• 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

炎症存在与不存在情况下趋化因子的神经元表达。

Neuronal expression of fractalkine in the presence and absence of inflammation.

作者信息

Schwaeble W J, Stover C M, Schall T J, Dairaghi D J, Trinder P K, Linington C, Iglesias A, Schubart A, Lynch N J, Weihe E, Schäfer M K

机构信息

Department of Microbiology and Immunology, University of Leicester, UK.

出版信息

FEBS Lett. 1998 Nov 20;439(3):203-7. doi: 10.1016/s0014-5793(98)01384-2.

DOI:10.1016/s0014-5793(98)01384-2
PMID:9845323
Abstract

Fractalkine is the only as yet known member of a novel class of chemokines. Besides its novel Cys-X-X-X-Cys motif, fractalkine exhibits features which have not been described for any other member of the chemokine family, including its unusual size (397 amino acids human, 395 mouse) and the possession of a transmembrane anchor, from which a soluble form may be released by extracellular cleavage. This report demonstrates the abundant mRNA and fractalkine protein expression in neuronal cells. The neuronal expression of fractalkine mRNA is unaffected by experimentally induced inflammation of central nervous tissue.

摘要

趋化因子是一类新型趋化因子中目前唯一已知的成员。除了其新颖的Cys-X-X-X-Cys基序外,趋化因子还具有趋化因子家族其他成员所没有描述过的特征,包括其不寻常的大小(人类为397个氨基酸,小鼠为395个氨基酸)以及拥有一个跨膜锚定结构,通过细胞外裂解可从中释放出一种可溶性形式。本报告证明了神经元细胞中趋化因子mRNA和趋化因子蛋白的大量表达。趋化因子mRNA的神经元表达不受实验诱导的中枢神经组织炎症的影响。

相似文献

1
Neuronal expression of fractalkine in the presence and absence of inflammation.炎症存在与不存在情况下趋化因子的神经元表达。
FEBS Lett. 1998 Nov 20;439(3):203-7. doi: 10.1016/s0014-5793(98)01384-2.
2
Fractalkine and macrophage-derived chemokine: T cell-attracting chemokines expressed in T cell area dendritic cells.fractalkine和巨噬细胞衍生趋化因子:在T细胞区树突状细胞中表达的T细胞吸引趋化因子
Eur J Immunol. 1999 Jun;29(6):1925-32. doi: 10.1002/(SICI)1521-4141(199906)29:06<1925::AID-IMMU1925>3.0.CO;2-U.
3
Enhanced expression of fractalkine in HIV-1 associated dementia.趋化因子在HIV-1相关痴呆中的表达增强。
J Neuroimmunol. 2001 Apr 2;115(1-2):168-75. doi: 10.1016/s0165-5728(01)00262-4.
4
Interferon-gamma stimulates the expression of CX3CL1/fractalkine in cultured human endothelial cells.干扰素-γ刺激培养的人内皮细胞中CX3CL1/趋化因子的表达。
Tohoku J Exp Med. 2000 Oct;192(2):127-39. doi: 10.1620/tjem.192.127.
5
CX3C-chemokine, fractalkine-enhanced adhesion of THP-1 cells to endothelial cells through integrin-dependent and -independent mechanisms.CX3C趋化因子(fractalkine)通过整合素依赖和非依赖机制增强THP-1细胞与内皮细胞的黏附。
J Immunol. 2000 Apr 15;164(8):4313-20. doi: 10.4049/jimmunol.164.8.4313.
6
Identification of fractalkine, a CX3C-type chemokine, as a direct target of p53.识别趋化因子(一种CX3C型趋化因子)为p53的直接靶点。
Cancer Res. 2000 Jul 15;60(14):3722-6.
7
Fractalkine is an epithelial and endothelial cell-derived chemoattractant for intraepithelial lymphocytes in the small intestinal mucosa.趋化因子是一种由上皮细胞和内皮细胞产生的趋化剂,可吸引小肠黏膜上皮内淋巴细胞。
J Immunol. 2000 Mar 15;164(6):3368-76. doi: 10.4049/jimmunol.164.6.3368.
8
Localization of fractalkine and CX3CR1 mRNAs in rat brain: does fractalkine play a role in signaling from neuron to microglia?大鼠脑中fractalkine和CX3CR1 mRNA的定位:fractalkine在神经元向小胶质细胞的信号传导中起作用吗?
FEBS Lett. 1998 Jun 12;429(2):167-72. doi: 10.1016/s0014-5793(98)00583-3.
9
Fractalkine cleavage from neuronal membranes represents an acute event in the inflammatory response to excitotoxic brain damage.从神经细胞膜上裂解趋化因子是对兴奋性毒性脑损伤炎症反应中的一个急性事件。
J Neurosci. 2000 Aug 1;20(15):RC87. doi: 10.1523/JNEUROSCI.20-15-j0004.2000.
10
Fractalkine modulates TNF-alpha secretion and neurotoxicity induced by microglial activation.趋化因子调节小胶质细胞激活诱导的肿瘤坏死因子-α分泌和神经毒性。
Glia. 2000 Feb 15;29(4):305-15.

