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Probing Intracellular Element Concentration Changes during Neutrophil Extracellular Trap Formation Using Synchrotron Radiation Based X-Ray Fluorescence

机译:使用基于同步辐射的X射线荧光探测中性粒细胞胞外陷阱形成过程中的细胞内元素浓度变化

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摘要

High pressure frozen (HPF), cryo-substituted microtome sections of 2 μm thickness containing human neutrophils (white blood cells) were analyzed using synchrotron radiation based X-ray fluorescence (SR nano-XRF) at a spatial resolution of 50 nm. Besides neutrophils from a control culture, we also analyzed neutrophils stimulated for 1–2 h with phorbol myristate acetate (PMA), a substance inducing the formation of so-called Neutrophil Extracellular Traps (or NETs), a defense system again pathogens possibly involving proteins with metal chelating properties. In order to gain insight in metal transport during this process, precise local evaluation of elemental content was performed reaching limits of detection (LODs) of 1 ppb. Mean weight fractions within entire neutrophils, their nuclei and cytoplasms were determined for the three main elements P, S and Cl, but also for the 12 following trace elements: K, Ca, Mn, Fe, Co, Ni, Cu, Zn, Se, Br, Sr and Pb. Statistical analysis, including linear regression provided objective analysis and a measure for concentration changes. The nearly linear Ca and Cl concentration changes in neutrophils could be explained by already known phenomena such as the induction of Ca channels and the uptake of Cl under activation of NET forming neutrophils. Linear concentration changes were also found for P, S, K, Mn, Fe, Co and Se. The observed linear concentration increase for Mn could be related to scavenging of this metal from the pathogen by means of the neutrophil protein calprotectin, whereas the concentration increase of Se may be related to its antioxidant function protecting neutrophils from the reactive oxygen species they produce against pathogens. We emphasize synchrotron radiation based nanoscopic X-ray fluorescence as an enabling analytical technique to study changing (trace) element concentrations throughout cellular processes, provided accurate sample preparation and data-analysis.
机译:使用基于同步辐射的X射线荧光(SR纳米XRF)在50 nm的空间分辨率下分析了包含人嗜中性粒细胞(白细胞)的2μm厚的高压冷冻(HPF)冷冻切片机切片。除了来自对照培养的嗜中性粒细胞外,我们还分析了佛波肉豆蔻酸酯醋酸盐(PMA)刺激1-2 h的嗜中性粒细胞,这种物质可诱导形成所谓的嗜中性白血球细胞外陷阱(或NETs),防御系统也是可能涉及蛋白质的病原体具有金属螯合性能。为了深入了解此过程中的金属传输,对元素含量进行了精确的局部评估,达到了1 ppb的检出限(LOD)。确定了中性粒细胞,其细胞核和细胞质中三个主要元素P,S和Cl的平均重量分数,还确定了以下12种微量元素的钾,钙,锰,铁,钴,镍,铜,锌,硒的平均重量分数,Br,Sr和Pb。包括线性回归在内的统计分析提供了客观分析和浓度变化的度量。中性粒细胞中Ca和Cl浓度的线性变化可以用已知的现象来解释,例如在形成NET的中性粒细胞活化下,Ca通道的诱导和Cl的吸收。还发现了P,S,K,Mn,Fe,Co和Se的线性浓度变化。观察到的锰线性浓度增加可能与通过嗜中性粒细胞钙卫蛋白清除这种金属有关,而硒的浓度增加可能与其抗氧化功能有关,该功能可以保护嗜中性粒细胞免受针对病原体产生的活性氧的影响。 。我们强调基于同步加速器辐射的纳米X射线荧光是一种使能的分析技术,可研究整个细胞过程中元素的浓度变化(痕量),提供准确的样品制备和数据分析。

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