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Feasibility of a self‐assembling peptide hydrogel scaffold for meniscal defect: An in vivo study in a rabbit model
Author(s) -
Okuno Nobuhiro,
Otsuki Shuhei,
Aoyama Jo,
Nakagawa Kosuke,
Murakami Tomohiko,
Ikeda Kuniaki,
Hirose Yoshinobu,
Wakama Hitoshi,
Okayoshi Tomohiro,
Okamoto Yoshinori,
Hirano Yoshiaki,
Neo Masashi
Publication year - 2021
Publication title -
journal of orthopaedic research®
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.041
H-Index - 155
eISSN - 1554-527X
pISSN - 0736-0266
DOI - 10.1002/jor.24841
Subject(s) - meniscus , medial meniscus , regeneration (biology) , in vivo , extracellular matrix , cartilage , self healing hydrogels , fibrocartilage , scaffold , adhesion , lesion , anatomy , biomedical engineering , osteoarthritis , medicine , pathology , chemistry , articular cartilage , microbiology and biotechnology , biology , biochemistry , physics , organic chemistry , optics , alternative medicine , incidence (geometry)
The inner avascular zone of the meniscus has limited healing capacity as the area is poorly vascularized. Although peptide hydrogels have been reported to regenerate bone and cartilage, their effect on meniscus regeneration remains unknown. We tested whether the self‐assembling peptide hydrogel scaffold KI24RGDS stays in the meniscal lesion and facilitates meniscal repair and regeneration in an induced rabbit meniscal defect model. Full‐thickness (2.0 mm diameter) cylindrical defects were introduced into the inner avascular zones of the anterior portions of the medial menisci of rabbit knees ( n = 40). Right knee defects were left empty (control group) while the left knee defects were transplanted with peptide hydrogel (KI24RGDS group). Macroscopic meniscus scores were significantly higher in the KI24RGDS group than in the control group at 2, 4, and 8 weeks after surgery. Histological examinations including quantitative and qualitative scores indicated that compared with the control group, the reparative tissue in the meniscus was significantly enhanced in the KI24RGDS group at 2, 4, 8, and 12 weeks after surgery. Immunohistochemical staining showed that the reparative tissue induced by KI24RGDS at 12 weeks postimplantation was positive for Type I and II collagen. KI24RGDS is highly biocompatible and biodegradable, with strong stiffness, and a three dimensional structure mimicking native extracellular matrix and RGDS sequences that enhance cell adhesion and proliferation. This in vivo study demonstrated that KI24RGDS remained in the meniscal lesion and facilitated the repair and regeneration in a rabbit meniscal defect model.