Repair of articular cartilage defect by autologous transplantation of basic fibroblast growth factor gene-transduced chondrocytes with adeno-associated virus vector

Arthritis Rheum. 2005 Jan;52(1):164-70. doi: 10.1002/art.20739.

Abstract

Objective: To examine the effects of basic fibroblast growth factor (bFGF) gene-transduced chondrocytes on the repair of articular cartilage defects.

Methods: LacZ gene or bFGF gene was transduced into primary isolated rabbit chondrocytes with the use of a recombinant adeno-associated virus (AAV) vector. These gene-transduced chondrocytes were embedded in collagen gel and transplanted into a full-thickness defect in the articular cartilage of the patellar groove of a rabbit. The efficiency of gene transduction was assessed according to the percentage of LacZ-positive cells among the total number of living cells. The concentration of bFGF in the culture supernatant was measured by enzyme-linked immunosorbent assay to confirm the production by bFGF gene-transduced chondrocytes. At 4, 8, and 12 weeks after transplantation, cartilage repair was evaluated histologically and graded semiquantitatively using a histologic scoring system ranging from 0 (complete regeneration) to 14 (no regeneration) points.

Results: LacZ gene expression by chondrocytes was maintained until 8 weeks in >85% of the in vitro population. LacZ-positive cells were found at the transplant sites for at least 4 weeks after surgery. The mean concentration of bFGF was significantly increased in bFGF gene-transduced cells compared with control cells (P < 0.01). Semiquantitative histologic scoring indicated that the total score was significantly lower in the bFGF-transduced group than in the control group throughout the observation period.

Conclusion: These results demonstrated that gene transfer to chondrocytes by an ex vivo method was established with the AAV vector, and transplantation of bFGF gene-transduced chondrocytes had a clear beneficial effect on the repair of rabbit articular cartilage defects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage, Articular / pathology
  • Cartilage, Articular / physiopathology
  • Cartilage, Articular / surgery*
  • Cells, Cultured
  • Chondrocytes / metabolism*
  • Chondrocytes / transplantation*
  • Dependovirus / genetics
  • Fibroblast Growth Factor 2 / genetics
  • Fibroblast Growth Factor 2 / metabolism*
  • Gene Expression
  • Gene Transfer Techniques*
  • Genetic Vectors
  • Knee Injuries / pathology
  • Knee Injuries / physiopathology
  • Knee Injuries / surgery*
  • Lac Operon
  • Rabbits
  • Regeneration
  • Transduction, Genetic
  • Transplantation, Autologous
  • Wounds, Penetrating / pathology
  • Wounds, Penetrating / physiopathology
  • Wounds, Penetrating / surgery*

Substances

  • Fibroblast Growth Factor 2