AI Article Synopsis

  • - The study aimed to assess if osteogenic matrix cell sheets (OMCS) could promote bone formation around grafted tendons in rabbits, which might aid in early tendon-to-bone healing after surgery.
  • - Researchers found that OMCS had strong osteogenic properties, demonstrated by high alkaline phosphatase activity and positive bone formation indicators when tested with grafted tendons.
  • - Results showed that OMCS significantly increased bone volume and pullout strength at the tendon-bone interface compared to controls, suggesting that OMCS can effectively enhance tendon-to-bone healing post-surgery.

Article Abstract

The objective of this study was to determine whether osteogenic matrix cell sheets (OMCS) could induce bone formation around grafted tendons, thereby enhancing early stage tendon to bone tunnel healing in skeletally mature male Japanese white rabbits. First, the osteogenic potential of rabbit OMCS was evaluated. Then, the OMCS were transplanted into the interface between the grafted tendon and the bone tunnel created at the tibia. Histological assessments and biomechanical tensile testing were performed after 3 weeks. The rabbit OMCS showed high alkaline phosphatase (ALP) activity, positive staining of ALP, and osteogenic potential when transplanted subcutaneously with beta tricalcium phosphate disks. Newly formed bony walls and positive collagen type I staining were seen around the grafted tendon with OMCS transplantation, whereas such bony walls were thinner or less frequent without OMCS transplantation. Micro-computed tomography images showed significantly higher bone volume in the OMCS transplantation group. The pullout strength was significantly higher with OMCS (0.74 ± 0.23 N/mm(2)) than without OMCS (0.58 ± 0.15 N/mm(2)). These results show that OMCS enhance early tendon to bone tunnel healing. This method can be applied to cases requiring early tendon to bone tunnel healing after ligament reconstruction surgery.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784076PMC
http://dx.doi.org/10.1155/2013/842192DOI Listing

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