• 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

M1/M2 巨噬细胞极化在自身免疫性疾病发展中的调控机制。

Regulatory Mechanism of M1/M2 Macrophage Polarization in the Development of Autoimmune Diseases.

机构信息

Shandong University of Traditional Chinese Medicine, Jinan 250002, China.

Qingdao Traditional Chinese Medicine Hospital (Qingdao Hiser Hospital), Qingdao 266033, China.

出版信息

Mediators Inflamm. 2023 Jun 8;2023:8821610. doi: 10.1155/2023/8821610. eCollection 2023.

DOI:10.1155/2023/8821610
PMID:37332618
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10270764/
Abstract

Macrophages are innate immune cells in the organism and can be found in almost tissues and organs. They are highly plastic and heterogeneous cells and can participate in the immune response, thereby playing a crucial role in maintaining the immune homeostasis of the body. It is well known that undifferentiated macrophages can polarize into classically activated macrophages (M1 macrophages) and alternatively activated macrophages (M2 macrophages) under different microenvironmental conditions. The directions of macrophage polarization can be regulated by a series of factors, including interferon, lipopolysaccharide, interleukin, and noncoding RNAs. To elucidate the role of macrophages in various autoimmune diseases, we searched the literature on macrophages with the PubMed database. Search terms are as follows: macrophages, polarization, signaling pathways, noncoding RNA, inflammation, autoimmune diseases, systemic lupus erythematosus, rheumatoid arthritis, lupus nephritis, Sjogren's syndrome, Guillain-Barré syndrome, and multiple sclerosis. In the present study, we summarize the role of macrophage polarization in common autoimmune diseases. In addition, we also summarize the features and recent advances with a particular focus on the immunotherapeutic potential of macrophage polarization in autoimmune diseases and the potentially effective therapeutic targets.

摘要

巨噬细胞是机体固有免疫细胞,几乎存在于各种组织和器官中。它们是高度可塑性和异质性的细胞,可以参与免疫反应,从而在维持机体免疫稳态方面发挥着至关重要的作用。众所周知,未分化的巨噬细胞可以在不同的微环境条件下极化为经典激活的巨噬细胞(M1 巨噬细胞)和选择性激活的巨噬细胞(M2 巨噬细胞)。巨噬细胞极化的方向可以受到一系列因素的调节,包括干扰素、脂多糖、白细胞介素和非编码 RNA。为了阐明巨噬细胞在各种自身免疫性疾病中的作用,我们使用 PubMed 数据库对巨噬细胞相关文献进行了检索。检索词如下:巨噬细胞、极化、信号通路、非编码 RNA、炎症、自身免疫性疾病、系统性红斑狼疮、类风湿关节炎、狼疮性肾炎、干燥综合征、格林-巴利综合征、多发性硬化。在本研究中,我们总结了巨噬细胞极化在常见自身免疫性疾病中的作用。此外,我们还总结了其特征和最新进展,特别关注了巨噬细胞极化在自身免疫性疾病中的免疫治疗潜力以及潜在的有效治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64d7/10270764/7184a26aefb2/MI2023-8821610.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64d7/10270764/7184a26aefb2/MI2023-8821610.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64d7/10270764/7184a26aefb2/MI2023-8821610.001.jpg

