Three-Dimensional Printed Silk Fibroin/Hyaluronic Acid Scaffold with Functionalized Modification Results in Excellent Mechanical Strength and Efficient Endogenous Cell Recruitment for Articular Cartilage Regeneration

被引:5
作者
Shi, Weili [1 ,2 ,3 ]
Zhang, Jiahao [1 ,2 ,3 ]
Gao, Zeyuan [1 ,2 ,3 ]
Hu, Fengyi [1 ,2 ,3 ]
Kong, Simin [1 ,2 ,3 ]
Hu, Xiaoqing [1 ,2 ,3 ]
Zhao, Fengyuan [1 ,2 ,3 ]
Ao, Yingfang [1 ,2 ,3 ]
Shao, Zhenxing [1 ,2 ,3 ]
机构
[1] Peking Univ Third Hosp, Inst Sports Med Peking Univ, Dept Sports Med, Beijing 100191, Peoples R China
[2] Beijing Key Lab Sports Injuries, Beijing 100191, Peoples R China
[3] Minist Educ, Engn Res Ctr Sports Trauma Treatment Technol & Dev, Beijing 100191, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
three-dimensional printing; double-network scaffolds; cell recruitment; bone marrow mesenchymal stem cell; cartilage repair; HYDROGELS; FIBROIN; GROWTH; REPAIR; KNEE;
D O I
10.3390/ijms251910523
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Treatment of articular cartilage remains a great challenge due to its limited self-repair capability. In tissue engineering, a scaffold with both mechanical strength and regenerative capacity has been highly desired. This study developed a double-network scaffold based on natural biomaterials of silk fibroin (SF) and methacrylated hyaluronic acid (MAHA) using three-dimensional (3D) printing technology. Structural and mechanical characteristics of the scaffold was first investigated. To enhance its ability of recruiting endogenous bone marrow mesenchymal stem cells (BMSCs), the scaffold was conjugated with a proven BMSC-specific-affinity peptide E7, and its biocompatibility and capacity of cell recruitment were assessed in vitro. Animal experiments were conducted to evaluate cartilage regeneration after transplantation of the described scaffolds. The SF/HA scaffolds exhibited a hierarchical macro-microporous structure with ideal mechanical properties, and offered a 3D spatial microenvironment for cell migration and proliferation. In vitro experiments demonstrated excellent biocompatibility of the scaffolds to support BMSCs proliferation, differentiation, and extracellular matrix production. In vivo, superior capacity of cartilage regeneration was displayed by the SF/MAHA + E7 scaffold as compared with microfracture and unconjugated SF/MAHA scaffold based on macroscopic, histologic and imaging evaluation. In conclusion, this structurally and functionally optimized SF/MAHA + E7 scaffold may provide a promising approach to repair articular cartilage lesions in situ.
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页数:16
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