Rossi Massimiliano, Lindken Ralph, Hierck Beerend P, Westerweel Jerry
Laboratory for Aero- and Hydrodynamics, Delft University of Technology, Delft, The Netherlands.
Lab Chip. 2009 May 21;9(10):1403-11. doi: 10.1039/b822270n. Epub 2009 Feb 27.
A lab-on-a-chip application for the investigation of biochemical and mechanical response of individual endothelial cells to different fluid dynamical conditions is presented. A microfluidic flow chamber design with a tapered geometry that creates a pre-defined, homogeneous shear stress gradient on the cell layer is described and characterized. A non-intrusive, non-tactile measurement method based on micro-PIV is used for the determination of the topography and shear stress distribution over individual cells with subcellular resolution. The cellular gene expression is measured simultaneously with the shape and shear stress distribution of the cell. With this set-up the response of the cells on different pre-defined shear stress levels is investigated without the influence of variations in repetitive experiments. Results are shown on cultured endothelial cells related to the promoter activity of the shear-responsive transcription factor KLF2 driving the marker gene for green fluorescent protein.
本文介绍了一种用于研究单个内皮细胞在不同流体动力学条件下的生化和机械反应的芯片实验室应用。描述并表征了一种具有锥形几何形状的微流控流动腔设计,该设计可在细胞层上产生预定义的均匀剪切应力梯度。基于微粒子图像测速技术(micro-PIV)的非侵入式、非接触式测量方法用于以亚细胞分辨率确定单个细胞上的形貌和剪切应力分布。同时测量细胞的基因表达以及细胞的形状和剪切应力分布。通过这种设置,研究了细胞在不同预定义剪切应力水平下的反应,而不受重复实验中变化的影响。结果显示在与驱动绿色荧光蛋白标记基因的剪切响应转录因子KLF2的启动子活性相关的培养内皮细胞上。