相似文献

1
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。
Mediators Inflamm. 2023 Jun 8;2023:8821610. doi: 10.1155/2023/8821610. eCollection 2023.
2
DNA-dependent activator of interferon-regulatory factors (DAI) promotes lupus nephritis by activating the calcium pathway.DNA 依赖性干扰素调节因子激活物 (DAI) 通过激活钙途径促进狼疮肾炎。
J Biol Chem. 2013 May 10;288(19):13534-50. doi: 10.1074/jbc.M113.457218. Epub 2013 Apr 3.
3
Paeonol interferes with lupus nephritis by regulating M1/M2 polarization of macrophages.丹皮酚通过调节巨噬细胞的M1/M2极化来干预狼疮性肾炎。
Mol Immunol. 2024 May;169:66-77. doi: 10.1016/j.molimm.2024.03.004. Epub 2024 Mar 18.
4
Regulation of macrophage polarization by targeted metabolic reprogramming for the treatment of lupus nephritis.靶向代谢重编程调控巨噬细胞极化治疗狼疮性肾炎。
Mol Med. 2024 Jun 25;30(1):96. doi: 10.1186/s10020-024-00866-z.
5
The Role of M1/M2 Macrophage Polarization in Rheumatoid Arthritis Synovitis.M1/M2 巨噬细胞极化在类风湿关节炎滑膜炎中的作用。
Front Immunol. 2022 May 19;13:867260. doi: 10.3389/fimmu.2022.867260. eCollection 2022.
6
Total Glucosides of Paeony Ameliorate Pristane-Induced Lupus Nephritis by Inducing PD-1 ligands Macrophages Activating IL-4/STAT6/PD-L2 Signaling.白芍总苷通过诱导 PD-1 配体巨噬细胞激活 IL-4/STAT6/PD-L2 信号通路改善马兜铃酸诱导的狼疮肾炎。
Front Immunol. 2021 Jul 5;12:683249. doi: 10.3389/fimmu.2021.683249. eCollection 2021.
7
Mesenchymal stem cell exosomal tsRNA-21109 alleviate systemic lupus erythematosus by inhibiting macrophage M1 polarization.间充质干细胞外泌体 tsRNA-21109 通过抑制巨噬细胞 M1 极化缓解系统性红斑狼疮。
Mol Immunol. 2021 Nov;139:106-114. doi: 10.1016/j.molimm.2021.08.015. Epub 2021 Aug 28.
8
Exosomes Derived from Human Umbilical Cord Mesenchymal Stem Cells Alleviate Diffuse Alveolar Hemorrhage Associated with Systemic Lupus Erythematosus in Mice by Promoting M2 Macrophage Polarization via the microRNA-146a-5p/NOTCH1 Axis.人脐带间充质干细胞来源的外泌体通过 microRNA-146a-5p/NOTCH1 轴促进 M2 巨噬细胞极化缓解系统性红斑狼疮相关弥漫性肺泡出血。
Immunol Invest. 2022 Oct;51(7):1975-1993. doi: 10.1080/08820139.2022.2090261. Epub 2022 Jun 20.
9
The roles of long noncoding RNA-mediated macrophage polarization in respiratory diseases.长非编码 RNA 调控的巨噬细胞极化在呼吸疾病中的作用。
Front Immunol. 2023 Jan 5;13:1110774. doi: 10.3389/fimmu.2022.1110774. eCollection 2022.
10
Mesenchymal Stem Cells-derived Exosomes Ameliorate Lupus by Inducing M2 Macrophage Polarization and Regulatory T Cell Expansion in MRL/lpr Mice.间充质干细胞衍生的外泌体通过诱导 M2 巨噬细胞极化和调节性 T 细胞扩增改善 MRL/lpr 小鼠的狼疮。
Immunol Invest. 2022 Aug;51(6):1785-1803. doi: 10.1080/08820139.2022.2055478. Epub 2022 Mar 25.

引用本文的文献

1
Biomimetic hydrogel scaffolds for stimulating fibrotic responses: development of an in-vitro assay for implant material testing.用于刺激纤维化反应的仿生水凝胶支架:用于植入材料测试的体外试验的开发
Front Bioeng Biotechnol. 2025 Aug 29;13:1628630. doi: 10.3389/fbioe.2025.1628630. eCollection 2025.
2
Comprehensive review of macrophage models: primary cells and immortalized lines across species.巨噬细胞模型的全面综述:跨物种的原代细胞和永生化细胞系
Front Immunol. 2025 Aug 20;16:1640935. doi: 10.3389/fimmu.2025.1640935. eCollection 2025.
3
IL-15 Promotes the Survival of Anti-Inflammatory (M2), Immunoinhibitory (IL-10+) Dermal Macrophages in Human Eyelid Skin Under IFNγ-Dominated Inflammatory Conditions.

