Repair of meniscal lesions using a scaffold-free tissue-engineered construct derived from allogenic synovial MSCs in a miniature swine model

弯月面 间充质干细胞 技术 医学 血管性 脚手架 解剖 软骨 关节炎 干细胞 病理 生物医学工程 生物 细胞生物学 内科学 电离层 物理 入射(几何) 天文 光学
作者
Yu Moriguchi,Kosuke Tateishi,Wataru Ando,Kazunori Shimomura,Yasukazu Yonetani,Yoshinari Tanaka,Keisuke Kita,David A. Hart,Alberto Gobbi,Konsei Shino,Hideki Yoshikawa,Norimasa Nakamura
出处
期刊:Biomaterials [Elsevier]
卷期号:34 (9): 2185-2193 被引量:110
标识
DOI:10.1016/j.biomaterials.2012.11.039
摘要

The menisci of the knee are fibro-cartilaginous tissues and play important roles in the joint, and the loss of the meniscus predisposes the knee to degenerative changes. However, the menisci have limited healing potential due to the paucity of vascularity. The purpose of the present study was to test the feasibility of a scaffold-free tissue-engineered construct (TEC) derived from synovial mesenchymal stem cells (MSCs) to repair incurable meniscal lesions. Porcine synovial MSCs were cultured in monolayers at high density in the presence of ascorbic acid followed by the suspension culture to develop a three-dimensional cell/matrix construct (TEC). A 4-mm cylindrical defect was created bilaterally in the medial meniscus of skeletally mature miniature pigs. The defects were implanted with an allogenic TEC or were left empty. After 6 months, the TEC-treated defects were consistently repaired by a fibro-cartilaginous tissue with good tissue integration to the adjacent host meniscal tissue, while the untreated were either partially or not repaired. The ratio of Safranin O positive area within the central body of the meniscus adjacent to the original defect was significantly higher in the TEC-treated group than in the control group. Moreover, TEC treatment significantly reduced the size and severity of post-traumatic chondral lesions on the tibial plateau. These results suggest that the TEC could be a promising stem cell-based implant to repair meniscal lesions with preventive effects from meniscal body degeneration and the development of post-traumatic arthritis.
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