Perfetto Stephen P, Chattopadhyay Pratip K, Lamoreaux Laurie, Nguyen Richard, Ambrozak David, Koup Richard A, Roederer Mario
Immunology Laboratory, Vaccine Research Center, NIAID, NIH, 40 Convent Dr, Room 5509, Bethesda, MD 20892, USA.
J Immunol Methods. 2006 Jun 30;313(1-2):199-208. doi: 10.1016/j.jim.2006.04.007. Epub 2006 May 19.
Membrane-damaged cells caused by either mechanical trauma or through normal biological processes can produce artifacts in immunophenotyping analysis by flow cytometry. Dead cells can nonspecifically bind monoclonal antibody conjugates, potentially leading to erroneous conclusions, particularly when cell frequencies are low. To date, DNA intercalating dyes (Ethidium monoazaide (EMA), Propidium Iodide, 7AAD, etc.) or Annexin V have been commonly used to exclude dead cells; however, each suffer from technical problems. The first issue with such dyes is the dependence on a consistent dead cell source for fluorescence compensation. Another major issue is the stability of the staining; except for EMA, fixation and permeablization used for intracellular staining procedures can cause loss of fluorescence. EMA requires a UV exposure to covalently bond to DNA; while this dye is effective and is not affected by intracellular treatments it is weakly fluorescent. Here we report on the optimization of a new class of viability dyes, the amine reactive viability dyes (ViD) as a dead cell exclusion marker. The inclusion of ViD into the staining panel was found to be simple, reproducible and can have a significant benefit on the accuracy of identifying appropriate cell populations. We show the fluorescence of cells stained with these dyes correlates with traditional dead cell discriminating markers, even after fixation and permeabilization. Amine reactive viability dyes are a powerful tool for fluorescence immunophenotyping experiments.
由机械创伤或正常生物学过程导致的膜损伤细胞,在通过流式细胞术进行免疫表型分析时会产生假象。死细胞可非特异性结合单克隆抗体偶联物,这可能导致错误结论,尤其是在细胞频率较低时。迄今为止,DNA嵌入染料(单叠氮溴化乙锭(EMA)、碘化丙啶、7-氨基放线菌素D等)或膜联蛋白V已被普遍用于排除死细胞;然而,每种方法都存在技术问题。此类染料的第一个问题是依赖一致的死细胞来源进行荧光补偿。另一个主要问题是染色的稳定性;除了EMA,用于细胞内染色程序的固定和通透处理会导致荧光损失。EMA需要紫外线照射才能与DNA共价结合;虽然这种染料有效且不受细胞内处理的影响,但它的荧光较弱。在此,我们报告了一类新型活力染料——胺反应性活力染料(ViD)作为死细胞排除标记的优化情况。发现将ViD纳入染色方案简单、可重复,并且对识别合适细胞群体的准确性有显著益处。我们表明,即使在固定和通透处理后,用这些染料染色的细胞的荧光也与传统的死细胞鉴别标记相关。胺反应性活力染料是荧光免疫表型分析实验的有力工具。