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CD169 macrophages are critical for osteoblast maintenance and promote intramembranous and endochondral ossification during bone repair.CD169 巨噬细胞对于成骨细胞的维持至关重要,并在骨修复过程中促进膜内和软骨内成骨。
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Macrophages in bone fracture healing: Their essential role in endochondral ossification.骨愈合过程中的巨噬细胞:它们在软骨内骨化中的重要作用。
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Fracture healing via periosteal callus formation requires macrophages for both initiation and progression of early endochondral ossification.通过骨膜骨痂形成的骨折愈合需要巨噬细胞来启动和促进早期软骨内成骨的进程。
Am J Pathol. 2014 Dec;184(12):3192-204. doi: 10.1016/j.ajpath.2014.08.017. Epub 2014 Oct 5.
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Modulating macrophage polarization for the enhancement of fracture healing, a systematic review.调节巨噬细胞极化以促进骨折愈合:一项系统综述
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Differential expression of inducible nitric oxide synthase and IL-12 between peritoneal and splenic macrophages stimulated with LPS plus IFN-gamma is associated with the activation of extracellular signal-related kinase.脂多糖加γ干扰素刺激的腹膜巨噬细胞和脾巨噬细胞之间,诱导型一氧化氮合酶和白细胞介素-12的差异表达与细胞外信号调节激酶的激活有关。
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The role of morphogens in endochondral ossification.形态发生素在软骨内骨化中的作用。
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Osteomacs and Bone Regeneration.成骨细胞与骨再生。
Curr Osteoporos Rep. 2017 Aug;15(4):385-395. doi: 10.1007/s11914-017-0384-x.

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Osteoimmunological Principles Adapted to Achieve Mechanically Superior Posterolateral Fusion in a New Zealand White Rabbit Model Using Antigen-Coated, Electrospun Beta-Tricalcium Phosphate.在新西兰白兔模型中,采用抗原包被的静电纺丝β-磷酸三钙,运用骨免疫学原理以实现机械性能更优的后外侧融合。
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本文引用的文献

1
Osteoimmunology: evolving concepts in bone-immune interactions in health and disease.骨免疫学:健康与疾病中骨-免疫相互作用的新概念。
Nat Rev Immunol. 2019 Oct;19(10):626-642. doi: 10.1038/s41577-019-0178-8. Epub 2019 Jun 11.
2
Discovery of a periosteal stem cell mediating intramembranous bone formation.发现一种骨膜干细胞介导膜内成骨。
Nature. 2018 Oct;562(7725):133-139. doi: 10.1038/s41586-018-0554-8. Epub 2018 Sep 24.
3
CD169 macrophages are critical for osteoblast maintenance and promote intramembranous and endochondral ossification during bone repair.CD169 巨噬细胞对于成骨细胞的维持至关重要,并在骨修复过程中促进膜内和软骨内成骨。
Biomaterials. 2019 Mar;196:51-66. doi: 10.1016/j.biomaterials.2017.10.033. Epub 2017 Oct 22.
4
Non-union bone fracture: a quicker fix.骨折不愈合:更快的修复方法。
Nature. 2017 Oct 25;550(7677):S193. doi: 10.1038/550S193a.
5
National incidence of traumatic fractures in China: a retrospective survey of 512 187 individuals.中国创伤性骨折的国家发病率:对 512187 人的回顾性调查。
Lancet Glob Health. 2017 Aug;5(8):e807-e817. doi: 10.1016/S2214-109X(17)30222-X. Epub 2017 Jun 27.
6
Osteoimmunology in Bone Fracture Healing.骨愈合中的骨免疫学。
Curr Osteoporos Rep. 2017 Aug;15(4):367-375. doi: 10.1007/s11914-017-0381-0.
7
Osteomacs and Bone Regeneration.成骨细胞与骨再生。
Curr Osteoporos Rep. 2017 Aug;15(4):385-395. doi: 10.1007/s11914-017-0384-x.
8
Macrophages and skeletal health.巨噬细胞与骨骼健康。
Pharmacol Ther. 2017 Jun;174:43-54. doi: 10.1016/j.pharmthera.2017.02.017. Epub 2017 Feb 7.
9
Implant-derived magnesium induces local neuronal production of CGRP to improve bone-fracture healing in rats.植入来源的镁可诱导局部神经元产生降钙素基因相关肽,以促进大鼠骨折愈合。
Nat Med. 2016 Oct;22(10):1160-1169. doi: 10.1038/nm.4162. Epub 2016 Aug 29.
10
Resting and injury-induced inflamed periosteum contain multiple macrophage subsets that are located at sites of bone growth and regeneration.静息和损伤诱导炎症的骨膜含有多种巨噬细胞亚群,这些亚群位于骨骼生长和再生部位。
Immunol Cell Biol. 2017 Jan;95(1):7-16. doi: 10.1038/icb.2016.74. Epub 2016 Nov 15.

