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A novel flow cytometry-based quantitative monocyte adhesion assay to estimate endothelial cell activation in vitro

机译:基于流式细胞术的数量单核细胞粘附测定,以估计体外内皮细胞活性

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One of the earliest events in the development of atherosclerosis is endothelial activation, which is estimated in vitro at the functional level by quantifying monocyte adhesion. This involves the incubation of fluorescently labeled monocytes on top of cultured endothelial cells and quantifying the number of adhered monocytes. Currently, the quantification of adhered monocytes is done using microscopy or by lysing the cells and estimating the fluorescence. Here we present a novel flow cytometry-based method for the quantification of monocyte adhesion. This method could quantify the average number of monocytes adhered to a single endothelial cell after monocyte adhesion assay, and was also sensitive to the level of activation of endothelial cells. Flow cytometry-based quantification requires less time and effort compared with microscopy-based quantification.
机译:动脉粥样硬化发展中最早的事件之一是内皮激活,通过量化单核细胞粘附来估计功能水平的体外。 这涉及在培养的内皮细胞顶部孵育荧光标记的单核细胞并定量粘附的单核细胞的数量。 目前,使用显微镜或通过裂解细胞并估计荧光来完成粘附的单核细胞的定量。 在这里,我们提出了一种基于流式细胞术的基于流体粘附性的方法。 该方法可以量化单核细胞粘附测定后粘附到单个内皮细胞的单核细胞的平均数量,并且对内皮细胞的活化水平也敏感。 与基于显微镜的量化相比,基于流式细胞术的定量需要更少的时间和精力。

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