Sequential delivery of immunomodulatory cytokines to facilitate the M1-to-M2 transition of macrophages and enhance vascularization of bone scaffolds
By K. Spiller, S. Nassiri, Claire E. Witherel, Rachel R Anfang, Johnathan Ng, Kenneth R. Nakazawa, T. Yu, G. Vunjak‐Novakovic. Biomaterials, 2014
692 citations recorded by the source corpus.
In normal tissue repair, macrophages exhibit a pro-inflammatory phenotype (M1) at early stages and a pro-healing phenotype (M2) at later stages. We have previously shown that M1 macrophages initiate angiogenesis while M2 macrophages promote vessel maturation. Therefore, we reasoned that scaffolds that promote sequential M1 and M2 polarization of infiltrating macrophages should result in enhanced angiogenesis and healing. To this end, we first analyzed the in vitro kinetics of macrophage phenotype switch using flow cytometry, gene expression, and cytokine secretion analysis. Then, we designed scaffolds for bone regeneration based on modifications of decellularized bone for a short release of interferon-gamma (IFNg) to promote the M1 phenotype, followed by a more sustained release of interleukin-4 (IL4) to promote the M2 phenotype. To achieve this sequential release profile, IFNg was physically adsorbed onto the scaffolds, while IL4 was attached via biotin-streptavidin binding. Interestingly, despite the strong interactions between biotin and streptavidin, release studies showed that biotinylated IL4 was released over 6 days. These scaffolds promoted sequential M1 and M2 polarization of primary human macrophages as measured by gene expression of ten M1 and M2 markers and secretion of four cytokines, although the overlapping phases of IFNg and IL4 release tempered polarization to some extent. Murine subcutaneous implantation model showed increased vascularization in scaffolds releasing IFNg compared to controls. This study demonstrates that scaffolds for tissue engineering can be designed to harness the angiogenic behavior of host macrophages towards scaffold vascularization.
Subfields: Immunology, Molecular Biology, Surgery
View Paper: https://www.semanticscholar.org/paper/b7a8988f18bf0c3d6f5337bb13327c871ab06728
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Citations in the corpus
- Biomaterial based modulation of macrophage polarization: A review and suggested design principles (2015, background): “, IL-4, IL-10, steroids) that overwhelm native signaling and direct polarization [92,93].”
- Inflammation, Fracture and Bone Repair (2016, background): “VEGF) [181] pathways, a growing number of reports involve modulating inflammation to improve tissue [90,182,183] and bone repair by biomimetic approaches [70,94,96].”