• 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

心脏瓣膜发育和疾病中的巨噬细胞谱系。

Macrophage lineages in heart valve development and disease.

机构信息

Division of Molecular Cardiovascular Biology, The Heart Institute, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, 240 Albert Sabin Way, Cincinnati, OH 45229, USA.

出版信息

Cardiovasc Res. 2021 Feb 22;117(3):663-673. doi: 10.1093/cvr/cvaa062.

DOI:10.1093/cvr/cvaa062
PMID:32170926
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8453806/
Abstract

Heterogeneous macrophage lineages are present in the aortic and mitral valves of the heart during development and disease. These populations include resident macrophages of embryonic origins and recruited monocyte-derived macrophages prevalent in disease. Soon after birth, macrophages from haematopoietic lineages are recruited to the heart valves, and bone marrow transplantation studies in mice demonstrate that haematopoietic-derived macrophages continue to invest adult valves. During myxomatous heart valve disease, monocyte-derived macrophages are recruited to the heart valves and they contribute to valve degeneration in a mouse model of Marfan syndrome. Here, we review recent studies of macrophage lineages in heart valve development and disease with discussion of clinical significance and therapeutic applications.

摘要

在心脏发育和疾病过程中,主动脉瓣和二尖瓣存在异质性的巨噬细胞谱系。这些群体包括胚胎来源的固有巨噬细胞和在疾病中普遍存在的募集而来的单核细胞衍生的巨噬细胞。出生后不久,造血谱系的巨噬细胞就被招募到心脏瓣膜,并且在小鼠的骨髓移植研究中表明,造血衍生的巨噬细胞持续浸润成年瓣膜。在黏液样心脏瓣膜病中,单核细胞衍生的巨噬细胞被招募到心脏瓣膜,并且它们在马凡综合征的小鼠模型中导致瓣膜退化。在这里,我们回顾了心脏瓣膜发育和疾病中巨噬细胞谱系的最新研究,并讨论了其临床意义和治疗应用。

相似文献

1
Macrophage lineages in heart valve development and disease.心脏瓣膜发育和疾病中的巨噬细胞谱系。
Cardiovasc Res. 2021 Feb 22;117(3):663-673. doi: 10.1093/cvr/cvaa062.
2
Macrophage Transitions in Heart Valve Development and Myxomatous Valve Disease.心脏瓣膜发育和黏液瘤性瓣膜病中的巨噬细胞转化。
Arterioscler Thromb Vasc Biol. 2018 Mar;38(3):636-644. doi: 10.1161/ATVBAHA.117.310667. Epub 2018 Jan 18.
3
Deficiency of Circulating Monocytes Ameliorates the Progression of Myxomatous Valve Degeneration in Marfan Syndrome.循环单核细胞缺乏可改善马凡综合征黏液瘤性瓣膜退行性变的进展。
Circulation. 2020 Jan 14;141(2):132-146. doi: 10.1161/CIRCULATIONAHA.119.042391. Epub 2020 Jan 13.
4
Twist1 promotes heart valve cell proliferation and extracellular matrix gene expression during development in vivo and is expressed in human diseased aortic valves.Twist1 在体内发育过程中促进心脏瓣膜细胞增殖和细胞外基质基因表达,并在人类病变主动脉瓣中表达。
Dev Biol. 2010 Nov 1;347(1):167-79. doi: 10.1016/j.ydbio.2010.08.021. Epub 2010 Sep 6.
5
Mechanisms of heart valve development and disease.心脏瓣膜发育和疾病的机制。
Development. 2020 Jul 3;147(13):dev183020. doi: 10.1242/dev.183020.
6
Endothelial Cell Lineage Analysis Does Not Provide Evidence for EMT in Adult Valve Homeostasis and Disease.内皮细胞谱系分析在成人瓣膜稳态和疾病中不提供 EMT 的证据。
Anat Rec (Hoboken). 2019 Jan;302(1):125-135. doi: 10.1002/ar.23916. Epub 2018 Oct 10.
7
Morphology, Clinicopathologic Correlations, and Mechanisms in Heart Valve Health and Disease.心脏瓣膜健康与疾病的形态学、临床病理相关性及机制
Cardiovasc Eng Technol. 2018 Jun;9(2):126-140. doi: 10.1007/s13239-016-0277-7. Epub 2016 Aug 8.
8
Heart valve development: regulatory networks in development and disease.心脏瓣膜发育:发育与疾病中的调控网络
Circ Res. 2009 Aug 28;105(5):408-21. doi: 10.1161/CIRCRESAHA.109.201566.
9
Editorial: Special Issue on Heart Valve Mechanobiology : New Insights into Mechanical Regulation of Valve Disease and Regeneration.社论:心脏瓣膜力学生物学特刊:瓣膜疾病与再生机械调节的新见解
Cardiovasc Eng Technol. 2018 Jun;9(2):121-125. doi: 10.1007/s13239-018-0360-3.
10
Cholesterol induced heart valve inflammation and injury: efficacy of cholesterol lowering treatment.胆固醇诱导的心脏瓣膜炎症与损伤:降低胆固醇治疗的疗效
Open Heart. 2020 Aug;7(2). doi: 10.1136/openhrt-2020-001274.

