Protocol for engineering bone organoids from mesenchymal stem cells

被引:1
|
作者
Wang, Jian [1 ,2 ,3 ,4 ,5 ,6 ]
Zhou, Dongyang [4 ,6 ]
Li, Ruiyang [1 ,2 ,3 ]
Sheng, Shihao [1 ,2 ,3 ]
Li, Guangfeng [4 ,5 ,6 ,7 ]
Sun, Yue [4 ,5 ,6 ]
Wang, Peng [1 ,2 ,3 ]
Mo, Yulin [4 ,5 ,6 ]
Liu, Han [4 ,6 ]
Chen, Xiao [1 ,2 ,3 ,4 ,6 ]
Geng, Zhen [4 ,6 ]
Zhang, Qin [4 ,6 ]
Jing, Yingying [4 ,6 ]
Bai, Long [4 ,6 ]
Xu, Ke [4 ,6 ]
Su, Jiacan [1 ,2 ,3 ,4 ,6 ]
机构
[1] Shanghai Jiao Tong Univ, Xinhua Hosp, Sch Med, Dept Orthoped, Shanghai 200092, Peoples R China
[2] Shanghai Jiao Tong Univ, Xinhua Hosp, Trauma Orthoped Ctr, Sch Med, Shanghai 200092, Peoples R China
[3] Shanghai Jiao Tong Univ, Xinhua Hosp, Inst Musculoskeletal Injury & Translat Med Organoi, Sch Med, Shanghai 200092, Peoples R China
[4] Shanghai Univ, Inst Translat Med, Shanghai 200444, Peoples R China
[5] Shanghai Univ, Sch Med, Shanghai 200444, Peoples R China
[6] Shanghai Univ, Natl Ctr Translat Med SHU Branch, SHU Branch, Shanghai 200444, Peoples R China
[7] Shanghai Zhongye Hosp, Dept Orthoped, Shanghai 200941, Peoples R China
基金
中国国家自然科学基金;
关键词
Bone organoids; 3D bioprinting; Bioink; Mineralization; Vascularization; REGENERATION;
D O I
10.1016/j.bioactmat.2024.11.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bone organoids are emerging as powerful tools for studying bone development and related diseases. However, the simplified design of current methods somewhat limits their application potential, as these methods produce single-tissue organoids that fail to replicate the bone microarchitecture or achieve effective mineralization. To address this issue, we propose a three-dimensional (3D) construction strategy for generating mineralized bone structures using bone marrow-derived mesenchymal stem cells (BMSCs). By mixing BMSCs with hydrogel to create a bone matrix-mimicking bioink and employing projection-based light-curing 3D printing technology, we constructed 3D-printed structures, which were then implanted subcutaneously into nude mice, away from the native bone microenvironment. Even without external stimulation, these implants spontaneously formed mineralized bone domains. With long-term culture, these structures gradually matured into fully differentiated bone tissue, completing both mineralization and vascularization. This in vivo bone organoid model offers a novel platform for studying bone development, exploring congenital diseases, testing drugs, and developing therapeutic applications.
引用
收藏
页码:388 / 400
页数:13
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