Choi Jong Seob, Seo Tae Seok
Department of Bioengineering, University of Washington, Seattle, Washington, DC 98195, USA.
Department of Chemical Engineering, College of Engineering, Kyung Hee University, 1 Seochon-dong, Giheung-gu, Yongin-si, Gyeonggi-do 17104, South Korea.
Biomicrofluidics. 2019 Feb 26;13(1):014115. doi: 10.1063/1.5068689. eCollection 2019 Jan.
Development of a three-dimensional (3D) vascular co-cultivation system is one of the major challenges to provide an advanced analytical platform for studying blood vessel related diseases. To date, however, the -like vessel system has not been fully realized due to the difficulty of co-cultivation of the cells with orthogonal alignment. In this study, we report the utilization of microfabrication technology to construct biomimetic 3D co-cultured vasculature. First, microwrinkle patterns whose direction was perpendicular to the axis of a circular microfluidic channel were fabricated, and vascular smooth muscle cells (VSMCs) were cultured inside the microchannel, leading to an -like circumferential VSMC layer. Then, human umbilical vein endothelial cells (HUVECs) were co-cultured on the circumferentially aligned VSMC, and the success of double layer formation of HUVEC-VSMC in the circular microchannel could be monitored. After HUVEC cultivation, we applied shear flow in order to induce the orientation of HUVEC parallel to the axis, and the analysis of orientation angle and spreading area of HUVECs indicated that they were changed by shear stress to be aligned to the direction of flow. Thus, the HUVEC and VSMC layer could be aligned with a distinct direction. The expression level of VE-Cadherin located at the boundary of HUVECs implies -like vascular behavior. The proposed microfluidic vascular assay platform would be valuable for studying vascular diseases with high reliability due to -likeness.
开发三维(3D)血管共培养系统是为研究血管相关疾病提供先进分析平台的主要挑战之一。然而,迄今为止,由于难以将细胞进行正交排列共培养,类血管系统尚未完全实现。在本研究中,我们报告了利用微加工技术构建仿生3D共培养脉管系统。首先,制作方向垂直于圆形微流控通道轴线的微皱纹图案,并在微通道内培养血管平滑肌细胞(VSMC),从而形成类圆周VSMC层。然后,将人脐静脉内皮细胞(HUVEC)与圆周排列的VSMC共培养,并监测圆形微通道中HUVEC-VSMC双层形成的成功情况。在HUVEC培养后,我们施加剪切流以诱导HUVEC平行于轴线方向排列,对HUVEC取向角和铺展面积的分析表明,它们会因剪切应力而改变,从而与流动方向对齐。因此,HUVEC和VSMC层可以沿不同方向排列。位于HUVEC边界的VE-钙黏蛋白的表达水平暗示了类血管行为。由于具有类血管特性,所提出的微流控血管检测平台对于可靠地研究血管疾病将具有重要价值。