• 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

小鼠动脉粥样硬化中的细胞因子与免疫反应

Cytokines and Immune Responses in Murine Atherosclerosis.

作者信息

Kusters Pascal J H, Lutgens Esther

机构信息

Department of Medical Biochemistry, Academic Medical Center, Amsterdam, The Netherlands.

Department of Medical Biochemistry, Academic Medical Center, L01-146.1, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

出版信息

Methods Mol Biol. 2015;1339:17-40. doi: 10.1007/978-1-4939-2929-0_2.

DOI:10.1007/978-1-4939-2929-0_2
PMID:26445779
Abstract

Atherosclerosis is an inflammatory disease of the vessel wall characterized by activation of the innate immune system, with macrophages as the main players, as well as the adaptive immune system, characterized by a Th1-dominant immune response. Cytokines play a major role in the initiation and regulation of inflammation. In recent years, many studies have investigated the role of these molecules in experimental models of atherosclerosis. While some cytokines such as TNF or IFNγ clearly had atherogenic effects, others such as IL-10 were found to be atheroprotective. However, studies investigating the different cytokines in experimental atherosclerosis revealed that the cytokine system is complex with both disease stage-dependent and site-specific effects. In this review, we strive to provide an overview of the main cytokines involved in atherosclerosis and to shed light on their individual role during atherogenesis.

摘要

动脉粥样硬化是一种血管壁炎症性疾病,其特征是先天性免疫系统激活,巨噬细胞是主要参与者,同时也是适应性免疫系统激活,其特征是以Th1为主导的免疫反应。细胞因子在炎症的启动和调节中起主要作用。近年来,许多研究调查了这些分子在动脉粥样硬化实验模型中的作用。虽然一些细胞因子如TNF或IFNγ明显具有致动脉粥样硬化作用,但其他细胞因子如IL-10被发现具有抗动脉粥样硬化保护作用。然而,在实验性动脉粥样硬化中研究不同细胞因子的研究表明,细胞因子系统很复杂,具有疾病阶段依赖性和位点特异性效应。在这篇综述中,我们力求概述参与动脉粥样硬化的主要细胞因子,并阐明它们在动脉粥样硬化发生过程中的各自作用。

相似文献

1
Cytokines and Immune Responses in Murine Atherosclerosis.小鼠动脉粥样硬化中的细胞因子与免疫反应
Methods Mol Biol. 2015;1339:17-40. doi: 10.1007/978-1-4939-2929-0_2.
2
Use of Mouse Models in Atherosclerosis Research.小鼠模型在动脉粥样硬化研究中的应用。
Methods Mol Biol. 2015;1339:1-16. doi: 10.1007/978-1-4939-2929-0_1.
3
Differentiation factors and cytokines in the atherosclerotic plaque micro-environment as a trigger for macrophage polarisation.动脉粥样硬化斑块微环境中的分化因子和细胞因子作为触发巨噬细胞极化的因素。
Thromb Haemost. 2011 Nov;106(5):763-71. doi: 10.1160/TH11-05-0320. Epub 2011 Sep 22.
4
Exploring immune checkpoints as potential therapeutic targets in atherosclerosis.探讨免疫检查点作为动脉粥样硬化潜在治疗靶点的研究进展。
Cardiovasc Res. 2018 Mar 1;114(3):368-377. doi: 10.1093/cvr/cvx248.
5
Macrophages and dendritic cells: the usual suspects in atherogenesis.巨噬细胞和树突状细胞:动脉粥样硬化形成中的常见嫌疑对象。
Curr Drug Targets. 2015;16(4):373-82. doi: 10.2174/1389450116666150330115809.
6
Macrophages and T cells in atherosclerosis: a translational perspective.动脉粥样硬化中的巨噬细胞和 T 细胞:转化视角。
Am J Physiol Heart Circ Physiol. 2019 Aug 1;317(2):H375-H386. doi: 10.1152/ajpheart.00206.2019. Epub 2019 Jun 14.
7
Atherosclerosis and immunity: A perspective.动脉粥样硬化与免疫:一个视角。
Trends Cardiovasc Med. 2019 Aug;29(6):363-371. doi: 10.1016/j.tcm.2018.09.017. Epub 2018 Sep 28.
8
Dendritic cells in atherosclerosis: functions in immune regulation and beyond.动脉粥样硬化中的树突状细胞:免疫调节及其他功能。
Thromb Haemost. 2011 Nov;106(5):772-8. doi: 10.1160/TH11-05-0296. Epub 2011 Sep 8.
9
Adaptive Response of T and B Cells in Atherosclerosis.动脉粥样硬化中 T 和 B 细胞的适应性反应。
Circ Res. 2016 Feb 19;118(4):668-78. doi: 10.1161/CIRCRESAHA.115.306427.
10
Immune and inflammatory mechanisms of atherosclerosis (*).动脉粥样硬化的免疫和炎症机制(*)
Annu Rev Immunol. 2009;27:165-97. doi: 10.1146/annurev.immunol.021908.132620.