引用本文的文献

1
Characterising Distinct Migratory Profiles of Infiltrating T-Cell Subsets in Human Glioblastoma.描绘人类脑胶质瘤浸润性 T 细胞亚群的不同迁移特征。
Front Immunol. 2022 Apr 6;13:850226. doi: 10.3389/fimmu.2022.850226. eCollection 2022.
2
Chemokine-Driven Migration of Pro-Inflammatory CD4 T Cells in CNS Autoimmune Disease.趋化因子驱动的促炎 CD4 T 细胞在中枢神经系统自身免疫疾病中的迁移。
Front Immunol. 2022 Feb 16;13:817473. doi: 10.3389/fimmu.2022.817473. eCollection 2022.
3
Fractalkine Attenuates Microglial Cell Activation Induced by Prenatal Stress.
fractalkine减轻产前应激诱导的小胶质细胞活化
Neural Plast. 2016;2016:7258201. doi: 10.1155/2016/7258201. Epub 2016 Apr 27.
4
Help-me signaling: Non-cell autonomous mechanisms of neuroprotection and neurorecovery.求助信号:神经保护和神经恢复的非细胞自主机制。
Prog Neurobiol. 2017 May;152:181-199. doi: 10.1016/j.pneurobio.2016.04.004. Epub 2016 Apr 11.
5
Analysis of the Role of CX3CL1 (Fractalkine) and Its Receptor CX3CR1 in Traumatic Brain and Spinal Cord Injury: Insight into Recent Advances in Actions of Neurochemokine Agents.CX3CL1(趋化因子)及其受体CX3CR1在创伤性脑损伤和脊髓损伤中的作用分析:深入了解神经趋化因子药物作用的最新进展
Mol Neurobiol. 2017 Apr;54(3):2167-2188. doi: 10.1007/s12035-016-9787-4. Epub 2016 Mar 1.
6
Changes in the expression of genes related to neuroinflammation over the course of sporadic Alzheimer's disease progression: CX3CL1, TREM2, and PPARγ.散发性阿尔茨海默病进展过程中神经炎症相关基因的表达变化:CX3CL1、TREM2和PPARγ。
J Neural Transm (Vienna). 2015 Jul;122(7):1069-76. doi: 10.1007/s00702-015-1369-5. Epub 2015 Jan 18.
7
Fractalkine promotes human monocyte survival via a reduction in oxidative stress.趋化因子通过降低氧化应激促进人单核细胞存活。
Arterioscler Thromb Vasc Biol. 2014 Dec;34(12):2554-62. doi: 10.1161/ATVBAHA.114.304717. Epub 2014 Oct 30.
8
Fractalkine regulation of microglial physiology and consequences on the brain and behavior.趋化因子对小胶质细胞生理功能的调节及其对大脑和行为的影响。
Front Cell Neurosci. 2014 May 13;8:129. doi: 10.3389/fncel.2014.00129. eCollection 2014.
9
Neuron-glia crosstalk in health and disease: fractalkine and CX3CR1 take centre stage.神经元-胶质细胞相互作用在健康和疾病中的作用: fractalkine 和 CX3CR1 占据中心舞台。
Open Biol. 2013 Dec 18;3(12):130181. doi: 10.1098/rsob.130181.
10
CX3CR1/CX3CL1 axis negatively controls glioma cell invasion and is modulated by transforming growth factor-β1.CX3CR1/CX3CL1 轴负向调控神经胶质瘤细胞侵袭,受转化生长因子-β1 调节。
Neuro Oncol. 2010 Jul;12(7):701-10. doi: 10.1093/neuonc/nop076. Epub 2010 Feb 8.