• 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

Toll样受体4缺陷会损害运动协调性。

Toll-Like Receptor 4 Deficiency Impairs Motor Coordination.

作者信息

Zhu Jian-Wei, Li Yi-Fei, Wang Zhao-Tao, Jia Wei-Qiang, Xu Ru-Xiang

机构信息

Affiliated Bayi Brain Hospital, Military General Hospital of Beijing PLA, Southern Medical University Beijing, China.

出版信息

Front Neurosci. 2016 Feb 16;10:33. doi: 10.3389/fnins.2016.00033. eCollection 2016.

DOI:10.3389/fnins.2016.00033
PMID:26909014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4754460/
Abstract

The cerebellum plays an essential role in balance and motor coordination. Purkinje cells (PCs) are the sole output neurons of the cerebellar cortex and are critical for the execution of its functions, including motor coordination. Toll-like receptor (TLR) 4 is involved in the innate immune response and is abundantly expressed in the central nervous system; however, little is known about its role in cerebellum-related motor functions. To address this question, we evaluated motor behavior in TLR4 deficient mice. We found that TLR4(-∕-) mice showed impaired motor coordination. Morphological analyses revealed that TLR4 deficiency was associated with a reduction in the thickness of the molecular layer of the cerebellum. TLR4 was highly expressed in PCs but not in Bergmann glia or cerebellar granule cells; however, loss of TLR4 decreased the number of PCs. These findings suggest a novel role for TLR4 in cerebellum-related motor coordination through maintenance of the PC population.

摘要

小脑在平衡和运动协调中起着至关重要的作用。浦肯野细胞(PCs)是小脑皮质的唯一输出神经元,对其功能的执行至关重要,包括运动协调。Toll样受体(TLR)4参与先天免疫反应,在中枢神经系统中大量表达;然而,其在小脑相关运动功能中的作用却知之甚少。为了解决这个问题,我们评估了TLR4缺陷小鼠的运动行为。我们发现TLR4(-∕-)小鼠表现出运动协调受损。形态学分析显示,TLR4缺陷与小脑分子层厚度的减少有关。TLR4在PCs中高表达,但在伯格曼胶质细胞或小脑颗粒细胞中不表达;然而,TLR4的缺失减少了PCs的数量。这些发现表明TLR4通过维持PC群体在小脑相关运动协调中具有新的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/cd5d48d523e5/fnins-10-00033-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/d13de3a6d12e/fnins-10-00033-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/56452adda922/fnins-10-00033-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/038e33bd1ca1/fnins-10-00033-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/550e5c1f624d/fnins-10-00033-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/37667f920ae7/fnins-10-00033-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/cd5d48d523e5/fnins-10-00033-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/d13de3a6d12e/fnins-10-00033-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/56452adda922/fnins-10-00033-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/038e33bd1ca1/fnins-10-00033-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/550e5c1f624d/fnins-10-00033-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/37667f920ae7/fnins-10-00033-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d65b/4754460/cd5d48d523e5/fnins-10-00033-g0006.jpg

