Department of Nutrition, Food, and Exercise Sciences, Florida State University, Tallahassee, FL 32304, USA.
Nutrients. 2020 Sep 30;12(10):2999. doi: 10.3390/nu12102999.
Over 200 million people suffer from osteoporosis worldwide. Individuals with osteoporosis have increased rates of bone resorption while simultaneously having impaired osteogenesis. Most current treatments for osteoporosis focus on anti-resorptive methods to prevent further bone loss. However, it is important to identify safe and cost-efficient treatments that not only inhibit bone resorption, but also stimulate anabolic mechanisms to upregulate osteogenesis. Recent data suggest that macrophage polarization may contribute to osteoblast differentiation and increased osteogenesis as well as bone mineralization. Macrophages exist in two major polarization states, classically activated macrophages (M1) and alternatively activated macrophage (M2) macrophages. The polarization state of macrophages is dependent on molecules in the microenvironment including several cytokines and chemokines. Mechanistically, M2 macrophages secrete osteogenic factors that stimulate the differentiation and activation of pre-osteoblastic cells, such as mesenchymal stem cells (MSC's), and subsequently increase bone mineralization. In this review, we cover the mechanisms by which M2 macrophages contribute to osteogenesis and postulate the hypothesis that regulating macrophage polarization states may be a potential treatment for the treatment of osteoporosis.
全世界有超过 2 亿人患有骨质疏松症。骨质疏松症患者的骨吸收率增加,同时成骨作用受损。大多数骨质疏松症的当前治疗方法侧重于抗吸收方法,以防止进一步的骨质流失。然而,重要的是要确定安全且具有成本效益的治疗方法,这些方法不仅可以抑制骨吸收,还可以刺激合成代谢机制来上调成骨作用。最近的数据表明,巨噬细胞极化可能有助于成骨细胞分化和增加成骨作用以及骨矿化。巨噬细胞存在于两种主要的极化状态下,经典激活的巨噬细胞(M1)和替代激活的巨噬细胞(M2)巨噬细胞。巨噬细胞的极化状态取决于微环境中的分子,包括几种细胞因子和趋化因子。从机制上讲,M2 巨噬细胞分泌成骨因子,刺激前成骨细胞(如间充质干细胞(MSC))的分化和激活,随后增加骨矿化。在这篇综述中,我们介绍了 M2 巨噬细胞促进成骨作用的机制,并假设调节巨噬细胞极化状态可能是骨质疏松症治疗的一种潜在治疗方法。