• 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

巨噬细胞极化及其对骨质疏松症的影响。

Macrophage Polarization and Its Impact on Osteoporosis.

机构信息

Department of Orthopedic Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.

Department of Biomedical Engineering, University of California, Irvine, CA, USA.

出版信息

Results Probl Cell Differ. 2024;74:291-296. doi: 10.1007/978-3-031-65944-7_11.

DOI:10.1007/978-3-031-65944-7_11
PMID:39406910
Abstract

Owing to its reduced bone density and higher risk for fractures, osteoporosis remains an international public health crisis. Research highlights the essential role played by macrophage polarization in osteoporosis and indicates that the balance between pro-inflammatory M1 macrophages and anti-inflammatory M2 macrophages influences bone metabolism. This review examines how M1 and M2 macrophages contribute to the development of osteoporosis and evaluates existing therapeutic approaches aimed at controlling macrophage polarization. It also describes future study areas that will allow improved management and treatment of osteoporosis.

摘要

由于其骨密度降低和骨折风险增加,骨质疏松症仍然是一个国际公共健康危机。研究强调了巨噬细胞极化在骨质疏松症中的重要作用,并表明促炎 M1 巨噬细胞和抗炎 M2 巨噬细胞之间的平衡影响着骨代谢。本综述探讨了 M1 和 M2 巨噬细胞如何促进骨质疏松症的发展,并评估了现有的控制巨噬细胞极化的治疗方法。它还描述了未来的研究领域,这将有助于改善骨质疏松症的管理和治疗。

相似文献

1
Macrophage Polarization and Its Impact on Osteoporosis.巨噬细胞极化及其对骨质疏松症的影响。
Results Probl Cell Differ. 2024;74:291-296. doi: 10.1007/978-3-031-65944-7_11.
2
The M2 Macrophages Importance Role in Psoriasis.M2巨噬细胞在银屑病中的重要作用
Immun Inflamm Dis. 2025 Jun;13(6):e70211. doi: 10.1002/iid3.70211.
3
Sphingosine-1-phosphate stimulates colorectal cancer tumor microenvironment angiogenesis and induces macrophage polarization via macrophage migration inhibitory factor.鞘氨醇-1-磷酸通过巨噬细胞迁移抑制因子刺激结直肠癌肿瘤微环境血管生成并诱导巨噬细胞极化。
Front Immunol. 2025 Jun 16;16:1564213. doi: 10.3389/fimmu.2025.1564213. eCollection 2025.
4
Adapting Safety Plans for Autistic Adults with Involvement from the Autism Community.在自闭症群体的参与下为成年自闭症患者调整安全计划。
Autism Adulthood. 2025 May 28;7(3):293-302. doi: 10.1089/aut.2023.0124. eCollection 2025 Jun.
5
KunMingShanHaiTang formula reprograms macrophage metabolism and promotes M2 polarization via the HIF-1α pathway to alleviate ulcerative colitis symptoms in a rat model.昆明山海丹方通过HIF-1α途径重编程巨噬细胞代谢并促进M2极化,以减轻大鼠模型中的溃疡性结肠炎症状。
J Bioenerg Biomembr. 2025 Apr 2. doi: 10.1007/s10863-025-10056-z.
6
Risedronate for the primary and secondary prevention of osteoporotic fractures in postmenopausal women.利塞膦酸钠用于绝经后妇女骨质疏松性骨折的一级和二级预防。
Cochrane Database Syst Rev. 2022 May 3;5(5):CD004523. doi: 10.1002/14651858.CD004523.pub4.
7
Targeting Decidual Macrophage Polarization through JNK Signaling Pathway Inhibition Alleviates Adverse Pregnancy Outcomes in Early Spontaneous Abortion.通过抑制JNK信号通路靶向蜕膜巨噬细胞极化可减轻早期自然流产中的不良妊娠结局。
Reprod Sci. 2025 Jun 23. doi: 10.1007/s43032-025-01915-6.
8
Regulation of macrophage plasticity by circCCDC719-13 through HSP90 inhibition suppresses prostate cancer progression and metastasis: a translational study.circCCDC719-13通过抑制HSP90对巨噬细胞可塑性的调控抑制前列腺癌进展和转移:一项转化研究
Int J Surg. 2025 Jun 27. doi: 10.1097/JS9.0000000000002895.
9
Wharton's jelly-derived mesenchymal stem cells ameliorate high altitude-induced heart injury by promoting type 2 macrophage polarization via COX2-PGE2 pathway.沃顿胶源性间充质干细胞通过COX2-PGE2途径促进2型巨噬细胞极化,改善高原诱导的心脏损伤。
Front Immunol. 2025 Jun 6;16:1538046. doi: 10.3389/fimmu.2025.1538046. eCollection 2025.
10
Glucocorticoid-induced osteoporosis: a systematic review and cost-utility analysis.糖皮质激素性骨质疏松症:一项系统评价与成本效用分析
Health Technol Assess. 2007 Mar;11(7):iii-iv, ix-xi, 1-231. doi: 10.3310/hta11070.

