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Updated: May 26, 2025

Polarization and Characterization of M1 and M2 Human Monocyte-Derived Macrophages on Implant Surfaces
Published on: December 6, 2024
Macrophage-related inflammatory responses to degradation products of biodegradable molybdenum implants
Danyang Liu1,2, Jiahao Chen3, Jiannan Zhou1,2
1School and Hospital of Stomatology, Guangdong Engineering Research Center of Oral Restoration and Reconstruction, Guangzhou Medical University, Guangzhou, 510182, PR China.
Abstract:
Metallic molybdenum (Mo) has been increasingly recognized as a potential biodegradable metal for biomedical implants. However, the macrophage-mediated inflammatory responses to Mo-based implants remain underexplored. This study examined the in vitro inflammatory reactions of macrophages to the degradation products of biodegradable Mo implants. The short-term and long-term biodegradation behavior and the subsequent impact on cytotoxicity, metabolism, and macrophage polarization were assessed. Both Mo and its degradation products were shown to be non-toxic within macrophage tolerance limits. Nevertheless, morphological changes and pro-inflammatory polarization were observed in cells around Mo-based specimen. Notably, matrix metalloproteinase 9 (Mmp9) was identified as a key gene influencing macrophage polarization in proximity to Mo. Additionally, pre-treating the Mo specimens in culture medium for 24 h significantly mitigated its stimulatory effects on cells. These results demonstrated the significance of optimizing Mo pre-treatment methods to prevent localized inflammation associated with its degradation. Specifically, pre-treatment of Mo can effectively mitigate the adverse impacts of its early degradation on macrophages and the surrounding immune environment. Our research into these early degradation phases introduces new avenues for studying molybdenum's immunomodulatory properties, potentially through precise control of its release and the targeted expression of pivotal genes.
Insights
Biodegradable molybdenum implants can cause inflammation. Pre-treating molybdenum (Mo) specimens reduces these adverse effects on macrophages, paving the way for safer biomedical applications.
Area of Science:
- Biomaterials Science
- Immunology
- Materials Science
Background:
- Metallic molybdenum (Mo) is a promising biodegradable metal for biomedical implants.
- Macrophage-mediated inflammatory responses to Mo implants are not well understood.
Purpose of the Study:
- To investigate the in vitro inflammatory reactions of macrophages to biodegradable Mo implant degradation products.
- To assess the impact of Mo biodegradation on macrophage cytotoxicity, metabolism, and polarization.
Main Methods:
- Evaluated short-term and long-term biodegradation of Mo.
- Assessed cytotoxicity, cellular metabolism, and macrophage polarization.
- Identified key genes involved in Mo-induced macrophage polarization, including matrix metalloproteinase 9 (Mmp9).
Main Results:
- Mo and its degradation products were non-toxic within macrophage tolerance limits.
- Observed morphological changes and pro-inflammatory polarization in macrophages near Mo.
- Pre-treating Mo specimens for 24 hours significantly reduced cellular stimulatory effects.
Conclusions:
- Optimizing Mo pre-treatment is crucial for preventing localized inflammation from implant degradation.
- Pre-treatment effectively mitigates adverse early degradation impacts on macrophages and the immune microenvironment.
- This research opens avenues for controlling Mo's immunomodulatory properties through controlled release and gene targeting.
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