引用本文的文献

1
Disruption of Notch1 and Gata5 in Mice Leads to Congenital Aortic Valve Disease.小鼠中Notch1和Gata5的破坏导致先天性主动脉瓣疾病。
JACC Basic Transl Sci. 2025 Jul 31;10(9):101354. doi: 10.1016/j.jacbts.2025.101354.
2
A Bibliometric and Visualization Analysis of Metabolic Reprogramming in Cardiovascular Diseases: Trends, Key Contributors, and Future Directions from 2000 to 2024.心血管疾病中代谢重编程的文献计量与可视化分析:2000年至2024年的趋势、主要贡献者及未来方向
Curr Cardiol Rev. 2025;21(4):e1573403X371021. doi: 10.2174/011573403X371021250109064231.
3
Exploring the Relationship Between Gut Microbiota and Aortic Stenosis: Role of Inflammatory Proteins, Blood Metabolites, and Immune Cells.探索肠道微生物群与主动脉瓣狭窄之间的关系:炎症蛋白、血液代谢物和免疫细胞的作用。
Int J Med Sci. 2025 Mar 10;22(8):1750-1761. doi: 10.7150/ijms.110392. eCollection 2025.
4
Autophagy regulates cellular senescence by mediating the degradation of CDKN1A/p21 and CDKN2A/p16 through SQSTM1/p62-mediated selective autophagy in myxomatous mitral valve degeneration.自噬通过在黏液瘤样二尖瓣退变中经由SQSTM1/p62介导的选择性自噬调节CDKN1A/p21和CDKN2A/p16的降解,从而调控细胞衰老。
Autophagy. 2025 Mar 4:1-23. doi: 10.1080/15548627.2025.2469315.
5
Cardiomyocyte proliferation: Advances and insights in macrophage-targeted therapy for myocardial injury.心肌细胞增殖:针对心肌损伤的巨噬细胞靶向治疗的进展与见解
Genes Dis. 2024 May 19;12(3):101332. doi: 10.1016/j.gendis.2024.101332. eCollection 2025 May.
6
Side- and Disease-Dependent Changes in Human Aortic Valve Cell Population and Transcriptomic Heterogeneity Determined by Single-Cell RNA Sequencing.通过单细胞RNA测序确定的人类主动脉瓣细胞群体和转录组异质性的侧别及疾病依赖性变化
Genes (Basel). 2024 Dec 19;15(12):1623. doi: 10.3390/genes15121623.
7
Cardiac macrophages in maintaining heart homeostasis and regulating ventricular remodeling of heart diseases.心脏中的巨噬细胞在维持心脏稳态和调节心脏疾病的心室重构中的作用。
Front Immunol. 2024 Sep 20;15:1467089. doi: 10.3389/fimmu.2024.1467089. eCollection 2024.
8
Recent advancements in polymeric heart valves: From basic research to clinical trials.聚合物心脏瓣膜的最新进展:从基础研究到临床试验。
Mater Today Bio. 2024 Aug 10;28:101194. doi: 10.1016/j.mtbio.2024.101194. eCollection 2024 Oct.
9
Facile engineering of interactive double network hydrogels for heart valve regeneration.用于心脏瓣膜再生的交互式双网络水凝胶的简易工程设计。
Nat Commun. 2024 Aug 29;15(1):7462. doi: 10.1038/s41467-024-51773-0.
10
Anti-IL-17 Inhibits PINK1/Parkin Autophagy and M1 Macrophage Polarization in Rheumatic Heart Disease.抗白细胞介素-17抑制风湿性心脏病中的PINK1/Parkin自噬和M1巨噬细胞极化。
Inflammation. 2025 Apr;48(2):870-884. doi: 10.1007/s10753-024-02094-3. Epub 2024 Jul 8.

