• 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

microRNAs 在炎症性关节炎中对巨噬细胞表型的功能调控

Functional Regulation of Macrophage Phenotypes by MicroRNAs in Inflammatory Arthritis.

机构信息

Department of Nephrology and Rheumatology, Shanghai Children's Hospital, The Children's Hospital of Shanghai Jiaotong University, Pudong, China.

Division of Rheumatology, Cincinnati Children's Hospital Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

出版信息

Front Immunol. 2019 Sep 13;10:2217. doi: 10.3389/fimmu.2019.02217. eCollection 2019.

DOI:10.3389/fimmu.2019.02217
PMID:31572403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6753331/
Abstract

Inflammatory arthritis including rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) exhibit the shared feature of changes in activation and polarization of circulating monocytes and tissue macrophages. Numerous microRNAs (miRs) have been found to have key functions in regulating inflammation and macrophage polarization. Although there is increasing interest in the roles of miRs in both RA and JIA, less is known regarding how miRs relate to functional properties of immune cells, including monocytes and macrophages. Interestingly, miRs can function both to promote inflammatory phenotypes and pro-inflammatory polarization, as well as through negative-feedback loops to limit inflammation. Here, we review the functional roles of several miRs in macrophages in inflammatory arthritis, with a particular focus on vivo effects of miR alteration in experimental arthritis. We also consider how current efforts to target miRs clinically could modify functional monocyte and macrophage polarization , and serve as novel therapies for diseases such as RA and JIA.

摘要

炎症性关节炎包括类风湿关节炎(RA)和幼年特发性关节炎(JIA),其特征为循环单核细胞和组织巨噬细胞的激活和极化发生变化。已经发现许多 microRNAs(miRs)在调节炎症和巨噬细胞极化方面具有关键功能。尽管人们对 RA 和 JIA 中 miRs 的作用越来越感兴趣,但对于 miRs 与包括单核细胞和巨噬细胞在内的免疫细胞的功能特性之间的关系知之甚少。有趣的是,miRs 既可以促进炎症表型和促炎极化,也可以通过负反馈环来限制炎症。在这里,我们综述了几种在炎症性关节炎中巨噬细胞中的 miRs 的功能作用,特别关注 miR 在实验性关节炎中改变的体内效应。我们还考虑了目前靶向 miRs 进行临床治疗的方法如何改变功能性单核细胞和巨噬细胞的极化,并作为 RA 和 JIA 等疾病的新型治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa3/6753331/bd6f4b6cabc7/fimmu-10-02217-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa3/6753331/bd6f4b6cabc7/fimmu-10-02217-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa3/6753331/bd6f4b6cabc7/fimmu-10-02217-g0001.jpg

