• 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

相似文献

1
Polarizing Macrophage Functional Phenotype to Foster Cardiac Regeneration.极化巨噬细胞功能表型以促进心脏再生。
Int J Mol Sci. 2023 Jun 28;24(13):10747. doi: 10.3390/ijms241310747.
2
Inflammation in cardiac injury, repair and regeneration.心脏损伤、修复与再生中的炎症
Curr Opin Cardiol. 2015 May;30(3):240-5. doi: 10.1097/HCO.0000000000000158.
3
Cortical bone stem cells modify cardiac inflammation after myocardial infarction by inducing a novel macrophage phenotype.皮质骨干细胞通过诱导新型巨噬细胞表型来改善心肌梗死后的心脏炎症。
Am J Physiol Heart Circ Physiol. 2021 Oct 1;321(4):H684-H701. doi: 10.1152/ajpheart.00304.2021. Epub 2021 Aug 20.
4
The Evolving Roles of Cardiac Macrophages in Homeostasis, Regeneration, and Repair.心脏巨噬细胞在稳态、再生和修复中的不断演变的作用。
Int J Mol Sci. 2021 Jul 25;22(15):7923. doi: 10.3390/ijms22157923.
5
Macrophages and regeneration: Lessons from the heart.巨噬细胞与再生:心脏的启示。
Semin Cell Dev Biol. 2016 Oct;58:26-33. doi: 10.1016/j.semcdb.2016.04.012. Epub 2016 Apr 23.
6
Regenerative cross talk between cardiac cells and macrophages.心肌细胞与巨噬细胞间的再生对话。
Am J Physiol Heart Circ Physiol. 2021 Jun 1;320(6):H2211-H2221. doi: 10.1152/ajpheart.00056.2021. Epub 2021 Mar 26.
7
Harnessing the innate and adaptive immune system for tissue repair and regeneration: Considering more than macrophages.利用固有和适应性免疫系统进行组织修复和再生:不仅仅考虑巨噬细胞。
Acta Biomater. 2021 Oct 1;133:208-221. doi: 10.1016/j.actbio.2021.02.023. Epub 2021 Feb 28.
8
Lgr4 Governs a Pro-Inflammatory Program in Macrophages to Antagonize Post-Infarction Cardiac Repair.Lgr4 调控巨噬细胞中的促炎程序以拮抗心肌梗死后的心脏修复。
Circ Res. 2020 Sep 25;127(8):953-973. doi: 10.1161/CIRCRESAHA.119.315807. Epub 2020 Jun 30.
9
Cells of the Immune System in Cardiac Remodeling: Main Players in Resolution of Inflammation and Repair After Myocardial Infarction.免疫系统细胞在心脏重构中的作用:心肌梗死后炎症消退和修复的主要参与者。
Front Immunol. 2021 Apr 2;12:664457. doi: 10.3389/fimmu.2021.664457. eCollection 2021.
10
Distinct macrophage lineages contribute to disparate patterns of cardiac recovery and remodeling in the neonatal and adult heart.不同的巨噬细胞谱系对新生儿和成年心脏的心脏恢复和重塑的不同模式有贡献。
Proc Natl Acad Sci U S A. 2014 Nov 11;111(45):16029-34. doi: 10.1073/pnas.1406508111. Epub 2014 Oct 27.

引用本文的文献

1
Effects and mechanisms of the myocardial microenvironment on cardiomyocyte proliferation and regeneration.心肌微环境对心肌细胞增殖和再生的影响及机制。
Front Cell Dev Biol. 2024 Jul 10;12:1429020. doi: 10.3389/fcell.2024.1429020. eCollection 2024.
2
Macrophage-based therapeutic approaches for cardiovascular diseases.基于巨噬细胞的心血管疾病治疗方法。
Basic Res Cardiol. 2024 Feb;119(1):1-33. doi: 10.1007/s00395-023-01027-9. Epub 2024 Jan 3.

