Multifunctional Roles of Magnesium Ions in Modulating Bone Regeneration-Related Cells.

IF 4.4 3区 医学 Q2 ENGINEERING, BIOMEDICAL
Xiangcheng Lei, Ruipeng Li, Yangyi Nie, Deju Gao, Wei Zhang, Yuxiao Lai, Cairong Li
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Abstract

Magnesium ions (Mg2+) play pivotal roles in bone regeneration by regulating the biological functions of multiple bone repair-related cells. However, the effective concentration ranges and optimal concentration of Mg2+ for different cell types remain incompletely defined, which limits the precise design of Mg-containing biomaterials with controllable ion release for repairing of bone defects. In this study, the concentration-dependent effects of Mg2+ on the biological functions of bone regeneration-related cells were systematically investigated. Human bone marrow mesenchymal stem cells (hBMSCs), human umbilical vein endothelial cells (HUVECs), rat Schwann cells (RSCs), and RAW264.7 macrophage were selected to evaluate the effective concentration of Mg2+ for promoting osteogenesis, angiogenesis, neuroregulation, and immunomodulation, respectively. The results demonstrated that Mg2+ concentrations ranging from to 16 mM, particularly 8 mM, significantly upregulated the expression of M2 macrophage-related markers, thereby promoting the polarization of RAW264.7 macrophages toward the anti-inflammatory M2 phenotype. Moreover, Mg2+ concentrations between 2 and 8 mM effectively enhanced the osteogenic activity of hBMSCs, the angiogenic activity of HUVECs, and the neuroregulatory function of RSCs, as confirmed by immunofluorescence staining and quantitative PCR analysis of osteogenic, angiogenic, and neuroregulation-related marker expression. These findings provide a comprehensive understanding of the concentration-dependent biological effects of Mg2+ on bone regeneration-related cells and establish a theoretical basis for the rational design of next-generation Mg2+-releasing biomaterials with precise biological regulation.

镁离子在骨再生相关细胞调控中的多功能作用。
镁离子(Mg2+)通过调节多种骨修复相关细胞的生物学功能,在骨再生中发挥关键作用。然而,不同细胞类型的Mg2+的有效浓度范围和最佳浓度尚未完全确定,这限制了精确设计具有可控离子释放的含镁生物材料用于骨缺损修复。本研究系统研究了Mg2+浓度依赖性对骨再生相关细胞生物学功能的影响。选择人骨髓间充质干细胞(hBMSCs)、人脐静脉内皮细胞(HUVECs)、大鼠雪旺细胞(RSCs)和RAW264.7巨噬细胞,分别评价Mg2+促进骨生成、血管生成、神经调节和免疫调节的有效浓度。结果表明,Mg2+浓度在16 mM,特别是8 mM范围内,可显著上调M2巨噬细胞相关标志物的表达,从而促进RAW264.7巨噬细胞向抗炎M2表型极化。此外,通过免疫荧光染色和成骨、血管生成和神经调节相关标志物表达的定量PCR分析,证实了2 ~ 8 mM浓度的Mg2+能有效增强hBMSCs的成骨活性、HUVECs的血管生成活性以及RSCs的神经调节功能。这些研究结果全面了解了Mg2+对骨再生相关细胞的浓度依赖性生物学效应,为合理设计具有精确生物学调控的下一代Mg2+释放生物材料奠定了理论基础。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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