Repair of full-thickness articular cartilage defects using injectable type II collagen gel embedded with cultured chondrocytes in a rabbit model

Atsushi Funayama, Yasuo Niki, Hideo Matsumoto, Shinichi Maeno, Taku Yatabe, Hideo Morioka, Shigeru Yanagimoto, Tetsushi Taguchi, Junzo Tanaka, Yoshiaki Toyama

Research output: Contribution to journalArticle

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Abstract

Background. Recently, tissue-engineered chondrocyte transplantation has been tried to treat full-thickness cartilage defects. We developed an injectable type II collagen gel scaffold by chemically reacting type II collagen with polyethylene glycol crosslinker. This type II collagen was prepared from the nasal septa of cattle. In the present study, chondrocytes embedded in type II collagen gel were injected into rabbit full-thickness cartilage defects without a periosteal graft, and the feasibility for clinical application of the gel was evaluated. Methods. Chondrocytes were isolated from 1-kg New Zealand white rabbits. A full-thickness articular cartilage defect (5 mm diameter, 4 mm depth) was created on the patellar groove of the femur of 16 male 3-kg New Zealand white rabbits. A type II collagen solution of mixed chondrocytes at a density of 1 × 107 cells/ml was injected and transplanted into the defect in the right knee. The controls were the defect only in the left knee. At 4, 8, 12, and 24 weeks after operation, four cases from each group were evaluated macroscopically and histologically. Results. After injection into the cartilage defect, the gel bonded to the adjacent cartilage and bone within several minutes. Macroscopic examination revealed that the surface of the transplanted area was smooth and exhibited similar coloration and good integration with the surrounding cartilage at 12 and 24 weeks after transplantation. Histological examination at 8 weeks revealed favorable hyaline cartilage regeneration with good chondrocyte morphology. At 12 and 24 weeks, reparative cartilage remained rich in type II collagen. According to O'Driscoll histological scores, significant differences between the transplanted and control groups were apparent at 12 and 24 weeks. Immunohistochemical staining indicated sufficient type II collagen synthesis in regenerated cartilage 8 weeks after transplantation, and it was maintained until 24 weeks. Conclusions. These results indicate that type II collagen gel is suitable for injection into cartilage defects without any covering of a graft and offers a useful scaffold during chondrocyte transplantation.

Original languageEnglish
Pages (from-to)225-232
Number of pages8
JournalJournal of Orthopaedic Science
Volume13
Issue number3
DOIs
Publication statusPublished - 2008 May

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Collagen Type II
Articular Cartilage
Chondrocytes
Cartilage
Gels
Rabbits
Injections
Transplantation
Knee
Hyaline Cartilage
Transplants
Nasal Septum
Femur
Regeneration
Staining and Labeling
Bone and Bones
Control Groups

ASJC Scopus subject areas

  • Surgery

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Repair of full-thickness articular cartilage defects using injectable type II collagen gel embedded with cultured chondrocytes in a rabbit model. / Funayama, Atsushi; Niki, Yasuo; Matsumoto, Hideo; Maeno, Shinichi; Yatabe, Taku; Morioka, Hideo; Yanagimoto, Shigeru; Taguchi, Tetsushi; Tanaka, Junzo; Toyama, Yoshiaki.

In: Journal of Orthopaedic Science, Vol. 13, No. 3, 05.2008, p. 225-232.

Research output: Contribution to journalArticle

Funayama, A, Niki, Y, Matsumoto, H, Maeno, S, Yatabe, T, Morioka, H, Yanagimoto, S, Taguchi, T, Tanaka, J & Toyama, Y 2008, 'Repair of full-thickness articular cartilage defects using injectable type II collagen gel embedded with cultured chondrocytes in a rabbit model', Journal of Orthopaedic Science, vol. 13, no. 3, pp. 225-232. https://doi.org/10.1007/s00776-008-1220-z
Funayama, Atsushi ; Niki, Yasuo ; Matsumoto, Hideo ; Maeno, Shinichi ; Yatabe, Taku ; Morioka, Hideo ; Yanagimoto, Shigeru ; Taguchi, Tetsushi ; Tanaka, Junzo ; Toyama, Yoshiaki. / Repair of full-thickness articular cartilage defects using injectable type II collagen gel embedded with cultured chondrocytes in a rabbit model. In: Journal of Orthopaedic Science. 2008 ; Vol. 13, No. 3. pp. 225-232.
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AU - Funayama, Atsushi

AU - Niki, Yasuo

AU - Matsumoto, Hideo

AU - Maeno, Shinichi

AU - Yatabe, Taku

AU - Morioka, Hideo

AU - Yanagimoto, Shigeru

AU - Taguchi, Tetsushi

AU - Tanaka, Junzo

AU - Toyama, Yoshiaki

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N2 - Background. Recently, tissue-engineered chondrocyte transplantation has been tried to treat full-thickness cartilage defects. We developed an injectable type II collagen gel scaffold by chemically reacting type II collagen with polyethylene glycol crosslinker. This type II collagen was prepared from the nasal septa of cattle. In the present study, chondrocytes embedded in type II collagen gel were injected into rabbit full-thickness cartilage defects without a periosteal graft, and the feasibility for clinical application of the gel was evaluated. Methods. Chondrocytes were isolated from 1-kg New Zealand white rabbits. A full-thickness articular cartilage defect (5 mm diameter, 4 mm depth) was created on the patellar groove of the femur of 16 male 3-kg New Zealand white rabbits. A type II collagen solution of mixed chondrocytes at a density of 1 × 107 cells/ml was injected and transplanted into the defect in the right knee. The controls were the defect only in the left knee. At 4, 8, 12, and 24 weeks after operation, four cases from each group were evaluated macroscopically and histologically. Results. After injection into the cartilage defect, the gel bonded to the adjacent cartilage and bone within several minutes. Macroscopic examination revealed that the surface of the transplanted area was smooth and exhibited similar coloration and good integration with the surrounding cartilage at 12 and 24 weeks after transplantation. Histological examination at 8 weeks revealed favorable hyaline cartilage regeneration with good chondrocyte morphology. At 12 and 24 weeks, reparative cartilage remained rich in type II collagen. According to O'Driscoll histological scores, significant differences between the transplanted and control groups were apparent at 12 and 24 weeks. Immunohistochemical staining indicated sufficient type II collagen synthesis in regenerated cartilage 8 weeks after transplantation, and it was maintained until 24 weeks. Conclusions. These results indicate that type II collagen gel is suitable for injection into cartilage defects without any covering of a graft and offers a useful scaffold during chondrocyte transplantation.

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