首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >IDENTIFICATION AND ANALYSIS OF MACROPHAGE-DERIVED FOAM CELLS FROM HUMAN ATHEROSCLEROTIC LESIONS BY USING A MOCK FL3 CHANNEL IN FLOW CYTOMETRY
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IDENTIFICATION AND ANALYSIS OF MACROPHAGE-DERIVED FOAM CELLS FROM HUMAN ATHEROSCLEROTIC LESIONS BY USING A MOCK FL3 CHANNEL IN FLOW CYTOMETRY

机译:流式细胞术中MOCK FL3通道从人动脉粥样硬化病变中识别和分析巨噬细胞源性泡沫细胞

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摘要

Macrophages are one of the major cell types in atherosclerotic lesions, They are believed to play an important role in the pathogenesis and development of the lesion, but their functional state and phenotypic characteristics are not well understood. Using flow cytometry, we analyzed surface markers of macrophages extracted from tissue digests, However, conventional techniques were hampered by the abundance of cell debris and extracellular Lipids, which co-localized with double-positive cells in all fluorescent plots, We therefore developed a method to overcome this problem by using a novel gating technique in multiparameter flow cytometry. This method utilized the third fluorescence channel (FL3) as a ''mock'' channel, since no antibody conjugated to an FL3-specific fluorochrome was added to the samples. Cells single-positive for macrophage-specific monoclonal antibodies (mAb) conjugated to phycoerythrin (PE) (FL2) were separated from nonspecific fluorescent particles in the FL2 versus FL3 fluorescent plot and a region excluding debris could be set. This was then used as a gate to exclude debris also in the first fluorescence channel (FL1) vs. FL2 plot in which expression of a panel of activation markers identified by fluorescein isothiocyanate (FITC)-conjugated mAb was analyzed, Using this strategy, we were able to identify and analyze the phenotype of macrophages from human atherosclerotic lesions. We were also able to sort these cells and in this way obtained a preparation of macrophage-derived foam cells from the tissue with little contamination of debris. (C) 1997 Wiley-Liss, Inc. [References: 39]
机译:巨噬细胞是动脉粥样硬化病变中的主要细胞类型之一,据信它们在病变的发病机理和发展中起着重要作用,但是它们的功能状态和表型特征尚未得到很好的理解。使用流式细胞仪,我们分析了从组织消化物中提取的巨噬细胞的表面标志物,但是,常规技术受到大量细胞碎片和细胞外脂质的阻碍,它们在所有荧光图中均与双阳性细胞共定位,因此我们开发了一种方法通过在多参数流式细胞术中使用新颖的门控技术来克服这个问题。此方法利用第三条荧光通道(FL3)作为“模拟”通道,因为没有将与FL3特异性荧光染料偶联的抗体添加到样品中。在FL2 vs FL3荧光图中,将与藻红蛋白(PE)(FL2)结合的巨噬细胞特异性单克隆抗体(mAb)单阳性的细胞与非特异性荧光颗粒分开,可以设置一个不包含碎片的区域。然后,在第一个荧光通道(FL1)与FL2图中,它也被用作排除碎片的门,在该图中,分析了由异硫氰酸荧光素(FITC)偶联的mAb鉴定的一组激活标记的表达,使用这种策略,我们能够鉴定和分析人类动脉粥样硬化病变中巨噬细胞的表型。我们还能够对这些细胞进行分选,并以此方式从组织中制备出巨噬细胞衍生的泡沫细胞,几乎没有碎片污染。 (C)1997 Wiley-Liss,Inc. [参考:39]

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