相似文献

1
Functional Regulation of Macrophage Phenotypes by MicroRNAs in Inflammatory Arthritis.microRNAs 在炎症性关节炎中对巨噬细胞表型的功能调控
Front Immunol. 2019 Sep 13;10:2217. doi: 10.3389/fimmu.2019.02217. eCollection 2019.
2
Monocyte MicroRNA Expression in Active Systemic Juvenile Idiopathic Arthritis Implicates MicroRNA-125a-5p in Polarized Monocyte Phenotypes.活性全身型幼年特发性关节炎中单核细胞 microRNA 表达谱分析提示 microRNA-125a-5p 参与极化单核细胞表型。
Arthritis Rheumatol. 2016 Sep;68(9):2300-13. doi: 10.1002/art.39694.
3
MicroRNA networks associated with active systemic juvenile idiopathic arthritis regulate CD163 expression and anti-inflammatory functions in macrophages through two distinct mechanisms.与活动系统性幼年特发性关节炎相关的 microRNA 网络通过两种不同机制调节巨噬细胞中的 CD163 表达和抗炎功能。
J Leukoc Biol. 2018 Jan;103(1):71-85. doi: 10.1002/JLB.2A0317-107R. Epub 2017 Dec 29.
4
MiR-146a modulates macrophage polarization in systemic juvenile idiopathic arthritis by targeting INHBA.微小RNA-146a通过靶向抑制素βA调节全身型幼年特发性关节炎中的巨噬细胞极化。
Mol Immunol. 2016 Sep;77:205-12. doi: 10.1016/j.molimm.2016.08.007. Epub 2016 Aug 16.
5
Children with oligoarticular juvenile idiopathic arthritis have skewed synovial monocyte polarization pattern with functional impairment-a distinct inflammatory pattern for oligoarticular juvenile arthritis.少关节型幼年特发性关节炎患儿滑膜单核细胞极化模式异常且伴有功能障碍——这是少关节型幼年关节炎独特的炎症模式。
Arthritis Res Ther. 2020 Aug 12;22(1):186. doi: 10.1186/s13075-020-02279-9.
6
PAQR11 modulates monocyte-to-macrophage differentiation and pathogenesis of rheumatoid arthritis.PAQR11 调节单核细胞向巨噬细胞的分化及类风湿关节炎的发病机制。
Immunology. 2021 May;163(1):60-73. doi: 10.1111/imm.13303. Epub 2021 Jan 24.
7
Signals and Mechanisms Regulating Monocyte and Macrophage Activation in the Pathogenesis of Juvenile Idiopathic Arthritis.调控幼年特发性关节炎发病机制中单核细胞和巨噬细胞活化的信号和机制。
Int J Mol Sci. 2021 Jul 26;22(15):7960. doi: 10.3390/ijms22157960.
8
Angiopoietin-2 promotes inflammatory activation of human macrophages and is essential for murine experimental arthritis.血管生成素-2 促进人巨噬细胞的炎症激活,并且是实验性关节炎小鼠模型所必需的。
Ann Rheum Dis. 2012 Aug;71(8):1402-10. doi: 10.1136/annrheumdis-2011-200718. Epub 2012 Jun 22.
9
Polarization of Rheumatoid Macrophages by TNF Targeting Through an IL-10/STAT3 Mechanism.通过 TNF 靶向作用通过 IL-10/STAT3 机制极化类风湿巨噬细胞。
Front Immunol. 2019 Jan 18;10:3. doi: 10.3389/fimmu.2019.00003. eCollection 2019.
10
Monocyte/Macrophage Abnormalities Specific to Rheumatoid Arthritis Are Linked to miR-155 and Are Differentially Modulated by Different TNF Inhibitors.类风湿关节炎特异性的单核细胞/巨噬细胞异常与 miR-155 相关,并受不同 TNF 抑制剂的差异调节。
J Immunol. 2019 Oct 1;203(7):1766-1775. doi: 10.4049/jimmunol.1900386. Epub 2019 Sep 4.

引用本文的文献

1
Macrophages polarization in renal inflammation and fibrosis animal models (Review).肾脏炎症和纤维化动物模型中的巨噬细胞极化(综述)。
Mol Med Rep. 2024 Feb;29(2). doi: 10.3892/mmr.2023.13152. Epub 2023 Dec 22.
2
Role of miRNAs in Rheumatoid Arthritis Therapy.miRNAs 在类风湿关节炎治疗中的作用。
Cells. 2023 Jun 30;12(13):1749. doi: 10.3390/cells12131749.
3
Regulatory Mechanism of M1/M2 Macrophage Polarization in the Development of Autoimmune Diseases.M1/M2 巨噬细胞极化在自身免疫性疾病发展中的调控机制。

