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Updated: Apr 29, 2026

Reprograming Model of Human Monocyte-derived Macrophages for In-vitro Assays
Published on: April 18, 2025
In vitro model to study the biomaterial-dependent reaction of macrophages in an inflammatory environment
N Grotenhuis1, H F E Vd Toom, N Kops
1Department of Otorhinolaryngology, Erasmus MC University Medical Centre Rotterdam, Rotterdam, The Netherlands; Department of General Surgery, Erasmus MC University Medical Centre Rotterdam, Rotterdam, The Netherlands.
Background:
Macrophages play an important role in the reaction to biomaterials, which sometimes have to be used in a surgical field at risk of contamination. The macrophage phenotype in reaction to biomaterials in an inflammatory environment was evaluated in both an in vivo and in vitro setting.
Methods:
In the in vivo setting, polypropylene (PP) biomaterial was implanted for 28 days in the contaminated abdominal wall of rats, and upon removal analysed by routine histology as well as immunohistochemistry for CD68 (marker for macrophages), inducible nitric oxide synthase (iNOS - a marker for proinflammatory M1 macrophages) and CD206 (marker for anti-inflammatory M2 macrophages). For the in vitro model, human peripheral blood monocytes were cultured for 3 days on biomaterials made from PP, collagen (COL), polyethylene terephthalate (PET) and PET coated with collagen (PET+COL). These experiments were performed both with and without lipopolysaccharide and interferon γ stimulation. Secretion of both M1- and M2-related proteins was measured, and a relative M1/M2 index was calculated.
Results:
In vivo, iNOS- and CD206-positive cells were found around the fibres of the implanted PP biomaterial. In vitro, macrophages on both PP and COL biomaterial had a relatively low M1/M2 index. Macrophages on the PET biomaterial had a high M1/M2 index, with the highest increase of M1 cytokines in an inflammatory environment. Macrophages on the PET+COL biomaterial also had a high M1/M2 index.
Conclusion:
Macrophages in an inflammatory environment in vitro still react in a biomaterial-dependent manner. This model can help to select biomaterials that are tolerated best in a surgical environment at risk of contamination.
Insights
Macrophages react to biomaterials differently based on the material type, even in contaminated surgical sites. This study evaluated macrophage responses in vivo and in vitro to guide selection of better-tolerated surgical materials.
Area of Science:
- Biomaterials Science
- Immunology
- Surgical Research
Background:
- Macrophages are crucial in the host response to biomaterials, especially in contaminated surgical fields.
- Understanding macrophage behavior is key for developing safe and effective surgical implants.
Purpose of the Study:
- To evaluate macrophage phenotype in response to various biomaterials within an inflammatory environment.
- To compare in vivo and in vitro models for assessing biomaterial-macrophage interactions.
Main Methods:
- In vivo: Polypropylene (PP) biomaterial implanted in contaminated rat abdominal walls, analyzed for macrophage markers (CD68, iNOS, CD206).
- In vitro: Human monocytes cultured on PP, collagen (COL), polyethylene terephthalate (PET), and PET+COL, with and without inflammatory stimulation.
- Quantified M1/M2 cytokine secretion to calculate a relative M1/M2 index.
Main Results:
- In vivo, both pro-inflammatory (iNOS) and anti-inflammatory (CD206) macrophages were present around PP implants.
- In vitro, PP and COL biomaterials showed a low M1/M2 index.
- PET and PET+COL biomaterials induced a high M1/M2 index, indicating a pro-inflammatory response, particularly with PET in an inflammatory setting.
Conclusions:
- Macrophage response to biomaterials is material-dependent, even under inflammatory conditions.
- The in vitro model effectively predicts biomaterial-macrophage interactions and can aid in selecting materials for contaminated surgical environments.
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