Zhu Wangwei, Wang Weidan, Yang Xing, Ran Chunxiao, Zhang Tianwei, Huang Shibo, Yang Jiahui, Wang Fuyang, Wang Huiya, Wan Peng, Piao Fengyuan, Lu Faqiang, Shi Shengbo, Li Ye, Zhang Xiuzhi, Zhao Dewei
Department of Orthopedics, Affiliated Zhongshan Hospital of Dalian University, Dalian 116001, China.
Orthopedic Medical Research Center, Dalian University, Dalian 116622, China.
Regen Biomater. 2025 Apr 26;12:rbaf026. doi: 10.1093/rb/rbaf026. eCollection 2025.
Continuous advancements in medical technology and biomaterials have underscored the significant advantages of biodegradable implant materials for bone repair and remodelling over traditional inert metallic implants. Notably, biodegradable magnesium-based materials have gained much attention because of their optimal corrosion rates. Importantly, extensive clinical experience has resulted in the use of biodegradable magnesium-based orthopaedic implants. Both preclinical and clinical studies have consistently demonstrated that Mg has an excellent ability to promote bone tissue formation, a process that is closely associated with the release of Mg and other degradation byproducts. Bone metabolism depends on a dynamic balance of bone formation and bone resorption. Mg has been shown to increase osteoblast (OB) activity while suppressing osteoclast (OC) formation, thus playing a crucial role in bone remodelling and regeneration. In terms of osteolysis inhibition, Mg plays a multifaceted role. First, Mg inhibits OC formation by modulating the activity of mature OCs, their migratory behaviour and the activity of precursor cells. Second, Mg influences OC production by regulating the expression of osteoprotegerin (OPG), receptor activator of nuclear factor kappa-Β ligand (RANKL) and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB). Additionally, Mg impacts bone resorption by altering the immune microenvironment and the levels of hormones and peptides within the body. Furthermore, the alkaline environment generated around the biodegradable magnesium implant and its degradation products (e.g. H) also significantly inhibit OC formation. Recent research on magnesium-based implants has focused predominantly on their osteogenic properties, with few systematic reviews addressing the mechanisms through which biodegradable magnesium alloys suppress osteoclastic activity. This article summarizes the latest clinical research progress concerning biodegradable magnesium implant materials and their significant regulatory effects and discusses recent advances in the understanding of the regulatory mechanisms of action Mg-based biomaterials on OCs, with the aim of providing a more theoretical basis for the clinical application of biodegradable magnesium-based implants.
医学技术和生物材料的不断进步凸显了可生物降解植入材料在骨修复和重塑方面相对于传统惰性金属植入物的显著优势。值得注意的是,可生物降解的镁基材料因其最佳的腐蚀速率而备受关注。重要的是,广泛的临床经验促使可生物降解的镁基骨科植入物得到应用。临床前和临床研究均一致表明,镁具有促进骨组织形成的出色能力,这一过程与镁及其他降解副产物的释放密切相关。骨代谢依赖于骨形成和骨吸收的动态平衡。已表明镁可增加成骨细胞(OB)活性,同时抑制破骨细胞(OC)形成,从而在骨重塑和再生中发挥关键作用。在抑制骨溶解方面,镁发挥着多方面作用。首先,镁通过调节成熟破骨细胞的活性、其迁移行为以及前体细胞的活性来抑制破骨细胞形成。其次,镁通过调节骨保护素(OPG)、核因子κB受体激活剂配体(RANKL)和活化B细胞核因子κ轻链增强子(NF-κB)的表达来影响破骨细胞生成。此外,镁通过改变免疫微环境以及体内激素和肽的水平来影响骨吸收。此外,可生物降解镁植入物及其降解产物(如氢气)周围产生的碱性环境也显著抑制破骨细胞形成。近期关于镁基植入物的研究主要集中在其成骨特性上,很少有系统综述探讨可生物降解镁合金抑制破骨细胞活性的机制。本文总结了可生物降解镁植入材料的最新临床研究进展及其显著的调节作用,并讨论了对镁基生物材料对破骨细胞调节作用机制的最新认识进展,旨在为可生物降解镁基植入物的临床应用提供更多理论依据。