Article: Griffin, DJ; Ortved, KF; Nixon, AJ; Bonassar, LJ; (2016) “Mechanical Properties and Structure-Function Relationships in Articular Cartilage Repaired Using IGF-I Gene-Enhanced Chondrocytes”, Journal of Orthopaedic Research, 34 (1); 149-153
Abstract: Several studies have demonstrated the benefits of IGF-I gene therapy in enhancing the histologic and biochemical content of cartilage repaired by chondrocyte transplantation. However, there is little to no data on the mechanical performance of IGF-I augmented cartilage grafts. This study evaluated the compressive properties of full-thickness chondral defects in the equine femur repaired with and without IGF-I gene therapy. Animals were randomly assigned to one of three study cohorts based on chondrocyte treatment provided in each defect: (i) IGF-I gene delivered by recombinant adeno-associated virus (rAAV)-5; (ii) AAV-5 delivering GFP as a reporter; (iii) naive cells without virus. In each case, the opposite limb was implanted with a fibrin carrier without cells. Samples were prepared for confined compression testing to measure the aggregate modulus and hydraulic permeability. All treatment groups, regardless of cell content or transduction, had mechanical properties inferior to native cartilage. Overexpression of IGF-I increased modulus and lowered permeability relative to other treatments. Investigation of structure-property relationships revealed that Ha and k were linearly correlated with GAG content but logarithmically correlated with collagen content. This provides evidence that IGF-I gene therapy can improve healing of articular cartilage and can greatly increase the mechanical properties of repaired grafts. (C) 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
Funding Acknowledgement: Cornell University, Cornell Vet. Medicine, Cornell University Provost Diversity Fellowship; NIH [5R01-AR055373]
Funding Text: Grant sponsor: Cornell University, Cornell Vet. Medicine, Cornell University Provost Diversity Fellowship; Grant sponsor: NIH; Grant number: 5R01-AR055373.