A VEGF/BMP-6-Functionalized PLGA Scaffold Combined with Mesenchymal Stem Cells Promotes Bone Regeneration in a Chicken Femoral Defect Model

Repair of critical-sized bone defects remains challenging because successful regeneration requires both osteogenesis and vascular support. This study investigated whether a biodegradable poly(lactic-co-glycolic acid) (PLGA) scaffold functionalized with vascular endothelial growth factor (VEGF) and bone morphogenetic protein-6 (BMP-6), combined with chicken bone marrow-derived mesenchymal stem cells (MSCs), could enhance bone regeneration. Porous PLGA scaffolds were functionalized with VEGF and BMP-6, seeded with MSCs, and implanted into surgically created chicken femoral defects. Bone regeneration was evaluated after eight weeks by micro-computed tomography (micro-CT) and histological analysis. The effects of VEGF and BMP-6 on MSC osteogenic differentiation were further assessed by Alizarin Red S staining and quantitative real-time PCR. Among the treatment groups, VEGF/BMP-6-functionalized scaffolds combined with MSCs produced the greatest bone volume and most extensive defect bridging. In vitro, VEGF and BMP-6 modulated matrix mineralization and osteogenic marker expression. These findings demonstrate the regenerative potential of a multifunctional PLGA-based construct integrating growth-factor functionalization and MSC transplantation. Because an MSC-only scaffold group was not included, the individual contributions of MSCs and growth-factor functionalization to the enhanced in vivo response cannot be distinguished.

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Publication Details

Journal
Biomolecules
Published
2026-10-26
DOI
https://doi.org/10.3390/biom16111556
Primary Topic
Bone Tissue Engineering Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

A VEGF/BMP-6-Functionalized PLGA Scaffold Combined with Mesenchymal Stem Cells Promotes Bone Regeneration in a Chicken Femoral Defect Model

Te‐Feng Arthur Chou, Quanjun Cui, Weitao Wang, Adam S. Wilson et al.
Biomolecules
Bone Tissue Engineering Materials
article

A VEGF/BMP-6-Functionalized PLGA Scaffold Combined with Mesenchymal Stem Cells Promotes Bone Regeneration in a Chicken Femoral Defect Model

Te‐Feng Arthur Chou, Quanjun Cui, Weitao Wang, Adam S. Wilson, Abhijit S. Dighe, Vedavathi Madhu, Xinlin Yang, Ching Ju Li, Jae Sung Suh
article en

Abstract

Repair of critical-sized bone defects remains challenging because successful regeneration requires both osteogenesis and vascular support. This study investigated whether a biodegradable poly(lactic-co-glycolic acid) (PLGA) scaffold functionalized with vascular endothelial growth factor (VEGF) and bone morphogenetic protein-6 (BMP-6), combined with chicken bone marrow-derived mesenchymal stem cells (MSCs), could enhance bone regeneration. Porous PLGA scaffolds were functionalized with VEGF and BMP-6, seeded with MSCs, and implanted into surgically created chicken femoral defects. Bone regeneration was evaluated after eight weeks by micro-computed tomography (micro-CT) and histological analysis. The effects of VEGF and BMP-6 on MSC osteogenic differentiation were further assessed by Alizarin Red S staining and quantitative real-time PCR. Among the treatment groups, VEGF/BMP-6-functionalized scaffolds combined with MSCs produced the greatest bone volume and most extensive defect bridging. In vitro, VEGF and BMP-6 modulated matrix mineralization and osteogenic marker expression. These findings demonstrate the regenerative potential of a multifunctional PLGA-based construct integrating growth-factor functionalization and MSC transplantation. Because an MSC-only scaffold group was not included, the individual contributions of MSCs and growth-factor functionalization to the enhanced in vivo response cannot be distinguished.

BiomoleculesVol. 16(11)
University of Virginia (US)
Arthritis National Research Foundation
Openalex Percentile: Top 24%
Bone Tissue Engineering Materials
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A VEGF/BMP-6-Functionalized PLGA Scaffold Combined with Mesenchymal Stem Cells Promotes Bone Regeneration in a Chicken Femoral Defect Model — Te‐Feng Arthur Chou, Quanjun Cui, et al. · Biomolecules (2026) | TGRS Research Map | TGRS