• 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
The role of glial cells in synapse elimination.胶质细胞在突触消除中的作用。
Curr Opin Neurobiol. 2012 Jun;22(3):438-45. doi: 10.1016/j.conb.2011.10.003. Epub 2011 Oct 27.
2
Errant gardeners: glial-cell-dependent synaptic pruning and neurodevelopmental disorders.错误的园丁:神经胶质细胞依赖性的突触修剪和神经发育障碍。
Nat Rev Neurosci. 2017 Nov;18(11):658-670. doi: 10.1038/nrn.2017.110. Epub 2017 Sep 21.
3
Glial cells in synaptic plasticity.突触可塑性中的神经胶质细胞。
J Physiol Paris. 2006 Mar-May;99(2-3):75-83. doi: 10.1016/j.jphysparis.2005.12.002. Epub 2006 Jan 30.
4
Neural activity, neuron-glia relationships, and synapse development.神经活动、神经元与神经胶质细胞的关系以及突触发育。
Perspect Dev Neurobiol. 1995;2(4):399-407.
5
Sculpting neural circuits by axon and dendrite pruning.通过轴突和树突修剪塑造神经回路。
Annu Rev Cell Dev Biol. 2015;31:779-805. doi: 10.1146/annurev-cellbio-100913-013038. Epub 2015 Oct 2.
6
[The updated advancements in synaptic plasticity mediated by glial cells].[由神经胶质细胞介导的突触可塑性的最新进展]
Sheng Li Ke Xue Jin Zhan. 2007 Apr;38(2):111-5.
7
The interplay between neurons and glia in synapse development and plasticity.神经元与神经胶质细胞在突触发育和可塑性方面的相互作用。
Curr Opin Neurobiol. 2017 Feb;42:1-8. doi: 10.1016/j.conb.2016.09.016. Epub 2016 Oct 24.
8
Sculpting the nervous system: glial control of neuronal development.塑造神经系统:神经胶质细胞对神经元发育的调控
Curr Opin Neurobiol. 2006 Feb;16(1):119-25. doi: 10.1016/j.conb.2005.12.004. Epub 2006 Jan 4.
9
Role of neuron-glia interactions in developmental synapse elimination.神经元-神经胶质细胞相互作用在发育性突触消除中的作用。
Brain Res Bull. 2017 Mar;129:74-81. doi: 10.1016/j.brainresbull.2016.08.017. Epub 2016 Sep 4.
10
Experience-dependent structural synaptic plasticity in the mammalian brain.哺乳动物大脑中依赖经验的结构性突触可塑性。
Nat Rev Neurosci. 2009 Sep;10(9):647-58. doi: 10.1038/nrn2699.

引用本文的文献

1
GABA-dependent microglial elimination of inhibitory synapses underlies neuronal hyperexcitability in epilepsy.γ-氨基丁酸(GABA)依赖的小胶质细胞对抑制性突触的清除是癫痫中神经元过度兴奋的基础。
Nat Neurosci. 2025 May 27. doi: 10.1038/s41593-025-01979-2.
2
Unraveling Neurodevelopment: Synergistic Effects of Intrinsic Genetic Programs and Extrinsic Environmental Cues.解析神经发育:内在遗传程序与外在环境线索的协同效应
Adv Sci (Weinh). 2025 Jun;12(22):e2414890. doi: 10.1002/advs.202414890. Epub 2025 May 5.
3
Aged Gut Microbiota Contributes to Cognitive Impairment and Hippocampal Synapse Loss in Mice.衰老的肠道微生物群导致小鼠认知障碍和海马体突触丧失。
Aging Cell. 2025 Jul;24(7):e70064. doi: 10.1111/acel.70064. Epub 2025 Apr 12.
4
Blood-Brain Barrier Dysfunction Predicts Microglial Activation After Traumatic Brain Injury in Juvenile Rats.血脑屏障功能障碍可预测幼年大鼠创伤性脑损伤后的小胶质细胞激活。
Neurotrauma Rep. 2024 Feb 8;5(1):95-116. doi: 10.1089/neur.2023.0057. eCollection 2024.
5
Astrocytes Are the Source of TNF Mediating Homeostatic Synaptic Plasticity.星形胶质细胞是介导稳态突触可塑性的 TNF 的来源。
J Neurosci. 2024 Apr 3;44(14):e2278222024. doi: 10.1523/JNEUROSCI.2278-22.2024.
6
Botulinum Neurotoxin Induces Neurotoxic Microglia Mediated by Exogenous Inflammatory Responses.肉毒杆菌神经毒素通过外源性炎症反应诱导神经毒性小胶质细胞。
Adv Sci (Weinh). 2024 Apr;11(15):e2305326. doi: 10.1002/advs.202305326. Epub 2024 Feb 11.
7
Molecular mechanisms underlying microglial sensing and phagocytosis in synaptic pruning.突触修剪中微胶质细胞感知与吞噬作用的分子机制
Neural Regen Res. 2024 Jun 1;19(6):1284-1290. doi: 10.4103/1673-5374.385854. Epub 2023 Sep 22.
8
A unique cell population expressing the Epithelial-Mesenchymal Transition-transcription factor Snail moderates microglial and astrocyte injury responses.一种表达上皮-间质转化转录因子Snail的独特细胞群可调节小胶质细胞和星形胶质细胞的损伤反应。
PNAS Nexus. 2023 Oct 12;2(10):pgad334. doi: 10.1093/pnasnexus/pgad334. eCollection 2023 Oct.
9
Early Draper-mediated glial refinement of neuropil architecture and synapse number in the Drosophila antennal lobe.早期德雷珀介导的果蝇触角叶中神经毡结构和突触数量的胶质细胞精细化过程。
Front Cell Neurosci. 2023 Jun 2;17:1166199. doi: 10.3389/fncel.2023.1166199. eCollection 2023.
10
Interrogating the Etiology of Sporadic Alzheimer's Disease Using Aging Rhesus Macaques: Cellular, Molecular, and Cortical Circuitry Perspectives.利用衰老恒河猴探究散发性阿尔茨海默病的病因:从细胞、分子和皮质回路角度。
J Gerontol A Biol Sci Med Sci. 2023 Aug 27;78(9):1523-1534. doi: 10.1093/gerona/glad134.

