• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

突触的突触后组织。

The postsynaptic organization of synapses.

机构信息

The Department of Neuroscience, Genentech Incorporated, San Francisco, California 94080, USA.

出版信息

Cold Spring Harb Perspect Biol. 2011 Dec 1;3(12):a005678. doi: 10.1101/cshperspect.a005678.

DOI:10.1101/cshperspect.a005678
PMID:22046028
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3225953/
Abstract

The postsynaptic side of the synapse is specialized to receive the neurotransmitter signal released from the presynaptic terminal and transduce it into electrical and biochemical changes in the postsynaptic cell. The cardinal functional components of the postsynaptic specialization of excitatory and inhibitory synapses are the ionotropic receptors (ligand-gated channels) for glutamate and γ-aminobutyric acid (GABA), respectively. These receptor channels are concentrated at the postsynaptic membrane and embedded in a dense and rich protein network comprised of anchoring and scaffolding molecules, signaling enzymes, cytoskeletal components, as well as other membrane proteins. Excitatory and inhibitory postsynaptic specializations are quite different in molecular organization. The postsynaptic density of excitatory synapses is especially complex and dynamic in composition and regulation; it contains hundreds of different proteins, many of which are required for cognitive function and implicated in psychiatric illness.

摘要

突触的突触后侧专门用于接收来自突触前末端释放的神经递质信号,并将其转导为突触后细胞的电和生化变化。兴奋性和抑制性突触的突触后特化的主要功能成分分别是谷氨酸和γ-氨基丁酸(GABA)的离子型受体(配体门控通道)。这些受体通道集中在突触后膜上,并嵌入由锚定和支架分子、信号酶、细胞骨架成分以及其他膜蛋白组成的丰富的蛋白质网络中。兴奋性和抑制性突触后特化在分子组织上有很大的不同。兴奋性突触的突触后密度在组成和调节上特别复杂和动态;它包含数百种不同的蛋白质,其中许多蛋白质是认知功能所必需的,并与精神疾病有关。

相似文献

1
The postsynaptic organization of synapses.突触的突触后组织。
Cold Spring Harb Perspect Biol. 2011 Dec 1;3(12):a005678. doi: 10.1101/cshperspect.a005678.
2
An opposing function of paralogs in balancing developmental synapse maturation.同源基因在平衡发育性突触成熟中的拮抗作用。
PLoS Biol. 2018 Dec 26;16(12):e2006838. doi: 10.1371/journal.pbio.2006838. eCollection 2018 Dec.
3
Essential contribution of the ligand-binding beta B/beta C loop of PDZ1 and PDZ2 in the regulation of postsynaptic clustering, scaffolding, and localization of postsynaptic density-95.PDZ1和PDZ2的配体结合βB/βC环在调节突触后聚集、支架作用以及突触后致密物95的定位方面的重要贡献。
J Neurosci. 2006 Jan 18;26(3):763-74. doi: 10.1523/JNEUROSCI.2489-05.2006.
4
PSD-95 family MAGUKs are essential for anchoring AMPA and NMDA receptor complexes at the postsynaptic density.PSD-95家族的膜相关鸟苷酸激酶对于将AMPA和NMDA受体复合物锚定在突触后致密区至关重要。
Proc Natl Acad Sci U S A. 2015 Dec 15;112(50):E6983-92. doi: 10.1073/pnas.1517045112. Epub 2015 Nov 24.
5
Hierarchical organization and genetically separable subfamilies of PSD95 postsynaptic supercomplexes.PSD95突触后超复合物的层次组织和基因可分离的亚家族。
J Neurochem. 2017 Aug;142(4):504-511. doi: 10.1111/jnc.14056. Epub 2017 Jul 25.
6
[Molecular mechanism underlying the formation and maintenance of excitatory synapses].[兴奋性突触形成与维持的分子机制]
Brain Nerve. 2011 Jan;63(1):51-8.
7
Neuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses.神经连接蛋白1是兴奋性突触的一种突触后细胞黏附分子。
Proc Natl Acad Sci U S A. 1999 Feb 2;96(3):1100-5. doi: 10.1073/pnas.96.3.1100.
8
Activity-dependent protein dynamics define interconnected cores of co-regulated postsynaptic proteins.活动依赖性蛋白动力学定义了相互关联的共同调节的突触后蛋白核心。
Mol Cell Proteomics. 2013 Jan;12(1):29-41. doi: 10.1074/mcp.M112.019976. Epub 2012 Oct 3.
9
MAGUKs, synaptic development, and synaptic plasticity.MAGUKs、突触发育和突触可塑性。
Neuroscientist. 2011 Oct;17(5):493-512. doi: 10.1177/1073858410386384. Epub 2011 Apr 15.
10
S-SCAM/MAGI-2 is an essential synaptic scaffolding molecule for the GluA2-containing maintenance pool of AMPA receptors.S-SCAM/MAGI-2 是 GluA2 含有的 AMPA 受体维持池的必需突触支架分子。
J Neurosci. 2012 May 16;32(20):6967-80. doi: 10.1523/JNEUROSCI.0025-12.2012.