本文引用的文献

1
A potential role of microvesicle-containing miR-223/142 in lung inflammation.微囊泡 miR-223/142 在肺部炎症中的潜在作用。
Thorax. 2019 Sep;74(9):865-874. doi: 10.1136/thoraxjnl-2018-212994. Epub 2019 Jul 22.
2
MiR-146a-5p Expression in Peripheral CD14⁺ Monocytes from Patients with Psoriatic Arthritis Induces Osteoclast Activation, Bone Resorption, and Correlates with Clinical Response.银屑病关节炎患者外周血CD14⁺单核细胞中MiR-146a-5p的表达诱导破骨细胞活化、骨吸收,并与临床反应相关。
J Clin Med. 2019 Jan 17;8(1):110. doi: 10.3390/jcm8010110.
3
Delivery of miR-146a to Ly6C Monocytes Inhibits Pathogenic Bone Erosion in Inflammatory Arthritis.
Mediators Inflamm. 2023 Jun 8;2023:8821610. doi: 10.1155/2023/8821610. eCollection 2023.
4
IL-12p40 deletion aggravates lipopolysaccharide-induced cardiac dysfunction in mice.白细胞介素-12 p40缺失加重脂多糖诱导的小鼠心脏功能障碍。
Front Cardiovasc Med. 2022 Sep 16;9:950029. doi: 10.3389/fcvm.2022.950029. eCollection 2022.
5
LNA-anti-miR-150 alleviates renal interstitial fibrosis by reducing pro-inflammatory M1/M2 macrophage polarization.LNA-anti-miR-150 通过减少促炎 M1/M2 巨噬细胞极化来减轻肾间质纤维化。
Front Immunol. 2022 Aug 5;13:913007. doi: 10.3389/fimmu.2022.913007. eCollection 2022.
6
Pathogenic role of microRNAs in atherosclerotic ischemic stroke: Implications for diagnosis and therapy.微小RNA在动脉粥样硬化性缺血性卒中中的致病作用:对诊断和治疗的启示。
Genes Dis. 2021 Jan 12;9(3):682-696. doi: 10.1016/j.gendis.2021.01.001. eCollection 2022 May.
7
Tuning Monocytes and Macrophages for Personalized Therapy and Diagnostic Challenge in Rheumatoid Arthritis.为类风湿关节炎的个性化治疗和诊断挑战而调整单核细胞和巨噬细胞。
Cells. 2021 Jul 22;10(8):1860. doi: 10.3390/cells10081860.
8
Signals and Mechanisms Regulating Monocyte and Macrophage Activation in the Pathogenesis of Juvenile Idiopathic Arthritis.调控幼年特发性关节炎发病机制中单核细胞和巨噬细胞活化的信号和机制。
Int J Mol Sci. 2021 Jul 26;22(15):7960. doi: 10.3390/ijms22157960.
9
IFN-γ is essential for alveolar macrophage-driven pulmonary inflammation in macrophage activation syndrome.IFN-γ 在巨噬细胞活化综合征中肺泡巨噬细胞驱动的肺部炎症中是必不可少的。
JCI Insight. 2021 Sep 8;6(17):e147593. doi: 10.1172/jci.insight.147593.
10
A narrative review of tumor-associated macrophages in lung cancer: regulation of macrophage polarization and therapeutic implications.肺癌中肿瘤相关巨噬细胞的叙述性综述:巨噬细胞极化的调控及其治疗意义
Transl Lung Cancer Res. 2021 Apr;10(4):1889-1916. doi: 10.21037/tlcr-20-1241.
miR-146a 递送至 Ly6C 单核细胞可抑制炎症性关节炎中的致病骨侵蚀。
Theranostics. 2018 Nov 13;8(21):5972-5985. doi: 10.7150/thno.29313. eCollection 2018.
4
A MicroRNA-29 Mimic (Remlarsen) Represses Extracellular Matrix Expression and Fibroplasia in the Skin.一种 microRNA-29 模拟物(雷马森)可抑制皮肤细胞外基质的表达和纤维化。
J Invest Dermatol. 2019 May;139(5):1073-1081. doi: 10.1016/j.jid.2018.11.007. Epub 2018 Nov 22.
5
Biology of MiR-17-92 Cluster and Its Progress in Lung Cancer.miR-17-92 簇的生物学特性及其在肺癌中的研究进展。
Int J Med Sci. 2018 Sep 7;15(13):1443-1448. doi: 10.7150/ijms.27341. eCollection 2018.
6
Evaluation of plasma microRNA expressions in patients with juvenile idiopathic arthritis.评估幼年特发性关节炎患者的血浆 microRNA 表达。
Clin Rheumatol. 2018 Dec;37(12):3255-3262. doi: 10.1007/s10067-018-4277-x. Epub 2018 Aug 31.
7
Systemic Juvenile Idiopathic Arthritis.全身型幼年特发性关节炎
Pediatr Clin North Am. 2018 Aug;65(4):691-709. doi: 10.1016/j.pcl.2018.04.005.
8
miR-155 is dispensable in monosodium urate-induced gouty inflammation in mice.miR-155 在小鼠尿酸单钠诱导的痛风性炎症中是可有可无的。
Arthritis Res Ther. 2018 Jul 11;20(1):144. doi: 10.1186/s13075-018-1550-y.
9
Transcriptional Regulation of Macrophages Polarization by MicroRNAs.miRNAs 对巨噬细胞极化的转录调控
Front Immunol. 2018 May 28;9:1175. doi: 10.3389/fimmu.2018.01175. eCollection 2018.
10
Critical Role of Alternative M2 Skewing in miR-155 Deletion-Mediated Protection of Colitis.miR-155 缺失介导的结肠炎保护作用中 M2 极化的关键作用
Front Immunol. 2018 May 3;9:904. doi: 10.3389/fimmu.2018.00904. eCollection 2018.