Acceleration of cartilage repair by genetically modified chondrocytes over expressing bone morphogenetic protein‐7
- 1 July 2003
- journal article
- Published by Wiley in Journal of Orthopaedic Research
- Vol. 21 (4) , 573-583
- https://doi.org/10.1016/s0736-0266(02)00264-4
Abstract
Cartilage has a limited capacity to heal. Although chondrocyte transplantation is a useful therapeutic strategy, the repair process can be lengthy. Previously we have shown that over expression of bone morphogenetic protein-7 (BMP-7) in chondrocytes by adenovirus-mediated gene transfer leads to increased matrix synthesis and cartilage-like tissue formation in vitro. In this context we hypothesized that implantation of genetically modified chondrocytes expressing BMP-7 would accelerate the formation of hyaline-like repair tissue in an equine model of cartilage defect repair. Chondrocytes treated with adenovirus vector encoding BMP-7 (AdBMP-7) or as control, an adenovirus vector encoding an irrelevant gene (Escherichia coli cytosine deaminase, AdCD) were implanted into extensive (15 mm diameter) articular cartilage defects in the patellofemoral joints of 10 horses. Biopsies were performed to evaluate early healing at 4 weeks. At the terminal time point of 8 months, repairs were assessed for morphology, MRI appearance, compressive strength, biochemical composition and persistence of implanted cells. Four weeks after surgery AdBMP-7-treated repairs showed an increased level of BMP-7 expression and accelerated healing, with markedly more hyaline-like morphology than control. Quantitative real-time polymerase chain reaction (PCR) analysis of the repair tissue 8 months after surgery showed that few implanted cells persisted. By this time, the controls had healed similarly to the AdBMP-7-treated defects, and no difference was detected in the morphologic, biochemical or biomechanical properties of the repair tissues from the two treatment groups. Implantation of genetically modified chondrocytes expressing BMP-7 accelerates the appearance of hyaline-like repair tissue in experimental cartilage defects. Rehabilitation after cell-based cartilage repair can be prolonged, leading to decreased patient productivity and quality of life. This study shows the feasibility of using genetically modified chondrocytes to accelerate cartilage healing.Keywords
This publication has 31 references indexed in Scilit:
- Enhanced matrix synthesis and in vitro formation of cartilage‐like tissue by genetically modified chondrocytes expressing BMP‐7Journal of Orthopaedic Research, 2001
- Use of Quantitative TaqMan Real-Time PCR to Track the Time-Dependent Distribution of Gene Transfer Vectors in VivoMolecular Therapy, 2000
- Enhanced repair of extensive articular defects by insulin‐like growth factor‐I‐laden fibrin compositesJournal of Orthopaedic Research, 1999
- Expression of human bone morphogenic protein 7 in primary rabbit periosteal cells: potential utility in gene therapy for osteochondral repairGene Therapy, 1998
- Detection of Cytosine Deaminase in Genetically Modified Tumor Cells by Specific AntibodiesHuman Gene Therapy, 1997
- Expression pattern of osteogenic protein-1 (bone morphogenetic protein-7) in human and mouse development.Journal of Histochemistry & Cytochemistry, 1995
- In VivoAdenovirus-Mediated Gene Transfer of theEscherichia coliCytosine Deaminase Gene to Human Colon Carcinoma-Derived Tumors Induces Chemosensitivity to 5-FluorocytosineHuman Gene Therapy, 1995
- Chondrocyte-laden collagen scaffolds for resurfacing extensive articular cartilage defectsOsteoarthritis and Cartilage, 1995
- In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epitheliumCell, 1992
- The repair of experimentally produced defects in rabbit articular cartilage by autologous chondrocyte transplantationJournal of Orthopaedic Research, 1989