Publication | Open Access
Immobilized Lentivirus Vector on Chondroitin Sulfate-Hyaluronate Acid-Silk Fibroin Hybrid Scaffold for Tissue-Engineered Ligament-Bone Junction
34
Citations
28
References
2014
Year
Tissue EngineeringCartilage LayerEngineeringBiomaterials DesignBone RepairBiomedical EngineeringOrthopaedic SurgeryAnterior Cruciate LigamentRegenerative MedicineRegenerative BiomaterialsTranslational Tissue EngineeringLentivirus VectorSilk CablesMatrix BiologyTissue RepairRegenerative EngineeringTissue-engineered Ligament-boneCartilage BiologyFunctional Tissue EngineeringCell BiologyMesenchymal Stem CellTissue RegenerationSoft Tissue ReconstructionMedicineBiomaterialsBiocompatible Material
The lack of a fibrocartilage layer between graft and bone remains the leading cause of graft failure after anterior cruciate ligament (ACL) reconstruction. The objective of this study was to develop a gene-modified silk cable-reinforced chondroitin sulfate-hyaluronate acid-silk fibroin (CHS) hybrid scaffold for reconstructing the fibrocartilage layer. The scaffold was fabricated by lyophilizing the CHS mixture with braided silk cables. The scanning electronic microscopy (SEM) showed that microporous CHS sponges were formed around silk cables. Each end of scaffold was modified with lentiviral-mediated transforming growth factor- β 3 (TGF- β 3) gene. The cells on scaffold were transfected by bonded lentivirus. In vitro culture demonstrated that mesenchymal stem cells (MSCs) on scaffolds proliferated vigorously and produced abundant collagen. The transcription levels of cartilage-specific genes also increased with culture time. After 2 weeks, the MSCs were distributed uniformly throughout scaffold. Deposited collagen was also found to increase. The chondral differentiation of MSCs was verified by expressions of collagen II and TGF- β 3 genes in mRNA and protein level. Histology also confirmed the production of cartilage extracellular matrix (ECM) components. The results demonstrated that gene-modified silk cable-reinforced CHS scaffold was capable of supporting cell proliferation and differentiation to reconstruct the cartilage layer of interface.
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