Zhao Yuqing, An Yanxin, Wu Fan, Liu Lipeng, Tay Franklin R, Jiao Yang, Wang Jing
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, National Clinical Research Center for Oral Diseases, Shaanxi Engineering Research Center for Dental Materials and Advanced Manufacture, Department of Oral Implants, School of Stomatology, The Fourth Military Medical University, Xi'an, 710032, PR China.
Department of General Surgery, The First Affiliated Hospital of Xi'an Medical University, Xi'an, 710077, PR China.
J Nanobiotechnology. 2025 Mar 11;23(1):199. doi: 10.1186/s12951-025-03272-7.
Optimizing the immune microenvironment is essential for successful implant osseointegration. In this study, four different nano/microstructures were fabricated on polyetheretherketone (PEEK) substrates by varying the agitation speed during sulfonation to influence osteoimmunomodulation and implant integration. The results indicate that nano/microstructures with minimal dimensions (SP450) inhibit actin polymerization by reducing calcium influx through PIEZO1, activating the anti-inflammatory M2 macrophage phenotype. Among the tested specimens, SP450 exhibited the lowest expression levels of tumor necrosis factor-α and interleukin-1β while releasing the highest levels of anti-inflammatory factors, including interleukin-4 and interleukin-10. This optimized immune environment promotes the osteogenesis of MC3T3-E1 pre-osteoblasts and enhances the osseointegration of PEEK implants. Transcriptomic analysis and validation experiment further revealed that SP450 inhibits osteoclastic differentiation by down-regulating transforming growth factor-β2 and suppressing the NF-κB signaling pathway. These findings suggest that manipulating the surface topography of PEEK implants is an effective strategy for enhancing osseointegration with promising clinical applications.
优化免疫微环境对于种植体骨整合的成功至关重要。在本研究中,通过在磺化过程中改变搅拌速度,在聚醚醚酮(PEEK)基底上制备了四种不同的纳米/微观结构,以影响骨免疫调节和种植体整合。结果表明,尺寸最小的纳米/微观结构(SP450)通过减少通过PIEZO1的钙内流来抑制肌动蛋白聚合,激活抗炎M2巨噬细胞表型。在测试样本中,SP450表现出最低水平的肿瘤坏死因子-α和白细胞介素-1β表达,同时释放出最高水平的抗炎因子,包括白细胞介素-4和白细胞介素-10。这种优化的免疫环境促进了MC3T3-E1前成骨细胞的成骨作用,并增强了PEEK种植体的骨整合。转录组分析和验证实验进一步表明,SP450通过下调转化生长因子-β2和抑制NF-κB信号通路来抑制破骨细胞分化。这些发现表明,操纵PEEK种植体的表面形貌是增强骨整合的有效策略,具有广阔的临床应用前景。