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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*
  • *Tämän työn vastaava kirjoittaja

Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

1 Sitaatiot (Scopus)

Abstrakti

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.

AlkuperäiskieliEnglanti
Artikkelie14351
JulkaisuAdvanced Functional Materials
Vuosikerta36
Numero16
Varhainen verkossa julkaisun päivämäärä6 lokak. 2025
DOI - pysyväislinkit
TilaJulkaistu - 23 helmik. 2026
OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

Rahoitus

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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