• 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

相似文献

1
Protracted and asynchronous accumulation of PSD95-family MAGUKs during maturation of nascent dendritic spines.PSD95 家族 MAGUKs 在新生树突棘成熟过程中的延长和异步积累。
Dev Neurobiol. 2017 Oct;77(10):1161-1174. doi: 10.1002/dneu.22503. Epub 2017 May 13.
2
SAP102 is a highly mobile MAGUK in spines.SAP102 是一种在脊柱中高度移动的 MAGUK。
J Neurosci. 2010 Mar 31;30(13):4757-66. doi: 10.1523/JNEUROSCI.6108-09.2010.
3
Ultrastructural modifications of spine and synapse morphology by SAP97.SAP97 对脊柱和突触形态的超微结构修饰。
Hippocampus. 2011 Sep;21(9):990-8. doi: 10.1002/hipo.20811. Epub 2010 May 20.
4
Plasma membrane Ca2+-atpase isoforms 2b and 4b interact promiscuously and selectively with members of the membrane-associated guanylate kinase family of PDZ (PSD95/Dlg/ZO-1) domain-containing proteins.质膜Ca2+ -ATP酶同工型2b和4b与含PDZ(PSD95/Dlg/ZO-1)结构域的膜相关鸟苷酸激酶家族成员进行杂乱且选择性的相互作用。
J Biol Chem. 2001 Jun 15;276(24):21594-600. doi: 10.1074/jbc.M101448200. Epub 2001 Mar 26.
5
Synapse-specific and developmentally regulated targeting of AMPA receptors by a family of MAGUK scaffolding proteins.一类膜相关鸟苷酸激酶(MAGUK)支架蛋白对AMPA受体的突触特异性及发育调控靶向作用。
Neuron. 2006 Oct 19;52(2):307-20. doi: 10.1016/j.neuron.2006.09.012.
6
Postsynaptic density scaffold SAP102 regulates cortical synapse development through EphB and PAK signaling pathway.突触后密度支架 SAP102 通过 EphB 和 PAK 信号通路调节皮质突触发育。
J Neurosci. 2013 Mar 13;33(11):5040-52. doi: 10.1523/JNEUROSCI.2896-12.2013.
7
Interaction between SAP97 and PSD-95, two Maguk proteins involved in synaptic trafficking of AMPA receptors.SAP97与PSD-95之间的相互作用,这两种膜相关鸟苷酸激酶(Maguk)蛋白参与AMPA受体的突触转运。
J Biol Chem. 2006 Feb 17;281(7):4267-73. doi: 10.1074/jbc.M505886200. Epub 2005 Dec 6.
8
NMDA receptor-dependent regulation of dendritic spine morphology by SAP102 splice variants.NMDA 受体依赖的 SAP102 剪接变异体对树突棘形态的调节。
J Neurosci. 2011 Jan 5;31(1):89-96. doi: 10.1523/JNEUROSCI.1034-10.2011.
9
Loss of PSD-95 enrichment is not a prerequisite for spine retraction.PSD-95 耗竭不是棘突回缩的必要前提。
J Neurosci. 2011 Aug 24;31(34):12129-38. doi: 10.1523/JNEUROSCI.6662-10.2011.
10
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.

