可生物降解镁调控破骨细胞的研究进展及其机制。

IF 5.6 1区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Regenerative Biomaterials Pub Date : 2025-04-26 eCollection Date: 2025-01-01 DOI:10.1093/rb/rbaf026
Wangwei Zhu, Weidan Wang, Xing Yang, Chunxiao Ran, Tianwei Zhang, Shibo Huang, Jiahui Yang, Fuyang Wang, Huiya Wang, Peng Wan, Fengyuan Piao, Faqiang Lu, Shengbo Shi, Ye Li, Xiuzhi Zhang, Dewei Zhao
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引用次数: 0

摘要

医学技术和生物材料的不断进步凸显了生物可降解植入材料在骨修复和重塑方面的显著优势,而不是传统的惰性金属植入物。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受到广泛关注。重要的是,广泛的临床经验导致了可生物降解镁基骨科植入物的使用。临床前和临床研究一致表明,Mg具有良好的促进骨组织形成的能力,这一过程与Mg2+和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。Mg2+已被证明可以增加成骨细胞(OB)活性,同时抑制破骨细胞(OC)的形成,因此在骨重塑和再生中起着至关重要的作用。在抑制骨溶解方面,Mg2+起着多方面的作用。首先,Mg2+通过调节成熟OC的活性、迁移行为和前体细胞的活性来抑制OC的形成。其次,Mg2+通过调节活化B细胞的骨保护素(OPG)、核因子κ pa-Β配体受体激活因子(RANKL)和核因子κ pa轻链增强子(NF-κB)的表达来影响OC的产生。此外,Mg2+通过改变免疫微环境和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H2)周围的碱性环境也显著抑制OC的形成。最近对镁基植入物的研究主要集中在其成骨特性上,很少有系统的综述解决可生物降解镁合金抑制破骨活性的机制。本文综述了生物可降解镁种植体材料的最新临床研究进展及其显著的调节作用,并讨论了近年来对镁基生物材料对OCs作用调节机制的认识进展,旨在为生物可降解镁基种植体的临床应用提供更多的理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research progress on osteoclast regulation by biodegradable magnesium and its mechanism.

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 Mg2+ and other degradation byproducts. Bone metabolism depends on a dynamic balance of bone formation and bone resorption. Mg2+ 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, Mg2+ plays a multifaceted role. First, Mg2+ inhibits OC formation by modulating the activity of mature OCs, their migratory behaviour and the activity of precursor cells. Second, Mg2+ 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, Mg2+ 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. H2) 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.

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来源期刊
Regenerative Biomaterials
Regenerative Biomaterials Materials Science-Biomaterials
CiteScore
7.90
自引率
16.40%
发文量
92
审稿时长
10 weeks
期刊介绍: Regenerative Biomaterials is an international, interdisciplinary, peer-reviewed journal publishing the latest advances in biomaterials and regenerative medicine. The journal provides a forum for the publication of original research papers, reviews, clinical case reports, and commentaries on the topics relevant to the development of advanced regenerative biomaterials concerning novel regenerative technologies and therapeutic approaches for the regeneration and repair of damaged tissues and organs. The interactions of biomaterials with cells and tissue, especially with stem cells, will be of particular focus.
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