Teilmann Anne C, Kalliokoski Otto, Jacobsen Kirsten R, Hau Jann, Abelson Klas S P
Department of Experimental Medicine, University of Copenhagen, Blegdamsvej 3B, Copenhagen DK-2200, Denmark.
Acta Vet Scand. 2014 May 20;56(1):33. doi: 10.1186/1751-0147-56-33.
Studies have reported that heparin may be unsuitable as an anticoagulant in human plasma samples when quantifying cytokines using multiplex bead array assays. For mouse samples, multiplex assays have been validated for serum and EDTA-plasma, but it remains to be elucidated whether heparin influences the quantification of cytokines, and if so - to what extent. Furthermore, laboratory mice are often anesthetized for blood sampling, which causes acute stress that may influence circulating cytokine concentrations and thus bias experimental results. The objectives of the present study were to identify whether specific cytokine concentrations varied between heparin-plasma, serum, and EDTA-plasma, and whether short isoflurane anesthesia would influence the concentrations of these cytokines in the circulation. Twenty-three acute phase and pro-inflammatory cytokines were quantified in matched serum, EDTA-plasma, and heparin-plasma samples from anesthetized and unanesthetized male NMRI mice using a multiplex assay. In addition, samples from unanesthetized mice were spiked with three levels of heparin.
The concentrations of five out of 23 cytokines were significantly different between sample types, but only one cytokine (IL-17A) differed between heparin-plasma and serum. When further spiking the heparin-plasma with increasing concentrations of heparin, there was a significant effect on 11 cytokines, where the cytokine recovery could be correlated to the heparin concentration for ten of these cytokines. Anesthesia resulted in lower concentrations of G-CSF, but had no significant impact on the concentrations of the other 22 cytokines.
In mice, heparin seems like a suitable anticoagulant for obtaining plasma for multiplex assays for the cytokines IL-1α, IL-1β, IL-2, IL-6, IL-9, IL-12p40, IL-12p70, IL-13, G-CSF, GM-CSF, IFN-γ, KC, MCP-1, MIP-1α, MIP-1β, RANTES and TNFα, but an effect of heparin in high concentrations should be considered for the cytokines IL-9, IL-12p40, IL-12p70, KC, MCP-1, MIP-1β and RANTES. Short isoflurane anesthesia had significant impact on G-CSF, but none of the other cytokines.
研究报告称,在使用多重微珠阵列分析法对细胞因子进行定量时,肝素可能不适用于人血浆样本的抗凝。对于小鼠样本,多重分析法已在血清和乙二胺四乙酸(EDTA)血浆中得到验证,但肝素是否会影响细胞因子的定量,若有影响,程度如何,仍有待阐明。此外,实验室小鼠采血时通常会进行麻醉,这会引发急性应激,可能影响循环中的细胞因子浓度,从而使实验结果产生偏差。本研究的目的是确定特定细胞因子浓度在肝素血浆、血清和EDTA血浆之间是否存在差异,以及短暂的异氟烷麻醉是否会影响这些细胞因子在循环中的浓度。使用多重分析法对麻醉和未麻醉的雄性NMRI小鼠的匹配血清、EDTA血浆和肝素血浆样本中的23种急性期和促炎细胞因子进行了定量。此外,对未麻醉小鼠的样本添加样本添加了三种浓度水平的肝素。
23种细胞因子中有5种在不同样本类型之间浓度存在显著差异,但肝素血浆和血清之间只有一种细胞因子(IL - 17A)不同。当向肝素血浆中进一步添加浓度递增的肝素时,对11种细胞因子有显著影响,其中10种细胞因子的回收率与肝素浓度相关。麻醉导致粒细胞集落刺激因子(G - CSF)浓度降低,但对其他22种细胞因子的浓度无显著影响。
在小鼠中,对于获取用于多重分析细胞因子IL - 1α、IL - 1β、IL - 2、IL - 6、IL - 9、IL - 12p40、IL - 12p70、IL - 13、G - CSF、粒细胞巨噬细胞集落刺激因子(GM - CSF)、干扰素 - γ(IFN - γ)、KC、单核细胞趋化蛋白 - 1(MCP - 1)、巨噬细胞炎性蛋白 - 1α(MIP - 1α)、巨噬细胞炎性蛋白 - 1β(MIP - 1β)、调节激活正常T细胞表达和分泌因子(RANTES)和肿瘤坏死因子α(TNFα)的血浆而言,肝素似乎是一种合适的抗凝剂,但对于细胞因子IL - 9、IL - 12p40、IL - 12p70、KC、MCP - 1、MIP - 1β和RANTES,应考虑高浓度肝素的影响。短暂的异氟烷麻醉对G - CSF有显著影响,但对其他细胞因子无影响。