Research Center for Stem Cell Engineering, National Institute of Advanced Industrial Science and Technology (AIST), Central 5th, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8565, Japan.
Frontier Research Laboratories, R&D Division, Daiichi Sankyo Co., Ltd., 1-2-58, Hiromachi, Shinagawa-ku, Tokyo 140-8710, Japan.
J Biosci Bioeng. 2014 Sep;118(3):327-32. doi: 10.1016/j.jbiosc.2014.02.006. Epub 2014 Jul 3.
We developed a microfluidic perfusion cell culture chip that provides three different shear stress strengths and a large cell culture area for the analysis of vascular endothelial functions. The microfluidic network was composed of shallow flow-control channels of three different depths and deep cell culture channels. The flow-control channels with high fluidic resistances created shear stress strengths ranging from 1.0 to 10.0 dyn/cm(2) in the cell culture channels. The large surface area of the culture channels enabled cultivation of a large number (approximately 6.0 × 10(5)) of cells. We cultured human umbilical vein endothelial cells (HUVECs) and evaluated the changes in cellular morphology and gene expression in response to applied shear stress. The HUVECs were aligned in the direction of flow when exposed to a shear stress of 10.0 dyn/cm(2). Compared with conditions of no shear stress, endothelial nitric oxide synthase mRNA expression increased by 50% and thrombomodulin mRNA expression increased by 8-fold under a shear stress of 9.5 dyn/cm(2).
我们开发了一种微流控灌注细胞培养芯片,可提供三种不同的切变应力强度和大面积的细胞培养区域,用于分析血管内皮功能。微流控网络由三个不同深度的浅流控通道和深细胞培养通道组成。具有高流体阻力的流控通道在细胞培养通道中产生了 1.0 至 10.0 dyn/cm(2) 的切变应力强度。培养通道的大表面积可培养大量(约 6.0×10(5))细胞。我们培养了人脐静脉内皮细胞(HUVEC),并评估了细胞形态和基因表达对施加切变应力的变化。当暴露于 10.0 dyn/cm(2)的切变应力时,HUVEC 沿流动方向排列。与无切变应力的条件相比,在 9.5 dyn/cm(2)的切变应力下,内皮型一氧化氮合酶 mRNA 表达增加了 50%,血栓调节蛋白 mRNA 表达增加了 8 倍。