本文引用的文献

1
Synaptic pruning by microglia is necessary for normal brain development.小胶质细胞的突触修剪对于正常的大脑发育是必要的。
Science. 2011 Sep 9;333(6048):1456-8. doi: 10.1126/science.1202529. Epub 2011 Jul 21.
2
Phagocytic clearance in neurodegeneration.神经退行性变中的吞噬清除作用。
Am J Pathol. 2011 Apr;178(4):1416-28. doi: 10.1016/j.ajpath.2010.12.051.
3
Experience-dependent structural plasticity in the cortex.皮层的经验依赖性结构可塑性。
Trends Neurosci. 2011 Apr;34(4):177-87. doi: 10.1016/j.tins.2011.02.001.
4
Molecular clustering identifies complement and endothelin induction as early events in a mouse model of glaucoma.分子聚类将补体和内皮素诱导鉴定为青光眼小鼠模型中的早期事件。
J Clin Invest. 2011 Apr;121(4):1429-44. doi: 10.1172/JCI44646. Epub 2011 Mar 7.
5
Myelination transition zone astrocytes are constitutively phagocytic and have synuclein dependent reactivity in glaucoma.少突胶质细胞髓鞘化过渡区星形胶质细胞具有固有吞噬作用,并在青光眼中有与突触核蛋白相关的反应性。
Proc Natl Acad Sci U S A. 2011 Jan 18;108(3):1176-81. doi: 10.1073/pnas.1013965108. Epub 2011 Jan 3.
6
Keeping the CNS clear: glial phagocytic functions in Drosophila.保持中枢神经系统清晰:果蝇中的神经胶质吞噬功能。
Glia. 2011 Sep;59(9):1304-11. doi: 10.1002/glia.21098. Epub 2010 Dec 6.
7
Microglial interactions with synapses are modulated by visual experience.小胶质细胞与突触的相互作用受视觉经验的调节。
PLoS Biol. 2010 Nov 2;8(11):e1000527. doi: 10.1371/journal.pbio.1000527.
8
Distinct presynaptic and postsynaptic dismantling processes of Drosophila neuromuscular junctions during metamorphosis.果蝇变态过程中神经肌肉接头的独特的突触前和突触后解体过程。
J Neurosci. 2010 Sep 1;30(35):11624-34. doi: 10.1523/JNEUROSCI.0410-10.2010.
9
Spine plasticity in the motor cortex.运动皮层中的脊柱可塑性。
Curr Opin Neurobiol. 2011 Feb;21(1):169-74. doi: 10.1016/j.conb.2010.07.010. Epub 2010 Aug 20.
10
Hematopoietic origin of pathological grooming in Hoxb8 mutant mice.Hoxb8 突变小鼠病理性梳理行为的造血起源。
Cell. 2010 May 28;141(5):775-85. doi: 10.1016/j.cell.2010.03.055.

胶质细胞在突触消除中的作用。

The role of glial cells in synapse elimination.

机构信息

Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.

出版信息

Curr Opin Neurobiol. 2012 Jun;22(3):438-45. doi: 10.1016/j.conb.2011.10.003. Epub 2011 Oct 27.

DOI:10.1016/j.conb.2011.10.003
PMID:22036016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3319527/
Abstract

Excessive synapses generated during early development are eliminated extensively to form functionally mature neural circuits. Synapses in juvenile and mature brains are highly dynamic, and undergo remodeling processes through constant formation and elimination of dendritic spines. Although neural activity has been implicated in initiating the synapse elimination process cell-autonomously, the cellular and molecular mechanisms that transduce changes in correlated neural activity into structural changes in synapses are largely unknown. Recently, however, new findings provide evidence that in different species, glial cells, non-neuronal cell types in the nervous system are crucial in eliminating neural debris and unwanted synapses through phagocytosis. Glial cells not only clear fragmented axons and synaptic debris produced during synapse elimination, but also engulf unwanted synapses thereby actively promoting synapse elimination non-cell autonomously. These new findings support the important role of glial cells in the formation and maintenance of functional neural circuits in development as well as in adult stages and neurodegenerative diseases.

摘要

在早期发育过程中产生的过多的突触会被大量消除,从而形成功能成熟的神经回路。幼年和成年大脑中的突触具有高度的动态性,通过树突棘的不断形成和消除来进行重塑过程。尽管神经活动已经被牵连到自主启动突触消除过程中,但将相关神经活动的变化转化为突触结构变化的细胞和分子机制在很大程度上仍是未知的。然而,最近的新发现提供了证据,表明在不同物种中,神经胶质细胞——神经系统中的非神经元细胞类型,通过吞噬作用来清除神经碎片和不需要的突触。神经胶质细胞不仅清除突触消除过程中产生的碎片化轴突和突触碎片,还吞噬不需要的突触,从而非自主地积极促进突触消除。这些新发现支持了神经胶质细胞在发育以及成年阶段和神经退行性疾病中形成和维持功能性神经回路中的重要作用。