Nashimoto Yuji, Hayashi Tomoya, Kunita Itsuki, Nakamasu Akiko, Torisawa Yu-Suke, Nakayama Masamune, Takigawa-Imamura Hisako, Kotera Hidetoshi, Nishiyama Koichi, Miura Takashi, Yokokawa Ryuji
Department of Micro Engineering, Kyoto University, Kyoto 615-8540, Japan.
Integr Biol (Camb). 2017 Jun 19;9(6):506-518. doi: 10.1039/c7ib00024c.
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.
在组织中构建血管网络对于组织工程至关重要。尽管最近的研究已证明在组织模型中形成了血管样结构,但由于血管网络缺乏主动灌注,长期培养仍然具有挑战性。在此,我们提出一种在微流控装置中创建具有可灌注血管网络的三维细胞球体的方法。通过定义球体中的人肺成纤维细胞(hLFs)与微通道中的人脐静脉内皮细胞(HUVECs)之间的细胞相互作用,诱导血管生成芽从微通道向球体生长;这些芽到达球体中的血管样结构以形成连续的管腔。我们证明了血管网络可以将生物物质输送到球体内部。由于球体中的细胞密度与组织相似,这种可灌注脉管系统模型为体外长期组织培养开辟了新的可能性。