骨骼巨噬细胞在骨折修复中的作用:一项系统综述。

Role of skeletal macrophages in fracture repair: A systematic review.

作者信息

Wan Zihao, Shin Lih-Ying, Wang Yu-Fan, Huang Zhihao, Dong Yanjing, Lee Chien-Wei, Kumta Shekhar-Madhukar, Lee Oscar Kuang-Sheng

机构信息

Department of Orthopaedics and Traumatology, The Chinese University of Hong Kong, Sha Tin, Hong Kong, SAR 999077, P.R. China.

Guangzhou Regenerative Medicine and Health Guangdong Laboratory, Guangzhou, Guangdong 510005, P.R. China.

出版信息

Biomed Rep. 2020 Dec;13(6):53. doi: 10.3892/br.2020.1360. Epub 2020 Sep 29.

DOI:10.3892/br.2020.1360
PMID:33082950
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7560542/
Abstract

In the field of bone research, the importance of the function of skeletal macrophages (sMΦ) and their crucial role in immune homeostasis and bone regeneration has been extensively studied. The aim of the present systematic review was to summarize the role of sMΦ in bone fracture healing and to evaluate their potential for immunoregulatory therapy in bone regeneration. A systematic literature search of PubMed and Embase was performed to retrieve studies on the role of sMΦ in bone injury repair. The Systematic Review Centre for Laboratory animal Experimentation tool was used to assess the risk of bias of the studies included. A total of four articles were included in the present review. A relatively high risk of bias was identified in the included articles as none of the assessors in these studies were blinded. sMΦ were defined by the surface markers F4/80, Mac-2 , TRAP, CD169, Ly6G and CD115. All of the studies provided support for the essential role of sMΦ in intramembranous ossification or endochondral ossification during fracture healing. F4/80Mac-2CD169 sMΦ are a promising therapeutic target for immunoregulatory therapy of bone repair due to their essential role in bone formation and homeostasis. Future studies aimed at profiling and modulating sMΦ to promote bone regeneration are required.

摘要

在骨研究领域,骨骼巨噬细胞(sMΦ)的功能及其在免疫稳态和骨再生中的关键作用已得到广泛研究。本系统综述的目的是总结sMΦ在骨折愈合中的作用,并评估其在骨再生免疫调节治疗中的潜力。通过对PubMed和Embase进行系统的文献检索,以获取关于sMΦ在骨损伤修复中作用的研究。使用实验动物系统综述中心工具来评估纳入研究的偏倚风险。本综述共纳入四篇文章。纳入的文章中存在较高的偏倚风险,因为这些研究中的评估者均未设盲。sMΦ由表面标志物F4/80、Mac-2、TRAP、CD169、Ly6G和CD115定义。所有研究均支持sMΦ在骨折愈合过程中膜内成骨或软骨内成骨中的重要作用。F4/80Mac-2CD169 sMΦ因其在骨形成和稳态中的重要作用,是骨修复免疫调节治疗的一个有前景的治疗靶点。未来需要开展旨在分析和调节sMΦ以促进骨再生的研究。