| Literature DB >> 24630614 |
Koji Hattori1, Yoichi Munehira2, Hideki Kobayashi2, Taku Satoh1, Shinji Sugiura3, Toshiyuki Kanamori1.
Abstract
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).Entities:
Keywords: Endothelial cell; Microfluidic device; Perfusion culture; Quantitative PCR; Shear stress
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Year: 2014 PMID: 24630614 DOI: 10.1016/j.jbiosc.2014.02.006
Source DB: PubMed Journal: J Biosci Bioeng ISSN: 1347-4421 Impact factor: 2.894