Development of a novel approach for restoration of the meniscus using silk-elastin in a rabbit meniscus injury model

被引:1
作者
Inoue, Tadashi [1 ]
Kano, Toshiya [1 ]
Nakasa, Tomoyuki [1 ]
Ishikawa, Masakazu [2 ]
Inoue, Keiichiro [4 ]
Kawabata, Shingo [4 ]
Miyaki, Shigeru [3 ]
Kamei, Naosuke [1 ]
Adachi, Nobuo [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Orthopaed Surg, 1-2-3 Kasumi,Minami Ku, Hiroshima 7348553, Japan
[2] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Artificial Joints & Biomat, Hiroshima, Japan
[3] Hiroshima Univ Hosp, Med Ctr Translat & Clin Res, Hiroshima, Japan
[4] Sanyo Chem Ind Ltd, Kyoto, Japan
关键词
Meniscal injury; Silk-elastin; Meniscal repair; Rabbit model; MESENCHYMAL STEM-CELLS; SCAFFOLD IMPLANTATION; MENISCECTOMY; COLLAGEN; REPAIR; OUTCOMES; KNEE; LESIONS; TRENDS; VIVO;
D O I
10.1186/s12891-024-07675-9
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
BackgroundLimited healing potential of the meniscus remains a burden for the successful repair of meniscus injuries in the orthopaedic fields. Silk-elastin (SE) is a novel recombinant protein with favorable properties for wound healing. This proof-of-concept study aimed to investigate the therapeutic effect of silk-elastin in a rabbit meniscal defect model.MethodsA migration assay using rabbit meniscus and synovial cells with various concentrations of SE in a culture medium was conducted to investigate the mechanism of meniscal healing by SE. Additionally, cylindrical defects with a 1.5 mm diameter were created at the anterior horn of the medial meniscus of rabbits. The animals were divided into three groups: 1) the Blank group; defect only, 2) the Col I group; implantation of type I atelocollagen sponge, and 3) the SE group; implantation of SE (150 mg/ml) sponge. Whole medial menisci were harvested at 4, 8, 12, and 24 weeks after surgery. Histological analyses including immunohistochemical staining were performed to assess meniscal healing.ResultsIn vitro study, Migration assay demonstrated a significantly higher number of migrated cells only in synovial cells. Especially, the SE concentration of 10 mu g/mL demonstrated the highest number of migrated cells compared with other concentrations. In vivo study, the SE group exhibited significantly higher Ishida scores than other groups at all time points. Furthermore, the SE group showed higher synovial coverage scores than the Col I group at 4 and 8 weeks. Immunohistochemical staining demonstrated higher type II collagen staining in the SE group compared to other groups at 12 weeks. Implanted SE was efficiently replaced by safranin-O staining positive tissue within 8 weeks.ConclusionsSE could effectively repair a meniscal defect by inducing coverage of synovial cells. SE has the potential to be a useful material for meniscal repair.
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页数:13
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