• 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

骨免疫学的最新进展:骨骼与免疫系统相互作用的新动态

Updates on Osteoimmunology: What's New on the Cross-Talk Between Bone and Immune System.

作者信息

Ponzetti Marco, Rucci Nadia

机构信息

Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

出版信息

Front Endocrinol (Lausanne). 2019 Apr 18;10:236. doi: 10.3389/fendo.2019.00236. eCollection 2019.

DOI:10.3389/fendo.2019.00236
PMID:31057482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6482259/
Abstract

The term osteoimmunology was coined many years ago to describe the research field that deals with the cross-regulation between bone cells and the immune system. As a matter of fact, many factors that are classically considered immune-related, such as InterLeukins (i.e., IL-6, -11, -17, and -23), Tumor Necrosis Factor (TNF)-α, Receptor-Activator of Nuclear factor Kappa B (RANK), and its Ligand (RANKL), Nuclear Factor of Activated T-cell, cytoplasmatic-1 (NFATc1), and others have all been found to be crucial in osteoclast and osteoblast biology. Conversely, bone cells, which we used to think would only regulate each other and take care of remodeling bone, actually regulate immune cells, by creating the so-called "endosteal niche." Both osteoblasts and osteoclasts participate to this niche, either by favoring engraftment, or mobilization of Hematopoietic Stem Cells (HSCs). In this review, we will describe the main milestones at the base of the osteoimmunology and present the key cellular players of the bone-immune system cross-talk, including HSCs, osteoblasts, osteoclasts, bone marrow macrophages, osteomacs, T- and B-lymphocytes, dendritic cells, and neutrophils. We will also briefly describe some pathological conditions in which the bone-immune system cross-talk plays a crucial role, with the final aim to portray the state of the art in the mechanisms regulating the bone-immune system interplay, and some of the latest molecular players in the field. This is important to encourage investigation in this field, to identify new targets in the treatment of bone and immune diseases.

摘要

“骨免疫学”这一术语是多年前创造的,用于描述研究骨细胞与免疫系统之间相互调节的研究领域。事实上,许多传统上被认为与免疫相关的因子,如白细胞介素(即IL-6、-11、-17和-23)、肿瘤坏死因子(TNF)-α、核因子κB受体激活剂(RANK)及其配体(RANKL)、活化T细胞核因子细胞质1(NFATc1)等,都已被发现对破骨细胞和成骨细胞生物学至关重要。相反,我们过去认为只会相互调节并负责骨重塑的骨细胞,实际上通过创造所谓的“骨内膜微环境”来调节免疫细胞。成骨细胞和破骨细胞都参与了这个微环境,要么通过促进造血干细胞(HSC)的植入,要么通过促进其动员。在这篇综述中,我们将描述骨免疫学基础的主要里程碑,并介绍骨-免疫系统相互作用的关键细胞参与者,包括造血干细胞、成骨细胞、破骨细胞、骨髓巨噬细胞、骨巨噬细胞、T和B淋巴细胞、树突状细胞和中性粒细胞。我们还将简要描述一些骨-免疫系统相互作用起关键作用的病理状况,最终目的是描绘调节骨-免疫系统相互作用机制的现状以及该领域一些最新的分子参与者。这对于鼓励该领域的研究、确定治疗骨和免疫疾病的新靶点很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/2dfe099240e5/fendo-10-00236-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/e3829e91a41c/fendo-10-00236-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/2dfe099240e5/fendo-10-00236-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/e3829e91a41c/fendo-10-00236-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3394/6482259/2dfe099240e5/fendo-10-00236-g0002.jpg

