Weckmann Markus, Becker Tim, Nissen Gyde, Pech Martin, Kopp Matthias V
Department of Pediatric Allergy and Pulmonology, Children's Hospital at the University of Lübeck, Lübeck, Germany.
Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Lübeck, Germany.
Cytometry A. 2017 Jul;91(7):675-685. doi: 10.1002/cyto.a.23114. Epub 2017 May 19.
In lung inflammation, neutrophils are the first leukocytes migrating to an inflammatory site, eliminating pathogens by multiple mechanisms. The term "migration" describes several stages of neutrophil movement to reach the site of inflammation, of which the passage of the interstitium and basal membrane of the airway are necessary to reach the site of bronchial inflammation. Currently, several methods exist (e.g., Boyden Chamber, under-agarose assay, or microfluidic systems) to assess neutrophil mobility. However, these methods do not allow for parameterization on single cell level, that is, the individual neutrophil pathway analysis is still considered challenging. This study sought to develop a simplified yet flexible method to monitor and quantify neutrophil chemotaxis by utilizing commercially available tissue culture hardware, simple video microscopic equipment and highly standardized tracking. A chemotaxis 3D µ-slide (IBIDI) was used with different chemoattractants [interleukin-8 (IL-8), fMLP, and Leukotriene B4 (LTB )] to attract neutrophils in different matrices like Fibronectin (FN) or human placental matrix. Migration was recorded for 60 min using phase contrast microscopy with an EVOS FL Cell Imaging System. The images were normalized and texture based image segmentation was used to generate neutrophil trajectories. Based on these spatio-temporal information a comprehensive parameter set is extracted from each time series describing the neutrophils motility, including velocity and directness and neutrophil chemotaxis. To characterize the latter one, a sector analysis was employed enabling the quantification of the neutrophils response to the chemoattractant. Using this hard- and software framework we were able to identify typical migration profiles of the chemoattractants IL-8, fMLP, and LTB , the effect of the matrices FN versus HEM as well as the response to different medications (Prednisolone). Additionally, a comparison of four asthmatic and three non-asthmatic patients gives a first hint to the capability of SiMA assay in the context of migration based diagnostics. Using SiMA we were able to identify typical migration profiles of the chemoattractants IL-8, fMLP, and LTB , the effect of the matrices FN versus HEM as well as the response to different medications, that is, Prednisolone induced a change of direction of migrating neutrophils in FN but no such effect was observed in human placental matrix. In addition, neutrophils of asthmatic individuals showed an increased proportion of cells migrating toward the vehicle. With the SiMA platform we presented a simplified but yet flexible platform for cost-effective tracking and quantification of neutrophil migration. The introduced method is based on a simple microscopic video stage, standardized, commercially available, µ-fluidic migration chambers and automated image analysis, and track validation software. © 2017 International Society for Advancement of Cytometry.
在肺部炎症中,中性粒细胞是最早迁移至炎症部位的白细胞,通过多种机制清除病原体。“迁移”一词描述了中性粒细胞移动至炎症部位的几个阶段,其中穿过气道间质和基底膜是到达支气管炎症部位的必要条件。目前,存在多种评估中性粒细胞迁移能力的方法(如Boyden小室法、琼脂糖下层分析法或微流控系统)。然而,这些方法无法在单细胞水平上进行参数化,也就是说,对单个中性粒细胞路径的分析仍具有挑战性。本研究旨在开发一种简化且灵活的方法,利用市售的组织培养硬件、简单的视频显微镜设备和高度标准化的追踪技术,来监测和量化中性粒细胞趋化性。使用趋化性3D微载玻片(IBIDI)搭配不同的趋化因子[白细胞介素-8(IL-8)、N-甲酰甲硫氨酸-亮氨酸-苯丙氨酸(fMLP)和白三烯B4(LTB₄)],在不同基质(如纤连蛋白(FN)或人胎盘基质)中吸引中性粒细胞。使用配备EVOS FL细胞成像系统的相差显微镜记录迁移60分钟。对图像进行归一化处理,并使用基于纹理的图像分割生成中性粒细胞轨迹。基于这些时空信息,从每个描述中性粒细胞运动性的时间序列中提取一套综合参数,包括速度、方向性和中性粒细胞趋化性。为了表征后者,采用扇形分析来量化中性粒细胞对趋化因子的反应。利用这个硬件和软件框架,我们能够识别趋化因子IL-8、fMLP和LTB₄的典型迁移图谱、基质FN与HEM的影响以及对不同药物(泼尼松龙)的反应。此外,对4例哮喘患者和3例非哮喘患者的比较首次提示了SiMA检测在基于迁移的诊断中的能力。使用SiMA,我们能够识别趋化因子IL-8、fMLP和LTB₄的典型迁移图谱、基质FN与HEM的影响以及对不同药物的反应,即泼尼松龙在FN中诱导迁移中性粒细胞的方向改变,但在人胎盘基质中未观察到这种效应。此外,哮喘个体的中性粒细胞向载体迁移的细胞比例增加。通过SiMA平台,我们提出了一个简化但灵活的平台,用于经济高效地追踪和量化中性粒细胞迁移。所介绍的方法基于一个简单的显微镜视频载物台、标准化的市售微流控迁移室以及自动图像分析和轨迹验证软件。© 2017国际细胞计量学协会。