引用本文的文献

1
A synapse-specific refractory period for plasticity at individual dendritic spines.单个树突棘可塑性的突触特异性不应期。
Proc Natl Acad Sci U S A. 2025 Jan 14;122(2):e2410433122. doi: 10.1073/pnas.2410433122. Epub 2025 Jan 7.
2
A synapse-specific refractory period for plasticity at individual dendritic spines.单个树突棘可塑性的突触特异性不应期。
bioRxiv. 2024 May 24:2024.05.24.595787. doi: 10.1101/2024.05.24.595787.
3
Activity-Dependent Stabilization of Nascent Dendritic Spines Requires Nonenzymatic CaMKIIα Function.活性依赖的新生树突棘稳定需要非酶 CaMKIIα 功能。
J Neurosci. 2024 Jan 10;44(2):e1393222023. doi: 10.1523/JNEUROSCI.1393-22.2023.
4
Unraveling the mysteries of dendritic spine dynamics: Five key principles shaping memory and cognition.揭开树突棘动力学的奥秘:塑造记忆和认知的五个关键原则。
Proc Jpn Acad Ser B Phys Biol Sci. 2023;99(8):254-305. doi: 10.2183/pjab.99.018.
5
Effects of Tropomodulin 2 on Dendritic Spine Reorganization and Dynamics.Tropomodulin 2 对树突棘重组和动力学的影响。
Biomolecules. 2023 Aug 11;13(8):1237. doi: 10.3390/biom13081237.
6
Editorial: New insights into schizophrenia-related neural and behavioral phenotypes.社论:对精神分裂症相关神经和行为表型的新见解
Front Cell Neurosci. 2023 May 10;17:1202230. doi: 10.3389/fncel.2023.1202230. eCollection 2023.
7
Dendritic spine loss deep in the neocortex and dendrite distortion with diffusion disturbances occur early in experimental pneumococcal meningitis.在实验性肺炎球菌性脑膜炎早期,新皮质深层的树突棘丢失以及伴有扩散障碍的树突畸变就会出现。
Front Neurosci. 2023 Jan 10;16:912445. doi: 10.3389/fnins.2022.912445. eCollection 2022.
8
Actin capping protein regulates postsynaptic spine development through CPI-motif interactions.肌动蛋白帽蛋白通过CPI基序相互作用调节突触后棘的发育。
Front Mol Neurosci. 2022 Sep 29;15:1020949. doi: 10.3389/fnmol.2022.1020949. eCollection 2022.
9
Fragile X Mental Retardation Protein Mediates the Effects of Androgen on Hippocampal PSD95 Expression and Dendritic Spines Density/Morphology and Autism-Like Behaviors Through miR-125a.脆性X智力低下蛋白通过miR-125a介导雄激素对海马PSD95表达、树突棘密度/形态及自闭症样行为的影响。
Front Cell Neurosci. 2022 Apr 22;16:872347. doi: 10.3389/fncel.2022.872347. eCollection 2022.
10
Ion flux-independent NMDA receptor signaling.离子流非依赖性 NMDA 受体信号转导。
Neuropharmacology. 2022 Jun 1;210:109019. doi: 10.1016/j.neuropharm.2022.109019. Epub 2022 Mar 9.

本文引用的文献

1
De novo synaptogenesis induced by GABA in the developing mouse cortex.γ-氨基丁酸(GABA)在发育中的小鼠皮层诱导的新生突触形成。
Science. 2016 Sep 2;353(6303):1037-1040. doi: 10.1126/science.aaf5206. Epub 2016 Aug 11.
2
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.
3
Labelling and optical erasure of synaptic memory traces in the motor cortex.运动皮层中突触记忆痕迹的标记与光学消除
Nature. 2015 Sep 17;525(7569):333-8. doi: 10.1038/nature15257. Epub 2015 Sep 9.
4
Synaptic Consolidation Normalizes AMPAR Quantal Size following MAGUK Loss.突触巩固在 MAGUK 缺失后使 AMPA 受体量子大小正常化。
Neuron. 2015 Aug 5;87(3):534-48. doi: 10.1016/j.neuron.2015.07.015.
5
Targeting protein-protein interactions with trimeric ligands: high affinity inhibitors of the MAGUK protein family.用三聚体配体靶向蛋白质-蛋白质相互作用:MAGUK蛋白家族的高亲和力抑制剂
PLoS One. 2015 Feb 6;10(2):e0117668. doi: 10.1371/journal.pone.0117668. eCollection 2015.
6
Structural and molecular remodeling of dendritic spine substructures during long-term potentiation.长期增强过程中树突棘亚结构的结构和分子重塑。
Neuron. 2014 Apr 16;82(2):444-59. doi: 10.1016/j.neuron.2014.03.021.
7
Sequential delivery of synaptic GluA1- and GluA4-containing AMPA receptors (AMPARs) by SAP97 anchored protein complexes in classical conditioning.在经典条件反射中,SAP97 锚定蛋白复合物依次传递含有突触 GluA1 和 GluA4 的 AMPA 受体(AMPAR)。
J Biol Chem. 2014 Apr 11;289(15):10540-10550. doi: 10.1074/jbc.M113.535179. Epub 2014 Feb 24.
8
The relationship between PSD-95 clustering and spine stability in vivo.PSD-95 聚集与体内脊柱稳定性的关系。
J Neurosci. 2014 Feb 5;34(6):2075-86. doi: 10.1523/JNEUROSCI.3353-13.2014.
9
Dynamics of dendritic spines in the mouse auditory cortex during memory formation and memory recall.在记忆形成和回忆过程中,小鼠听觉皮层树突棘的动力学。
Proc Natl Acad Sci U S A. 2013 Nov 5;110(45):18315-20. doi: 10.1073/pnas.1312508110. Epub 2013 Oct 22.
10
Postsynaptic density scaffold SAP102 regulates cortical synapse development through EphB and PAK signaling pathway.突触后密度支架 SAP102 通过 EphB 和 PAK 信号通路调节皮质突触发育。
J Neurosci. 2013 Mar 13;33(11):5040-52. doi: 10.1523/JNEUROSCI.2896-12.2013.

