Objective To review the research progress on the application of magnesium element and magnesium materials in the repair and reconstruction of tendon-bone interface injuries. Methods Relevant research literature at home and abroad in recent years was retrieved. Focusing on the physiological functions of magnesium element, the classification and advantages of magnesium materials, the core mechanisms of magnesium element in regulating the proliferation and differentiation of stem cells, up-regulating the expression of healing markers, activating key signaling pathways, and regulating the inflammatory response were systematically analyzed. At the same time, the current application status and challenges of non-alloyed magnesium materials and magnesium alloys in tendon-bone interface healing were summarized. Results As an essential element in the human body, the elastic modulus of magnesium is close to that of natural bone. The magnesium ions released during degradation can promote the healing of the tendon-bone interface through multiple pathways. Non-alloyed magnesium materials can promote the formation of fibrocartilage and regulate the inflammatory microenvironment. Magnesium alloys have further optimized the mechanical properties and biocompatibility through alloying, surface coating and modification techniques. Both of them have shown good effects in promoting tendon-bone interface healing in animal experiments and preliminary clinical studies. Conclusion Magnesium element and magnesium materials have significant advantages and application potential in the repair of tendon-bone interface injuries. However, it is still necessary to optimize their mechanical strength and degradation behavior through material design, clarify the molecular mechanism, and carry out large-scale long-term clinical trials to further promote their clinical transformation and wide application.
This review systematically examines the mechanisms and recent research progress of magnesium ions in promoting tendon-bone interface repair by regulating stem cell functions. Firstly, the analysis indicates that magnesium ions synergistically regulate stem cell proliferation, migration, and multidirectional differentiation through multiple signaling pathways, while simultaneously promoting angiogenesis and optimizing the immune microenvironment. Subsequently, a summary of existing research findings confirms that magnesium-based biodegradable biomaterials demonstrate favorable tissue repair-promoting effects in animal experiments. Finally, this article proposes that, given the spatiotemporal sequential characteristics of magnesium ion regulation on stem cells and the healing microenvironment, future research should focus on developing novel smart materials capable of precisely controlling magnesium ion release to match the healing process, thereby advancing its clinical translation and precision medicine applications in the field of tendon-bone repair.