| Original Article | |
| Collagen Type I, II and CD Markers Gene Expression of Articular Cartilage Repair Following Wedge Resection Trochleoplasty | |
| Peyman Farrahi1, Soroush Mohitmafi1, Fariborz Moayer2 | |
| 1Department of Clinical Science, Karaj Branch, Islamic Azad University, Karaj, Iran 2Department of Pathobiology, Karaj Branch, Islamic Azad University, Karaj, Iran |
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DOI: 10.34172/cjmb.2026.5062 Viewed : 61 times Downloaded : 76 times. Keywords : Trochleoplasty, Articular cartilage, Repair, Collagen type II, Collagen type I, CD31, CD45 |
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| Introduction | |
Objectives: Articular cartilage injury poses a significant clinical challenge due to its limited intrinsic regenerative capacity. Wedge resection trochleoplasty is a common technique for correcting patellar instability, but the biological quality of the repaired cartilage remains unclear. This study aimed to investigate the gene expression patterns of collagen type I, II and CD markers (CD31 and CD45) in cartilage repair following wedge resection trochleoplasty in a rabbit model. Materials and Methods: In this experimental study, 18 adult male New Zealand White rabbits underwent wedge resection trochleoplasty of the femoral trochlea. Animals were divided into three postoperative groups: 4, 8, and 16 weeks. Gene expression of COL1A1, COL2A1, CD45, and CD31 in the repair tissue was quantified using real-time polymerase chain reaction (PCR). Results: Results showed that COL1A1 expression was significantly elevated at 4 weeks and then declined, but remained higher than baseline at all time points. In contrast, COL2A1 expression progressively and significantly increased up to 16 weeks. The COL2A1/COL1A1 ratio improved over time. Expression of both CD45 and CD31 peaked at 4 weeks and subsequently declined significantly. Conclusions: Wedge-resection trochleoplasty promotes progressive cartilage remodeling over time, with the most pronounced chondrogenic response observed at 16 weeks. These findings may help guide interpretation of postoperative healing after trochlear reconstruction and provide a molecular benchmark for future translational studies. |
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