Dual-functional 3D-printed polyetheretherketone scaffolds with immunomodulatory nano‑calcium silicate/interleukin-4 coating synergistically enhance osteogenesis through macrophage M2 polarization and NF-κB pathway suppression

化学 间充质干细胞 巨噬细胞极化 偷看 表面改性 碱性磷酸酶 生物医学工程 细胞生物学 再生医学 涂层 免疫系统 间质细胞 生物物理学 组织工程 细胞 壳聚糖 共焦激光扫描显微镜 巨噬细胞 骨髓 脐静脉 细胞生长 干细胞 共焦 骨形态发生蛋白2 共焦显微镜 材料科学 纳米技术 祖细胞 细胞疗法 M2巨噬细胞 骨愈合
作者
Xiaoyu Guo,Yanwen Su,Zixuan Wu,Zhiyuan Wu,Kaili Liu,Junyu Yue,Yuning Qu,Kunzheng Wang,Jiankang He,Rui Ma,Pei Yang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:525: 170004-170004 被引量:1
标识
DOI:10.1016/j.cej.2025.170004
摘要

Despite its biomechanical advantages, polyetheretherketone (PEEK) exhibits bioinertness and pro-inflammatory responses, which limit its efficacy in bone-defect repair. Therefore, we aimed to engineer three-dimensional-printed PEEK scaffolds functionalized with a polydopamine (PDA)-assisted nano‑calcium silicate (n-CS)/interleukin-4 (IL-4) coating (PEEK/PCS/IL-4) to synergistically modulate immune responses and osteogenesis to overcome the challenges associated with PEEK. The scaffolds were fabricated through fused deposition modeling under optimized conditions and subsequently subjected to sequential surface functionalization involving PDA-mediated n-CS immobilization followed by IL-4 impregnation. In vitro, the PEEK/PCS/IL-4 scaffolds significantly enhanced human bone marrow mesenchymal stem cell (hBMSCs) spreading, alkaline phosphatase activity, mineralization, and osteogenic gene expression compared with the controls. The scaffolds also promoted human umbilical vein endothelial cell migration and tube formation, suggesting potent pro-angiogenic effects. RAW264.7 macrophages cultured on PEEK/PCS/IL-4 exhibited M2 polarization, elevated transforming growth factor-β1 (TGFβ1), and suppressed tumor necrotic factor-α levels (TNFα), which correlated with the non-canonical NF-κB pathway inhibition. The conditioned medium from PEEK/PCS/IL-4-primed macrophages further amplified hBMSCs osteogenesis, confirming immune-osteogenic coupling. In vivo, PEEK/PCS/IL-4 scaffolds reduced fibrous encapsulation and enhanced M2 macrophage polarization in a rat subcutaneous implantation model. In rabbit femoral defects, micro-CT, confocal laser scanning microscopy, histology, and biomechanical testing results revealed that the PEEK/PCS/IL-4 scaffolds exhibited enhanced osteogenesis and superior osseointegration. This study pioneers an immuno-engineering approach to transform bioinert PEEK into a bioactive platform, leveraging n-CS/IL-4 coatings to harmonize immune homeostasis, bone regeneration, and revascularization, offering a transformative strategy for bone defect repair. • 3D-printed PEEK scaffolds are modified with nano-CaSiO₃/IL-4 for bone repair. • M2 macrophage polarization enhances osteogenesis via immunomodulation. • NF-κB pathway suppression underpins the anti-inflammatory/osteogenic effects. • Dual-functional n-CS/IL-4 coating synergizes immunomodulatory and osteogenesis.
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