相似文献

1
Toll-Like Receptor 4 Deficiency Impairs Motor Coordination.Toll样受体4缺陷会损害运动协调性。
Front Neurosci. 2016 Feb 16;10:33. doi: 10.3389/fnins.2016.00033. eCollection 2016.
2
Deficiency of TRIM32 Impairs Motor Function and Purkinje Cells in Mid-Aged Mice.TRIM32 缺乏会损害中年小鼠的运动功能和浦肯野细胞。
Front Aging Neurosci. 2021 Aug 6;13:697494. doi: 10.3389/fnagi.2021.697494. eCollection 2021.
3
Transcriptional Regulator ZEB2 Is Essential for Bergmann Glia Development.转录调控因子 ZEB2 对于 Bergmann 神经胶质细胞的发育是必需的。
J Neurosci. 2018 Feb 7;38(6):1575-1587. doi: 10.1523/JNEUROSCI.2674-17.2018. Epub 2018 Jan 11.
4
Review on Cross Talk between Neurotransmitters and Neuroinflammation in Striatum and Cerebellum in the Mediation of Motor Behaviour.纹状体和小脑中介运动行为中神经递质与神经炎症的串扰综述。
Biomed Res Int. 2019 Nov 14;2019:1767203. doi: 10.1155/2019/1767203. eCollection 2019.
5
Lack of Connexin43-mediated bergmann glial gap junctional coupling does not affect cerebellar long-term depression, motor coordination, or eyeblink conditioning.缺乏连接蛋白43介导的伯格曼胶质细胞间隙连接耦合并不影响小脑长时程抑制、运动协调或眨眼条件反射。
Front Behav Neurosci. 2008 Apr 23;2:1. doi: 10.3389/neuro.08.001.2008. eCollection 2008.
6
Ablation of TFR1 in Purkinje Cells Inhibits mGlu1 Trafficking and Impairs Motor Coordination, But Not Autistic-Like Behaviors.浦肯野细胞中TFR1的消融抑制mGlu1转运并损害运动协调,但不影响自闭症样行为。
J Neurosci. 2017 Nov 22;37(47):11335-11352. doi: 10.1523/JNEUROSCI.1223-17.2017. Epub 2017 Oct 20.
7
[Importance of diacylglycerol signaling in cerebellar motor coordination].[二酰基甘油信号在小脑运动协调中的重要性]
Nihon Yakurigaku Zasshi. 2018;152(2):90-93. doi: 10.1254/fpj.152.90.
8
Close homologue of adhesion molecule L1 promotes survival of Purkinje and granule cells and granule cell migration during murine cerebellar development.黏附分子L1的紧密同源物在小鼠小脑发育过程中促进浦肯野细胞和颗粒细胞的存活以及颗粒细胞迁移。
J Comp Neurol. 2009 Apr 10;513(5):496-510. doi: 10.1002/cne.21981.
9
Ccdc134 deficiency impairs cerebellar development and motor coordination.Ccdc134 缺失会损害小脑的发育和运动协调能力。
Genes Brain Behav. 2021 Sep;20(7):e12763. doi: 10.1111/gbb.12763. Epub 2021 Aug 23.
10
Altered cerebellar development in nuclear receptor TAK1/ TR4 null mice is associated with deficits in GLAST(+) glia, alterations in social behavior, motor learning, startle reactivity, and microglia.核受体 TAK1/TR4 缺失小鼠小脑发育改变与 GLAST(+)胶质细胞减少、社会行为改变、运动学习障碍、惊跳反应和小胶质细胞改变有关。
Cerebellum. 2010 Sep;9(3):310-23. doi: 10.1007/s12311-010-0163-z.

引用本文的文献

1
UBE3A reinstatement restores behaviorand proteome in an Angelman syndrome mouse model of imprinting defects.UBE3A 恢复可在印记缺陷的天使综合征小鼠模型中恢复行为和蛋白质组。
Mol Autism. 2025 Aug 28;16(1):45. doi: 10.1186/s13229-025-00675-z.
2
A Longitudinal Study of Sex Differences in a TDP-43 Mouse Model Reveals STI1 Regulation of TDP-43 Proteinopathy and Motor Deficits.TDP-43小鼠模型中性别差异的纵向研究揭示了STI1对TDP-43蛋白病和运动缺陷的调节作用。
J Neurochem. 2025 Aug;169(8):e70204. doi: 10.1111/jnc.70204.
3
Multi-site investigation of gut microbiota in CDKL5 deficiency disorder mouse models: Targeting dysbiosis to improve neurological outcomes.

