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Mechanically robust and personalized silk fibroin-magnesium composite scaffolds with water-responsive shape-memory for irregular bone regeneration

Author

Listed:
  • Zhinan Mao

    (Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center
    Peking University)

  • Xuewei Bi

    (Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center
    Peking University)

  • Chunhao Yu

    (Peking University)

  • Lei Chen

    (Capital Medical University)

  • Jie Shen

    (Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center)

  • Yongcan Huang

    (Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center)

  • Zihong Wu

    (TUM School of Life Sciences)

  • Hui Qi

    (Capital Medical University)

  • Juan Guan

    (Beihang University)

  • Xiong Shu

    (Capital Medical University)

  • Binsheng Yu

    (Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center)

  • Yufeng Zheng

    (Peking University)

Abstract

The regeneration of critical-size bone defects, especially those with irregular shapes, remains a clinical challenge. Various biomaterials have been developed to enhance bone regeneration, but the limitations on the shape-adaptive capacity, the complexity of clinical operation, and the unsatisfied osteogenic bioactivity have greatly restricted their clinical application. In this work, we construct a mechanically robust, tailorable and water-responsive shape-memory silk fibroin/magnesium (SF/MgO) composite scaffold, which is able to quickly match irregular defects by simple trimming, thus leading to good interface integration. We demonstrate that the SF/MgO scaffold exhibits excellent mechanical stability and structure retention during the degradative process with the potential for supporting ability in defective areas. This scaffold further promotes the proliferation, adhesion and migration of osteoblasts and the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) in vitro. With suitable MgO content, the scaffold exhibits good histocompatibility, low foreign-body reactions (FBRs), significant ectopic mineralisation and angiogenesis. Skull defect experiments on male rats demonstrate that the cell-free SF/MgO scaffold markedly enhances bone regeneration of cranial defects. Taken together, the mechanically robust, personalised and bioactive scaffold with water-responsive shape-memory may be a promising biomaterial for clinical-size and irregular bone defect regeneration.

Suggested Citation

  • Zhinan Mao & Xuewei Bi & Chunhao Yu & Lei Chen & Jie Shen & Yongcan Huang & Zihong Wu & Hui Qi & Juan Guan & Xiong Shu & Binsheng Yu & Yufeng Zheng, 2024. "Mechanically robust and personalized silk fibroin-magnesium composite scaffolds with water-responsive shape-memory for irregular bone regeneration," Nature Communications, Nature, vol. 15(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48417-8
    DOI: 10.1038/s41467-024-48417-8
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    References listed on IDEAS

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    1. Tao Wang & Jiaxiang Bai & Min Lu & Chenglong Huang & Dechun Geng & Gang Chen & Lei Wang & Jin Qi & Wenguo Cui & Lianfu Deng, 2022. "Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    2. Feng-Yen Li & Benjamin Chaigne-Delalande & Chrysi Kanellopoulou & Jeremiah C. Davis & Helen F. Matthews & Daniel C. Douek & Jeffrey I. Cohen & Gulbu Uzel & Helen C. Su & Michael J. Lenardo, 2011. "Second messenger role for Mg2+ revealed by human T-cell immunodeficiency," Nature, Nature, vol. 475(7357), pages 471-476, July.
    3. Lizhen Wang & Kaixiang Jin & Nan Li & Peng Xu & Hao Yuan & Harsha Ramaraju & Scott J. Hollister & Yubo Fan, 2023. "Innovative design of minimal invasive biodegradable poly(glycerol-dodecanoate) nucleus pulposus scaffold with function regeneration," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
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