A 3D vascularized bone remodeling model combining osteoblasts and osteoclasts in a CaP nanoparticle-enriched matrix

被引:49
作者
Bongio, Matilde [1 ]
Lopa, Silvia [1 ]
Gilardi, Mara [1 ,2 ]
Bersini, Simone [1 ]
Moretti, Matteo [1 ,3 ,4 ,5 ]
机构
[1] IRCCS Galeazzi Orthopaed Inst, Cell & Tissue Engn Lab, I-20161 Milan, Italy
[2] Univ Milano Bicocca, Sch Life Sci, Dept Biotechnol & Biosci, I-20126 Milan, Italy
[3] EOC, Regenerat Med Technol Lab, CH-6900 Lugano, Switzerland
[4] SIRM, CH-6900 Lugano, Switzerland
[5] Fdn Cardiocentro Ticino, CH-6900 Lugano, Switzerland
关键词
3D model; bone remodeling; vascularization; MESENCHYMAL STEM-CELLS; TROPHIC FACTOR SECRETION; IN-VITRO; GROWTH-FACTOR; MICROVASCULAR NETWORKS; GENE-EXPRESSION; DIFFERENTIATION; COCULTURE; HYDROXYAPATITE; ANGIOGENESIS;
D O I
10.2217/nnm-2015-0021
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: We aimed to establish a 3D vascularized in vitro bone remodeling model. Materials & methods: Human umbilical endothelial cells (HUVECs), bone marrow mesenchymal stem cells (BMSCs), and osteoblast (OBs) and osteoclast (OCs) precursors were embedded in collagen/fibrin hydrogels enriched with calcium phosphate nanoparticles (CaPn). We assessed vasculogenesis in HUVEC-BMSC coculture, osteogenesis with OBs, osteoclastogenesis with OCs, and, ultimately, cell interplay in tetraculture. Results: HUVECs developed a robust microvascular network and BMSCs differentiated into mural cells. Noteworthy, OB and OC differentiation was increased by their reciprocal coculture and by CaPn, and even more by the combination of the tetraculture and CaPn. Conclusion: We successfully developed a vascularized 3D bone remodeling model, whereby cells interacted and exerted their specific function.
引用
收藏
页码:1073 / 1091
页数:19
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