本文引用的文献

1
Lipopolysaccharide stimulation upregulated Toll-like receptor 4 expression in chicken cerebellum.脂多糖刺激上调了鸡小脑Toll样受体4的表达。
Vet Immunol Immunopathol. 2015 Aug 15;166(3-4):145-50. doi: 10.1016/j.vetimm.2015.05.004. Epub 2015 May 27.
2
Sun1 deficiency leads to cerebellar ataxia in mice.Sun1基因缺陷导致小鼠出现小脑性共济失调。
Dis Model Mech. 2015 Aug 1;8(8):957-67. doi: 10.1242/dmm.019240. Epub 2015 May 5.
3
High-fat diet induces toll-like receptor 4-dependent macrophage/microglial cell activation and retinal impairment.
CDKL5缺陷障碍小鼠模型中肠道微生物群的多中心研究:针对生态失调改善神经学结局。
Cell Rep. 2025 Apr 22;44(4):115546. doi: 10.1016/j.celrep.2025.115546. Epub 2025 Apr 10.
4
Deciphering motor dysfunction and microglial activation in mThy1--synuclein mice: a comprehensive study of behavioral, gene expression, and methylation changes.解析mThy1-突触核蛋白小鼠的运动功能障碍和小胶质细胞激活:行为、基因表达和甲基化变化的综合研究
Front Mol Neurosci. 2025 Feb 13;18:1544971. doi: 10.3389/fnmol.2025.1544971. eCollection 2025.
5
Toll-like receptor 4 deficiency in Purkinje neurons drives cerebellar ataxia by impairing the BK channel-mediated after-hyperpolarization and cytosolic calcium homeostasis.浦肯野神经元中 Toll 样受体 4 的缺失通过损害 BK 通道介导的超极化后电位和细胞溶质钙稳态来驱动小脑共济失调。
Cell Death Dis. 2024 Aug 15;15(8):594. doi: 10.1038/s41419-024-06988-w.
6
Gut dysbiosis impairs intestinal renewal and lipid absorption in Scarb2 deficiency-associated neurodegeneration.肠道菌群失调损害 Scarb2 缺乏相关神经退行性变中的肠道更新和脂质吸收。
Protein Cell. 2024 Nov 1;15(11):818-839. doi: 10.1093/procel/pwae016.
7
Real-time field-programmable gate array-based closed-loop deep brain stimulation platform targeting cerebellar circuitry rescues motor deficits in a mouse model of cerebellar ataxia.基于实时现场可编程门阵列的闭环深部脑刺激平台针对小脑回路,可挽救小脑共济失调小鼠模型的运动缺陷。
CNS Neurosci Ther. 2024 Mar;30(3):e14638. doi: 10.1111/cns.14638.
8
Microbiota-mediated effects of Parkinson's disease medications on Parkinsonian non-motor symptoms in male transgenic mice.微生物群介导的帕金森病药物对雄性转基因小鼠帕金森病非运动症状的影响。
mSphere. 2024 Jan 30;9(1):e0037923. doi: 10.1128/msphere.00379-23. Epub 2023 Dec 11.
9
Cerebellar axonopathy in Shivers horses identified by spatial transcriptomic and proteomic analyses.空间转录组学和蛋白质组学分析鉴定的颤抖马小脑轴突病。
J Vet Intern Med. 2023 Jul-Aug;37(4):1568-1579. doi: 10.1111/jvim.16784. Epub 2023 Jun 8.
10
Toll-Like Receptor 4 Plays a Significant Role in the Biochemical and Neurological Alterations Observed in Two Distinct Mice Models of Huntington's Disease.Toll样受体4在两种不同的亨廷顿舞蹈病小鼠模型中观察到的生化和神经学改变中起重要作用。
Mol Neurobiol. 2023 May;60(5):2678-2690. doi: 10.1007/s12035-023-03234-w. Epub 2023 Jan 26.
高脂饮食诱导Toll样受体4依赖性巨噬细胞/小胶质细胞活化及视网膜损伤。
Invest Ophthalmol Vis Sci. 2015 May;56(5):3041-50. doi: 10.1167/iovs.15-16504.
4
Disease-related microglia heterogeneity in the hippocampus of Alzheimer's disease, dementia with Lewy bodies, and hippocampal sclerosis of aging.阿尔茨海默病、路易体痴呆和老年海马硬化症中海马内与疾病相关的小胶质细胞异质性。
Acta Neuropathol Commun. 2015 May 23;3:32. doi: 10.1186/s40478-015-0209-z.
5
Intracellular FGF14 (iFGF14) Is Required for Spontaneous and Evoked Firing in Cerebellar Purkinje Neurons and for Motor Coordination and Balance.细胞内成纤维细胞生长因子14(iFGF14)是小脑浦肯野神经元自发和诱发放电以及运动协调和平衡所必需的。
J Neurosci. 2015 Apr 29;35(17):6752-69. doi: 10.1523/JNEUROSCI.2663-14.2015.
6
Prenatal stress is a vulnerability factor for altered morphology and biological activity of microglia cells.产前应激是导致小胶质细胞形态和生物学活性改变的易感性因素。
Front Cell Neurosci. 2015 Mar 12;9:82. doi: 10.3389/fncel.2015.00082. eCollection 2015.
7
Cerebellar transcriptional alterations with Purkinje cell dysfunction and loss in mice lacking PGC-1α.在缺乏PGC-1α的小鼠中,小脑转录改变伴浦肯野细胞功能障碍和缺失。
Front Cell Neurosci. 2015 Jan 6;8:441. doi: 10.3389/fncel.2014.00441. eCollection 2014.
8
Toll-like receptor 4: innate immune regulator of neuroimmune and neuroendocrine interactions in stress and major depressive disorder.Toll 样受体 4:应激和重度抑郁症中神经免疫和神经内分泌相互作用的先天免疫调节剂。
Front Neurosci. 2014 Sep 30;8:309. doi: 10.3389/fnins.2014.00309. eCollection 2014.
9
Lgr4 protein deficiency induces ataxia-like phenotype in mice and impairs long term depression at cerebellar parallel fiber-Purkinje cell synapses.Lgr4蛋白缺乏会在小鼠中诱发共济失调样表型,并损害小脑平行纤维-浦肯野细胞突触处的长时程抑制。
J Biol Chem. 2014 Sep 19;289(38):26492-26504. doi: 10.1074/jbc.M114.564138. Epub 2014 Jul 25.
10
Innate immune activation in neurodegenerative disease.神经退行性疾病中的先天免疫激活。
Nat Rev Immunol. 2014 Jul;14(7):463-77. doi: 10.1038/nri3705.