• 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

靶向巨噬细胞表型治疗心力衰竭:一种新方法。

Targeting Macrophage Phenotype for Treating Heart Failure: A New Approach.

机构信息

School of Chinese Medicine, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.

Hunan Key Laboratory of Colleges and Universities of Intelligent TCM Diagnosis and Preventive Treatment of Chronic Diseases, Hunan University of Chinese Medicine, Changsha, 410208, People's Republic of China.

出版信息

Drug Des Devel Ther. 2024 Nov 5;18:4927-4942. doi: 10.2147/DDDT.S486816. eCollection 2024.

DOI:10.2147/DDDT.S486816
PMID:39525046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11549885/
Abstract

Heart failure (HF) is a disease with high morbidity and mortality rates worldwide and significantly affects human health. Currently, the treatment options for HF are limited, and there is an urgent need to discover new therapeutic targets and strategies. Macrophages are innate immune cells involved in the development of HF. They play a crucial role in maintaining cardiac homeostasis and regulating cardiac stress. Recently, macrophages have received increasing attention as potential targets for treating HF. With the improvement of technological means, the study of macrophages in HF has made great progress. This article discusses the biological functions of macrophage phagocytosis, immune response, and tissue repair. The polarization, pyroptosis, autophagy, and apoptosis are of macrophages, deeply involved in the pathogenesis of HF. Modulation of the phenotypic changes of macrophages can improve immune-inflammation, myocardial fibrosis, energy metabolism, apoptosis, and angiogenesis in HF.

摘要

心力衰竭(HF)是一种全球范围内发病率和死亡率都很高的疾病,严重影响人类健康。目前,HF 的治疗选择有限,迫切需要发现新的治疗靶点和策略。巨噬细胞是参与 HF 发生发展的固有免疫细胞。它们在维持心脏内稳态和调节心脏应激方面发挥着关键作用。最近,巨噬细胞作为治疗 HF 的潜在靶点受到了越来越多的关注。随着技术手段的提高,巨噬细胞在 HF 中的研究取得了很大进展。本文讨论了巨噬细胞吞噬、免疫应答和组织修复的生物学功能。巨噬细胞的极化、细胞焦亡、自噬和凋亡与 HF 的发病机制密切相关。调节巨噬细胞的表型变化可以改善 HF 中的免疫炎症、心肌纤维化、能量代谢、细胞凋亡和血管生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/950ae32b63a9/DDDT-18-4927-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/56e4fec31358/DDDT-18-4927-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/b6f6f78374e8/DDDT-18-4927-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/c82b2d53db11/DDDT-18-4927-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/7512bec4b30a/DDDT-18-4927-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/950ae32b63a9/DDDT-18-4927-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/56e4fec31358/DDDT-18-4927-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/b6f6f78374e8/DDDT-18-4927-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/c82b2d53db11/DDDT-18-4927-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/7512bec4b30a/DDDT-18-4927-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a0/11549885/950ae32b63a9/DDDT-18-4927-g0005.jpg

相似文献

1
Targeting Macrophage Phenotype for Treating Heart Failure: A New Approach.靶向巨噬细胞表型治疗心力衰竭:一种新方法。
Drug Des Devel Ther. 2024 Nov 5;18:4927-4942. doi: 10.2147/DDDT.S486816. eCollection 2024.
2
[Role of macrophages in heart failure and traditional Chinese medicine intervention].[巨噬细胞在心力衰竭中的作用及中医干预]
Zhongguo Zhong Yao Za Zhi. 2023 May;48(9):2379-2386. doi: 10.19540/j.cnki.cjcmm.20230105.601.
3
Macrophage-mediated heart repair and remodeling: A promising therapeutic target for post-myocardial infarction heart failure.巨噬细胞介导的心脏修复和重构:心肌梗死后心力衰竭有前景的治疗靶点。
J Cell Physiol. 2024 Nov;239(11):e31372. doi: 10.1002/jcp.31372. Epub 2024 Jul 16.
4
Cardiac resident macrophages: The core of cardiac immune homeostasis.心肌驻留巨噬细胞:心脏免疫稳态的核心。
Cell Signal. 2024 Jul;119:111169. doi: 10.1016/j.cellsig.2024.111169. Epub 2024 Apr 8.
5
Macrophage-specific lipoxygenase deletion amplify cardiac repair activating Treg cells in chronic heart failure.巨噬细胞特异性脂氧合酶缺失可扩增慢性心力衰竭心脏修复激活的 Treg 细胞。
J Leukoc Biol. 2024 Oct 1;116(4):864-875. doi: 10.1093/jleuko/qiae113.
6
Role of macrophage polarization in heart failure and traditional Chinese medicine treatment.巨噬细胞极化在心力衰竭及中医治疗中的作用
Front Pharmacol. 2024 Jul 18;15:1434654. doi: 10.3389/fphar.2024.1434654. eCollection 2024.
7
Multiple roles of cardiac macrophages in heart homeostasis and failure.心脏巨噬细胞在心脏稳态和衰竭中的多重作用。
Heart Fail Rev. 2022 Jul;27(4):1413-1430. doi: 10.1007/s10741-021-10156-z. Epub 2021 Aug 13.
8
Nuanxinkang protects against ischemia/reperfusion-induced heart failure through regulating IKKβ/IκBα/NF-κB-mediated macrophage polarization.暖心康通过调节 IKKβ/IκBα/NF-κB 介导的巨噬细胞极化来防治缺血/再灌注诱导的心力衰竭。
Phytomedicine. 2022 Jul;101:154093. doi: 10.1016/j.phymed.2022.154093. Epub 2022 Mar 30.
9
Macrophages: The Good, the Bad, and the Gluttony.巨噬细胞:亦善亦恶亦饕餮。
Front Immunol. 2021 Aug 12;12:708186. doi: 10.3389/fimmu.2021.708186. eCollection 2021.
10
Single-cell transcriptomics reveals writers of RNA modification-mediated immune microenvironment and cardiac resident Macro-MYL2 macrophages in heart failure.单细胞转录组学揭示了 RNA 修饰介导的免疫微环境的书写者和心力衰竭中心肌驻留的 Macro-MYL2 巨噬细胞。
BMC Cardiovasc Disord. 2024 Aug 16;24(1):432. doi: 10.1186/s12872-024-04080-x.

