首页> 外文期刊>Cytometry, Part B. Clinical cytometry: the journal of the International Society for Analytical Cytology >Imaging flow cytometry for morphologic and phenotypic characterization of rare circulating endothelial cells
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Imaging flow cytometry for morphologic and phenotypic characterization of rare circulating endothelial cells

机译:成像流式细胞仪用于罕见循环内皮细胞的形态和表型鉴定

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Endothelial cells in the peripheral circulation are rare events that require technically rigorous approaches for detection by flow cytometry. Visualization of these cells has been even more demanding, as this has historically required extensive enrichment and processing prior to attempting imaging. As a result, few, if any, examples exist on images of peripheral blood circulating endothelial cells (CECs) that include verification of the cell lineage both phenotypically and genomically. In this study, we have devised a method whereby CECs can be directly visualized after lysis of red blood cells and staining, without pre-enrichment or additional processing. Peripheral blood is stained with CD45, CD146, CD3, Hoechst, and DAPI to permit identification of CD146 positive, nonleukocyte, nucleated, and live cells that fit the description of CECs. These cells are imaged using the Amnis ImageStream~X, an imaging flow cytometer. Genomic verification of the endothelial nature of these cells is accomplished by using an aliquot of the same stained samples for sorting CECs using similar gating strategies. This proof of principle of direct imaging of CECs by imaging flow cytometry will permit studies to be conducted heretofore not possible, as the ImageStreamX~ has the capability of detecting additional fluorochromes other than those used to identify the CECs. Such potential investigations include antigen colocalization or capping, autophagy and apoptosis, morphologic changes in response to therapy, and others. Thus, this method will enable a broad range of novel studies to be conducted using CECs as surrogates of the endothelium. Published 2013 Wiley-Periodicals, Inc.?
机译:外周循环中的内皮细胞是罕见事件,需要技术上严格的方法才能通过流式细胞仪进行检测。这些细胞的可视化要求更高,因为历史上一直要求在尝试成像之前进行大量富集和处理。结果,在外周血循环内皮细胞(CEC)的图像上几乎没有(包括表型和基因组的)细胞核实实例。在这项研究中,我们设计了一种方法,通过该方法可以在裂解红细胞和染色后直接可视化CEC,而无需进行预富集或其他处理。外周血用CD45,CD146,CD3,Hoechst和DAPI染色,以鉴定符合CEC描述的CD146阳性,非白细胞,有核和活细胞。这些细胞使用成像流式细胞仪Amnis ImageStream_X成像。这些细胞的内皮特性的基因组验证是通过使用相同染色样品的等分试样,使用相似的门控策略对CEC进行分选来完成的。通过成像流式细胞术对CEC进行直接成像的原理证明将允许迄今无法进行研究,因为ImageStreamX具有检测除用于识别CEC的荧光染料以外的其他荧光染料的能力。这样的潜在研究包括抗原共定位或加帽,自噬和凋亡,对治疗反应的形态变化等。因此,这种方法将使使用CEC作为内皮替代物进行广泛的新颖研究。 2013年发布的Wiley-Periodicals,Inc.?

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