Integrating perfusable vascular networks with a three-dimensional tissue in a microfluidic device

被引:204
作者
Nashimoto, Yuji [1 ]
Hayashi, Tomoya [1 ]
Kunita, Itsuki [2 ]
Nakamasu, Akiko [3 ]
Torisawa, Yu-suke [1 ,4 ,5 ]
Nakayama, Masamune [1 ]
Takigawa-Imamura, Hisako [3 ]
Kotera, Hidetoshi [1 ]
Nishiyama, Koichi [2 ]
Miura, Takashi [3 ]
Yokokawa, Ryuji [1 ]
机构
[1] Kyoto Univ, Dept Micro Engn, Kyoto 6158540, Japan
[2] Kumamoto Univ, IRCMS, Kumamoto 8608556, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Fukuoka 8128582, Japan
[4] Hakubi Ctr Adv Res, Kyoto 6158540, Japan
[5] Japan Agcy Med Res & Dev AMED, AMED PRIME, Tokyo 1000004, Japan
关键词
ENDOTHELIAL-CELLS; HYDROGELS; CULTURE; PERMEABILITY; MICROVESSELS; FIBROBLASTS; FABRICATION; MORPHOGENESIS; ANGIOGENESIS; GELATIN;
D O I
10.1039/c7ib00024c
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Creating vascular networks in tissues is crucial for tissue engineering. Although recent studies have demonstrated the formation of vessel-like structures in a tissue model, long-term culture is still challenging due to the lack of active perfusion in vascular networks. Here, we present a method to create a three-dimensional cellular spheroid with a perfusable vascular network in a microfluidic device. By the definition of the cellular interaction between human lung fibroblasts (hLFs) in a spheroid and human umbilical vein endothelial cells (HUVECs) in microchannels, angiogenic sprouts were induced from microchannels toward the spheroid; the sprouts reached the vessel-like structures in a spheroid to form a continuous lumen. We demonstrated that the vascular network could administer biological substances to the interior of the spheroid. As cell density in the spheroid is similar to that of a tissue, the perfusable vasculature model opens up new possibilities for a long-term tissue culture in vitro.
引用
收藏
页码:506 / 518
页数:13
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