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Published on: February 23, 2024
PHBV wet-spun scaffold coated with ELR-REDV improves vascularization for bone tissue engineering
Ayse Selcen Alagoz1, Jose Carlos Rodriguez-Cabello2, Vasif Hasirci1,3
1Middle East Technical University (METU), Department of Biological Sciences, Ankara, Turkey.
This study developed a 3D bone tissue engineering scaffold using poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) coated with an elastin-like recombinamer (ELR) peptide. The modified scaffold significantly enhanced early vascularization by attracting endothelial cells, addressing a key challenge in bone regeneration.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Regenerative Medicine
Background:
- Large-scale bone tissue replacement requires 3D scaffolds, but limited nutrient and oxygen transport hinders cell survival.
- Vascularization is crucial for scaffold survival but cannot be immediately established post-implantation.
- Developing strategies for early vascularization is essential for the success of bone tissue engineering.
Purpose of the Study:
- To develop a 3D wet-spun bone tissue engineering scaffold promoting early vascularization.
- To functionalize poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) scaffolds with an elastin-like recombinamer (ELR) peptide containing a REDV sequence.
- To evaluate the effect of ELR-REDV coating on scaffold properties and endothelial cell attraction.
Main Methods:
- Fabrication of 3D PHBV scaffolds using wet-spinning.
- Surface modification of PHBV scaffolds via oxygen plasma treatment and subsequent ELR-REDV peptide immobilization (PHBV-O2-ELR-REDV).
- Characterization of surface properties (wettability, topography, composition) and in vitro assessment of cell adhesion, proliferation, and migration using mesenchymal stem cells and human umbilical vein endothelial cells (HUVECs).
Main Results:
- Oxygen plasma treatment and ELR-REDV coating altered scaffold wettability, topography, and surface composition, creating a moderately hydrophilic surface.
- FTIR-ATR confirmed successful ELR-REDV immobilization on the PHBV scaffolds.
- While ELR modification did not significantly impact bone marrow mesenchymal cell adhesion or proliferation, it markedly increased HUVEC adhesion and migration (approx. 2.5-fold higher than untreated scaffolds after 14 days).
Conclusions:
- The developed PHBV-O2-ELR-REDV scaffolds demonstrate significant potential for inducing early vascularization in bone tissue engineering.
- The REDV sequence on the ELR peptide effectively promotes endothelial cell recruitment, a critical factor for nutrient supply in 3D implants.
- These findings suggest a promising approach to overcome vascularization limitations in large-scale bone regeneration applications.
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