相似文献

1
Updates on Osteoimmunology: What's New on the Cross-Talk Between Bone and Immune System.骨免疫学的最新进展:骨骼与免疫系统相互作用的新动态
Front Endocrinol (Lausanne). 2019 Apr 18;10:236. doi: 10.3389/fendo.2019.00236. eCollection 2019.
2
Osteoimmunology.骨免疫学
Int Arch Allergy Immunol. 2007;143(1):31-48. doi: 10.1159/000098223. Epub 2006 Dec 22.
3
Mechanistic insight into osteoclast differentiation in osteoimmunology.骨免疫学中破骨细胞分化的机制性见解。
J Mol Med (Berl). 2005 Mar;83(3):170-9. doi: 10.1007/s00109-004-0612-6. Epub 2005 Jan 26.
4
Inflammatory bone destruction and osteoimmunology.炎症性骨破坏与骨免疫学
J Periodontal Res. 2005 Aug;40(4):287-93. doi: 10.1111/j.1600-0765.2005.00814.x.
5
Cross-talk between the interleukin-6 and prostaglandin E(2) signaling systems results in enhancement of osteoclastogenesis through effects on the osteoprotegerin/receptor activator of nuclear factor-{kappa}B (RANK) ligand/RANK system.白细胞介素-6与前列腺素E2信号系统之间的相互作用,通过影响骨保护素/核因子-κB受体激活因子配体(RANKL)/核因子-κB受体激活因子(RANK)系统,导致破骨细胞生成增强。
Endocrinology. 2005 Apr;146(4):1991-8. doi: 10.1210/en.2004-1167. Epub 2004 Dec 23.
6
Osteoclasts, rheumatoid arthritis, and osteoimmunology.破骨细胞、类风湿性关节炎与骨免疫学
Curr Opin Rheumatol. 2006 Jul;18(4):419-26. doi: 10.1097/01.bor.0000231912.24740.a5.
7
Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families.肿瘤坏死因子受体和配体家族新成员对破骨细胞分化和功能的调节
Endocr Rev. 1999 Jun;20(3):345-57. doi: 10.1210/edrv.20.3.0367.
8
New immune connections in osteoclast formation.破骨细胞形成中的新免疫连接。
Ann N Y Acad Sci. 2010 Mar;1192:117-23. doi: 10.1111/j.1749-6632.2009.05303.x.
9
Osteoimmunology: The Conceptual Framework Unifying the Immune and Skeletal Systems.骨免疫学:统一免疫系统和骨骼系统的概念框架。
Physiol Rev. 2017 Oct 1;97(4):1295-1349. doi: 10.1152/physrev.00036.2016.
10
Osteoporosis in Rheumatoid Arthritis: Dangerous Liaisons.类风湿关节炎中的骨质疏松:危险关联。
Front Med (Lausanne). 2020 Nov 23;7:601618. doi: 10.3389/fmed.2020.601618. eCollection 2020.

引用本文的文献

1
Identification and validation of the cellular senescence-associated molecular pattern and diagnostic markers for osteoporosis.骨质疏松症细胞衰老相关分子模式及诊断标志物的鉴定与验证
BMC Med Genomics. 2025 Sep 2;18(1):140. doi: 10.1186/s12920-025-02205-5.
2
Role and mechanism of botanical drugs and their metabolites in osteoporosis: new strategies for clinical application.植物药及其代谢产物在骨质疏松症中的作用与机制:临床应用新策略
Front Pharmacol. 2025 Aug 12;16:1530194. doi: 10.3389/fphar.2025.1530194. eCollection 2025.
3
Immunomodulatory and Regenerative Functions of MSC-Derived Exosomes in Bone Repair.