本文引用的文献

1
Development of a Fluorescent Probe for M2 Macrophages Gating-Oriented Live-Cell Distinction.用于M2巨噬细胞门控定向活细胞区分的荧光探针的开发
J Am Chem Soc. 2023 Feb 8;145(5):2951-2957. doi: 10.1021/jacs.2c11393. Epub 2023 Jan 27.
2
Cathepsin B/NLRP3/GSDMD axis-mediated macrophage pyroptosis induces inflammation and fibrosis in systemic sclerosis.组织蛋白酶 B/NLRP3/GSDMD 轴介导线粒体介导的巨噬细胞焦亡诱导系统性硬皮病中的炎症和纤维化。
J Dermatol Sci. 2022 Dec;108(3):127-137. doi: 10.1016/j.jdermsci.2022.12.006. Epub 2022 Dec 24.
3
ADAR1 promotes systemic sclerosis modulating classic macrophage activation.
在以干扰素γ为主导的炎症条件下,白细胞介素-15促进人眼睑皮肤中抗炎性(M2型)、免疫抑制性(白细胞介素-10阳性)真皮巨噬细胞的存活。
Int J Mol Sci. 2025 Aug 13;26(16):7811. doi: 10.3390/ijms26167811.
4
RBM15 enhances paclitaxel resistance in triple-negative breast cancer by targeting mA methylation of TNFSF9 and inducing polarization of tumor-associated macrophages to M2 phenotype.RBM15通过靶向TNFSF9的mA甲基化并诱导肿瘤相关巨噬细胞极化为M2表型来增强三阴性乳腺癌对紫杉醇的耐药性。
Hereditas. 2025 Aug 19;162(1):167. doi: 10.1186/s41065-025-00534-0.
5
Therapeutic potential of extracellular vesicles in systemic lupus erythematosus: a systematic review.细胞外囊泡在系统性红斑狼疮中的治疗潜力:一项系统综述
Immunol Res. 2025 Aug 15;73(1):120. doi: 10.1007/s12026-025-09680-z.
6
Macrophages in chronic infections: regulation and remodeling.慢性感染中的巨噬细胞:调控与重塑
Front Immunol. 2025 Jul 17;16:1594988. doi: 10.3389/fimmu.2025.1594988. eCollection 2025.
7
An auxiliary diagnostic strategy for distinguishing Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy: combining platelet-to-lymphocyte ratio and cerebrospinal fluid interleukin-8 levels.一种区分吉兰-巴雷综合征和慢性炎症性脱髓鞘性多发性神经病的辅助诊断策略:联合血小板与淋巴细胞比值和脑脊液白细胞介素-8水平
BMC Neurol. 2025 Jul 30;25(1):314. doi: 10.1186/s12883-025-04330-1.
8
Uncovering bifurcation behaviors of biochemical reaction systems from network topology.从网络拓扑结构中揭示生化反应系统的分岔行为。
Sci Rep. 2025 Jul 29;15(1):27596. doi: 10.1038/s41598-025-10688-6.
9
Macrophages at the Crossroads of Chronic Stress and Cancer.处于慢性应激与癌症交叉点的巨噬细胞。
Int J Mol Sci. 2025 Jul 16;26(14):6838. doi: 10.3390/ijms26146838.
10
Dynamic macrophage phenotypes in autoimmune and inflammatory rheumatic diseases.自身免疫性和炎性风湿性疾病中的动态巨噬细胞表型
Nat Rev Rheumatol. 2025 Jul 28. doi: 10.1038/s41584-025-01279-w.
ADAR1 促进系统性硬皮病,调节经典的巨噬细胞活化。
Front Immunol. 2022 Dec 1;13:1051254. doi: 10.3389/fimmu.2022.1051254. eCollection 2022.
4
Autoimmune pre-disease.自身免疫性前驱疾病。
Autoimmun Rev. 2023 Feb;22(2):103236. doi: 10.1016/j.autrev.2022.103236. Epub 2022 Nov 24.
5
Inhibition of angiogenetic macrophages reduces disc degeneration-associated pain.抑制血管生成性巨噬细胞可减轻椎间盘退变相关疼痛。
Front Bioeng Biotechnol. 2022 Oct 11;10:962155. doi: 10.3389/fbioe.2022.962155. eCollection 2022.
6
siRNA Accelerates M2 Macrophage Polarization and Alleviates Oxidative Stress via Inhibiting Gene Alternative Splicing.siRNA 通过抑制基因选择性剪接加速 M2 巨噬细胞极化并减轻氧化应激。
Oxid Med Cell Longev. 2022 Sep 23;2022:4942519. doi: 10.1155/2022/4942519. eCollection 2022.
7
Natural variation in macrophage polarization and function impact pneumocyte senescence and susceptibility to fibrosis.巨噬细胞极化和功能的自然变化影响肺细胞衰老和纤维化易感性。
Aging (Albany NY). 2022 Sep 28;14(19):7692-7717. doi: 10.18632/aging.204309.
8
Circular RNA ACTR2 activates M2 polarization of macrophages through activating Yes-associated protein signalling and contributes to renal fibrosis.环状 RNA ACTR2 通过激活 Yes 相关蛋白信号通路激活巨噬细胞 M2 极化,并促进肾脏纤维化。
Immunology. 2022 Dec;167(4):606-621. doi: 10.1111/imm.13558. Epub 2022 Sep 7.
9
MSC-Derived Small Extracellular Vesicles Attenuate Autoimmune Dacryoadenitis by Promoting M2 Macrophage Polarization and Inducing Tregs miR-100-5p.MSC 来源的小细胞外囊泡通过促进 M2 巨噬细胞极化和诱导 Tregs 来减轻自身免疫性干眼病 miR-100-5p。
Front Immunol. 2022 Jul 6;13:888949. doi: 10.3389/fimmu.2022.888949. eCollection 2022.
10
Efficacy of plasma exchange on top of standard immunosuppressive therapy in adult autoimmune inflammatory rheumatic diseases-associated macrophage activation syndrome, a single center real-world analysis.血浆置换联合标准免疫抑制疗法治疗成人自身免疫性炎症性风湿病相关巨噬细胞活化综合征的疗效:一项单中心真实世界分析。
Semin Arthritis Rheum. 2022 Aug;55:152043. doi: 10.1016/j.semarthrit.2022.152043. Epub 2022 Jun 7.