3D bioprinting of osteon-mimetic scaffolds with hierarchical microchannels for vascularized bone tissue regeneration

被引:28
|
作者
Sun, Xin [1 ]
Jiao, Xin [1 ]
Yang, Xue [2 ]
Ma, Jie [1 ]
Wang, Tianchang [1 ]
Jin, Wenjie [1 ]
Li, Wentao [1 ]
Yang, Han [3 ]
Mao, Yuanqing [1 ]
Gan, Yaokai [1 ]
Zhou, Xiaojun [4 ]
Li, Tao [5 ]
Li, Shuai [1 ]
Chen, Xiaodong [5 ]
Wang, Jinwu [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 9, Dept Orthopaed Surg, Shanghai Key Lab Orthopaed Implants,Sch Med, 639 Zhizaoju Rd, Shanghai 200001, Peoples R China
[2] Southwest Jiaotong Univ, Coll Med, 111 2nd Ring Rd, Chengdu 610031, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Biomed Engn, 1954 Huashan Rd, Shanghai 200030, Peoples R China
[4] Donghua Univ, Coll Chem Chem Engn & Biotechnol, 2999 North Renmin Rd, Shanghai 201620, Peoples R China
[5] Shanghai Jiao Tong Univ, Dept Orthopaed, Xinhua Hosp, Sch Med, 1665 Kongjiang Rd, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划; 中国博士后科学基金;
关键词
3D bioprinting; bone defect repair; osteon-mimetic scaffolds; hierarchical microchannels; vascularized bone regeneration; MESENCHYMAL STEM-CELLS; ENDOTHELIAL-CELLS; MORPHOGENETIC PROTEIN-4; IN-VITRO; OSTEOGENESIS; GELATIN; GROWTH;
D O I
10.1088/1758-5090/ac6700
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The integration of three-dimensional (3D) bioprinted scaffold's structure and function for critical-size bone defect repair is of immense significance. Inspired by the basic component of innate cortical bone tissue-osteons, many studies focus on biomimetic strategy. However, the complexity of hierarchical microchannels in the osteon, the requirement of mechanical strength of bone, and the biological function of angiogenesis and osteogenesis remain challenges in the fabrication of osteon-mimetic scaffolds. Therefore, we successfully built mimetic scaffolds with vertically central medullary canals, peripheral Haversian canals, and transverse Volkmann canals structures simultaneously by 3D bioprinting technology using polycaprolactone and bioink loading with bone marrow mesenchymal stem cells and bone morphogenetic protein-4. Subsequently, endothelial progenitor cells were seeded into the canals to enhance angiogenesis. The porosity and compressive properties of bioprinted scaffolds could be well controlled by altering the structure and canal numbers of the scaffolds. The osteon-mimetic scaffolds showed satisfactory biocompatibility and promotion of angiogenesis and osteogenesis in vitro and prompted the new blood vessels and new bone formation in vivo. In summary, this study proposes a biomimetic strategy for fabricating structured and functionalized 3D bioprinted scaffolds for vascularized bone tissue regeneration.
引用
收藏
页数:20
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