本文引用的文献

1
Deficiency of Circulating Monocytes Ameliorates the Progression of Myxomatous Valve Degeneration in Marfan Syndrome.循环单核细胞缺乏可改善马凡综合征黏液瘤性瓣膜退行性变的进展。
Circulation. 2020 Jan 14;141(2):132-146. doi: 10.1161/CIRCULATIONAHA.119.042391. Epub 2020 Jan 13.
2
An acute immune response underlies the benefit of cardiac stem cell therapy.急性免疫反应是心脏干细胞治疗获益的基础。
Nature. 2020 Jan;577(7790):405-409. doi: 10.1038/s41586-019-1802-2. Epub 2019 Nov 27.
3
Stress-induced remodelling of the mitral valve: a model for leaflet thickening and superimposed tissue formation in mitral valve disease.压力诱导的二尖瓣重构:二尖瓣疾病中瓣叶增厚和叠加组织形成的模型。
Cardiovasc Res. 2020 Apr 1;116(5):931-943. doi: 10.1093/cvr/cvz204.
4
Adaptive immune cells in calcific aortic valve disease.在钙化性主动脉瓣疾病中的适应性免疫细胞。
Am J Physiol Heart Circ Physiol. 2019 Jul 1;317(1):H141-H155. doi: 10.1152/ajpheart.00100.2019. Epub 2019 May 3.
5
Structural basis for ligand modulation of the CCR2 conformational landscape.配体调节 CCR2 构象景观的结构基础。
Proc Natl Acad Sci U S A. 2019 Apr 23;116(17):8131-8136. doi: 10.1073/pnas.1814131116. Epub 2019 Apr 11.
6
Endocardially Derived Macrophages Are Essential for Valvular Remodeling.心内膜衍生的巨噬细胞对于瓣膜重塑是必需的。
Dev Cell. 2019 Mar 11;48(5):617-630.e3. doi: 10.1016/j.devcel.2019.01.021. Epub 2019 Feb 21.
7
Maturation of heart valve cell populations during postnatal remodeling.心脏瓣膜细胞群体在出生后重塑过程中的成熟。
Development. 2019 Mar 12;146(12):dev173047. doi: 10.1242/dev.173047.
8
Chemokines as Therapeutic Targets in Cardiovascular Disease.趋化因子作为心血管疾病的治疗靶点。
Arterioscler Thromb Vasc Biol. 2019 Apr;39(4):583-592. doi: 10.1161/ATVBAHA.118.312037.
9
Tissue Resident CCR2- and CCR2+ Cardiac Macrophages Differentially Orchestrate Monocyte Recruitment and Fate Specification Following Myocardial Injury.组织驻留的 CCR2-和 CCR2+心脏巨噬细胞在心肌损伤后通过不同的方式募集单核细胞并决定其命运。
Circ Res. 2019 Jan 18;124(2):263-278. doi: 10.1161/CIRCRESAHA.118.314028.
10
The Macrophage in Cardiac Homeostasis and Disease: JACC Macrophage in CVD Series (Part 4).心肌稳态和疾病中的巨噬细胞:JACC 巨噬细胞在 CVD 系列中的应用(第 4 部分)。
J Am Coll Cardiol. 2018 Oct 30;72(18):2213-2230. doi: 10.1016/j.jacc.2018.08.2149.