引用本文的文献

1
Immunogenic cell death-related biomarkers in heart failure probed by transcriptome and single-cell sequencing.通过转录组和单细胞测序探究心力衰竭中免疫原性细胞死亡相关生物标志物
Front Immunol. 2025 Jun 24;16:1560903. doi: 10.3389/fimmu.2025.1560903. eCollection 2025.

本文引用的文献

1
Murine exosomal miR-30a aggravates cardiac function after acute myocardial infarction via regulating cell fate of cardiomyocytes and cardiac resident macrophages.鼠源细胞外体 miR-30a 通过调控心肌细胞和心脏固有巨噬细胞的命运加重急性心肌梗死后的心功能障碍。
Int J Cardiol. 2024 Nov 1;414:132395. doi: 10.1016/j.ijcard.2024.132395. Epub 2024 Jul 27.
2
M1 macrophage-derived exosomes inhibit cardiomyocyte proliferation through delivering miR-155.M1巨噬细胞衍生的外泌体通过传递miR-155抑制心肌细胞增殖。
BMC Cardiovasc Disord. 2024 Jul 16;24(1):365. doi: 10.1186/s12872-024-03893-0.
3
Deleterious Anti-Inflammatory Macrophage Recruitment in Early Post-Infarction Phase: Unraveling the IL-6/MCP-1/STAT3 Axis.
梗死早期有害的抗炎性巨噬细胞募集:解析白细胞介素-6/单核细胞趋化蛋白-1/信号转导和转录激活因子3轴
JACC Basic Transl Sci. 2024 Apr 24;9(5):593-604. doi: 10.1016/j.jacbts.2024.01.019. eCollection 2024 May.
4
Dissection of pro-tumoral macrophage subtypes and immunosuppressive cells participating in M2 polarization.解析参与 M2 极化的促肿瘤巨噬细胞亚型和免疫抑制细胞。
Inflamm Res. 2024 Sep;73(9):1411-1423. doi: 10.1007/s00011-024-01907-3. Epub 2024 Jun 27.
5
A simplified herbal decoction attenuates myocardial infarction by regulating macrophage metabolic reprogramming and phenotypic differentiation via modulation of the HIF-1α/PDK1 axis.一种简化的草药煎剂通过调节HIF-1α/PDK1轴来调控巨噬细胞代谢重编程和表型分化,从而减轻心肌梗死。
Chin Med. 2024 May 30;19(1):75. doi: 10.1186/s13020-024-00933-x.
6
Nicorandil-Pretreated Mesenchymal Stem Cell-Derived Exosomes Facilitate Cardiac Repair After Myocardial Infarction via Promoting Macrophage M2 Polarization by Targeting miR-125a-5p/TRAF6/IRF5 Signaling Pathway.尼可地尔预处理的间充质干细胞来源的外泌体通过靶向miR-125a-5p/TRAF6/IRF5信号通路促进巨噬细胞M2极化,从而促进心肌梗死后的心脏修复。
Int J Nanomedicine. 2024 Feb 29;19:2005-2024. doi: 10.2147/IJN.S441307. eCollection 2024.
7
Concurrent Left Ventricular Myocardial Diffuse Fibrosis and Left Atrial Dysfunction Strongly Predict Incident Heart Failure.同时存在的左心室心肌弥漫性纤维化和左心房功能障碍强烈预测心力衰竭的发生。
JACC Cardiovasc Imaging. 2024 May;17(5):560-562. doi: 10.1016/j.jcmg.2023.11.006. Epub 2024 Jan 3.
8
Inducible nitric oxide synthase accelerates nonalcoholic fatty liver disease progression by regulating macrophage autophagy.诱导型一氧化氮合酶通过调节巨噬细胞自噬加速非酒精性脂肪性肝病进展。
Immun Inflamm Dis. 2023 Dec;11(12):e1114. doi: 10.1002/iid3.1114.
9
Autophagy-modulating biomembrane nanostructures: A robust anticancer weapon by modulating the inner and outer cancer environment.自噬调节生物膜纳米结构:通过调节内外肿瘤微环境的新型抗肿瘤武器
J Control Release. 2024 Feb;366:85-103. doi: 10.1016/j.jconrel.2023.12.032. Epub 2023 Dec 29.
10
Dapagliflozin protects against chronic heart failure in mice by inhibiting macrophage-mediated inflammation, independent of SGLT2.达格列净通过抑制巨噬细胞介导体液炎症来预防小鼠慢性心力衰竭,与 SGLT2 无关。
Cell Rep Med. 2023 Dec 19;4(12):101334. doi: 10.1016/j.xcrm.2023.101334.