Chitosan hydrogel/3D-printed poly(ε-caprolactone) hybrid scaffold containing synovial mesenchymal stem cells for cartilage regeneration based on tetrahedral framework nucleic acid recruitment

被引:114
|
作者
Li, Pinxue [1 ,2 ]
Fu, Liwei [1 ,2 ]
Liao, Zhiyao [1 ,2 ]
Peng, Yu [1 ]
Ning, Chao [2 ]
Gao, Cangjian [1 ,2 ]
Zhang, Daxu [2 ]
Sui, Xiang [2 ]
Lin, Yunfeng [3 ]
Liu, Shuyun [2 ]
Hao, Chunxiang [4 ]
Guo, Quanyi [1 ,2 ]
机构
[1] Nankai Univ, Sch Med, Tianjin 300071, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Inst Orthoped, Beijing Key Lab Regenerat Med Orthoped, Key Lab Musculoskeletal Trauma & War Injuries PLA, 28 Fuxing Rd, Beijing 100853, Peoples R China
[3] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, State Key Lab Oral Dis, Chengdu 610041, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Inst Anesthesia, 28 Fuxing Rd,Haidian Dist, Beijing 100853, Peoples R China
基金
国家重点研发计划;
关键词
Tetrahedral framework nucleic acid; Chitosan; Chondrogenesis; Mesenchymal stem cells; Cartilage tissue engineering; DNA NANOSTRUCTURES; TISSUE; REPAIR; DELIVERY; ACTIVATION; DIFFERENTIATION; PROLIFERATION; MICROFRACTURE; HYDROGEL; DEFECTS;
D O I
10.1016/j.biomaterials.2021.121131
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Articular cartilage (AC) injury repair has always been a difficult problem for clinicians and researchers. Recently, a promising therapy based on mesenchymal stem cells (MSCs) has been developed for the regeneration of cartilage defects. As endogenous articular stem cells, synovial MSCs (SMSCs) possess strong chondrogenic dif-ferentiation ability and articular specificity. In this study, a cartilage regenerative system was developed based on a chitosan (CS) hydrogel/3D-printed poly(epsilon-caprolactone) (PCL) hybrid containing SMSCs and recruiting tetrahedral framework nucleic acid (TFNA) injected into the articular cavity. TFNA, which is a promising DNA nanomaterial for improving the regenerative microenvironment, could be taken up into SMSCs and promoted the proliferation and chondrogenic differentiation of SMSCs. CS, as a cationic polysaccharide, can bind to DNA through electrostatic action and recruit free TFNA after articular cavity injection in vivo. The 3D-printed PCL scaffold provided basic mechanical support, and TFNA provided a good microenvironment for the proliferation and chondrogenic differentiation of the delivered SMSCs and promoted cartilage regeneration, thus greatly improving the repair of cartilage defects. In conclusion, this study confirmed that a CS hydrogel/3D-printed PCL hybrid scaffold containing SMSCs could be a promising strategy for cartilage regeneration based on chitosan-directed TFNA recruitment and TFNA-enhanced cell proliferation and chondrogenesis.
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页数:13
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