骨关节炎
透明质酸
软骨
离体
归巢(生物学)
间充质干细胞
化学
体内
病理
细胞生物学
体外
生物化学
医学
解剖
生物
替代医学
生物技术
生态学
作者
Chin‐Yu Lin,Yung‐Li Wang,Yu-Jen Chen,Chun-Te Ho,Yi-Hsuan Chi,Long Yi Chan,Guanwen Chen,Horng‐Chaung Hsu,Dennis W. Hwang,Han‐Chung Wu,Shih‐Chieh Hung
标识
DOI:10.1038/s41551-022-00948-5
摘要
Treatments for osteoarthritis would benefit from the enhanced visualization of injured articular cartilage and from the targeted delivery of disease-modifying drugs to it. Here, by using ex vivo human osteoarthritic cartilage and live rats and minipigs with induced osteoarthritis, we report the application of collagen-binding peptides, identified via phage display, that are home to osteoarthritic cartilage and that can be detected via magnetic resonance imaging when conjugated with a superparamagnetic iron oxide. Compared with the use of peptides with a scrambled sequence, hyaluronic acid conjugated with the collagen-binding peptides displayed enhanced retention in osteoarthritic cartilage and better lubricated human osteoarthritic tissue ex vivo. Mesenchymal stromal cells encapsulated in the modified hyaluronic acid and injected intra-articularly in rats showed enhanced homing to osteoarthritic tissue and improved its regeneration. Molecular docking revealed WXPXW as the consensus motif that binds to the α1 chain of collagen type XII. Peptides that specifically bind to osteoarthritic tissue may aid the diagnosis and treatment of osteoarthritic joints.
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