Strategies of Macrophages to Maintain Bone Homeostasis and Promote Bone Repair: A Narrative Review

被引:10
作者
Hu, Yingkun [1 ]
Huang, Jinghuan [2 ]
Chen, Chunying [1 ]
Wang, Yi [1 ]
Hao, Zhuowen [1 ]
Chen, Tianhong [1 ]
Wang, Junwu [1 ]
Li, Jingfeng [1 ]
机构
[1] Wuhan Univ, Dept Orthoped, Zhongnan Hosp, Wuhan 430000, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Orthoped Surg, Affiliated Peoples Hosp 6, Shanghai 200000, Peoples R China
基金
中国国家自然科学基金;
关键词
bone homeostasis; bone remodeling; macrophage; macrophage polarization; bone repair; MESENCHYMAL STROMAL CELLS; OSTEOBLAST DIFFERENTIATION; ALTERNATIVE ACTIVATION; TRANSCRIPTION FACTOR; OSTEOCLAST FORMATION; SIGNALING PATHWAY; MOUSE MODEL; STEM-CELLS; ERR-ALPHA; IN-VITRO;
D O I
10.3390/jfb14010018
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone homeostasis (a healthy bone mass) is regulated by maintaining a delicate balance between bone resorption and bone formation. The regulation of physiological bone remodeling by a complex system that involves multiple cells in the skeleton is closely related to bone homeostasis. Loss of bone mass or repair of bone is always accompanied by changes in bone homeostasis. However, due to the complexity of bone homeostasis, we are currently unable to identify all the mechanisms that affect bone homeostasis. To date, bone macrophages have been considered a third cellular component in addition to osteogenic spectrum cells and osteoclasts. As confirmed by co-culture models or in vivo experiments, polarized or unpolarized macrophages interact with multiple components within the bone to ensure bone homeostasis. Different macrophage phenotypes are prone to resorption and formation of bone differently. This review comprehensively summarizes the mechanisms by which macrophages regulate bone homeostasis and concludes that macrophages can control bone homeostasis from osteoclasts, mesenchymal cells, osteoblasts, osteocytes, and the blood/vasculature system. The elaboration of these mechanisms in this narrative review facilitates the development of macrophage-based strategies for the treatment of bone metabolic diseases and bone defects.
引用
收藏
页数:27
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