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Stem Cell Fishing at Bone-Implant Interface: A Cell-Clicking Bioadhesion Strategy to Enhance Osteointegration

  • Junjie Niu
  • , Yu Zhang
  • , Zhenhuan Jiang
  • , Tao Feng
  • , Hao Shen
  • , Yingkang Huang
  • , Yin Zhang
  • , Yufan Ying
  • , Wenguo Cui*
  • , Guoqing Pan*
  • , Qin Shi*
  • *Korresponderande författare för detta arbete

Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

1 Citeringar (Scopus)

Sammanfattning

Insufficient mesenchymal stem cells (MSCs) at bone-implant interfaces hinder osseointegration and implant success. Although stem cell therapies are promising, in situ recruitment and high-efficiency localization of target cells remain challenging. This study proposes a “cell-clicking” strategy for in situ “fishing” bone marrow MSCs (BMSCs) at the bone-implant interface. The bidirectional binding, based on a clickable biomimetic peptide with mussel-like adhesive and bioorthogonal molecular binding abilities, enables rapid, precise, and stable chemical tethering of azide-modified BMSCs (BMSCs-Az) at the initial phase after implantation. Thereafter, a steady transition of the tethered stem cells into chemo-biological co-adhesion states improves interfacial osteogenesis. This study first verifies that BMSCs-Az can be captured and stably bound to the surface of clickable biomimetic peptide-modified implants both in vitro and in vivo. Additionally, the immunomodulatory activity of BMSCs-Az can alter macrophage polarization. The synergistic effect of BMSCs-Az immunomodulation and in situ cell fishing-mediated recruitment enhances osteogenic efficiency and reinforces biomechanical integration at the bone-implant interface. In conclusion, this study provides a new inspiration for osteo-implants in stem cell-based regenerative medicine to develop rapid, precise, and stable stem cell recruitment strategies for high-efficiency tissue regeneration.

OriginalspråkEngelska
Artikelnummere14351
TidskriftAdvanced Functional Materials
Volym36
Nummer16
Tidigt onlinedatum6 okt. 2025
DOI
StatusPublicerad - 23 feb. 2026
MoE-publikationstypA1 Tidskriftsartikel-refererad

Finansiering

J.N., Y.Z., Z.J., and T.F. contributed equally to this work. This work was supported by the National Natural Science Foundation of China (82472426, 81902181, 82172485, 32222041); the National Key R&D Program of China, MOST (2023YFC2509900); the Natural Science Foundation of Jiangsu Province (BK20220059); the Suzhou Basic Research Pilot Program (SSD2024048, SSD2024028); the Suzhou Medical Application Basic Research (SKY2023147).

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