Donor cell fate in tissue engineering for articular cartilage repair

• Published in: Clinical orthopaedics and related research no. 389; p. 228
• Main Authors: Ostrander, R V, Goomer, R S, Tontz, W L, Khatod, M, Harwood, F L, Maris, T M, Amiel, D
• Format: Journal Article
• Language: English
• Published: United States 01.08.2001
• Subjects: Animals; Biomedical Engineering; Cartilage, Articular; Cell Count; Cells, Cultured; Culture Techniques; Male; Rabbits
• ISSN: 0009-921X; 1528-1132
• DOI: 10.1097/00003086-200108000-00032

Articular cartilage repair is a clinical challenge because of its limited intrinsic healing potential. Considerable research has focused on tissue engineering and transplantation of viable chondrogenic cells to enhance cartilage regeneration. However, the question remains: do transplanted allogenic cells survive in the repair with time? This study assessed donor cell fate after transplantation of male New Zealand White rabbit perichondrium cell and polylactic acid constructs into osteochondral defects created in the medial femoral condyles of female New Zealand White rabbits. Repair tissue was harvested at 0, 1, 2, 3, 7, and 28 days after implantation and was evaluated for cell viability and total cell number using confocal microscopic analysis. The number of donor cells in each sample was estimated using quantitative polymerase chain reaction targeting a gender-specific gene present on the Y-chromosome, the sex-determining region Y gene, and a control deoxyribonucleic acid present in male and female cell deoxyribonucleic acid, the matrix metalloproteinase-1 gene promoter. Average cell viability was found to be 87% or more at all times. Donor cells were present in repair tissue for 28 days after implantation. However, the number of donor cells declined from approximately 1 million at Time 0 to approximately 140,000 at 28 days. This decline in donor cells was accompanied by a significant influx of host cells into the repair tissue. This study shows that the sex-determining region Y gene is a valuable marker for tracking the fate of transplanted allogenic cells in tissue engineering.