本文引用的文献

1
An interferon gamma response signature links myocardial aging and immunosenescence.干扰素 γ 反应特征可将心肌衰老与免疫衰老联系起来。
Cardiovasc Res. 2023 Nov 15;119(14):2458-2468. doi: 10.1093/cvr/cvad068.
2
Streptozotocin-Induced Type 1 and 2 Diabetes Mellitus Mouse Models Show Different Functional, Cellular and Molecular Patterns of Diabetic Cardiomyopathy.链脲佐菌素诱导的 1 型和 2 型糖尿病心肌病小鼠模型表现出不同的糖尿病心肌病的功能、细胞和分子特征。
Int J Mol Sci. 2023 Jan 6;24(2):1132. doi: 10.3390/ijms24021132.
3
Pharmacological clearance of senescent cells improves cardiac remodeling and function after myocardial infarction in female aged mice.
衰老细胞的药理学清除可改善老年雌性小鼠心肌梗死后的心脏重构和功能。
Mech Ageing Dev. 2022 Dec;208:111740. doi: 10.1016/j.mad.2022.111740. Epub 2022 Sep 20.
4
The negative regulation of gene expression by microRNAs as key driver of inducers and repressors of cardiomyocyte differentiation.微小 RNA 对基因表达的负调控作为心肌细胞分化诱导物和抑制剂的关键驱动因素。
Clin Sci (Lond). 2022 Aug 31;136(16):1179-1203. doi: 10.1042/CS20220391.
5
Myocardial regeneration protocols towards the routine clinical scenario: An unseemly path from bench to bedside.面向常规临床应用的心肌再生方案:从实验室到临床的艰难之路。
EClinicalMedicine. 2022 Jun 27;50:101530. doi: 10.1016/j.eclinm.2022.101530. eCollection 2022 Aug.
6
Adult T-cells impair neonatal cardiac regeneration.成人 T 细胞损害新生儿心脏再生。
Eur Heart J. 2022 Jul 21;43(28):2698-2709. doi: 10.1093/eurheartj/ehac153.
7
Lyotropic Liquid Crystals: A Biocompatible and Safe Material for Local Cardiac Application.溶致液晶:一种用于局部心脏应用的生物相容性和安全性良好的材料。
Pharmaceutics. 2022 Feb 20;14(2):452. doi: 10.3390/pharmaceutics14020452.
8
Unraveling and Targeting Myocardial Regeneration Deficit in Diabetes.揭示和靶向糖尿病中的心肌再生缺陷
Antioxidants (Basel). 2022 Jan 22;11(2):208. doi: 10.3390/antiox11020208.
9
Diabetes-Induced Cellular Senescence and Senescence-Associated Secretory Phenotype Impair Cardiac Regeneration and Function Independently of Age.糖尿病诱导的细胞衰老和衰老相关分泌表型独立于年龄损害心脏再生和功能。
Diabetes. 2022 May 1;71(5):1081-1098. doi: 10.2337/db21-0536.
10
Heart Disease and Stroke Statistics-2022 Update: A Report From the American Heart Association.《心脏病与卒中统计-2022 更新:美国心脏协会报告》。
Circulation. 2022 Feb 22;145(8):e153-e639. doi: 10.1161/CIR.0000000000001052. Epub 2022 Jan 26.

极化巨噬细胞功能表型以促进心脏再生。

Polarizing Macrophage Functional Phenotype to Foster Cardiac Regeneration.

机构信息

Department of Medical and Surgical Sciences, Magna Graecia University, 88100 Catanzaro, Italy.

Department of Experimental and Clinical Medicine, Magna Graecia University, 88100 Catanzaro, Italy.

出版信息

Int J Mol Sci. 2023 Jun 28;24(13):10747. doi: 10.3390/ijms241310747.

DOI:10.3390/ijms241310747
PMID:37445929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10341872/
Abstract

There is an increasing interest in understanding the connection between the immune and cardiovascular systems, which are highly integrated and communicate through finely regulated cross-talking mechanisms. Recent evidence has demonstrated that the immune system does indeed have a key role in the response to cardiac injury and in cardiac regeneration. Among the immune cells, macrophages appear to have a prominent role in this context, with different subtypes described so far that each have a specific influence on cardiac remodeling and repair. Similarly, there are significant differences in how the innate and adaptive immune systems affect the response to cardiac damage. Understanding all these mechanisms may have relevant clinical implications. Several studies have already demonstrated that stem cell-based therapies support myocardial repair. However, the exact role that cardiac macrophages and their modulation may have in this setting is still unclear. The current need to decipher the dual role of immunity in boosting both heart injury and repair is due, at least for a significant part, to unresolved questions related to the complexity of cardiac macrophage phenotypes. The aim of this review is to provide an overview on the role of the immune system, and of macrophages in particular, in the response to cardiac injury and to outline, through the modulation of the immune response, potential novel therapeutic strategies for cardiac regeneration.

摘要

人们越来越关注理解免疫系统和心血管系统之间的联系,这两个系统高度整合,并通过精细调节的相互交流机制进行通讯。最近的证据表明,免疫系统确实在心脏损伤反应和心脏再生中起着关键作用。在免疫细胞中,巨噬细胞在这方面似乎起着突出的作用,迄今为止已经描述了不同的亚型,它们各自对心脏重构和修复有特定的影响。同样,先天免疫系统和适应性免疫系统对心脏损伤反应的影响也存在显著差异。了解所有这些机制可能具有相关的临床意义。已有多项研究表明,基于干细胞的疗法支持心肌修复。然而,心脏巨噬细胞及其调节在这种情况下可能发挥的具体作用仍不清楚。目前需要阐明免疫在促进心脏损伤和修复方面的双重作用,这至少在很大程度上是由于与心脏巨噬细胞表型的复杂性相关的一些未解决的问题。本篇综述的目的是概述免疫系统,特别是巨噬细胞,在心脏损伤反应中的作用,并通过调节免疫反应,为心脏再生概述潜在的新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/4e7588d6dec3/ijms-24-10747-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/c90a471357c6/ijms-24-10747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/78e550f2f7ae/ijms-24-10747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/4e7588d6dec3/ijms-24-10747-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/c90a471357c6/ijms-24-10747-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/78e550f2f7ae/ijms-24-10747-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15ae/10341872/4e7588d6dec3/ijms-24-10747-g003.jpg