引用本文的文献

1
The Role of Cytokines in Cholesterol Accumulation in Cells and Atherosclerosis Progression.细胞因子在细胞胆固醇蓄积和动脉粥样硬化进展中的作用。
Int J Mol Sci. 2023 Mar 29;24(7):6426. doi: 10.3390/ijms24076426.
2
Pro-efferocytic macrophage membrane biomimetic nanoparticles for the synergistic treatment of atherosclerosis via competition effect.基于噬泡形成的巨噬细胞膜仿生纳米粒通过竞争效应协同治疗动脉粥样硬化
J Nanobiotechnology. 2022 Dec 1;20(1):506. doi: 10.1186/s12951-022-01720-2.
3
Increased Level of Tim-3PD-1CD4T Cells With Altered Function Might Be Associated With Lower Extremity Arteriosclerosis Obliterans.
Tim-3PD-1CD4T 细胞水平升高伴功能改变可能与下肢动脉硬化闭塞症有关。
Front Immunol. 2022 Jun 10;13:871362. doi: 10.3389/fimmu.2022.871362. eCollection 2022.
4
Targeting Inflammatory Pathways in Cardiovascular Disease: The Inflammasome, Interleukin-1, Interleukin-6 and Beyond.靶向心血管疾病中的炎症途径:炎症小体、白细胞介素-1、白细胞介素-6 及其他。
Cells. 2021 Apr 20;10(4):951. doi: 10.3390/cells10040951.
5
Antibody-Mediated Inhibition of CTLA4 Aggravates Atherosclerotic Plaque Inflammation and Progression in Hyperlipidemic Mice.抗体介导的 CTLA4 抑制加重了高脂血症小鼠动脉粥样硬化斑块的炎症和进展。
Cells. 2020 Aug 29;9(9):1987. doi: 10.3390/cells9091987.
6
Development of a tunable method to generate various three-dimensional microstructures by replenishing macromolecules such as extracellular matrix components and polysaccharides.开发一种可调节的方法,通过补充细胞外基质成分和多糖等大分子来生成各种三维微结构。
Sci Rep. 2020 Apr 16;10(1):6567. doi: 10.1038/s41598-020-63621-4.
7
Anti-Atherosclerotic Properties of Wild Rice in Low-Density Lipoprotein Receptor Knockout Mice: The Gut Microbiome, Cytokines, and Metabolomics Study.野生稻米在 LDLR 敲除小鼠中的抗动脉粥样硬化特性:肠道微生物组、细胞因子和代谢组学研究。
Nutrients. 2019 Nov 28;11(12):2894. doi: 10.3390/nu11122894.
8
Yangyin Qingre Huoxue Method in Traditional Chinese Medicine Ameliorates Atherosclerosis in ApoE Mice Suffering from High-Fat Diet and HSP65 Aggression.中医养阴清热活血法改善高脂饮食并受HSP65攻击的载脂蛋白E基因敲除小鼠的动脉粥样硬化
Evid Based Complement Alternat Med. 2019 Jan 1;2019:2531979. doi: 10.1155/2019/2531979. eCollection 2019.
9
Oxidation of methionine residues in human apolipoprotein A-I generates a potent pro-inflammatory molecule.蛋氨酸残基在人载脂蛋白 A-I 中的氧化产生了一种强效的促炎分子。
J Biol Chem. 2019 Mar 8;294(10):3634-3646. doi: 10.1074/jbc.RA118.005663. Epub 2019 Jan 11.