引用本文的文献

1
Deficiency of Kif15 impairing synaptic development leads to mood disorder in mice.Kif15缺乏导致突触发育受损,进而引发小鼠情绪障碍。
PLoS Genet. 2025 Sep 2;21(9):e1011839. doi: 10.1371/journal.pgen.1011839. eCollection 2025 Sep.
2
Calpain in Traumatic Brain Injury: From Cinderella to Central Player.钙蛋白酶在创伤性脑损伤中的作用:从灰姑娘到核心角色
Cells. 2025 Aug 14;14(16):1253. doi: 10.3390/cells14161253.
3
Selective life-long suppression of an odor processing channel in response to critical period experience.响应关键期经历对气味处理通道进行选择性终身抑制。
bioRxiv. 2025 Jul 20:2025.07.18.665601. doi: 10.1101/2025.07.18.665601.
4
Phosphoinositide- and Collybistin-Dependent Synaptic Clustering of Gephyrin.磷酸肌醇和结肠直肠癌缺失蛋白依赖性的甘氨酸受体聚集蛋白突触聚集
J Neurochem. 2025 Aug;169(8):e70169. doi: 10.1111/jnc.70169.
5
The pathogenic factor of ZC4H2-associated rare disorder is a postsynaptic regulator for synaptic activity and cognitive function.与ZC4H2相关的罕见疾病的致病因素是一种用于突触活动和认知功能的突触后调节因子。
Proc Natl Acad Sci U S A. 2025 Jul 15;122(28):e2426375122. doi: 10.1073/pnas.2426375122. Epub 2025 Jul 9.
6
Ultrafast endocytosis in mouse cortical inhibitory synapses.小鼠皮层抑制性突触中的超快内吞作用。
bioRxiv. 2025 Jun 8:2025.06.06.658279. doi: 10.1101/2025.06.06.658279.
7
Cannabinol (CBN) alleviates age-related cognitive decline by improving synaptic and mitochondrial health.大麻酚(CBN)通过改善突触和线粒体健康来缓解与年龄相关的认知衰退。
Redox Biol. 2025 Jul;84:103692. doi: 10.1016/j.redox.2025.103692. Epub 2025 May 20.
8
Neuroplasticity After Hypoxic-Ischemic Brain Injury in Neonatal Pigs Based on Time-Dependent Behavior of H-MRS-Tau Protein and Synaptic Associated Proteins and Synaptic Structure Analysis.基于H-MRS- Tau蛋白和突触相关蛋白的时间依赖性行为及突触结构分析的新生仔猪缺氧缺血性脑损伤后的神经可塑性
Neurochem Res. 2025 May 23;50(3):169. doi: 10.1007/s11064-025-04421-y.
9
MicroRNA-138-5p suppresses excitatory synaptic strength at the cerebellar input layer.微小RNA-138-5p抑制小脑输入层的兴奋性突触强度。
J Physiol. 2025 May;603(10):3161-3179. doi: 10.1113/JP288019. Epub 2025 May 11.
10
The unique biology of catch muscles: insights into structure, function, and robotics innovations.捕捉肌肉的独特生物学特性:对结构、功能及机器人技术创新的见解
Front Bioeng Biotechnol. 2025 Apr 16;13:1478626. doi: 10.3389/fbioe.2025.1478626. eCollection 2025.

本文引用的文献

1
NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD).N-甲基-D-天冬氨酸受体依赖性长时程增强和长时程抑制(LTP/LTD)。
Cold Spring Harb Perspect Biol. 2012 Jun 1;4(6):a005710. doi: 10.1101/cshperspect.a005710.
2
Synapses and Alzheimer's disease.突触与阿尔茨海默病。
Cold Spring Harb Perspect Biol. 2012 May 1;4(5):a005777. doi: 10.1101/cshperspect.a005777.
3
Synaptic cell adhesion.突触细胞黏附。
Cold Spring Harb Perspect Biol. 2012 Apr 1;4(4):a005694. doi: 10.1101/cshperspect.a005694.
4
Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities.神经发育障碍相关自闭症和智力残疾的突触功能障碍。
Cold Spring Harb Perspect Biol. 2012 Mar 1;4(3):a009886. doi: 10.1101/cshperspect.a009886.
5
Synaptic neurotransmitter-gated receptors.突触神经递质门控受体。
Cold Spring Harb Perspect Biol. 2012 Mar 1;4(3):a009662. doi: 10.1101/cshperspect.a009662.
6
Homeostatic synaptic plasticity: local and global mechanisms for stabilizing neuronal function.稳态突触可塑性:稳定神经元功能的局部和全局机制。
Cold Spring Harb Perspect Biol. 2012 Jan 1;4(1):a005736. doi: 10.1101/cshperspect.a005736.
7
GABAA receptor trafficking-mediated plasticity of inhibitory synapses.GABAA 受体转运介导的抑制性突触可塑性。
Neuron. 2011 May 12;70(3):385-409. doi: 10.1016/j.neuron.2011.03.024.
8
PSD-95 and PSD-93 play critical but distinct roles in synaptic scaling up and down.PSD-95 和 PSD-93 在突触的上调和下调中发挥关键但不同的作用。
J Neurosci. 2011 May 4;31(18):6800-8. doi: 10.1523/JNEUROSCI.5616-10.2011.
9
Functional dependence of neuroligin on a new non-PDZ intracellular domain.神经黏附素依赖于一个新的非 PDZ 细胞内结构域发挥功能。
Nat Neurosci. 2011 Jun;14(6):718-26. doi: 10.1038/nn.2825. Epub 2011 May 1.
10
PSD-95 is required to sustain the molecular organization of the postsynaptic density.PSD-95 对于维持突触后密度的分子结构是必需的。
J Neurosci. 2011 Apr 27;31(17):6329-38. doi: 10.1523/JNEUROSCI.5968-10.2011.