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Surface microstructure of PEEK scaffolds regulates osteogenic differentiation via the βPIX–RAC1–NOX1 pathway

  • Zijian Yang
  • , Bowen Zhang
  • , Yihao Liu
  • , Kaiting Chen
  • , Qing Zhang
  • , Changning Sun
  • , Ling Wang
  • , Dichen Li
  • , Qingchu Li
  • , Huiyu Zhao
  • Southern Medical University
  • Xi'an Jiaotong University
  • National Medical Products Administration

科研成果: 期刊稿件文章同行评审

摘要

Polyetheretherketone (PEEK) is widely applied in orthopedic implants, yet its intrinsic surface bioinertness limits stable osseointegration. Although a nature solution is modifying its surface to enhance cellular adhesion, other pathways related to osseointegration also hold significant value. Here, we combined fused deposition modeling (FDM) 3D printing with a two-step poly (acrylic acid)–ethylenediamine (PAA–EDA) grafting method to engineer porous PEEK scaffolds with bioactive surface microstructures. Beyond improving hydrophilicity to optimize cellular adhesion, the modified surface activated the βPIX-mediated signaling cascade, which suppressed ITGB1–RAC1–NOX1 activity, potentially delaying bone mesenchymal stem cell (BMSC) senescence and promoting osteogenic differentiation. In vivo implantation further validated that the modified scaffolds promoted bone formation and integration. Together, this work highlights a new pathway on osseointegration for PEEK surface engineering, revealing the potential of βPIX-mediated regulation as a new direction for durable bone–implant integration.

源语言英语
文章编号214718
期刊Biomaterials Advances
182
DOI
出版状态已出版 - 5月 2026

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