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首页> 外文期刊>Cytometry, Part A: the journal of the International Society for Analytical Cytology >Single and three-color flow cytometry assay for intracellular zinc ion availability in human lymphocytes with Zinpyr-1 and double immunofluorescence: Relationship with metallothioneins
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Single and three-color flow cytometry assay for intracellular zinc ion availability in human lymphocytes with Zinpyr-1 and double immunofluorescence: Relationship with metallothioneins

机译:单和三色流式细胞仪检测人淋巴细胞中具有Zinpyr-1和双重免疫荧光的细胞内锌离子可用性:与金属硫蛋白的关系

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摘要

Background: The amount of available intracellular zinc is pivotal to regulate many cellular processes, including oxidative stress response and apoptotic mechanisms. Therefore it is not surprising that zinc homeostasis and dyshomeostasis is involved in many physiological and pathological states, respectively. Cell permeable zinc probes allow intracellular applications with microscopy technology, but flow cytometry (FC) applications have been scarcely explored, albeit they can be suited to study zinc homeostasis in different cell types, including rare cells. Methods: We describe a FC method able to estimate intracellular zinc ion availability and the intracellular capability to activate a zinc signal after treatment with an NO-donor (AcOM-DEA/NO) in human PBMCs, using the fluorescent zinc-specific probe, Zinpyr-1 (ZP1), alone or in association with CD4-PE and CD8-Cychrome mAb. Results: This method was able to detect an increase/decrease of intracellular zinc available in human fresh cultured PBMC and in immune subsets using AcOM-DEA/NO or TPEN, respectively. ZP1 mean fluorescence on gated histograms was sensitive to the amount of zinc added in the culture medium and significantly correlated to metallothioneins and total intracellular zinc. Conclusions: FC applications using ZP1 may be a fast and useful tool to study zinc homeostasis in immune cells. (c) 2006 International Society for Analytical Cytology.
机译:背景:可用的细胞内锌的量对于调节许多细胞过程(包括氧化应激反应和凋亡机制)至关重要。因此,锌稳态和异常动态分别涉及许多生理和病理状态就不足为奇了。具有细胞渗透性的锌探针可通过显微镜技术应用于细胞内,但几乎未研究流式细胞术(FC)的应用,尽管它们适合研究不同细胞类型(包括稀有细胞)中的锌稳态。方法:我们描述了一种使用荧光锌特异性探针Zinpyr的FC方法,该方法能够估计人PBMC中细胞内锌离子的可用性和细胞内激活NO受体(AcOM-DEA / NO)后激活锌信号的能力。 -1(ZP1),单独或与CD4-PE和CD8-Cychrome mAb结合使用。结果:该方法能够分别使用AcOM-DEA / NO或TPEN检测人新鲜培养的PBMC和免疫亚群中可用的细胞内锌的增加/减少。门控直方图上的ZP1平均荧光对培养基中添加的锌量敏感,并且与金属硫蛋白和细胞内总锌显着相关。结论:使用ZP1的FC应用可能是研究免疫细胞中锌稳态的快速而有用的工具。 (c)2006年国际分析细胞学学会。

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