本文引用的文献

1
Glucocorticoid-Induced Osteoporosis.糖皮质激素性骨质疏松症
N Engl J Med. 2018 Dec 27;379(26):2547-2556. doi: 10.1056/NEJMcp1800214.
2
LIGHT/TNFSF14 as a New Biomarker of Bone Disease in Multiple Myeloma Patients Experiencing Therapeutic Regimens.LIGHT/TNFSF14 作为多发性骨髓瘤患者接受治疗方案时骨病的新生物标志物。
Front Immunol. 2018 Oct 23;9:2459. doi: 10.3389/fimmu.2018.02459. eCollection 2018.
3
Update on Neutrophil Function in Severe Inflammation.严重炎症中性粒细胞功能的最新研究进展。
间充质干细胞来源的外泌体在骨修复中的免疫调节和再生功能
Bioengineering (Basel). 2025 Aug 5;12(8):844. doi: 10.3390/bioengineering12080844.
4
Paracrine Bone-Derived Senescent Secretome Induces Spatially Patterned ECM and Biomechanical Vulnerability in Human Brain Organoids.旁分泌的骨源衰老分泌组在人脑类器官中诱导空间模式化的细胞外基质和生物力学脆弱性。
bioRxiv. 2025 Aug 12:2025.08.11.669674. doi: 10.1101/2025.08.11.669674.
5
Bone mineral density changes following immune checkpoint inhibitor therapy: insights from a case series analysis.免疫检查点抑制剂治疗后的骨矿物质密度变化:来自病例系列分析的见解
Osteoporos Int. 2025 Aug 10. doi: 10.1007/s00198-025-07647-2.
6
Osteoclast-like multinucleated giant cells reinforce polycaprolactone grafts.破骨细胞样多核巨细胞增强聚己内酯移植物。
Front Immunol. 2025 May 21;16:1572238. doi: 10.3389/fimmu.2025.1572238. eCollection 2025.
7
Impact of Antibody Immune Response and Immune Cells on Osteoporosis and Fractures.抗体免疫反应和免疫细胞对骨质疏松症及骨折的影响
Clin Orthop Surg. 2025 Jun;17(3):530-545. doi: 10.4055/cios24445. Epub 2025 Mar 21.
8
Identification of senescence-related biomarkers for osteoporosis based on microarray analysis, Mendelian randomization, and experimental validation.基于微阵列分析、孟德尔随机化和实验验证的骨质疏松症衰老相关生物标志物的鉴定
Mamm Genome. 2025 May 24. doi: 10.1007/s00335-025-10116-0.
9
Swimming induces bone loss via regulating mechanical sensing pathways in bone marrow.游泳通过调节骨髓中的机械传感通路导致骨质流失。
Mechanobiol Med. 2025 Mar 12;3(2):100125. doi: 10.1016/j.mbm.2025.100125. eCollection 2025 Jun.
10
Association between triglyceride‑glucose index and lumbar bone mineral density among Chinese individuals with osteoporotic fractures: a cross sectional study.中国骨质疏松性骨折患者甘油三酯-葡萄糖指数与腰椎骨密度的相关性:一项横断面研究
Sci Rep. 2025 May 5;15(1):15686. doi: 10.1038/s41598-025-98089-7.
Front Immunol. 2018 Oct 2;9:2171. doi: 10.3389/fimmu.2018.02171. eCollection 2018.
4
Interferon-Gamma-Mediated Osteoimmunology.干扰素-γ介导的骨免疫学
Front Immunol. 2018 Jun 29;9:1508. doi: 10.3389/fimmu.2018.01508. eCollection 2018.
5
NR4A1 Regulates Motility of Osteoclast Precursors and Serves as Target for the Modulation of Systemic Bone Turnover.NR4A1 调节破骨细胞前体细胞的迁移并作为系统性骨转换调节的靶点。
J Bone Miner Res. 2018 Nov;33(11):2035-2047. doi: 10.1002/jbmr.3533. Epub 2018 Jul 24.
6
Regulation of Osteoclast Differentiation by Cytokine Networks.细胞因子网络对破骨细胞分化的调控
Immune Netw. 2018 Feb 7;18(1):e8. doi: 10.4110/in.2018.18.e8. eCollection 2018 Feb.
7
A Complex Role for Lipocalin 2 in Bone Metabolism: Global Ablation in Mice Induces Osteopenia Caused by an Altered Energy Metabolism.载脂蛋白 2 在骨代谢中的复杂作用:小鼠的全局敲除导致能量代谢改变引起的骨质疏松症。
J Bone Miner Res. 2018 Jun;33(6):1141-1153. doi: 10.1002/jbmr.3406. Epub 2018 Mar 24.
8
Osteomacs interact with megakaryocytes and osteoblasts to regulate murine hematopoietic stem cell function.破骨细胞相关巨噬细胞与巨核细胞和成骨细胞相互作用,以调节小鼠造血干细胞功能。
Blood Adv. 2017 Dec 5;1(26):2520-2528. doi: 10.1182/bloodadvances.2017011304. eCollection 2017 Dec 12.
9
Impairment of Bone Remodeling in LIGHT/TNFSF14-Deficient Mice.LIGHT/TNFSF14 缺陷小鼠的骨重塑损伤。
J Bone Miner Res. 2018 Apr;33(4):704-719. doi: 10.1002/jbmr.3345. Epub 2017 Dec 11.
10
MC4R-dependent suppression of appetite by bone-derived lipocalin 2.骨源视黄醇结合蛋白2通过MC4R抑制食欲
Nature. 2017 Mar 16;543(7645):385-390. doi: 10.1038/nature21697. Epub 2017 Mar 8.