Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Orthopaedic Institute, Medical College, Soochow University, Suzhou 215000, China.
Oxid Med Cell Longev. 2022 Jun 6;2022:2485959. doi: 10.1155/2022/2485959. eCollection 2022.
Millions of people worldwide suffer from osteoporosis, which causes bone fragility and increases the risk of fractures. Osteoporosis is closely related to the inhibition of osteogenesis and the enhancement of osteoclastogenesis. In addition, chronic inflammation and macrophage polarization may contribute to osteoporosis as well. Macrophages, crucial to inflammatory responses, display different phenotypes under the control of microenvironment. There are two major phenotypes, classically activated macrophages (M1) and alternatively activated macrophages (M2). Generally, M1 macrophages mainly lead to bone resorption, while M2 macrophages result in osteogenesis. M1/M2 ratio reflects the "fluid" state of macrophage polarization, and the imbalance of M1/M2 ratio may cause disease such as osteoporosis. Additionally, antioxidant drugs, such as melatonin, are applied to change the state of macrophage polarization and to treat osteoporosis. In this review, we introduce the mechanisms of macrophage polarization-mediated bone resorption and bone formation and the contribution to the clinical strategies of osteoporosis treatment.
全世界有数百万骨质疏松症患者,这种疾病会导致骨骼脆弱,增加骨折风险。骨质疏松症与成骨抑制和破骨细胞形成增强密切相关。此外,慢性炎症和巨噬细胞极化也可能导致骨质疏松症。巨噬细胞在炎症反应中至关重要,其表型在微环境的控制下会发生不同的变化。有两种主要的表型,经典激活的巨噬细胞(M1)和替代激活的巨噬细胞(M2)。一般来说,M1 巨噬细胞主要导致骨吸收,而 M2 巨噬细胞则导致成骨。M1/M2 比值反映了巨噬细胞极化的“流动”状态,M1/M2 比值的失衡可能导致骨质疏松等疾病。此外,抗氧化药物,如褪黑素,被应用于改变巨噬细胞极化状态,以治疗骨质疏松症。在这篇综述中,我们介绍了巨噬细胞极化介导的骨吸收和骨形成的机制及其对骨质疏松症治疗临床策略的贡献。