巨噬细胞极化
骨重建
巨噬细胞
极化(电化学)
新陈代谢
医学
生物
化学
内科学
生物化学
物理化学
体外
作者
Qiqi Yan,Haixia Liu,Ruyuan Zhu,Zhiguo Zhang
出处
期刊:Cytokine
[Elsevier]
日期:2024-09-27
卷期号:184: 156768-156768
标识
DOI:10.1016/j.cyto.2024.156768
摘要
Macrophage polarization divides macrophages into two main cell subpopulations, classically and alternatively activated macrophages (M1 and M2, respectively). M1 polarization promotes osteoclastogenesis, while M2 polarization promotes osteogenesis. The physiological homeostasis of bone metabolism involves a high dynamic balance between osteoclastic-mediated bone resorption and formation. Reportedly, M1/M2 imbalance causes the onset and persistence of inflammation-related bone diseases. Therefore, understanding the research advances in functions and roles of macrophages in such diseases will provide substantial guidance for improved treatment of bone diseases. In this review, we underscore and summarize the research advances in macrophage polarization, and bone-related diseases, such as rheumatoid arthritis, osteoarthritis, and osteoporosis, over the last 5 years. Our findings showed that targeting macrophages and balancing macrophage polarization can effectively reduce inflammation and decrease bone destruction while promoting bone formation and vascular repair. These results indicate that regulating macrophage and macrophage polarization to restore homeostasis is a prospective approach for curing bone-related diseases.
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