首页> 外文期刊>Cytometry, Part A: the journal of the International Society for Analytical Cytology >Quantifying the Dynamics of Hematopoiesis by In Vivo IdU Pulse-Chase, Mass Cytometry, and Mathematical Modeling
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Quantifying the Dynamics of Hematopoiesis by In Vivo IdU Pulse-Chase, Mass Cytometry, and Mathematical Modeling

机译:通过体内抗脉冲脉冲,质量细胞仪和数学建模量化血缺肌的动态

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摘要

We present a new method to directly quantify the dynamics of differentiation of multiple cellular subsets in unperturbed mice. We combine a pulse-chase protocol of 5-iodo-2 '-deoxyuridine (IdU) injections with subsequent analysis by mass cytometry (CyTOF) and mathematical modeling of the IdU dynamics. Measurements by CyTOF allow for a wide range of cells to be analyzed at once, due to the availability of a large staining panel without the complication of fluorescence spillover. These are also compatible with direct detection of integrated iodine signal, with minimal impact on immunophenotyping based on the surface markers. Mathematical modeling beyond a binary classification of surface marker abundance allows for a continuum of cellular states as the cells transition from one state to another. Thus, we present a complete and robust method for directly quantifying differentiation at the systemic level, allowing for system-wide comparisons between different mouse strains and/or experimental conditions. Published 2019. This article is a U.S. Government work and is in the public domain in the USA.
机译:我们提出了一种新方法,可以直接量化多个细胞亚群中的多次细胞小鼠的差异的动态。我们将5-Iodo-2'-丁氧基脲(IDU)注射的脉冲序列协议结合在随后的质量细胞测定法(CYTOF)和IDU动力学的数学建模分析。由于大染色面板的可用性而没有荧光溢出并发症,Cytof的测量允许立即分析各种细胞。这些也与集成碘信号的直接检测相容,对基于表面标志物的免疫渗透性影响最小。除了表面标记丰度的二进制分类之外的数学建模允许电池从一个状态转换到另一个状态时的蜂窝状态连续。因此,我们提出了一种用于直接定量系统水平的分化的完整和稳健的方法,允许在不同的小鼠菌株和/或实验条件之间进行系统宽的比较。 2019年出版。本文是美国政府工作,并在美国的公共领域。

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