本文引用的文献

1
Alterations in Alzheimer's disease microglia transcriptome might be involved in bone pathophysiology.阿尔茨海默病小胶质细胞转录组的改变可能与骨病理生理学有关。
Neurobiol Dis. 2024 Feb;191:106404. doi: 10.1016/j.nbd.2024.106404. Epub 2024 Jan 4.
2
Macrophage efferocytosis in health and disease.健康与疾病中的巨噬细胞吞噬作用
Cell Biochem Funct. 2023 Mar;41(2):152-165. doi: 10.1002/cbf.3780. Epub 2023 Feb 16.
3
The role of macrophage subtypes and exosomes in immunomodulation.巨噬细胞亚型和外泌体在免疫调节中的作用。
Cell Mol Biol Lett. 2022 Oct 3;27(1):83. doi: 10.1186/s11658-022-00384-y.
4
Latitudinal and longitudinal regulation of tissue macrophages in inflammatory diseases.炎症性疾病中组织巨噬细胞的纬度和经度调节
Genes Dis. 2021 Jul 13;9(5):1194-1207. doi: 10.1016/j.gendis.2021.06.007. eCollection 2022 Sep.
5
Engineering immune-responsive biomaterials for skin regeneration.用于皮肤再生的工程化免疫反应性生物材料。
Biomater Transl. 2021 Mar 28;2(1):61-71. doi: 10.3877/cma.j.issn.2096-112X.2021.01.008. eCollection 2021.
6
Macrophage Polarization and Alveolar Bone Healing Outcome: Despite a Significant M2 Polarizing Effect, VIP and PACAP Treatments Present a Minor Impact in Alveolar Bone Healing in Homeostatic Conditions.巨噬细胞极化与牙槽骨愈合结局:尽管 VIP 和 PACAP 有显著的 M2 极化作用,但在稳态条件下,它们对牙槽骨愈合的影响较小。
Front Immunol. 2021 Dec 21;12:782566. doi: 10.3389/fimmu.2021.782566. eCollection 2021.
7
Macrophage Polarization and Osteoporosis: A Review.巨噬细胞极化与骨质疏松症:综述。
Nutrients. 2020 Sep 30;12(10):2999. doi: 10.3390/nu12102999.
8
Biomimetic osteogenic peptide with mussel adhesion and osteoimmunomodulatory functions to ameliorate interfacial osseointegration under chronic inflammation.具有贻贝粘附和骨免疫调节功能的仿生成骨肽可改善慢性炎症下的界面骨整合。
Biomaterials. 2020 Oct;255:120197. doi: 10.1016/j.biomaterials.2020.120197. Epub 2020 Jun 13.
9
Macrophage Polarization: Different Gene Signatures in M1(LPS+) vs. Classically and M2(LPS-) vs. Alternatively Activated Macrophages.巨噬细胞极化:M1(LPS+)与经典激活和 M2(LPS-)与替代激活巨噬细胞的不同基因特征。
Front Immunol. 2019 May 24;10:1084. doi: 10.3389/fimmu.2019.01084. eCollection 2019.
10
Modulation of macrophage subtypes by IRF5 determines osteoclastogenic potential.IRF5 调节巨噬细胞亚型决定破骨细胞生成潜能。
J Cell Physiol. 2019 Dec;234(12):23033-23042. doi: 10.1002/jcp.28863. Epub 2019 May 24.