In vitro vascularization of a combined system based on a 3D printing technique

被引:66
作者
Zhao, Xinru [1 ,2 ]
Liu, Libiao [1 ,2 ]
Wang, Jiayin [1 ,2 ]
Xu, Yufan [1 ,2 ]
Zhang, Weiming [1 ,2 ]
Khang, Gilson [3 ,4 ]
Wang, Xiaohong [1 ,2 ,5 ]
机构
[1] Tsinghua Univ, Minist Educ, Key Lab Adv Mat Proc Technol, Beijing, Peoples R China
[2] Tsinghua Univ, Ctr Organ Mfg, Dept Mech Engn, Beijing 100084, Peoples R China
[3] Chonbuk Natl Univ, Dept BIN Fus Technol, Jeonju, South Korea
[4] Chonbuk Natl Univ, Dept Polymer Nano Sci Technol, Jeonju, South Korea
[5] Huazhong Univ Sci & Technol, State Key Lab Mat Proc & Die & Mould Technol, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
adipose-derived stem cells (ADSCs); combined construct; endothelial cells; fibrin/collagen hydrogel; poly(DL-lactic-co-glycolic acid) (PLGA); three-dimensional (3D) printing; CELL/HYDROGEL CONSTRUCT; PHOSPHORYLATED CHITOSAN; POLYURETHANE; FIBRIN; MATRICES; FABRICATION; RESPONSES; GELATIN; CONDUIT; RABBITS;
D O I
10.1002/term.1863
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A vital challenge in complex organ manufacturing is to vascularize large combined tissues. The aim of this study is to vascularize in vitro an adipose-derived stem cell (ADSC)/fibrin/collagen incorporated three-dimensional (3D) poly(D,L-lactic-co-glycolic acid) (PLGA) scaffold (10x10x10mm(3)) with interconnected channels. A low-temperature 3D printing technique was employed to build the PLGA scaffold. A step-by-step cocktail procedure was designed to engage or steer the ADSCs in the PLGA channels towards both endothelial and smooth muscle cell lineages. The combined system had sufficient mechanical properties to support the cell/fibrin/collagen hydrogel inside the predefined PLGA channels. The ADSCs encapsulated in the fibrin/collagen hydrogel differentiated to endothelial and smooth muscle cell lineage, respectively, corresponding to their respective locations in the construct and formed vascular-like structures. This technique allows in vitro vascularization of the predefined PLGA channels and provides a choice for complex organ manufacture. Copyright (C) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:833 / 842
页数:10
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