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Pitfalls and solutions in assaying anandamide transport in cells

机译:分析细胞中二十烷酰胺转运的陷阱和解决方案

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摘要

Nonspecific binding of anandamide to plastic exhibits many features that could be mistaken as biological processes, thereby representing an important source of conflicting data on the uptake and release of this lipophilic substance. Herein, we propose an improved method to assay anandamide transport, by using glass slides (i.e., coverslips) as physical support to grow cells. Although the results obtained using plastic do not differ significantly from those obtained using glass, the new procedure has the advantage of being faster, simpler, and more accurate. In fact, the lack of aspecific adsorption of anandamide to the glass surface yields a lower background and a higher precision and accuracy in determining transport kinetics, especially for the export process. Remarkably, the kinetic parameters of anandamide uptake obtained with the old and the new procedures may be similar or different depending on the cell type, thus demonstrating the complexity of the interference of plastic on the transport process. In addition, the novel procedure is particularly suitable for visualization and measurement of anandamide transport in intact cells by using a biotinylated derivative in confocal fluorescence microscopy.
机译:Anandamide与塑料的非特异性结合表现出许多可能被误认为是生物学过程的特征,从而代表了有关该亲脂性物质摄取和释放的相互矛盾的数据的重要来源。本文中,我们提出了一种改进的方法,其通过使用载玻片(即盖玻片)作为生长细胞的物理支持物来测定anandamide的转运。尽管使用塑料获得的结果与使用玻璃获得的结果没有显着差异,但是新过程具有更快,更简单和更准确的优势。实际上,在玻璃表面上缺乏对氨基甲酰胺的非特异性吸附会产生较低的背景,并在确定运输动力学(尤其是对于出口工艺)时具有较高的精确度和准确性。值得注意的是,根据细胞类型的不同,旧方法和新方法获得的花生四烯酸摄取动力学参数可能相似或不同,因此证明了塑料对运输过程的干扰非常复杂。另外,通过在共聚焦荧光显微镜中使用生物素化的衍生物,该新方法特别适用于可视化和测量完整细胞中的anandamide转运。

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