Biomimetic Wavy-Crimped Porous Structure Enhances Tendon Attachment Reconstruction via Integrin-FAK/Src-MAPK
Jinbo Zhang1, Hao Chen1, Xingzhen Li1
1Department of Orthopedics, The Second Hospital of Jilin University, Changchun, China.
Advanced Healthcare Materials
|May 6, 2026
Summary
A novel biomimetic wavy-crimped titanium scaffold (BT) enhances tendon-to-implant healing by promoting organized tissue growth and reducing fibrosis. This biomimetic approach significantly improves the mechanical strength of tendon-prosthesis integration for better joint reconstruction outcomes.
Area of Science:
- Biomaterials Engineering
- Tissue Engineering
- Orthopedic Surgery
Background:
- Porous prostheses are used for large bone defects, but often cause fibrotic healing at the tendon interface.
- This fibrotic healing leads to poor tissue organization and insufficient mechanical strength, limiting joint function recovery.
- Native tendons have a wavy-crimped collagen structure that guides cell alignment and promotes healing.
Purpose of the Study:
- To develop a biomimetic wavy-crimped porous titanium scaffold (BT) to improve tendon-prosthesis integration.
- To investigate the effects of the BT scaffold on cellular behavior and tissue formation at the tendon-implant interface.
- To elucidate the molecular mechanisms underlying enhanced tendon integration facilitated by the BT scaffold.
Main Methods:
- Fabrication of a biomimetic wavy-crimped porous titanium scaffold (BT).
- Evaluation of BT scaffold performance in a rabbit patellar tendon attachment reconstruction model.
- In vitro studies using tendon-derived stem cells (TDSCs) to assess cell alignment, tenogenic differentiation, and fibrotic markers.
- Transcriptomic analysis to identify molecular pathways involved in tendon-prosthesis integration.
Main Results:
- BT scaffolds promoted ordered interfacial tissue arrangement and significantly strengthened tendon attachment in vivo.
- In vitro, BT scaffolds guided TDSC alignment, enhanced tenogenic marker expression (COL I, SCX, TNMD), and suppressed fibrotic markers (α-SMA).
- BT scaffolds upregulated antifibrotic factor TGF-β3 and activated the integrin-FAK/Src-MAPK signaling axis, promoting tenogenesis and suppressing fibrogenesis.
Conclusions:
- The biomimetic wavy-crimped BT scaffold effectively overcomes fibrotic healing at the tendon-prosthesis interface.
- BT scaffolds provide a promising strategy to enhance interfacial mechanics for improved tendon-prosthesis reconstruction.
- This approach offers a potential solution for the long-standing challenge of insufficient mechanical stability in tendon repair and reconstruction.
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