PSD95 家族 MAGUKs 在新生树突棘成熟过程中的延长和异步积累。

Protracted and asynchronous accumulation of PSD95-family MAGUKs during maturation of nascent dendritic spines.

机构信息

Center for Neuroscience, University of California Davis, Davis, California, 95618.

出版信息

Dev Neurobiol. 2017 Oct;77(10):1161-1174. doi: 10.1002/dneu.22503. Epub 2017 May 13.

DOI:10.1002/dneu.22503
PMID:28388013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5605399/
Abstract

The formation and stabilization of new dendritic spines is a key component of the experience-dependent neural circuit plasticity that supports learning, but the molecular maturation of nascent spines remains largely unexplored. The PSD95-family of membrane-associated guanylate kinases (PSD-MAGUKs), most notably PSD95, has a demonstrated role in promoting spine stability. However, nascent spines contain low levels of PSD95, suggesting that other members of the PSD-MAGUK family might act to stabilize nascent spines in the early stages of spiny synapse formation. Here, we used GFP-fusion constructs to quantitatively define the molecular composition of new spines, focusing on the PSD-MAGUK family. We found that PSD95 levels in new spines were as low as those previously associated with rapid subsequent spine elimination, and new spines did not achieve mature levels of PSD95 until between 12 and 20 h following new spine identification. Surprisingly, we found that the PSD-MAGUKs PSD93, SAP97, and SAP102 were also substantially less enriched in new spines. However, they accumulated in new spines more quickly than PSD95: SAP102 enriched to mature levels within 3 h, SAP97 and PSD93 enriched gradually over the course of 6 h. Intriguingly, when we restricted our analysis to only those new spines that persisted, SAP97 was the only PSD-MAGUK already present at mature levels in persistent new spines when first identified. Our findings uncover a key structural difference between nascent and mature spines, and suggest a mechanism for the stabilization of nascent spines through the sequential arrival of PSD-MAGUKs. © 2017 Wiley Periodicals, Inc. Develop Neurobiol 77: 1161-1174, 2017.

摘要

新树突棘的形成和稳定是支持学习的经验依赖性神经回路可塑性的关键组成部分,但新生棘突的分子成熟在很大程度上仍未得到探索。突触后密度蛋白 95 家族(PSD-MAGUKs)的膜相关鸟苷酸激酶(PSD-MAGUKs),尤其是 PSD95,已被证明在促进棘突稳定性方面具有作用。然而,新生棘突中 PSD95 的水平较低,这表明 PSD-MAGUK 家族的其他成员可能在棘突突触形成的早期阶段发挥作用,以稳定新生棘突。在这里,我们使用 GFP 融合构建体来定量定义新棘突的分子组成,重点是 PSD-MAGUK 家族。我们发现,新棘突中的 PSD95 水平低至先前与快速随后的棘突消除相关的水平,并且新棘突在新棘突鉴定后 12 至 20 小时之间才达到成熟的 PSD95 水平。令人惊讶的是,我们发现 PSD-MAGUKs PSD93、SAP97 和 SAP102 在新棘突中也明显含量较低。然而,它们在新棘突中更快地积累:SAP102 在 3 小时内富集到成熟水平,SAP97 和 PSD93 在 6 小时内逐渐富集。有趣的是,当我们将分析仅限于那些持续存在的新棘突时,当首次鉴定时,SAP97 是仅有的在持续存在的新棘突中已经存在成熟水平的 PSD-MAGUK。我们的研究结果揭示了新生和成熟棘突之间的关键结构差异,并提出了一种通过 PSD-MAGUK 的顺序到达来稳定新生棘突的机制。 © 2017 Wiley Periodicals, Inc. 发展神经生物学 77:1161-1174,2017 年。