activity, synaptic targeting and recycling: role in synaptic plasticity.AMPA受体活性、突触定位及再循环的调控:在突触可塑性中的作用
Neurochem Res. 2003 Oct;28(10):1459-73. doi: 10.1023/a:1025610122776.
7
Regulation of AMPA receptors and synaptic plasticity.AMPA 受体的调节与突触可塑性
Neuroscience. 2009 Jan 12;158(1):105-25. doi: 10.1016/j.neuroscience.2008.02.037. Epub 2008 Feb 29.
8
Experience strengthening transmission by driving AMPA receptors into synapses.通过驱动AMPA受体进入突触来增强传递的经验。
Science. 2003 Mar 7;299(5612):1585-8. doi: 10.1126/science.1079886.
9
miR-124-dependent tagging of synapses by synaptopodin enables input-specific homeostatic plasticity.miR-124 通过突触足蛋白对突触的标记作用实现了输入特异性的平衡型可塑性。
EMBO J. 2022 Oct 17;41(20):e109012. doi: 10.15252/embj.2021109012. Epub 2022 Jul 25.
10
Synaptic AMPA receptor plasticity and behavior.突触AMPA受体可塑性与行为
Neuron. 2009 Feb 12;61(3):340-50. doi: 10.1016/j.neuron.2009.01.015.

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Ligand-directed two-step labeling to quantify neuronal glutamate receptor trafficking.配体导向的两步标记法定量检测神经元谷氨酸受体转运。
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UPF2 leads to degradation of dendritically targeted mRNAs to regulate synaptic plasticity and cognitive function.

本文引用的文献

1
X-ray structure, symmetry and mechanism of an AMPA-subtype glutamate receptor.X 射线结构、对称性和 AMPA 型谷氨酸受体的机制。
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Subunit composition of synaptic AMPA receptors revealed by a single-cell genetic approach.单细胞遗传学方法揭示的突触AMPA受体亚基组成
Neuron. 2009 Apr 30;62(2):254-68. doi: 10.1016/j.neuron.2009.02.027.
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Functional proteomics identify cornichon proteins as auxiliary subunits of AMPA receptors.功能蛋白质组学鉴定出柯尼希氏蛋白为AMPA受体的辅助亚基。
UPF2导致树突靶向mRNA的降解,以调节突触可塑性和认知功能。
Mol Psychiatry. 2020 Dec;25(12):3360-3379. doi: 10.1038/s41380-019-0547-5. Epub 2019 Oct 21.
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Effect of Damaging Rare Mutations in Synapse-Related Gene Sets on Response to Short-term Antipsychotic Medication in Chinese Patients With Schizophrenia: A Randomized Clinical Trial.突触相关基因集的有害罕见突变对中国精神分裂症患者短期抗精神病药物治疗反应的影响:一项随机临床试验。
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The Synaptic Theory of Memory: A Historical Survey and Reconciliation of Recent Opposition.记忆的突触理论:历史回顾与近期反对观点的调和
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Mechanism of Action for rTMS: A Working Hypothesis Based on Animal Studies.重复经颅磁刺激的作用机制:基于动物研究的一个工作假说
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Chemical labelling for visualizing native AMPA receptors in live neurons.用于可视化活神经元中天然 AMPA 受体的化学标记。
Nat Commun. 2017 Apr 7;8:14850. doi: 10.1038/ncomms14850.
8
Allosteric activation of membrane-bound glutamate receptors using coordination chemistry within living cells.利用活细胞内的配位化学对膜结合型谷氨酸受体进行别构激活。
Nat Chem. 2016 Oct;8(10):958-67. doi: 10.1038/nchem.2554. Epub 2016 Jun 27.
9
AMPA receptors as a molecular target in epilepsy therapy.AMPA受体作为癫痫治疗的分子靶点。
Acta Neurol Scand Suppl. 2013(197):9-18. doi: 10.1111/ane.12099.
10
AMPA receptor mediated behavioral plasticity in the isolated rat spinal cord.AMPA 受体介导的孤立大鼠脊髓中的行为可塑性。
Behav Brain Res. 2013 Jan 1;236(1):319-326. doi: 10.1016/j.bbr.2012.09.007. Epub 2012 Sep 12.
Science. 2009 Mar 6;323(5919):1313-9. doi: 10.1126/science.1167852.
4
Synaptic AMPA receptor plasticity and behavior.突触AMPA受体可塑性与行为
Neuron. 2009 Feb 12;61(3):340-50. doi: 10.1016/j.neuron.2009.01.015.
5
Silent synapses and the emergence of a postsynaptic mechanism for LTP.沉默突触与长时程增强的突触后机制的出现。
Nat Rev Neurosci. 2008 Nov;9(11):813-25. doi: 10.1038/nrn2501. Epub 2008 Oct 15.
6
AMPA receptor subunit-specific regulation by a distinct family of type II TARPs.AMPA受体亚基由不同的II型跨膜AMPAR调节蛋白家族进行特异性调节。
Neuron. 2008 Sep 25;59(6):986-96. doi: 10.1016/j.neuron.2008.07.034.
7
Kainate receptors: pharmacology, function and therapeutic potential.海人藻酸受体:药理学、功能及治疗潜力。
Neuropharmacology. 2009 Jan;56(1):90-113. doi: 10.1016/j.neuropharm.2008.08.023. Epub 2008 Aug 28.
8
Mechanism and time course of cocaine-induced long-term potentiation in the ventral tegmental area.可卡因诱导腹侧被盖区长期增强效应的机制及时间进程。
J Neurosci. 2008 Sep 10;28(37):9092-100. doi: 10.1523/JNEUROSCI.1001-08.2008.
9
6-Azido-7-nitro-1,4-dihydroquinoxaline-2,3-dione (ANQX) forms an irreversible bond to the active site of the GluR2 AMPA receptor.6-叠氮基-7-硝基-1,4-二氢喹喔啉-2,3-二酮(ANQX)与谷氨酸受体2(GluR2)α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体的活性位点形成不可逆的结合。
J Med Chem. 2008 Sep 25;51(18):5856-60. doi: 10.1021/jm701517b.
10
New concepts in synaptic biology derived from single-molecule imaging.源自单分子成像的突触生物学新概念。
Neuron. 2008 Aug 14;59(3):359-74. doi: 10.1016/j.neuron.2008.06.022.